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C6orf89

From Wikipedia, the free encyclopedia
C6orf89
Identifiers
AliasesC6orf89, BRAP, chromosome 6 open reading frame 89, PS1TP5TP1
External IDsOMIM: 616642; MGI: 2136782; HomoloGene: 12728; GeneCards: C6orf89; OMA:C6orf89 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001286635
NM_001286636
NM_001286637
NM_152734

NM_030561

RefSeq (protein)

NP_001273564
NP_001273565
NP_001273566
NP_689947
NP_001273564.1

NP_085038

Location (UCSC)Chr 6: 36.87 – 36.93 MbChr 17: 29.27 – 29.31 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Uncharacterized protein C6orf89 is a protein that in humans is encoded by the C6orf89 gene.[5]

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000198663Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000052712Ensembl, 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: C6orf89 chromosome 6 open reading frame 89".
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Further reading

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