CHMP2B
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 3[13]
- Cytogenetic location
- 3p11.2[16]
- Expressed in
- internal globus pallidus, amniotic fluid, mucosa of sigmoid colon, jejunal mucosa, palpebral conjunctiva, pons, oocyte, secondary oocyte, subthalamic nucleus, germinal epithelium[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- amyotrophic lateral sclerosis type 17[14]
- HomoloGene ID
- 8534[3]
- Strand orientation
- forward strand[15]
🏷️ Also known as
en VPS2B
en ALS17
en charged multivesicular body protein 2B
en CHMP2.5
en CHMP2B
en DMT1
en FTDALS7
en VPS2-2
ar CHMP٢B
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000083937
- Ensembl transcript ID
- ENST00000494980, ENST00000263780, ENST00000466696, ENST00000471660, ENST00000472024, ENST00000676705, ENST00000676947, ENST00000677929, ENST00000678818, ENST00000678859
- Entrez Gene ID
- 25978
- Exact match
- identifiers.org
- Freebase ID
- /m/03gx6s3
- HGNC ID
- 24537
- HGNC gene symbol
- CHMP2B
- OMIM ID
- 609512
- RefSeq RNA ID
- XM_011533576, NM_001244644, NM_014043
- UMLS CUI
- C1538456
🔗 Connections
Expressed in 5
← Genetic association 2
Chromosome 1
Found in taxon 1
Instance of 1
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Summary
CHMP2B is a gene[1].