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CAPRIN2

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CAPRIN2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesCAPRIN2, C1QDC1, EEG-1, EEG1, RNG140, caprin family member 2
External IDsOMIM: 610375; MGI: 2448541; HomoloGene: 11393; GeneCards: CAPRIN2; OMA:CAPRIN2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001301351
NM_181541

RefSeq (protein)

NP_001288280
NP_853519

Location (UCSC)Chr 12: 30.71 – 30.75 MbChr 6: 148.74 – 148.8 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

caprin family member 2, also known as CAPRIN2, is a human gene.[5]

The protein encoded by this gene may be involved in the transitioning of erythroblasts from a highly proliferative state to a terminal phase of differentiation. High level expression of the encoded protein can lead to apoptosis. Several transcript variants encoding different isoforms have been found for this gene.[5]

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000110888Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000030309Ensembl, 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. ^ a b "Entrez Gene: caprin family member 2". Retrieved 2011-08-30.
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Further reading

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