KCNMB2
protein-coding gene in the species Homo sapiens
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Summary
KCNMB2 is a gene[1]. KCNMB2 ranks in the top 2% of gene entities by monthly Wikipedia readership (24 views/month).[2]
Key Facts
- Subclass of: protein-coding gene[3]
- HomoloGene ID: 4257[4]
- Genomic start: 178272932[5], 177990720[6]
- Genomic end: 178844429[7], 178562217[8]
- Ortholog: Kcnmb2[9], si:ch211-247n2.1[10]
- Encodes: Potassium calcium-activated channel subfamily M regulatory beta subunit 2[11]
- Found in taxon: Homo sapiens[12]
- Chromosome: human chromosome 3[13]
- Genetic association: amyotrophic lateral sclerosis[14], bipolar disorder[15], schizophrenia[16], lymphoblastic leukemia[17]
- Strand orientation: forward strand[18]
- Exact match: http://identifiers.org/ncbigene/10242[19]
- Cytogenetic location: 3q26.32[20]
- Expressed in: islet of Langerhans[21], right uterine tube[22], testicle[23], bronchial epithelial cell[24], caput epididymis[25], corpus epididymis[26], cingulate gyrus[27], anterior cingulate cortex[28], prefrontal cortex[29], left ovary[30]