Genes | GeDiPNet - Gene Disease Pathway & Associations

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1291 to 1300 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1291	63035	BCORL1	BCL6 corepressor like 1	BCoR-L1, CXorf10, SHUVER	Adenoid cystic carcinoma, Global developmental delay, Intellectual developmental disorder, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Periodontitis, Shukla-vernon syndrome, Wilms tumor
1292	613	BCR	BCR activator of RhoGEF and GTPase	ALL, BCR1, CML, D22S11, D22S662, PHL	Bipolar disorder, Blast crisis, B-lymphoblastic leukemia/lymphoma, Myelogenous leukemia, Myeloid leukemia, Melanoma, Chromosome 22q11.2 microdeletion syndrome, Lymphoblastic leukemia, Major depressive disorder, Myeloproliferative disorder, Necrosis, Skin disease, Depression
1293	617	BCS1L	BCS1 ubiquinol-cytochrome c reductase complex chaperone	BCS, BCS1, BJS, FLNMS, GRACILE, Hs.6719, MC3DN1, PTD, h-BCS, h-BCS1	Bjornstad syndrome, Intellectual developmental disorder, Leigh syndrome, Mitochondrial complex deficiency, Movement disorder, Neuromuscular disease, Intellectual disability
1294	622	BDH1	3-hydroxybutyrate dehydrogenase 1	BDH, SDR9C1	Neurodevelopmental disorder
1295	623	BDKRB1	Bradykinin receptor B1	B1BKR, B1R, BKB1R, BKR1, BRADYB1	Temporal lobe epilepsy, Esophageal cancer, Gastric cancer, Hyperalgesia, Hypertension, Kidney failure, Pulmonary fibrosis, Splenomegaly, Vascular system injury
1296	624	BDKRB2	Bradykinin receptor B2	B2R, BK-2, BK2, BKR2, BRB2	Angioedema, Rheumatoid arthritis, Asthma, Bipolar disorder, Cardiomyopathy, Obstructive airway disease, Corneal astigmatism, Occupational dermatitis, Temporal lobe epilepsy, Extravasation of diagnostic and therapeutic materials, Gout, Hemorrhage, Hyperalgesia, Hyperemia, Hypertension View all (7 more)
1297	627	BDNF	Brain derived neurotrophic factor	ANON2, BULN2	Alzheimer disease, Amphetamine or sympathomimetic abuse, Asthma, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Body weight, Brain injuries, Brain ischemia, Cannabis abuse, Haddad syndrome, Color vision deficiency, Congenital central hypoventilation syndrome, Coronary artery disease, Deafness View all (35 more)
1298	55814	BDP1	BDP1 general transcription factor IIIB subunit	DFNB112, HSA238520, TAF3B1, TFC5, TFIIIB'', TFIIIB150, TFIIIB90, TFNR	Isolated sensorineural deafness, Deafness, Hearing impairment, Hearing loss, Obesity, Waardenburg syndrome
1299	146227	BEAN1	Brain expressed associated with NEDD4 1	BEAN, SCA31	Spinocerebellar ataxia
1300	8678	BECN1	Beclin 1	ATG6, VPS30, beclin1	Brain injuries, Colonic neoplasms, Lewy body disease, Lung neoplasms, Machado-joseph disease, Myocardial infarction, Schizophrenia, Status epilepticus, Diabetes mellitus type 2

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