DEL17P13.1

DEL17P13.1
Identifiers
AliasesC17DELp13.1Chromosome 17p13.1 deletion syndrome
External IDsGeneCards:
Orthologs
SpeciesHumanMouse
Entrez

100653374

n/a

Ensembl

n/a

n/a

UniProt

n/a

n/a

RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)n/an/a
PubMed search[1]n/a
Wikidata
View/Edit Human

Chromosome 17p13.1 deletion syndrome is a protein in humans that is encoded by the DEL17P13.1 gene. [2]

References

  1. ↑ "Human PubMed Reference:".
  2. ↑ "Entrez Gene: Chromosome 17p13.1 deletion syndrome". Retrieved 2012-12-09.


This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.