CHMP2B
protein-coding gene in the species Homo sapiens
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Summary
CHMP2B is a gene[1]. CHMP2B is known by 9 alternative names across languages and contexts.[2]
Key Facts
- Subclass of: protein-coding gene[3]
- HomoloGene ID: 8534[4]
- Genomic start: 87227271[5], 87276421[6]
- Genomic end: 87304698[7], 87255556[8]
- Ortholog: Chmp2b[9], chmp2bb[10], C01A2.4[11]
- Encodes: Charged multivesicular body protein 2B[12]
- Found in taxon: Homo sapiens[13]
- Chromosome: human chromosome 3[14]
- Genetic association: amyotrophic lateral sclerosis type 17[15]
- Strand orientation: forward strand[16]
- Exact match: http://identifiers.org/ncbigene/25978[17]
- Cytogenetic location: 3p11.2[18]
- Expressed in: internal globus pallidus[19], amniotic fluid[20], mucosa of sigmoid colon[21], jejunal mucosa[22], palpebral conjunctiva[23], pons[24], oocyte[25], secondary oocyte[26], subthalamic nucleus[27], germinal epithelium[28]