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"
51 to 60 of 1170 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

51
ATP binding cassette subfamily C member 12
MRP9
Bone marrow diseases, Colonic neoplasms, Amyotrophic lateral sclerosis

52
ATP binding cassette subfamily C member 2
ABC30, CMOAT, DJS, MRP2, cMRP
Rheumatoid arthritis, Pseudoxanthoma elasticum, Biliary cirrhosis, Cardiomyopathy, Cholelithiasis, Colorectal neoplasms, Diarrhea, Digestive system disease, Dubin-johnson syndrome, Dysentery, Esophageal squamous cell carcinoma, Gastrointestinal disease, Heart disease, Hyperbilirubinemia, Liver cirrhosis
View all (6 more)

53
ATP binding cassette subfamily C member 3
ABC31, EST90757, MLP2, MOAT-D, MRP3, cMOAT2
Rheumatoid arthritis, Autism, Cholelithiasis, Colorectal neoplasms, Hepatomegaly, Osteonecrosis

54
ATP binding cassette subfamily C member 4 (PEL blood group)
MOAT-B, MOATB, MRP4
Rheumatoid arthritis, Breast cancer, Cognition disorder, Colorectal cancer, Colorectal neoplasms, Complications of diabetes mellitus, Delirium, dementia, and cognitive disorders, Diabetes complications, Endometriosis, Major depressive disorder, Oligodendroglioma, Prostatic neoplasms, Psychotic disorders, Stroke, Tietz syndrome

55
ATP binding cassette subfamily C member 5
ABC33, EST277145, MOAT-C, MOATC, MRP5, SMRP, pABC11
Rheumatoid arthritis, Bone remodeling disease, Clonal hematopoiesis, Colorectal neoplasms, Liver cirrhosis, Metabolic syndrome, Diabetes mellitus type 2

56
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 neoplasms, Coronary artery disease, Cutis laxa, Myocardial ischemia, Nephrolithiasis, Optic atrophy, Retinitis pigmentosa, Urolithiasis

57
ATP binding cassette subfamily C member 8
ABC36, HHF1, HI, HRINS, MODY12, MRP8, PHHI, PNDM3, SUR, SUR1, SUR1delta2, TNDM2
Atrial septal defect, Hyperinsulinism, Colorectal neoplasms, Congenital hyperinsulinism, Congenital retrognathism, Congestive heart failure, Dend syndrome, Diabetes mellitus, Diabetes mellitus type 1, Diabetes mellitus type 2, Diabetes mellitus permanent neonatal, Diabetes mellitus transient neonatal, Diazoxide-resistant focal hyperinsulinism due to sulfonylurea receptor 1 deficiency, Diazoxide-resistant focal hyperinsulinism due to sur1 deficiency, Gout
View all (8 more)

58
ATP binding cassette subfamily C member 9
ABC37, ATFB12, CANTU, CMD1O, IDMYS, SUR2
Acromegaloid facial appearance syndrome, Arrhythmogenic right ventricular cardiomyopathy, Atrial fibrillation, Brugada syndrome, Cantu syndrome, Cardiomyopathy, Dilated cardiomyopathy, Congenital epicanthus, Desbuquois syndrome, Endometrial neoplasms, Endometriosis, Epilepsy, Gout, Hereditary atrial fibrillation, Hypertrichosis
View all (11 more)

59
ATP binding cassette subfamily D member 1
ABC42, ALD, ALDP, AMN
Adrenoleukodystrophy, Bipolar disorder, Congenital neurologic anomalies, Deafness, dystonia, and cerebral hypomyelination, Ehlers-danlos syndrome, Encephalitis, Hirschsprung disease, Intellectual developmental disorder, Major depressive disorder, Myocarditis, Peroxisome biogenesis disorder, Schizophrenia, Spastic paraplegia, Hereditary spastic paraplegia, Spondyloepimetaphyseal dysplasia
View all (1 more)

60
ATP binding cassette subfamily D member 2
ABC39, ALDL1, ALDR, ALDRP, hALDR
Alzheimer disease, Colorectal neoplasms