Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "A"
461 to 470 of 912 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

461
Aquaporin 1 (Colton blood group)
AQP-CHIP, CHIP28, CO
Polycystic kidney disease, Bladder calculus, Bone fracture, Carcinoma, Adenoid cystic carcinoma, Cholecystolithiasis, Edema, Huntington disease, Hypertension, Hyperthyroidism, Nephrolithiasis, Osteoporosis, Pulmonary arterial hypertension, Salivary gland disease, Toxic shock syndrome
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462
Aquaporin 2
AQP-CD, NDI2, WCH-CD
Arginine vasopressin resistance, Asthma, Cardiomyopathy, Diabetes insipidus, Neurogenic diabetes insipidus , Nephrogenic diabetes insipidus, Seasonal allergic rhinitis

463
Acyl-CoA dehydrogenase short/branched chain
2-MEBCAD, ACAD7, SBCAD
2-methylbutyryl-coa dehydrogenase deficiency, Autism, Lewy body disease, Periodontitis, Rheumatic disease

464
Aquaporin 3 (Gill blood group)
AQP-3, GIL
Eczema, Squamous cell carcinoma, Melanoma, Esophageal neoplasm, Lung cancer, Lymphatic metastasis, Major depressive disorder, Neuroblastoma, Non-small cell lung carcinoma, Ovarian neoplasm, Scoliosis, Skin neoplasm, Tongue cancer, Urinary bladder cancer

465
Aquaporin 4
MIWC, MLC4, WCH4, hAQP4
Autism, Blindness, Major depressive disorder, Temporal lobe epilepsy, Intellectual developmental disorder, Meniere disease, Depression, Optic neuritis, Schizophrenia, Status epilepticus

466
Aquaporin 5
AQP-5, PPKB
Diffuse palmoplantar keratoderma

467
Aquaporin 7
AQP7L, AQPap, GLYCQTL
Eczema, Color vision deficiency, Liver cirrhosis, Lung cancer, Major depressive disorder, Non-small cell lung carcinoma, Obesity, Scoliosis

468
Aquaporin 9
AQP-9, HsT17287, SSC1, T17287
Juvenile arthritis, Autism, Juvenile idiopathic arthritis, Lethal congenital contracture syndrome, Myeloid leukemia, Promyelocytic leukemia, Oligoarticular juvenile idiopathic arthritis

469
Androgen receptor
AIS, AR8, DHTR, HUMARA, HYSP1, KD, NR3C4, SBMA, SMAX1, TFM
Androgen insensitivity syndrome, Androgenetic alopecia, Astrocytoma, Attention deficit hyperactivity disorder, Autism, Breast neoplasm, Bulbo-spinal atrophy, x-linked, Hepatocellular carcinoma, Cryptorchidism, Major depressive disorder, Gestational diabetes, Hypertension, Hypogonadism, Hypospadias, Female infertility
View all (12 more)

470
ATP binding cassette subfamily C member 6
ABC34, ARA, EST349056, GACI2, MLP1, MOAT-E, MOATE, MRP6, PXE, PXE1, URG7
Pseudoxanthoma elasticum, Bladder calculus, Ischemic heart disease, Colorectal neoplasm, Coronary artery disease, Cutis laxa, Myocardial ischemia, Nephrolithiasis, Optic atrophy, Retinitis pigmentosa, Urolithiasis