Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
1311 to 1320 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1311
Bet1 golgi vesicular membrane trafficking protein
HBET1, MDRP
Breast cancer, Cancer

1312
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

1313
Brain expressed X-linked 4
BEXL1
Cholelithiasis

1314
Bifunctional apoptosis regulator
BAR, RNF47
Scoliosis

1315
Beaded filament structural protein 1
CP115, CP94, CTRCT33, LIFL-H
Cataract, Congenital cataract, Congenital ocular coloboma, Nuclear cataract, Sleep apnea, Sleep disorder

1316
Beaded filament structural protein 2
CP47, CP49, CTRCT12, LIFL-L, PHAKOSIN
Alzheimer disease, Cataract, Congenital cataract, Lamellar cataract, Non-syndromic cataract, Sutural cataract, Global developmental delay, Intellectual developmental disorder, Nystagmus, Strabismus

1317
Bone gamma-carboxyglutamate protein
BGP, OC, OCN
Asthma, Calcinosis, Heart valve disease, Heart valve prolapse, Nephrolithiasis, Osteoporosis, Prostatic neoplasms, Rheumatoid arthritis, Vitamin k deficiency

1318
Biglycan
DSPG1, MRLS, PG-S1, PGI, SEMDX, SLRR1A
Androgenetic alopecia, Rheumatoid arthritis, Breast neoplasms, Congenital contractural arachnodactyly, Desbuquois syndrome, Thoracic aortic aneurysm and aortic dissection, Marfan syndrome, Spondyloepimetaphyseal dysplasia, X-linked thoracic aortic aneurysm, X-linked spondyloepimetaphyseal dysplasia

1319
Basic helix-loop-helix family member a9
BHLHF42, CCSPD
Camptosynpolydactyly, Desbuquois syndrome, Gollop-wolfgang complex, Split hand-foot malformation, Syndactyly

1320
Basic helix-loop-helix family member e22
BHLHB5, Beta3, Beta3a, CAGL85, TNRC20
Attention deficit hyperactivity disorder