CHMP1B

Charged multivesicular body protein 1b is a protein that in humans is encoded by the CHMP1B gene.[5][6]

CHMP1B
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesCHMP1B, C10orf2, C18-ORF2, C18orf2, CHMP1.5, Vps46-2, Vps46B, hVps46-2, charged multivesicular body protein 1B
External IDsOMIM: 606486 MGI: 1914314 HomoloGene: 41374 GeneCards: CHMP1B
Gene location (Human)
Chr.Chromosome 18 (human)[1]
Band18p11.21Start11,851,413 bp[1]
End11,854,444 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

57132

67064

Ensembl

ENSG00000255112

ENSMUSG00000109901

UniProt

Q7LBR1

Q99LU0

RefSeq (mRNA)

NM_020412

NM_024190

RefSeq (protein)

NP_065145

NP_077152

Location (UCSC)Chr 18: 11.85 – 11.85 MbChr 18: 67.21 – 67.21 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse


References

  1. GRCh38: Ensembl release 89: ENSG00000255112 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000109901 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Reid E, Connell J, Edwards TL, Duley S, Brown SE, Sanderson CM (Dec 2004). "The hereditary spastic paraplegia protein spastin interacts with the ESCRT-III complex-associated endosomal protein CHMP1B". Hum Mol Genet. 14 (1): 19–38. doi:10.1093/hmg/ddi003. PMID 15537668.
  6. "Entrez Gene: CHMP1B chromatin modifying protein 1B".

Further reading


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