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PHF10

From Wikipedia, the free encyclopedia
PHF10
Identifiers
AliasesPHF10, BAF45A, XAP135, PHD finger protein 10, SMARCG4
External IDsOMIM: 613069; MGI: 1919307; HomoloGene: 10112; GeneCards: PHF10; OMA:PHF10 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_133325
NM_018288

NM_024250
NM_001360983

RefSeq (protein)

NP_060758
NP_579866

NP_077212
NP_001347912

Location (UCSC)Chr 6: 169.7 – 169.73 MbChr 17: 15.17 – 15.18 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

PHD finger protein 10 is a protein that in humans is encoded by the PHF10 gene.[5][6]

Function

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This gene contains a predicted ORF that encodes a protein with two zinc finger domains. The function of the encoded protein is not known. Sequence analysis suggests that multiple alternatively spliced transcript variants are derived from this gene but the full-length nature of only two of them is known. These two splice variants encode different isoforms. A pseudogene for this gene is located on Xq28.[6]

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000130024Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000023883Ensembl, 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. ^ Aradhya S, Woffendin H, Bonnen P, Heiss NS, Yamagata T, Esposito T, Bardaro T, Poustka A, D'Urso M, Kenwrick S, Nelson DL (January 2002). "Physical and genetic characterization reveals a pseudogene, an evolutionary junction, and unstable loci in distal Xq28". Genomics. 79 (1): 31–40. doi:10.1006/geno.2001.6680. PMID 11827455.
  6. ^ a b "Entrez Gene: PHF10 PHD finger protein 10".

Further reading

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