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"
1021 to 1030 of 1165 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1021
Autophagy related 3
APG3, APG3-LIKE, APG3L, PC3-96, hApg3
Asthma

1022
Autophagy related 4B cysteine peptidase
APG4B, AUTL1, HsAPG4B
Atherosclerosis, Sialolithiasis

1023
Autophagy related 4C cysteine peptidase
APG4-C, APG4C, AUTL1, AUTL3, HsAPG4C
Crohn disease, Hyperlipidemia, Inflammatory bowel disease

1024
Autophagy related 4D cysteine peptidase
APG4-D, APG4D, AUTL4, HsAPG4D, SPGF101
Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Spermatogenic failure, Venous thromboembolism

1025
Autophagy related 5
APG5, APG5-LIKE, APG5L, ASP, SCAR25, hAPG5
Androgenetic alopecia, Anemia, Ankylosing spondylitis, Asthma, Biliary cirrhosis, Crohn disease, Hepatomegaly, Inflammatory bowel disease, Insomnia, Crest syndrome, Liver cirrhosis, Multiple myeloma, Myositis, Necrosis, Ovarian neoplasms
View all (12 more)

1026
Autophagy related 7
APG7-LIKE, APG7L, GSA7, SCAR31
Anemia, Hepatocellular carcinoma, Cardiovascular disease, Color vision deficiency, Hypertension, Hepatomegaly, Insomnia, Kidney disease, Liver failure, Major depressive disorder, Necrosis, Non-melanoma skin carcinoma, Osteoarthritis, Premature ovarian failure, Ovarian neoplasms
View all (4 more)

1027
Autophagy related 9B
APG9L2, NOS3AS, SONE
Premature ovarian failure

1028
5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase
AICAR, AICARFT, HEL-S-70p, IMPCHASE, PURH
Aica-ribosiduria, Rheumatoid arthritis, Blindness, Kidney disease, Nephrotic syndrome, Osteoporosis, Spondylometaphyseal dysplasia

1029
Atlastin GTPase 1
AD-FSP, ATL-1, FSP1, GBP3, HSN1D, SPG3, SPG3A, atlastin1
Spastic paraplegia, Cardiovascular disease, Charcot-marie-tooth disease, Obstructive pulmonary disease, Congenital neurologic anomalies, Dupuytren contracture, Hereditary sensory and autonomic neuropathy, Potassium deficiency, Hereditary spastic paraplegia

1030
Atlastin GTPase 2
ARL3IP2, ARL6IP2, ATL-2, aip-2, atlastin2
Tourette syndrome, Insomnia