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PLEKHM2

From Wikipedia, the free encyclopedia
PLEKHM2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesPLEKHM2, SKIP, pleckstrin homology and RUN domain containing M2
External IDsOMIM: 609613; MGI: 1916832; HomoloGene: 19575; GeneCards: PLEKHM2; OMA:PLEKHM2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_015164

NM_001033150
NM_001347237

RefSeq (protein)

NP_055979

NP_001028322
NP_001334166

Location (UCSC)Chr 1: 15.68 – 15.73 MbChr 4: 141.35 – 141.39 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Pleckstrin homology domain-containing family M member 2 is a protein that in humans is encoded by the PLEKHM2 gene.[5]

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000116786Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000028917Ensembl, 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: pleckstrin homology domain containing, family M (with RUN domain) member 2". Retrieved 2011-08-30.

Further reading

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