Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "A"
791 to 800 of 1170 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

791
Apoptosis resistant E3 ubiquitin protein ligase 1
FIEL1, KIAA0317
Bipolar disorder, Glaucoma, Major depressive disorder, Mitral valve prolapse, Mood disorder, Neurotic disorder, Open angle glaucoma, Parkinson disease, Stroke

792
ARF GTPase 1
PVNH8
Breast neoplasms, Charcot-marie-tooth disease, Periventricular heterotopia, x-linked, Periventricular nodular heterotopia, Scoliosis

793
ARF GTPase 3
-
Autism, Nonsyndromic intellectual disability, Bifid uvula, Clinodactyly, Neurodevelopmental disorder, Congenital heart defects, Global developmental delay, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Scoliosis

794
ARF GTPase 5
-
Diabetes mellitus type 2

795
ARF GTPase activating protein 1
ARF1GAP, HRIHFB2281
Developmental disability, Nervous system disease

796
ARF GTPase activating protein 2
IRZ, NBLA10535, ZFP289, ZNF289
Alzheimer disease, Bone fracture, Major depressive disorder, Mood disorder, Stomach neoplasms

797
ARF guanine nucleotide exchange factor 1
ARFGEP1, BIG1, DEDISB, P200
Central serous retinopathy, Developmental delay with impaired growth and dysmorphic facies, Developmental disability, Global developmental delay, Intellectual developmental disorder, Joubert syndrome, Neurodevelopmental disorder, Schizophrenia, Seizures

798
ARF guanine nucleotide exchange factor 2
BIG2, PVNH2, dJ1164I10.1
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Coronary artery disease, Dyskinesia, Global developmental delay, Periventricular nodular heterotopia, Hydrocephalus, Intellectual developmental disorder, Major depressive disorder, Myocardial infarction, Periventricular heterotopia with microcephaly, autosomal recessive, Periventricular heterotopia, x-linked, Periventricular laminar heterotopia, Post-traumatic stress disorder
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799
ARFGEF family member 3
A7322, BIG3, C6orf92, KIAA1244, PPP1R33, dJ171N11.1
Alzheimer disease, Febrile convulsion, Neurodevelopmental disorder

800
ARF related protein 1
ARL18, ARP, Arp1
Asthma, Eczema, Diverticular disease, Dyskeratosis congenita, Prostate cancer, Diabetes mellitus type 2