Genes?

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?All genes including those with curated and unreviewed disease associations.
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41 to 50 of 15388 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

41
ATP binding cassette subfamily B member 11
ABC16, BRIC2, BSEP, PFIC-2, PFIC2, PGY4, SPGP
Benign recurrent intrahepatic cholestasis, Cholelithiasis, Colorectal neoplasms, Gout, Intrahepatic cholestasis, Intrahepatic cholestasis of pregnancy, Liver cirrhosis, Liver disease, Metabolic syndrome, Progressive intrahepatic cholestasis, Pruritus

42
ATP binding cassette subfamily B member 4
ABC21, GBD1, ICP3, MDR2, MDR2/3, MDR3, PFIC-3, PGY3
Biliary cirrhosis, Hepatocellular carcinoma, Cholangitis, Cholecystolithiasis, Cholelithiasis, Colorectal neoplasms, Gallbladder disease, Gallbladder neoplasms, Gallstones, Gastrointestinal disease, Intrahepatic cholestasis, Intrahepatic cholestasis of pregnancy, Liver cirrhosis, Liver disease, Nonalcoholic fatty liver disease
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43
ATP binding cassette subfamily B member 5
ABCB5alpha, ABCB5beta, EST422562
Colorectal neoplasms, Dental caries, Melanoma, Metabolic syndrome, Diabetes mellitus type 2

44
ATP binding cassette subfamily B member 6 (LAN blood group)
ABC, LAN, MTABC3, PRP, umat
Cleft eyelid, Coloboma, Colobomatous microphthalmia, Colorectal neoplasms, Congenital iris coloboma, Dyschromatosis symmetrica hereditaria, Microphthalmia, Microphthalmos, Polycystic ovary syndrome, Retinitis pigmentosa, Thyroid neoplasms, microphthalmia, isolated, with coloboma 7

45
ATP binding cassette subfamily B member 7
ABC7, ASAT, Atm1p, EST140535
Sideroblastic anemia, Ataxia, Mitochondrial disease, Spinocerebellar ataxia, x-linked, X-linked sideroblastic anemia

46
ATP binding cassette subfamily B member 8
EST328128, M-ABC1, MABC1, MITOSUR
Thyroid neoplasms

47
ATP binding cassette subfamily B member 9
EST122234, TAPL
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Insomnia, Osteoarthritis, Diabetes mellitus type 2, Venous thromboembolism

48
ATP binding cassette subfamily C member 1 (ABCC1 blood group)
ABC29, ABCC, DFNA77, GS-X, MRP, MRP1
Isolated sensorineural deafness, Nonsyndromic hearing loss, Breast neoplasms, Obstructive airway disease, Colorectal neoplasms, Deafness, Hearing loss, Heart disease, Hypertension, Non-neoplastic peripheral nervous system disease, Oligodendroglioma, Peripheral nervous system disease, Peripheral neuropathy, Psychiatric disorders, Squamous cell carcinoma
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49
ATP binding cassette subfamily C member 10
EST182763, MRP7, SIMRP7
Atrial fibrillation, Autism, Cardiovascular disease, Clonal hematopoiesis, Coronary artery disease, Hypertension, Heart failure, Idiopathic pulmonary fibrosis, Kidney failure, Schizophrenia, Skin neoplasms, Thyroid neoplasms

50
ATP binding cassette subfamily C member 11
EWWD, MRP8, WW
Breast neoplasms, Breast fibrocystic disease