Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
361 to 370 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

361
AAA ATPase AFG2B
DFNB119, NEDHLS, SPATA5L1
Isolated sensorineural deafness, Kidney disease, Deafness, Global developmental delay, Hearing impairment, Hearing loss, Neurodevelopmental disorder, Nonsyndromic hearing loss,

362
AFG3 like matrix AAA peptidase subunit 2
OPA12, SCA28, SPAX5
Spinocerebellar ataxia, Cerebellar ataxia, Central nervous system cancer, Chorea, Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome, Glioblastoma, Glioma, Glycogen storage disease, Hyperkinesia, Intellectual developmental disorder, Optic atrophy, Retinitis pigmentosa, Hearing loss, Spastic ataxia

363
173
AFM
Afamin
ALB2, ALBA, ALF
Kidney failure, Liver cirrhosis, Prostate cancer

364
Arylformamidase
FKF, KF, KFA
Diverticular disease

365
174
AFP
Alpha fetoprotein
AFPD, FETA, HPAFP
Breast neoplasm, Hepatocellular carcinoma, Congenital alpha-fetoprotein deficiency, Hepatitis c, Liver cirrhosis, Liver disease, Liver neoplasm, Premature ovarian failure, Stomach neoplasms

366
175
AGA
Aspartylglucosaminidase
AGU, ASRG, GA
Autism, Desbuquois syndrome, Intellectual developmental disorder, Neurodevelopmental disorder, Schizophrenia

367
ArfGAP with GTPase domain, ankyrin repeat and PH domain 1
AGAP-1, CENTG2, GGAP1, cnt-g2
Alzheimer disease, Autism, Cardiovascular disease, Corneal disease, Craniofacial microsomia, Dementia, Diabetic retinopathy, Insomnia, Metabolic syndrome, Obesity, Orofacial cleft, Osteoarthritis, Parkinson disease, Schizophrenia, Stroke
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368
ArfGAP with GTPase domain, ankyrin repeat and PH domain 2
CENTG1, GGAP2, PIKE
Insomnia, Multiple sclerosis

369
ArfGAP with GTPase domain, ankyrin repeat and PH domain 3
AGAP-3, CENTG3, CRAG, MRIP-1, cnt-g3
Diabetes mellitus, type 2

370
AGBL carboxypeptidase 1
CCP4, FECD8
Alzheimer disease, Astrocytoma, Barrett esophagus, Bulimia, Central nervous system cancer, Chagas cardiomyopathy, Color vision deficiency, Corneal dystrophy, Fuchs endothelial dystrophy, Gestational diabetes, Glioblastoma, Glioma, Idiopathic pulmonary fibrosis, Insomnia, Metabolic syndrome
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