Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "B"

131 to 140 of 258 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
131	581	BAX	BCL2 associated X, apoptosis regulator	BCL2L4	Alzheimer disease, Asthma, Ataxia telangiectasia, Breast neoplasm, Cerebral hemorrhage, Colonic neoplasm, Colorectal cancer, Colorectal neoplasm, Experimental diabetes, Diabetes mellitus type 2, Esophageal neoplasm, Human immunodeficiency virus infection, Male infertility, Intestinal neoplasm, Kidney failure View all (4 more)
132	582	BBS1	Bardet-Biedl syndrome 1	BBS2L2	Bardet-biedl syndrome, Ciliopathies, Insomnia, Retinitis pigmentosa, Usher syndrome
133	583	BBS2	Bardet-Biedl syndrome 2	BBS, RP74	Retinitis pigmentosa, Bardet-biedl syndrome, Breast cancer, Ciliopathies, Hearing loss, Insomnia, Metabolic syndrome, Obesity, Diabetes mellitus, type 2
134	585	BBS4	Bardet-Biedl syndrome 4	-	Bardet-biedl syndrome, Ciliopathies, Major depressive disorder, Obesity, Retinitis pigmentosa, Diabetes mellitus, type 2
135	586	BCAT1	Branched chain amino acid transaminase 1	BCATC, BCT1, ECA39, MECA39, PNAS121, PP18	Breast cancer, Cholelithiasis, Color vision deficiency
136	587	BCAT2	Branched chain amino acid transaminase 2	BCAM, BCATM, BCT2, HVLI, PP18	Hypervalinemia, Maple syrup urine disease, Scoliosis
137	590	BCHE	Butyrylcholinesterase	BCHED, CHE1, CHE2, E1	Alzheimer disease, Apnea, Astrocytoma, Autism, Bipolar disorder, Breast neoplasm, Bves-related limb-girdle muscular dystrophy, Renal cell carcinoma, Cardiovascular disease, Ischemic heart disease, Obstructive pulmonary disease, Cognition disorder, Coronary artery disease, Coronary restenosis, Butyrylcholinesterase deficiency View all (19 more)
138	593	BCKDHA	Branched chain keto acid dehydrogenase E1 subunit alpha	BCKDE1A, MSU, MSUD1, MSUD1A, OVD1A	Androgenetic alopecia, Intellectual developmental disorder, Maple syrup urine disease
139	594	BCKDHB	Branched chain keto acid dehydrogenase E1 subunit beta	BCKDE1B, BCKDH E1-beta, E1B, MSUD1B, OVD1B	Amblyopia, Color vision deficiency, Maple syrup urine disease, Nonalcoholic fatty liver disease, Severe acute respiratory syndrome, Diabetes mellitus, type 2
140	596	BCL2	BCL2 apoptosis regulator	Bcl-2, PPP1R50	Alzheimer disease, Androgenetic alopecia, Asthma, Autism, Azoospermia, Benign neoplasm, Bipolar disorder, Breast cancer, Breast neoplasm, Carcinoma, Cerebral hemorrhage, Chondrosarcoma, Lymphocytic leukemia, Colonic neoplasm, Colorectal neoplasm View all (47 more)

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