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CAPRIN2

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Protein-coding gene in humans
CAPRIN2
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

4OUL, 4OUM

Identifiers
AliasesCAPRIN2, C1QDC1, EEG-1, EEG1, RNG140, caprin family member 2
External IDsOMIM: 610375; MGI: 2448541; HomoloGene: 11393; GeneCards: CAPRIN2; OMA:CAPRIN2 - orthologs
Gene location (Human)
Chromosome 12 (human)
Chr.Chromosome 12 (human)
Chromosome 12 (human)Genomic location for CAPRIN2Genomic location for CAPRIN2
Band12p11.21Start30,709,552 bp
End30,754,951 bp
Gene location (Mouse)
Chromosome 6 (mouse)
Chr.Chromosome 6 (mouse)
Chromosome 6 (mouse)Genomic location for CAPRIN2Genomic location for CAPRIN2
Band6|6 G3Start148,743,990 bp
End148,797,735 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • spinal ganglia

  • cerebellar vermis

  • right hemisphere of cerebellum

  • trigeminal ganglion

  • testicle

  • sural nerve

  • lateral nuclear group of thalamus

  • pars compacta

  • pars reticulata

  • external globus pallidus
Top expressed in
  • lens

  • epithelium of lens

  • zygote

  • primary oocyte

  • secondary oocyte

  • tail of embryo

  • neural layer of retina

  • lumbar spinal ganglion

  • supraoptic nucleus

  • paraventricular nucleus of hypothalamus
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

65981

232560

Ensembl

ENSG00000110888

ENSMUSG00000030309

UniProt

Q6IMN6

Q05A80

RefSeq (mRNA)
NM_001002259
NM_001206856
NM_023925
NM_032156
NM_001319842

NM_001319843
NM_001319844
NM_001319845
NM_001319846

NM_001301351
NM_181541

RefSeq (protein)
NP_001002259
NP_001193785
NP_001306771
NP_001306772
NP_001306773

NP_001306774
NP_001306775
NP_076414
NP_115532

NP_001288280
NP_853519

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

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

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.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000110888Ensembl, May 2017
  2. ^ 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. ^ "Entrez Gene: caprin family member 2". Retrieved 2011-08-30.

External links

Further reading

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