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"
1121 to 1130 of 1165 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1121
ATPase phospholipid transporting 9A (putative)
ATPIIA, NEDGBA
Dupuytren contracture, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Obsessive-compulsive disorder, Osteoarthritis, Tourette syndrome

1122
ATPase phospholipid transporting 9B (putative)
ATPASEP, ATPIIB, HUSSY-20, NEO1L, hMMR1
Color vision deficiency, Frontotemporal dementia, Prostate cancer

1123
ATP synthase mitochondrial F1 complex assembly factor 1
ATP11, ATP11p
Obesity, Sinusitis

1124
ATP synthase mitochondrial F1 complex assembly factor 2
ATP12, ATP12p, LP3663, MC5DN1
Mitochondrial complex deficiency, Mitochondrial disease, Schizophrenia

1125
ATP synthase c subunit lysine N-methyltransferase
FAM173B, JS-2, hFAM173B
Astrocytoma, Cardiac embolism, Cardioembolic stroke, Duchenne muscular dystrophy

1126
ATR checkpoint kinase
FCTCS, FRP1, MEC1, SCKL, SCKL1
Familial telangiectasia cancer syndrome, Desbuquois syndrome, Prostate cancer, Prostatic neoplasms, Sarcoma, Seckel syndrome, Urologic neoplasms

1127
ATR interacting protein
-
Breast cancer, Cadasil, Chilblain lupus erythematosus, Vascular dementia, Hereditary breast cancer, Systemic lupus erythematosus, Migraine, Neurodevelopmental disorder, Obesity, Prion disease, Seckel syndrome, Retinal vasculopathy with cerebral leukodystrophy

1128
Attractin
DPPT-L, MGCA
Asthma, Autism, Colorectal cancer, Global developmental delay, Lung cancer, Thrombocytopenia

1129
Attractin like 1
ALP, bA338L11.1, bA454H24.1
Attention deficit hyperactivity disorder, Bipolar disorder, Bone remodeling disease, Central nervous system cancer, Glioma, Huntington disease, Oligodendroglioma, Osteoarthritis, Ovarian cancer, Willis-ekbom disease

1130
ATRX chromatin remodeler
JMS, MRX52, RAD54, RAD54L, XH2, XNP, ZNF-HX
Alpha thalassemia x-linked intellectual disability, Atr-x syndrome, Adenoid cystic carcinoma, Congenital neurologic anomalies, Craniofacial abnormalities, Cryptorchidism, Cushing syndrome, Developmental disability, Glioma, Global developmental delay, Growth disorder, Hemoglobin barts fetalis syndrome, Hemoglobin h disease, Intellectual developmental disorder, Intellectual developmental disorder hypotonic x-linked
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