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"
101 to 110 of 1170 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

101
Ankyrin repeat and BTB domain containing 2
ABTB2A, BTBD22, CCA3
Brain infarction, Cerebral amyloid angiopathy, Color vision deficiency, Insomnia, Lewy body disease, Ocular hypotension

102
Ankyrin repeat and BTB domain containing 3
ABTB2B, BTBD11
Coronary artery disease, Diabetic neuropathy, Eosinophilia, Essential tremor, Liver neoplasms, Metabolic syndrome, Myocardial infarction, Oral cavity carcinoma, Oropharyngeal cancer, Scoliosis, Diabetes mellitus type 2

103
Acetyl-CoA acyltransferase 2
DSAEC, T1
Anterior uveitis, Basal cell carcinoma, Coronary artery disease, Ovarian epithelial cancer, Myocardial infarction, Oligodendroglioma, Osteoarthritis, Ovarian cancer, Prostate cancer, Scoliosis, Sinusitis

104
Acetyl-CoA carboxylase alpha
ACAC, ACACAD, ACACalpha, ACC, ACC1, ACCA, ACCalpha, Acac1, hACC1
Acetyl-coa carboxylase deficiency, Hepatocellular carcinoma, Celiac disease, Congestive heart failure, Erectile dysfunction, Heart failure, Insomnia

105
Acetyl-CoA carboxylase beta
ACACbeta, ACC-beta, ACC2, ACCB, ACCbeta, HACC275
Autism, Breast neoplasms, Cervical cancer, Cleft palate, Diabetes mellitus type 2, Obesity, Vascular dementia

106
Acyl-CoA dehydrogenase family member 10
-
Atrial fibrillation, Atrophic macular degeneration, Kidney disease, Obstructive pulmonary disease, Colorectal cancer, Coronary artery disease, Esophageal cancer, Gout, Graves disease, Heart failure, Kidney failure, Major depressive disorder, Myocardial infarction, Stroke, Diabetes mellitus type 2
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107
Acyl-CoA dehydrogenase family member 11
ACAD-11
Coronary artery disease, Developmental and epileptic encephalopathy, Gout

108
Acyl-CoA dehydrogenase family member 8
ACAD-8, ARC42, IBDH
Isobutyryl-coa dehydrogenase deficiency, Obesity, Stomach neoplasms

109
Acyl-CoA dehydrogenase family member 9
MC1DN20, NPD002
Acyl-coa dehydrogenase deficiency, Mitochondrial complex deficiency

110
Acyl-CoA dehydrogenase long chain
ACAD4, LCAD
Basal cell carcinoma, Insomnia, Very long chain acyl-coa dehydrogenase deficiency