PCSK7

Source: Wikipedia, the free encyclopedia.
PCSK7
Identifiers
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Ensembl
UniProt
RefSeq (mRNA)

NM_004716

NM_001281934
NM_008794

RefSeq (protein)

NP_004707

NP_001268863
NP_032820

Location (UCSC)Chr 11: 117.2 – 117.23 MbChr 9: 45.82 – 45.84 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Proprotein convertase subtilisin/kexin type 7 is an enzyme that in humans is encoded by the PCSK7 gene.[5][6][7]

The protein encoded by this gene belongs to the

gp160
and gp140.

This gene has been implicated in the transcriptional regulation of housekeeping genes. Multiple alternatively spliced transcripts are described for this gene but their full length nature is not yet known. Downstream of this gene's map location at 11q23-q24,

nucleotides that match part of this gene's 3' end are duplicated and inverted. A translocation breakpoint associated with lymphoma occurs between this gene and its inverted counterpart.[7]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000160613Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000035382Ensembl, 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. PMID 8615762
    .
  6. .
  7. ^ a b "Entrez Gene: PCSK7 proprotein convertase subtilisin/kexin type 7".

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Further reading

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