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 "B"
151 to 160 of 321 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

151
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

152
Bone gamma-carboxyglutamate protein
BGP, OC, OCN
Asthma, Calcinosis, Heart valve disease, Heart valve prolapse, Nephrolithiasis, Osteoporosis, Prostatic neoplasms, Rheumatoid arthritis, Vitamin k deficiency

153
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, Liver cirrhosis, Marfan syndrome, Spondyloepimetaphyseal dysplasia, X-linked thoracic aortic aneurysm, X-linked spondyloepimetaphyseal dysplasia

154
Basic helix-loop-helix family member a9
BHLHF42, CCSPD
Camptosynpolydactyly, Desbuquois syndrome, Gollop-wolfgang complex, Split hand-foot malformation, Syndactyly

155
Basic helix-loop-helix family member e22
BHLHB5, Beta3, Beta3a, CAGL85, TNRC20
Attention deficit hyperactivity disorder

156
Basic helix-loop-helix family member e40
BHLHB2, Clast5, DEC1, HLHB2, SHARP-2, SHARP2, STRA13, Stra14
Androgenetic alopecia, Eczema, Bipolar disorder, Bipolar depression, Glioblastoma, Hypothyroidism, Myocardial ischemia, Osteoarthritis, Psoriasis vulgaris, Schizophrenia, Sleep disorder

157
Basic helix-loop-helix family member e41
BHLHB3, DEC2, FNSS1, SHARP1, hDEC2
Bipolar disorder, Lung neoplasms, Major depressive disorder, Mood disorder, Diabetes mellitus type 2

158
Betaine--homocysteine S-methyltransferase
BHMT1, HEL-S-61p
Ischemic stroke, Obstructive pulmonary disease, Diabetes mellitus type 2, Gastric ulcer, Hepatolenticular degeneration, Neural tube defect, Neural tube defects, x-linked

159
Betaine--homocysteine S-methyltransferase 2
-
Cleft lip, Cleft palate, Complete unilateral cleft lip, Congenital heart defects

160
BicC family RNA binding protein 1
BICC
Polycystic kidney disease, Congenital anomalies of the kidney and urinary tract, Cardiovascular disease, Kidney disease, Colorectal cancer, Renal agenesis, Corneal astigmatism, Coronary artery disease, Major depressive disorder, Developmental disability, Eye disease, Glaucoma, Gout, Hypertension, Hyperuricemia
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