R-HSA-1222387	Tolerance of reactive oxygen produced by macrophages
R-HSA-1222449	Mtb iron assimilation by chelation
R-HSA-1222499	Latent infection - Other responses of Mtb to phagocytosis
R-HSA-1222538	Tolerance by Mtb to nitric oxide produced by macrophages
R-HSA-1222541	Cell redox homeostasis
R-HSA-1226099	Signaling by FGFR in disease
R-HSA-1227990	Signaling by ERBB2 in Cancer
R-HSA-1236382	Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants
R-HSA-162585	Uncoating of the HIV Virion
R-HSA-162587	HIV Life Cycle
R-HSA-162588	Budding and maturation of HIV virion
R-HSA-162589	Reverse Transcription of HIV RNA
R-HSA-162592	Integration of provirus
R-HSA-162594	Early Phase of HIV Life Cycle
R-HSA-162599	Late Phase of HIV Life Cycle
R-HSA-162906	HIV Infection
R-HSA-162909	Host Interactions of HIV factors
R-HSA-1643685	Disease
R-HSA-1643713	Signaling by EGFR in Cancer
R-HSA-164516	Minus-strand DNA synthesis
R-HSA-164525	Plus-strand DNA synthesis
R-HSA-164843	2-LTR circle formation
R-HSA-164938	Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters
R-HSA-164939	Nef mediated downregulation of CD28 cell surface expression
R-HSA-164940	Nef mediated downregulation of MHC class I complex cell surface expression
R-HSA-164944	Nef and signal transduction
R-HSA-165054	Rev-mediated nuclear export of HIV RNA
R-HSA-167152	Formation of HIV elongation complex in the absence of HIV Tat
R-HSA-167158	Formation of the HIV-1 Early Elongation Complex
R-HSA-167160	RNA Pol II CTD phosphorylation and interaction with CE during HIV infection
R-HSA-167161	HIV Transcription Initiation
R-HSA-167162	RNA Polymerase II HIV Promoter Escape
R-HSA-167169	HIV Transcription Elongation
R-HSA-167172	Transcription of the HIV genome
R-HSA-167200	Formation of HIV-1 elongation complex containing HIV-1 Tat
R-HSA-167238	Pausing and recovery of Tat-mediated HIV elongation
R-HSA-167242	Abortive elongation of HIV-1 transcript in the absence of Tat
R-HSA-167243	Tat-mediated HIV elongation arrest and recovery
R-HSA-167246	Tat-mediated elongation of the HIV-1 transcript
R-HSA-167287	HIV elongation arrest and recovery
R-HSA-167290	Pausing and recovery of HIV elongation
R-HSA-167590	Nef Mediated CD4 Down-regulation
R-HSA-168255	Influenza Infection
R-HSA-168268	Virus Assembly and Release
R-HSA-168270	Fusion and Uncoating of the Influenza Virion
R-HSA-168271	Transport of Ribonucleoproteins into the Host Nucleus
R-HSA-168273	Influenza Viral RNA Transcription and Replication
R-HSA-168274	Export of Viral Ribonucleoproteins from Nucleus
R-HSA-168275	Entry of Influenza Virion into Host Cell via Endocytosis
R-HSA-168276	NS1 Mediated Effects on Host Pathways
R-HSA-168277	Influenza Virus Induced Apoptosis
R-HSA-168288	Fusion of the Influenza Virion to the Host Cell Endosome
R-HSA-168298	Release
R-HSA-168302	Budding
R-HSA-168303	Packaging of Eight RNA Segments
R-HSA-168305	Inhibition of Interferon Synthesis
R-HSA-168315	Inhibition of Host mRNA Processing and RNA Silencing
R-HSA-168316	Assembly of Viral Components at the Budding Site
R-HSA-168325	Viral Messenger RNA Synthesis
R-HSA-168330	Viral RNP Complexes in the Host Cell Nucleus
R-HSA-168333	NEP/NS2 Interacts with the Cellular Export Machinery
R-HSA-168336	Uncoating of the Influenza Virion
R-HSA-168799	Neurotoxicity of clostridium toxins
R-HSA-168874	Transport of HA trimer, NA tetramer and M2 tetramer from the endoplasmic reticulum to the Golgi Apparatus
R-HSA-168888	Inhibition of IFN-beta
R-HSA-169131	Inhibition of PKR
R-HSA-171286	Synthesis and processing of ENV and VPU
R-HSA-173107	Binding and entry of HIV virion
R-HSA-174490	Membrane binding and targetting of GAG proteins
R-HSA-174495	Synthesis And Processing Of GAG, GAGPOL Polyproteins
R-HSA-175474	Assembly Of The HIV Virion
R-HSA-175567	Integration of viral DNA into host genomic DNA
R-HSA-176033	Interactions of Vpr with host cellular proteins
R-HSA-176034	Interactions of Tat with host cellular proteins
R-HSA-177243	Interactions of Rev with host cellular proteins
R-HSA-177539	Autointegration results in viral DNA circles
R-HSA-180534	Vpu mediated degradation of CD4
R-HSA-180585	Vif-mediated degradation of APOBEC3G
R-HSA-180689	APOBEC3G mediated resistance to HIV-1 infection
R-HSA-180746	Nuclear import of Rev protein
R-HSA-180897	Vpr-mediated induction of apoptosis by mitochondrial outer membrane permeabilization
R-HSA-180910	Vpr-mediated nuclear import of PICs
R-HSA-182218	Nef Mediated CD8 Down-regulation
R-HSA-1839117	Signaling by cytosolic FGFR1 fusion mutants
R-HSA-1839120	Signaling by FGFR1 amplification mutants
R-HSA-1839122	Signaling by activated point mutants of FGFR1
R-HSA-1839124	FGFR1 mutant receptor activation
R-HSA-1839126	FGFR2 mutant receptor activation
R-HSA-1839128	FGFR4 mutant receptor activation
R-HSA-1839130	Signaling by activated point mutants of FGFR3
R-HSA-192814	vRNA Synthesis
R-HSA-192823	Viral mRNA Translation
R-HSA-192869	cRNA Synthesis
R-HSA-192905	vRNP Assembly
R-HSA-2023837	Signaling by FGFR2 amplification mutants
R-HSA-2033514	FGFR3 mutant receptor activation
R-HSA-2033515	t(4;14) translocations of FGFR3
R-HSA-2033519	Activated point mutants of FGFR2
R-HSA-2160456	Phenylketonuria
R-HSA-2206280	MPS IX - Natowicz syndrome
R-HSA-2206281	Mucopolysaccharidoses
R-HSA-2206282	MPS IIIB - Sanfilippo syndrome B
R-HSA-2206285	MPS VI - Maroteaux-Lamy syndrome
R-HSA-2206290	MPS IV - Morquio syndrome A
R-HSA-2206291	MPS IIIC - Sanfilippo syndrome C
R-HSA-2206292	MPS VII - Sly syndrome
R-HSA-2206296	MPS II - Hunter syndrome
R-HSA-2206302	MPS I - Hurler syndrome
R-HSA-2206305	MPS IIID - Sanfilippo syndrome D
R-HSA-2206307	MPS IIIA - Sanfilippo syndrome A
R-HSA-2206308	MPS IV - Morquio syndrome B
R-HSA-2219528	PI3K/AKT Signaling in Cancer
R-HSA-2219530	Constitutive Signaling by Aberrant PI3K in Cancer
R-HSA-2453864	Retinoid cycle disease events
R-HSA-2466712	Biosynthesis of A2E, implicated in retinal degradation
R-HSA-2474795	Diseases associated with visual transduction
R-HSA-2644602	Signaling by NOTCH1 PEST Domain Mutants in Cancer
R-HSA-2644603	Signaling by NOTCH1 in Cancer
R-HSA-2644605	FBXW7 Mutants and NOTCH1 in Cancer
R-HSA-2644606	Constitutive Signaling by NOTCH1 PEST Domain Mutants
R-HSA-2644607	Loss of Function of FBXW7 in Cancer and NOTCH1 Signaling
R-HSA-2660825	Signaling by NOTCH1 t(7;9)(NOTCH1:M1580_K2555) Translocation Mutant
R-HSA-2660826	Constitutive Signaling by NOTCH1 t(7;9)(NOTCH1:M1580_K2555) Translocation Mutant
R-HSA-2691230	Signaling by NOTCH1 HD Domain Mutants in Cancer
R-HSA-2691232	Constitutive Signaling by NOTCH1 HD Domain Mutants
R-HSA-2894858	Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer
R-HSA-2894862	Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants
R-HSA-2978092	Abnormal conversion of 2-oxoglutarate to 2-hydroxyglutarate
R-HSA-3229121	Glycogen storage diseases
R-HSA-3229133	Glycogen storage disease type Ib (SLC37A4)
R-HSA-3274531	Glycogen storage disease type Ia (G6PC)
R-HSA-3282872	Severe congenital neutropenia type 4 (G6PC3)
R-HSA-3296469	Defects in cobalamin (B12) metabolism
R-HSA-3296482	Defects in vitamin and cofactor metabolism
R-HSA-3304347	Loss of Function of SMAD4 in Cancer
R-HSA-3304349	Loss of Function of SMAD2/3 in Cancer
R-HSA-3304351	Signaling by TGF-beta Receptor Complex in Cancer
R-HSA-3304356	SMAD2/3 Phosphorylation Motif Mutants in Cancer
R-HSA-3311021	SMAD4 MH2 Domain Mutants in Cancer
R-HSA-3315487	SMAD2/3 MH2 Domain Mutants in Cancer
R-HSA-3323169	Defects in biotin (Btn) metabolism
R-HSA-3359454	Defective TCN2 causes TCN2 deficiency
R-HSA-3359457	Defective CBLIF causes IFD
R-HSA-3359462	Defective AMN causes MGA1
R-HSA-3359463	Defective CUBN causes MGA1
R-HSA-3359467	Defective MTRR causes HMAE
R-HSA-3359469	Defective MTR causes HMAG
R-HSA-3359471	Defective MMAB causes MMA, cblB type
R-HSA-3359473	Defective MMADHC causes MMAHCD
R-HSA-3359474	Defective MMACHC causes MAHCC
R-HSA-3359475	Defective MMAA causes MMA, cblA type
R-HSA-3359478	Defective MUT causes MMAM
R-HSA-3359485	Defective CD320 causes MMATC
R-HSA-3371598	Defective BTD causes biotidinase deficiency
R-HSA-3371599	Defective HLCS causes multiple carboxylase deficiency
R-HSA-3560782	Diseases associated with glycosaminoglycan metabolism
R-HSA-3560783	Defective B4GALT7 causes EDS, progeroid type
R-HSA-3560792	Defective SLC26A2 causes chondrodysplasias
R-HSA-3560796	Defective PAPSS2 causes SEMD-PA
R-HSA-3560801	Defective B3GAT3 causes JDSSDHD
R-HSA-3595172	Defective CHST3 causes SEDCJD
R-HSA-3595174	Defective CHST14 causes EDS, musculocontractural type
R-HSA-3595177	Defective CHSY1 causes TPBS
R-HSA-3642278	Loss of Function of TGFBR2 in Cancer
R-HSA-3642279	TGFBR2 MSI Frameshift Mutants in Cancer
R-HSA-3645790	TGFBR2 Kinase Domain Mutants in Cancer
R-HSA-3656225	Defective CHST6 causes MCDC1
R-HSA-3656234	Defective HEXA causes GM2G1
R-HSA-3656237	Defective EXT2 causes exostoses 2
R-HSA-3656243	Defective ST3GAL3 causes MCT12 and EIEE15
R-HSA-3656244	Defective B4GALT1 causes B4GALT1-CDG (CDG-2d)
R-HSA-3656248	Defective HEXB causes GM2G2
R-HSA-3656253	Defective EXT1 causes exostoses 1, TRPS2 and CHDS
R-HSA-3656532	TGFBR1 KD Mutants in Cancer
R-HSA-3656534	Loss of Function of TGFBR1 in Cancer
R-HSA-3656535	TGFBR1 LBD Mutants in Cancer
R-HSA-3781860	Diseases associated with N-glycosylation of proteins
R-HSA-3781865	Diseases of glycosylation
R-HSA-3785653	Myoclonic epilepsy of Lafora
R-HSA-3814836	Glycogen storage disease type XV (GYG1)
R-HSA-3828062	Glycogen storage disease type 0 (muscle GYS1)
R-HSA-3858516	Glycogen storage disease type 0 (liver GYS2)
R-HSA-3878781	Glycogen storage disease type IV (GBE1)
R-HSA-3906995	Diseases associated with O-glycosylation of proteins
R-HSA-4043911	Defective PMM2 causes PMM2-CDG
R-HSA-4043916	Defective MPI causes MPI-CDG
R-HSA-4085011	Defective GNE causes sialuria, NK and IBM2
R-HSA-4085023	Defective GFPT1 causes CMSTA1
R-HSA-4341670	Defective NEU1 causes sialidosis
R-HSA-4420332	Defective B3GALT6 causes EDSP2 and SEMDJL1
R-HSA-4549349	Defective ALG2 causes CDG-1i
R-HSA-4549356	Defective DPAGT1 causes CDG-1j, CMSTA2
R-HSA-4549380	Defective ALG1 causes CDG-1k
R-HSA-4551295	Defective ALG11 causes CDG-1p
R-HSA-4570571	Defective RFT1 causes CDG-1n
R-HSA-4687000	Defective MPDU1 causes CDG-1f
R-HSA-4717374	Defective DPM1 causes DPM1-CDG
R-HSA-4719360	Defective DPM3 causes DPM3-CDG
R-HSA-4719377	Defective DPM2 causes DPM2-CDG
R-HSA-4720454	Defective ALG9 causes CDG-1l
R-HSA-4720475	Defective ALG3 causes CDG-1d
R-HSA-4720489	Defective ALG12 causes CDG-1g
R-HSA-4724289	Defective ALG6 causes CDG-1c
R-HSA-4724325	Defective ALG8 causes CDG-1h
R-HSA-4755579	Defective SRD5A3 causes SRD5A3-CDG, KHRZ
R-HSA-4755583	Defective DOLK causes DOLK-CDG
R-HSA-4755609	Defective DHDDS causes RP59
R-HSA-4791275	Signaling by WNT in cancer
R-HSA-4793950	Defective MAN1B1 causes MRT15
R-HSA-4793952	Defective MGAT2 causes CDG-2a
R-HSA-4793953	Defective B4GALT1 causes CDG-2d
R-HSA-4793954	Defective MOGS causes CDG-2b
R-HSA-4839735	Signaling by AXIN mutants
R-HSA-4839743	Signaling by CTNNB1 phospho-site mutants
R-HSA-4839744	Signaling by APC mutants
R-HSA-4839748	Signaling by AMER1 mutants
R-HSA-5083625	Defective GALNT3 causes HFTC
R-HSA-5083627	Defective LARGE causes MDDGA6 and MDDGB6
R-HSA-5083628	Defective POMGNT1 causes MDDGA3, MDDGB3 and MDDGC3
R-HSA-5083629	Defective POMT2 causes MDDGA2, MDDGB2 and MDDGC2
R-HSA-5083630	Defective LFNG causes SCDO3
R-HSA-5083632	Defective C1GALT1C1 causes TNPS
R-HSA-5083633	Defective POMT1 causes MDDGA1, MDDGB1 and MDDGC1
R-HSA-5083635	Defective B3GALTL causes PpS
R-HSA-5083636	Defective GALNT12 causes CRCS1
R-HSA-5210891	Uptake and function of anthrax toxins
R-HSA-5250955	Toxicity of botulinum toxin type D (botD)
R-HSA-5250958	Toxicity of botulinum toxin type B (botB)
R-HSA-5250968	Toxicity of botulinum toxin type A (botA)
R-HSA-5250971	Toxicity of botulinum toxin type C (botC)
R-HSA-5250981	Toxicity of botulinum toxin type F (botF)
R-HSA-5250982	Toxicity of tetanus toxin (tetX)
R-HSA-5250989	Toxicity of botulinum toxin type G (botG)
R-HSA-5250992	Toxicity of botulinum toxin type E (botE)
R-HSA-5260271	Diseases of Immune System
R-HSA-5336415	Uptake and function of diphtheria toxin
R-HSA-5339562	Uptake and actions of bacterial toxins
R-HSA-5339700	Signaling by TCF7L2 mutants
R-HSA-5339716	Signaling by GSK3beta mutants
R-HSA-5339717	Signaling by LRP5 mutants 
R-HSA-5340573	LGK974 inhibits PORCN
R-HSA-5340588	Signaling by RNF43 mutants
R-HSA-5357609	Glycogen storage disease type II (GAA)
R-HSA-5358747	CTNNB1 S33 mutants aren't phosphorylated
R-HSA-5358749	CTNNB1 S37 mutants aren't phosphorylated
R-HSA-5358751	CTNNB1 S45 mutants aren't phosphorylated
R-HSA-5358752	CTNNB1 T41 mutants aren't phosphorylated
R-HSA-5362768	Hh mutants are degraded by ERAD
R-HSA-5387390	Hh mutants abrogate ligand secretion
R-HSA-5423599	Diseases of Mismatch Repair (MMR)
R-HSA-5467333	APC truncation mutants are not K63 polyubiquitinated
R-HSA-5467337	APC truncation mutants have impaired AXIN binding
R-HSA-5467340	AXIN missense mutants destabilize the destruction complex
R-HSA-5467343	Deletions in the AMER1 gene destabilize the destruction complex
R-HSA-5467345	Deletions in the AXIN1 gene destabilize the destruction complex
R-HSA-5467348	Truncations of AMER1 destabilize the destruction complex
R-HSA-5545483	Defective Mismatch Repair Associated With MLH1
R-HSA-5545619	XAV939 stabilizes AXIN
R-HSA-5578995	Defective TPMT causes TPMT deficiency
R-HSA-5578996	Defective CYP27A1 causes CTX
R-HSA-5578997	Defective AHCY causes HMAHCHD
R-HSA-5578998	Defective OPLAH causes OPLAHD
R-HSA-5578999	Defective GCLC causes HAGGSD
R-HSA-5579000	Defective CYP1B1 causes Glaucoma
R-HSA-5579002	Defective UGT1A1 causes hyperbilirubinemia
R-HSA-5579004	Defective CYP26C1 causes FFDD4
R-HSA-5579005	Defective CYP4F22 causes ARCI5
R-HSA-5579006	Defective GSS causes GSS deficiency
R-HSA-5579007	Defective ACY1 causes encephalopathy
R-HSA-5579009	Defective CYP11B2 causes CMO-1 deficiency
R-HSA-5579010	Defective CYP24A1 causes HCAI
R-HSA-5579011	Defective CYP2U1 causes SPG56
R-HSA-5579012	Defective MAOA causes BRUNS
R-HSA-5579013	Defective CYP7B1 causes SPG5A and CBAS3
R-HSA-5579014	Defective CYP27B1 causes VDDR1A
R-HSA-5579015	Defective CYP26B1 causes RHFCA
R-HSA-5579016	Defective UGT1A4 causes hyperbilirubinemia
R-HSA-5579017	Defective CYP11B1 causes AH4
R-HSA-5579019	Defective FMO3 causes TMAU
R-HSA-5579020	Defective SLC35D1 causes SCHBCKD
R-HSA-5579021	Defective CYP21A2 causes AH3
R-HSA-5579022	Defective GGT1 causes GLUTH
R-HSA-5579024	Defective MAT1A causes MATD
R-HSA-5579026	Defective CYP11A1 causes AICSR
R-HSA-5579027	Defective CYP27B1 causes VDDR1B
R-HSA-5579028	Defective CYP17A1 causes AH5
R-HSA-5579029	Metabolic disorders of biological oxidation enzymes
R-HSA-5579030	Defective CYP19A1 causes AEXS
R-HSA-5579031	Defective ACTH causes obesity and POMCD
R-HSA-5579032	Defective TBXAS1 causes GHDD
R-HSA-5602358	Diseases associated with the TLR signaling cascade
R-HSA-5602410	TLR3 deficiency - HSE
R-HSA-5602415	UNC93B1 deficiency - HSE
R-HSA-5602498	MyD88 deficiency (TLR2/4)
R-HSA-5602566	TICAM1 deficiency - HSE
R-HSA-5602571	TRAF3 deficiency - HSE
R-HSA-5602636	IKBKB deficiency causes SCID
R-HSA-5602680	MyD88 deficiency (TLR5)
R-HSA-5603027	IKBKG deficiency causes anhidrotic ectodermal dysplasia with immunodeficiency (EDA-ID) (via TLR)
R-HSA-5603029	IkBA variant leads to EDA-ID
R-HSA-5603037	IRAK4 deficiency (TLR5)
R-HSA-5603041	IRAK4 deficiency (TLR2/4)
R-HSA-5609974	Defective PGM1 causes PGM1-CDG
R-HSA-5609975	Diseases associated with glycosylation precursor biosynthesis
R-HSA-5609976	Defective GALK1 causes GALCT2
R-HSA-5609977	Defective GALE causes EDG
R-HSA-5609978	Defective GALT can cause GALCT
R-HSA-5619035	Defective SLC17A5 causes Salla disease (SD) and ISSD
R-HSA-5619036	Defective SLC24A5 causes oculocutaneous albinism 6 (OCA6)
R-HSA-5619037	Defective SLC35A1 causes congenital disorder of glycosylation 2F (CDG2F)
R-HSA-5619039	Defective SLC12A6 causes agenesis of the corpus callosum, with peripheral neuropathy (ACCPN)
R-HSA-5619040	Defective SLC34A1 causes hypophosphatemic nephrolithiasis/osteoporosis 1 (NPHLOP1)
R-HSA-5619041	Defective SLC36A2 causes iminoglycinuria (IG) and hyperglycinuria (HG)
R-HSA-5619042	Defective RHAG causes regulator type Rh-null hemolytic anemia (RHN)
R-HSA-5619043	Defective SLC2A1 causes GLUT1 deficiency syndrome 1 (GLUT1DS1)
R-HSA-5619044	Defective SLC6A19 causes Hartnup disorder (HND)
R-HSA-5619045	Defective SLC34A2 causes pulmonary alveolar microlithiasis (PALM)
R-HSA-5619046	Defective SLC26A4 causes Pendred syndrome (PDS)
R-HSA-5619047	Defective SLC2A9 causes hypouricemia renal 2 (RHUC2)
R-HSA-5619048	Defective SLC11A2 causes hypochromic microcytic anemia, with iron overload 1 (AHMIO1)
R-HSA-5619049	Defective SLC40A1 causes hemochromatosis 4 (HFE4) (macrophages)
R-HSA-5619050	Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4),  distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA)
R-HSA-5619052	Defective SLC9A9 causes autism 16 (AUTS16)
R-HSA-5619053	Defective SLC22A5 causes systemic primary carnitine deficiency (CDSP)
R-HSA-5619054	Defective SLC4A4 causes renal tubular acidosis, proximal, with ocular abnormalities and mental retardation (pRTA-OA)
R-HSA-5619055	Defective SLC24A4 causes hypomineralized amelogenesis imperfecta (AI)
R-HSA-5619056	Defective HK1 causes hexokinase deficiency (HK deficiency)
R-HSA-5619058	Defective SLCO1B3 causes hyperbilirubinemia, Rotor type (HBLRR)
R-HSA-5619060	Defective CP causes aceruloplasminemia (ACERULOP)
R-HSA-5619061	Defective SLC33A1 causes spastic paraplegia 42 (SPG42)
R-HSA-5619062	Defective SLC1A3 causes episodic ataxia 6 (EA6)
R-HSA-5619063	Defective SLC29A3 causes histiocytosis-lymphadenopathy plus syndrome (HLAS)
R-HSA-5619066	Defective SLC22A18 causes lung cancer (LNCR) and embryonal rhabdomyosarcoma 1 (RMSE1)
R-HSA-5619067	Defective SLC1A1 is implicated in schizophrenia 18 (SCZD18) and dicarboxylic aminoaciduria (DCBXA)
R-HSA-5619068	Defective SLC2A10 causes arterial tortuosity syndrome (ATS)
R-HSA-5619070	Defective SLC16A1 causes symptomatic deficiency in lactate transport (SDLT)
R-HSA-5619071	Defective SLC22A12 causes renal hypouricemia 1 (RHUC1)
R-HSA-5619072	Defective SLC35A2 causes congenital disorder of glycosylation 2M (CDG2M)
R-HSA-5619073	Defective GCK causes maturity-onset diabetes of the young 2 (MODY2)
R-HSA-5619076	Defective SLC17A8 causes autosomal dominant deafness 25 (DFNA25)
R-HSA-5619077	Defective SLC24A1 causes congenital stationary night blindness 1D (CSNB1D)
R-HSA-5619078	Defective SLC35C1 causes congenital disorder of glycosylation 2C (CDG2C)
R-HSA-5619079	Defective SLC6A18 may confer susceptibility to iminoglycinuria and/or hyperglycinuria
R-HSA-5619081	Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)
R-HSA-5619083	Defective SLC35A3 causes arthrogryposis, mental retardation, and seizures (AMRS)
R-HSA-5619084	ABC transporter disorders
R-HSA-5619085	Defective SLC26A3 causes congenital secretory chloride diarrhea 1 (DIAR1)
R-HSA-5619087	Defective SLC12A3 causes Gitelman syndrome (GS)
R-HSA-5619088	Defective SLC39A4 causes acrodermatitis enteropathica, zinc-deficiency type (AEZ)
R-HSA-5619089	Defective SLC6A5 causes hyperekplexia 3 (HKPX3)
R-HSA-5619092	Defective SLC9A6 causes  X-linked, syndromic mental retardation,, Christianson type (MRXSCH)
R-HSA-5619094	Variant SLC6A14 may confer susceptibility towards obesity
R-HSA-5619095	Defective SLCO2A1 causes primary, autosomal recessive hypertrophic osteoarthropathy 2 (PHOAR2)
R-HSA-5619096	Defective SLC5A5 causes thyroid dyshormonogenesis 1 (TDH1)
R-HSA-5619097	Defective SLC34A3 causes Hereditary hypophosphatemic rickets with hypercalciuria (HHRH)
R-HSA-5619098	Defective SLC2A2 causes Fanconi-Bickel syndrome (FBS)
R-HSA-5619099	Defective AVP does not bind AVPR1A,B and causes neurohypophyseal diabetes insipidus (NDI)
R-HSA-5619101	Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG)
R-HSA-5619102	SLC transporter disorders
R-HSA-5619104	Defective SLC12A1 causes Bartter syndrome 1 (BS1)
R-HSA-5619107	Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC)
R-HSA-5619108	Defective SLC27A4 causes ichthyosis prematurity syndrome (IPS)
R-HSA-5619109	Defective SLC6A2 causes orthostatic intolerance (OI)
R-HSA-5619110	Defective SLCO1B1 causes hyperbilirubinemia, Rotor type (HBLRR)
R-HSA-5619111	Defective SLC20A2 causes idiopathic basal ganglia calcification 1 (IBGC1)
R-HSA-5619113	Defective SLC3A1 causes cystinuria (CSNU)
R-HSA-5619114	Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)
R-HSA-5619115	Disorders of transmembrane transporters
R-HSA-5632927	Defective Mismatch Repair Associated With MSH3
R-HSA-5632928	Defective Mismatch Repair Associated With MSH2
R-HSA-5632968	Defective Mismatch Repair Associated With MSH6
R-HSA-5632987	Defective Mismatch Repair Associated With PMS2
R-HSA-5633231	Defective ALG14 causes ALG14-CMS
R-HSA-5637810	Constitutive Signaling by EGFRvIII
R-HSA-5637812	Signaling by EGFRvIII in Cancer
R-HSA-5637815	Signaling by Ligand-Responsive EGFR Variants in Cancer
R-HSA-5638302	Signaling by Overexpressed Wild-Type EGFR in Cancer
R-HSA-5638303	Inhibition of Signaling by Overexpressed EGFR
R-HSA-5655253	Signaling by FGFR2 in disease
R-HSA-5655291	Signaling by FGFR4 in disease
R-HSA-5655302	Signaling by FGFR1 in disease
R-HSA-5655332	Signaling by FGFR3 in disease
R-HSA-5655799	Defective SLC40A1 causes hemochromatosis 4 (HFE4) (duodenum)
R-HSA-5656364	Defective SLC5A1 causes congenital glucose/galactose malabsorption (GGM)
R-HSA-5657560	Hereditary fructose intolerance
R-HSA-5657562	Essential fructosuria
R-HSA-5658034	HHAT G278V doesn't palmitoylate Hh-Np
R-HSA-5658208	Defective SLC5A2 causes renal glucosuria (GLYS1)
R-HSA-5658471	Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)
R-HSA-5659729	Defective SLC6A18 may confer susceptibility to iminoglycinuria and/or hyperglycinuria
R-HSA-5659735	Defective SLC6A19 causes Hartnup disorder (HND)
R-HSA-5659898	Intestinal saccharidase deficiencies
R-HSA-5659996	RPIA deficiency: failed conversion of R5P to RU5P
R-HSA-5660686	Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG)
R-HSA-5660724	Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)
R-HSA-5660862	Defective SLC7A7 causes lysinuric protein intolerance (LPI)
R-HSA-5660883	Defective SLC7A9 causes cystinuria (CSNU)
R-HSA-5662853	Essential pentosuria
R-HSA-5663020	Defective SLC35A1 causes congenital disorder of glycosylation 2F (CDG2F)
R-HSA-5663084	Diseases of carbohydrate metabolism
R-HSA-5663202	Diseases of signal transduction by growth factor receptors and second messengers
R-HSA-5663205	Infectious disease
R-HSA-5668914	Diseases of metabolism
R-HSA-5674400	Constitutive Signaling by AKT1 E17K in Cancer
R-HSA-5674404	PTEN Loss of Function in Cancer
R-HSA-5678420	Defective ABCC9 causes CMD10, ATFB12 and Cantu syndrome
R-HSA-5678520	Defective ABCB11 causes PFIC2 and BRIC2
R-HSA-5678771	Defective ABCB4 causes PFIC3, ICP3 and GBD1
R-HSA-5678895	Defective CFTR causes cystic fibrosis
R-HSA-5679001	Defective ABCC2 causes DJS
R-HSA-5679090	Defective ABCG8 causes GBD4 and sitosterolemia
R-HSA-5679096	Defective ABCG5 causes sitosterolemia
R-HSA-5682113	Defective ABCA1 causes TGD
R-HSA-5682294	Defective ABCA12 causes ARCI4B
R-HSA-5683177	Defective ABCC8 can cause hypo- and hyper-glycemias
R-HSA-5683329	Defective ABCD4 causes MAHCJ
R-HSA-5683371	Defective ABCB6 causes MCOPCB7
R-HSA-5683678	Defective ABCA3 causes SMDP3
R-HSA-5684045	Defective ABCD1 causes ALD
R-HSA-5687583	Defective SLC34A2 causes PALM
R-HSA-5687613	Diseases associated with surfactant metabolism
R-HSA-5687868	Defective SFTPA2 causes IPF
R-HSA-5688031	Defective pro-SFTPB causes SMDP1 and RDS
R-HSA-5688354	Defective pro-SFTPC causes SMDP2 and RDS
R-HSA-5688399	Defective ABCA3 causes SMDP3
R-HSA-5688849	Defective CSF2RB causes SMDP5
R-HSA-5688890	Defective CSF2RA causes SMDP4
R-HSA-5690338	Defective ABCC6 causes PXE
R-HSA-6791055	TALDO1 deficiency: failed conversion of SH7P, GA3P to Fru(6)P, E4P
R-HSA-6791461	RPIA deficiency: failed conversion of RU5P to R5P
R-HSA-6791462	TALDO1 deficiency: failed conversion of  Fru(6)P, E4P to SH7P, GA3P
R-HSA-6791465	Pentose phosphate pathway disease
R-HSA-6802946	Signaling by moderate kinase activity BRAF mutants
R-HSA-6802948	Signaling by high-kinase activity BRAF mutants
R-HSA-6802949	Signaling by RAS mutants
R-HSA-6802952	Signaling by BRAF and RAF1 fusions
R-HSA-6802953	RAS signaling downstream of NF1 loss-of-function variants
R-HSA-6802955	Paradoxical activation of RAF signaling by kinase inactive BRAF
R-HSA-6802957	Oncogenic MAPK signaling
R-HSA-6809583	Retinoid metabolism disease events
R-HSA-8851708	Signaling by FGFR2 IIIa TM
R-HSA-8853333	Signaling by FGFR2 fusions
R-HSA-8853334	Signaling by FGFR3 fusions in cancer
R-HSA-8853336	Signaling by plasma membrane FGFR1 fusions
R-HSA-8862803	Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models
R-HSA-8863678	Neurodegenerative Diseases
R-HSA-8875360	InlB-mediated entry of Listeria monocytogenes into host cell
R-HSA-8876384	Listeria monocytogenes entry into host cells
R-HSA-8876493	InlA-mediated entry of Listeria monocytogenes into host cells
R-HSA-8942233	Intestinal infectious diseases
R-HSA-9005891	Loss of function of MECP2 in Rett syndrome
R-HSA-9005895	Pervasive developmental disorders
R-HSA-9006821	Alternative Lengthening of Telomeres (ALT)
R-HSA-9022534	Loss of MECP2 binding ability to 5hmC-DNA
R-HSA-9022535	Loss of phosphorylation of MECP2 at T308
R-HSA-9022537	Loss of MECP2 binding ability to the NCoR/SMRT complex
R-HSA-9022538	Loss of MECP2 binding ability to 5mC-DNA
R-HSA-9035968	Defective GGT1 in aflatoxin detoxification causes GLUTH
R-HSA-9036092	Defective AVP does not bind AVPR2 and causes neurohypophyseal diabetes insipidus (NDI)
R-HSA-9605308	Diseases of Base Excision Repair
R-HSA-9605310	Defective Base Excision Repair Associated with MUTYH
R-HSA-9608287	Defective MUTYH substrate binding
R-HSA-9608290	Defective MUTYH substrate processing
R-HSA-9609646	HCMV Infection
R-HSA-9609690	HCMV Early Events
R-HSA-9610379	HCMV Late Events
R-HSA-9616333	Defective Base Excision Repair Associated with NTHL1
R-HSA-9616334	Defective Base Excision Repair Associated with NEIL1
R-HSA-9629232	Defective Base Excision Repair Associated with NEIL3
R-HSA-9630221	Defective NTHL1 substrate processing
R-HSA-9630222	Defective NTHL1 substrate binding
R-HSA-9630747	Diseases of Cellular Senescence
R-HSA-9630750	Evasion of Oncogene Induced Senescence Due to p16INK4A Defects
R-HSA-9630791	Evasion of Oncogene Induced Senescence Due to Defective p16INK4A binding to CDK4
R-HSA-9630794	Evasion of Oncogene Induced Senescence Due to Defective p16INK4A binding to CDK4 and CDK6
R-HSA-9632693	Evasion of Oxidative Stress Induced Senescence Due to p16INK4A Defects
R-HSA-9632697	Evasion of Oxidative Stress Induced Senescence Due to Defective p16INK4A binding to CDK4
R-HSA-9632700	Evasion of Oxidative Stress Induced Senescence Due to Defective p16INK4A binding to CDK4 and CDK6
R-HSA-9634285	Constitutive Signaling by Overexpressed ERBB2
R-HSA-9635465	Suppression of apoptosis
R-HSA-9635486	Infection with Mycobacterium tuberculosis
R-HSA-9635644	Inhibition of membrane repair
R-HSA-9636249	Inhibition of nitric oxide production
R-HSA-9636383	Prevention of phagosomal-lysosomal fusion
R-HSA-9636467	Blockage of phagosome acidification
R-HSA-9636569	Suppression of autophagy
R-HSA-9636667	Manipulation of host energy metabolism
R-HSA-9637628	Modulation by Mtb of host immune system
R-HSA-9637679	Escape of Mtb from the phagocyte
R-HSA-9637687	Suppression of phagosomal maturation
R-HSA-9637690	Response of Mtb to phagocytosis
R-HSA-9637698	Phagocyte cell death caused by cytosolic Mtb
R-HSA-9639775	Antimicrobial action and antimicrobial resistance in Mtb
R-HSA-9645722	Defective Intrinsic Pathway for Apoptosis Due to p14ARF Loss of Function
R-HSA-9645723	Diseases of programmed cell death
R-HSA-9646303	Evasion of Oncogene Induced Senescence Due to p14ARF Defects
R-HSA-9646304	Evasion of Oxidative Stress Induced Senescence Due to p14ARF Defects
R-HSA-9649913	RAS GTPase cycle mutants
R-HSA-9649948	Signaling downstream of RAS mutants
R-HSA-9651496	Defects of contact activation system (CAS) and kallikrein/kinin system (KKS)
R-HSA-9652169	Signaling by MAP2K mutants
R-HSA-9652817	Signaling by MAPK mutants
R-HSA-9656223	Signaling by RAF1 mutants
R-HSA-9656249	Defective Base Excision Repair Associated with OGG1
R-HSA-9656255	Defective OGG1 Substrate Binding
R-HSA-9656256	Defective OGG1 Substrate Processing
R-HSA-9657050	Defective OGG1 Localization
R-HSA-9657688	Defective factor XII causes hereditary angioedema
R-HSA-9657689	Defective SERPING1 causes hereditary angioedema
R-HSA-9658195	Leishmania infection
R-HSA-9659787	Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects
R-HSA-9660537	Signaling by MRAS-complex mutants
R-HSA-9660821	ADORA2B mediated anti-inflammatory cytokines production
R-HSA-9660826	Purinergic signaling in leishmaniasis infection
R-HSA-9661069	Defective binding of RB1 mutants to E2F1,(E2F2, E2F3)
R-HSA-9661070	Defective translocation of RB1 mutants to the nucleus
R-HSA-9662001	Defective factor VIII causes hemophilia A
R-HSA-9662834	CD163 mediating an anti-inflammatory response
R-HSA-9662851	Anti-inflammatory response favouring Leishmania parasite infection
R-HSA-9663199	Defective DNA double strand break response due to BRCA1 loss of function
R-HSA-9664323	FCGR3A-mediated IL10 synthesis
R-HSA-9664407	Parasite infection
R-HSA-9664417	Leishmania phagocytosis
R-HSA-9664420	Killing mechanisms
R-HSA-9664422	FCGR3A-mediated phagocytosis
R-HSA-9664424	Cell recruitment (pro-inflammatory response)
R-HSA-9664433	Leishmania parasite growth and survival
R-HSA-9664535	LTC4-CYSLTR mediated IL4 production
R-HSA-9664565	Signaling by ERBB2 KD Mutants
R-HSA-9665230	Drug resistance in ERBB2 KD mutants
R-HSA-9665233	Resistance of ERBB2 KD mutants to trastuzumab
R-HSA-9665244	Resistance of ERBB2 KD mutants to sapitinib
R-HSA-9665245	Resistance of ERBB2 KD mutants to tesevatinib
R-HSA-9665246	Resistance of ERBB2 KD mutants to neratinib
R-HSA-9665247	Resistance of ERBB2 KD mutants to osimertinib
R-HSA-9665249	Resistance of ERBB2 KD mutants to afatinib
R-HSA-9665250	Resistance of ERBB2 KD mutants to AEE788
R-HSA-9665251	Resistance of ERBB2 KD mutants to lapatinib
R-HSA-9665348	Signaling by ERBB2 ECD mutants
R-HSA-9665686	Signaling by ERBB2 TMD/JMD mutants
R-HSA-9665737	Drug resistance in ERBB2 TMD/JMD mutants
R-HSA-9668250	Defective factor IX causes hemophilia B
R-HSA-9669914	Dasatinib-resistant KIT mutants
R-HSA-9669917	Imatinib-resistant KIT mutants
R-HSA-9669921	KIT mutants bind TKIs
R-HSA-9669924	Masitinib-resistant KIT mutants
R-HSA-9669926	Nilotinib-resistant KIT mutants
R-HSA-9669929	Regorafenib-resistant KIT mutants
R-HSA-9669933	Signaling by kinase domain mutants of KIT
R-HSA-9669934	Sunitinib-resistant KIT mutants
R-HSA-9669935	Signaling by juxtamembrane domain KIT mutants
R-HSA-9669936	Sorafenib-resistant KIT mutants
R-HSA-9669937	Drug resistance of KIT mutants
R-HSA-9669938	Signaling by KIT in disease
R-HSA-9670439	Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants
R-HSA-9670613	Defective Inhibition of DNA Recombination at Telomere Due to DAXX Mutations
R-HSA-9670615	Defective Inhibition of DNA Recombination at Telomere Due to ATRX Mutations
R-HSA-9670621	Defective Inhibition of DNA Recombination at Telomere
R-HSA-9671555	Signaling by PDGFR in disease
R-HSA-9671793	Diseases of hemostasis
R-HSA-9672383	Defective factor IX causes thrombophilia
R-HSA-9672387	Defective F8 accelerates dissociation of the A2 domain
R-HSA-9672391	Defective F8 cleavage by thrombin
R-HSA-9672393	Defective F8 binding to von Willebrand factor
R-HSA-9672395	Defective F8 binding to the cell membrane
R-HSA-9672396	Defective cofactor function of FVIIIa variant
R-HSA-9672397	Defective F8 secretion
R-HSA-9673013	Diseases of Telomere Maintenance
R-HSA-9673202	Defective F9 variant does not activate FX
R-HSA-9673218	Defective F9 secretion
R-HSA-9673221	Defective F9 activation
R-HSA-9673240	Defective gamma-carboxylation of F9
R-HSA-9673324	WNT5:FZD7-mediated leishmania damping
R-HSA-9673766	Signaling by cytosolic PDGFRA and PDGFRB fusion proteins
R-HSA-9673767	Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants
R-HSA-9673768	Signaling by membrane-tethered fusions of PDGFRA or PDGFRB
R-HSA-9673770	Signaling by PDGFRA extracellular domain mutants
R-HSA-9674396	Imatinib-resistant PDGFR mutants
R-HSA-9674401	Sunitinib-resistant PDGFR mutants
R-HSA-9674403	Regorafenib-resistant PDGFR mutants
R-HSA-9674404	Sorafenib-resistant PDGFR mutants
R-HSA-9674415	Drug resistance of PDGFR mutants
R-HSA-9674428	PDGFR mutants bind TKIs
R-HSA-9674519	Defective F8 sulfation at Y1699
R-HSA-9675126	Diseases of mitotic cell cycle
R-HSA-9675132	Diseases of cellular response to stress
R-HSA-9675135	Diseases of DNA repair
R-HSA-9675136	Diseases of DNA Double-Strand Break Repair
R-HSA-9675143	Diseases of the neuronal system
R-HSA-9675151	Disorders of Developmental Biology
R-HSA-9678108	SARS-CoV-1 Infection
R-HSA-9678110	Attachment and Entry
R-HSA-9679191	Potential therapeutics for SARS
R-HSA-9679504	Translation of Replicase and Assembly of the Replication Transcription Complex
R-HSA-9679506	SARS-CoV Infections
R-HSA-9679509	Virion Assembly and Release
R-HSA-9679514	SARS-CoV-1 Genome Replication and Transcription
R-HSA-9680187	Signaling by extracellular domain mutants of KIT
R-HSA-9682385	FLT3 signaling in disease
R-HSA-9682706	Replication of the SARS-CoV-1 genome
R-HSA-9682708	Transcription of SARS-CoV-1 sgRNAs
R-HSA-9683439	Assembly of the SARS-CoV-1 Replication-Transcription Complex (RTC)
R-HSA-9683610	Maturation of nucleoprotein
R-HSA-9683612	Maturation of protein M
R-HSA-9683673	Maturation of protein 3a
R-HSA-9683683	Maturation of protein E
R-HSA-9683686	Maturation of spike protein
R-HSA-9683701	Translation of Structural Proteins
R-HSA-9684325	Maturation of replicase proteins
R-HSA-9686347	Microbial modulation of RIPK1-mediated regulated necrosis
R-HSA-9687136	Aberrant regulation of mitotic exit in cancer due to RB1 defects
R-HSA-9687139	Aberrant regulation of mitotic cell cycle due to RB1 defects
R-HSA-9692912	SARS-CoV-1 targets PDZ proteins in cell-cell junction
R-HSA-9692913	SARS-CoV-1-mediated effects on programmed cell death
R-HSA-9692914	SARS-CoV-1-host interactions
R-HSA-9692916	SARS-CoV-1 activates/modulates innate immune responses
R-HSA-9693928	Defective RIPK1-mediated regulated necrosis
R-HSA-9694271	Assembly of the SARS-CoV-2 Replication-Transcription Complex (RTC)
R-HSA-9694301	Maturation of replicase proteins
R-HSA-9694322	Virion Assembly and Release
R-HSA-9694493	Maturation of protein E
R-HSA-9694516	SARS-CoV-2 Infection
R-HSA-9694548	Maturation of spike protein
R-HSA-9694594	Maturation of protein M
R-HSA-9694614	Attachment and Entry
R-HSA-9694631	Maturation of nucleoprotein
R-HSA-9694635	Translation of Structural Proteins
R-HSA-9694676	Translation of Replicase and Assembly of the Replication Transcription Complex
R-HSA-9694682	SARS-CoV-2 Genome Replication and Transcription
R-HSA-9694686	Replication of the SARS-CoV-2 genome
R-HSA-9694719	Maturation of protein 3a
R-HSA-9694786	Transcription of SARS-CoV-2 sgRNAs
R-HSA-9697154	Disorders of Nervous System Development
R-HSA-9699150	Defective DNA double strand break response due to BARD1 loss of function
R-HSA-9700206	Signaling by ALK in cancer
R-HSA-9700645	ALK mutants bind TKIs
R-HSA-9700649	Drug resistance of ALK mutants
R-HSA-9701190	Defective homologous recombination repair (HRR) due to BRCA2 loss of function
R-HSA-9701192	Defective homologous recombination repair (HRR) due to BRCA1 loss of function
R-HSA-9701193	Defective homologous recombination repair (HRR) due to PALB2 loss of function
R-HSA-9702506	Drug resistance of FLT3 mutants
R-HSA-9702509	FLT3 mutants bind TKIs
R-HSA-9702518	STAT5 activation downstream of FLT3 ITD mutants
R-HSA-9702569	KW2449-resistant FLT3 mutants
R-HSA-9702577	semaxanib-resistant FLT3 mutants
R-HSA-9702581	crenolanib-resistant FLT3 mutants
R-HSA-9702590	gilteritinib-resistant FLT3 mutants
R-HSA-9702596	lestaurtinib-resistant FLT3 mutants
R-HSA-9702600	midostaurin-resistant FLT3 mutants
R-HSA-9702605	pexidartinib-resistant FLT3 mutants
R-HSA-9702614	ponatinib-resistant FLT3 mutants
R-HSA-9702620	quizartinib-resistant FLT3 mutants
R-HSA-9702624	sorafenib-resistant FLT3 mutants
R-HSA-9702632	sunitinib-resistant FLT3 mutants
R-HSA-9702636	tandutinib-resistant FLT3 mutants
R-HSA-9702998	linifanib-resistant FLT3 mutants
R-HSA-9703009	tamatinib-resistant FLT3 mutants
R-HSA-9703465	Signaling by FLT3 fusion proteins
R-HSA-9703648	Signaling by FLT3 ITD and TKD mutants
R-HSA-9704331	Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function
R-HSA-9704646	Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function
R-HSA-9705671	SARS-CoV-2 activates/modulates innate and adaptive immune responses
R-HSA-9705677	SARS-CoV-2 targets PDZ proteins in cell-cell junction
R-HSA-9705683	SARS-CoV-2-host interactions
R-HSA-9706377	FLT3 signaling by CBL mutants
R-HSA-9709275	Impaired BRCA2 translocation to the nucleus
R-HSA-9709570	Impaired BRCA2 binding to RAD51
R-HSA-9709603	Impaired BRCA2 binding to PALB2
R-HSA-9710421	Defective pyroptosis
R-HSA-9717264	ASP-3026-resistant ALK mutants
R-HSA-9717301	NVP-TAE684-resistant ALK mutants
R-HSA-9717316	alectinib-resistant ALK mutants
R-HSA-9717319	brigatinib-resistant ALK mutants
R-HSA-9717323	ceritinib-resistant ALK mutants
R-HSA-9717326	crizotinib-resistant ALK mutants
R-HSA-9717329	lorlatinib-resistant ALK mutants
R-HSA-9723905	Loss of function of TP53 in cancer due to loss of tetramerization ability
R-HSA-9723907	Loss of Function of TP53 in Cancer
R-HSA-9725370	Signaling by ALK fusions and activated point mutants
R-HSA-9725371	Nuclear events stimulated by ALK signaling in cancer
R-HSA-9726840	SHOC2 M1731 mutant abolishes MRAS complex function
R-HSA-9726842	Gain-of-function MRAS complexes activate RAF signaling
R-HSA-9727281	Translation of Accessory Proteins
R-HSA-9733458	Induction of Cell-Cell Fusion
R-HSA-9734009	Defective Intrinsic Pathway for Apoptosis
R-HSA-9734195	Defective APRT disrupts adenine salvage
R-HSA-9734207	Nucleotide salvage defects
R-HSA-9734281	Defective HPRT1 disrupts guanine and hypoxanthine salvage
R-HSA-9734735	Defective ADA disrupts (deoxy)adenosine deamination
R-HSA-9735763	Defective PNP disrupts phosphorolysis of (deoxy)guanosine and (deoxy)inosine
R-HSA-9735786	Nucleotide catabolism defects
R-HSA-9735804	Diseases of nucleotide metabolism
R-HSA-9735869	SARS-CoV-1 modulates host translation machinery
R-HSA-9735871	SARS-CoV-1 targets host intracellular signalling and regulatory pathways
R-HSA-9753510	Signaling by RAS GAP mutants
R-HSA-9753512	Signaling by RAS GTPase mutants
R-HSA-9754560	SARS-CoV-2 modulates autophagy
R-HSA-9754678	SARS-CoV-2 modulates host translation machinery
R-HSA-9755779	SARS-CoV-2 targets host intracellular signalling and regulatory pathways
R-HSA-9759774	Diseases of mitochondrial beta oxidation
R-HSA-9759785	Diseases of propionyl-CoA catabolism
R-HSA-9763198	Impaired BRCA2 binding to SEM1 (DSS1)
R-HSA-9772572	Early SARS-CoV-2 Infection Events
R-HSA-9772573	Late SARS-CoV-2 Infection Events
R-HSA-9820952	Respiratory Syncytial Virus Infection Pathway
R-HSA-9820960	Respiratory syncytial virus (RSV) attachment and entry
R-HSA-9820962	Assembly and release of respiratory syncytial virus (RSV) virions
R-HSA-9820965	Respiratory syncytial virus (RSV) genome replication, transcription and translation
R-HSA-9823587	Defects of platelet adhesion to exposed collagen
R-HSA-9824439	Bacterial Infection Pathways
R-HSA-9824443	Parasitic Infection Pathways
R-HSA-9824446	Viral Infection Pathways
R-HSA-9824856	Defective regulation of TLR7 by endogenous ligand
R-HSA-9828642	Respiratory syncytial virus genome transcription
R-HSA-9828721	Translation of respiratory syncytial virus mRNAs
R-HSA-9828806	Maturation of hRSV A proteins
R-HSA-9833109	Evasion by RSV of host interferon responses
R-HSA-9833110	RSV-host interactions
R-HSA-9834752	Respiratory syncytial virus genome replication
R-HSA-9842640	Signaling by LTK in cancer
R-HSA-9845619	Enhanced cleavage of VWF variant by ADAMTS13
R-HSA-9845620	Enhanced binding of GP1BA variant to VWF multimer:collagen 
R-HSA-9845621	Defective VWF cleavage by ADAMTS13 variant
R-HSA-9845622	Defective VWF binding to collagen type I 
R-HSA-9846298	Defective binding of VWF variant to GPIb:IX:V
R-HSA-9865113	Loss-of-function mutations in DBT cause MSUD2
R-HSA-9865114	Maple Syrup Urine Disease
R-HSA-9865118	Diseases of branched-chain amino acid catabolism
R-HSA-9865125	Loss-of-function mutations in BCKDHA or BCKDHB cause MSUD
R-HSA-9907570	Loss-of-function mutations in DLD cause MSUD3/DLDD
R-HSA-9909438	3-Methylcrotonyl-CoA carboxylase deficiency
R-HSA-9912481	Branched-chain ketoacid dehydrogenase kinase deficiency
R-HSA-9912529	H139Hfs13* PPM1K causes a mild variant of  MSUD
R-HSA-9914274	3-methylglutaconic aciduria
R-HSA-9914355	Isovaleric acidemia
R-HSA-9915355	Beta-ketothiolase deficiency
R-HSA-9916720	Mitochondrial short-chain enoyl-CoA hydratase deficiency 1
R-HSA-9916722	3-hydroxyisobutyryl-CoA hydrolase deficiency
R-HSA-9918436	Defective visual phototransduction due to OPN1MW loss of function
R-HSA-9918438	Defective visual phototransduction due to RDH5 loss of function
R-HSA-9918440	Defective visual phototransduction due to RDH12 loss of function
R-HSA-9918442	Defective visual phototransduction due to LRAT loss of function
R-HSA-9918443	Defective visual phototransduction due to OPN1SW loss of function
R-HSA-9918449	Defective visual phototransduction due to STRA6 loss of function
R-HSA-9918450	Defective visual phototransduction due to OPN1LW loss of function
R-HSA-9918454	Defective visual phototransduction due to ABCA4 loss of function