PWP2

Periodic tryptophan protein 2 homolog is a protein that in humans is encoded by the PWP2 gene.[3][4]

PWP2
Identifiers
AliasesPWP2, EHOC-17, PWP2H, UTP1, PWP2 periodic tryptophan protein homolog (yeast), small subunit processome component, PWP2 small subunit processome component
External IDsOMIM: 601475 HomoloGene: 136786 GeneCards: PWP2
Gene location (Human)
Chr.Chromosome 21 (human)[1]
Band21q22.3Start44,107,373 bp[1]
End44,131,181 bp[1]
RNA expression pattern
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez

5822

n/a

Ensembl

ENSG00000241945

n/a

UniProt

Q15269

n/a

RefSeq (mRNA)

NM_005049

n/a

RefSeq (protein)

NP_005040

n/a

Location (UCSC)Chr 21: 44.11 – 44.13 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human

References

  1. GRCh38: Ensembl release 89: ENSG00000241945 - Ensembl, May 2017
  2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. Yamakawa K, Gao DQ, Korenberg JR (Dec 1996). "A periodic tryptophan protein 2 gene homologue (PWP2H) in the candidate region of progressive myoclonus epilepsy on 21q22.3". Cytogenet Cell Genet. 74 (1–2): 140–5. doi:10.1159/000134402. PMID 8893822.
  4. "Entrez Gene: PWP2 PWP2 periodic tryptophan protein homolog (yeast)".

Further reading


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