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HEPACAM2

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Protein-coding gene in the species Homo sapiens
HEPACAM2
Identifiers
AliasesHEPACAM2, MIKI, HEPACAM family member 2
External IDsOMIM: 614133; MGI: 2141520; HomoloGene: 18724; GeneCards: HEPACAM2; OMA:HEPACAM2 - orthologs
Gene location (Human)
Chromosome 7 (human)
Chr.Chromosome 7 (human)
Chromosome 7 (human)Genomic location for HEPACAM2Genomic location for HEPACAM2
Band7q21.2Start93,188,534 bp
End93,226,469 bp
Gene location (Mouse)
Chromosome 6 (mouse)
Chr.Chromosome 6 (mouse)
Chromosome 6 (mouse)Genomic location for HEPACAM2Genomic location for HEPACAM2
Band6|6 A1Start3,457,096 bp
End3,498,298 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • mucosa of ileum

  • mucosa of sigmoid colon

  • rectum

  • islet of Langerhans

  • palpebral conjunctiva

  • mucosa of transverse colon

  • jejunal mucosa

  • testicle

  • duodenum

  • human kidney
Top expressed in
  • islet of Langerhans

  • left colon

  • crypt of lieberkuhn of small intestine

  • ileum

  • jejunum

  • duodenum

  • intestinal villus

  • Paneth cell

  • right kidney

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

253012

101202

Ensembl

ENSG00000188175

ENSMUSG00000044156

UniProt

A8MVW5

Q4VAH7

RefSeq (mRNA)

NM_001039372
NM_001288804
NM_001288810
NM_198151
NM_001346642

NM_178899

RefSeq (protein)

NP_001034461
NP_001275733
NP_001275739
NP_001333571
NP_937794

NP_849230

Location (UCSC)Chr 7: 93.19 – 93.23 MbChr 6: 3.46 – 3.5 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

HEPACAM family member 2 is a protein that in humans is encoded by the HEPACAM2 gene.

Function

This gene encodes a protein related to the immunoglobulin superfamily that plays a role in mitosis. Knockdown of this gene results in prometaphase arrest, abnormal nuclear morphology, and apoptosis.

Poly (ADP-ribosylation) of the encoded protein promotes its translocation to centrosomes, which may stimulate centrosome maturation. A chromosomal deletion including this gene may be associated with myeloid leukemia and myelodysplastic syndrome in human patients.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000188175Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000044156Ensembl, 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: HEPACAM family member 2". Retrieved 2017-09-13.

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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