Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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1311 to 1320 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1311
BEN domain containing 6
C6orf65
Dementia, Psoriasis

1312
BEN domain containing 7
C10orf30
Attention deficit hyperactivity disorder, Color vision deficiency, Insomnia, Schizophrenia, Substance abuse, Diabetes mellitus type 2

1313
Bestrophin 1
ARB, BEST, BMD, Best1V1Delta2, RP50, TU15B, VMD2
Distal myopathy, Vitreoretinochoroidopathy, Bestrophinopathy, Iron overload, Macular degeneration, Macular dystrophy, Nanophthalmos, Neurodegeneration with brain iron accumulation, Retinal cone dystrophy, Retinitis pigmentosa, Rod-cone dystrophy, Stargardt disease, Vitelliform macular dystrophy

1314
Bestrophin 2
VMD2L1
Neoplasms

1315
Bestrophin 3
VMD2L3
Atrial fibrillation, Orofacial cleft, Psychiatric disorders, Scoliosis

1316
Bet1 golgi vesicular membrane trafficking protein
HBET1, MDRP
Breast cancer, Cancer

1317
Bet1 golgi vesicular membrane trafficking protein like
BET1L1, GOLIM3, GS15, HSPC197
Aortic stenosis, Benign prostatic hyperplasia, Brain aneurysm, Cataract, Coronary artery disease, Lipoma, Uterine benign neoplasm, Uterine fibroid

1318
Brain expressed X-linked 4
BEXL1
Cholelithiasis

1319
Bifunctional apoptosis regulator
BAR, RNF47
Scoliosis

1320
Beaded filament structural protein 1
CP115, CP94, CTRCT33, LIFL-H
Cataract, Congenital cataract, Congenital ocular coloboma, Nuclear cataract, Sleep apnea, Sleep disorder