Genes | GeDiPNet - Gene Disease Pathway & Associations

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1321 to 1330 of 15448 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1321	8419	BFSP2	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
1322	632	BGLAP	Bone gamma-carboxyglutamate protein	BGP, OC, OCN	Asthma, Calcinosis, Heart valve disease, Heart valve prolapse, Nephrolithiasis, Osteoporosis, Prostatic neoplasms, Rheumatoid arthritis, Vitamin k deficiency
1323	633	BGN	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
1324	727857	BHLHA9	Basic helix-loop-helix family member a9	BHLHF42, CCSPD	Camptosynpolydactyly, Desbuquois syndrome, Gollop-wolfgang complex, Split hand-foot malformation, Syndactyly
1325	27319	BHLHE22	Basic helix-loop-helix family member e22	BHLHB5, Beta3, Beta3a, CAGL85, TNRC20	Attention deficit hyperactivity disorder
1326	8553	BHLHE40	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
1327	79365	BHLHE41	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
1328	635	BHMT	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
1329	23743	BHMT2	Betaine--homocysteine S-methyltransferase 2	-	Cleft lip, Cleft palate, Complete unilateral cleft lip, Congenital heart defects
1330	80114	BICC1	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 View all (8 more)

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