DEL17P13.1
Chromosome 17p13.1 deletion syndrome is a protein in humans that is encoded by the DEL17P13.1 gene. [2]
DEL17P13.1 | |||||||
---|---|---|---|---|---|---|---|
Identifiers | |||||||
Aliases | C17DELp13.1Chromosome 17p13.1 deletion syndrome | ||||||
External IDs | GeneCards: | ||||||
Orthologs | |||||||
Species | Human | Mouse | |||||
Entrez |
| ||||||
Ensembl |
|
| |||||
UniProt |
|
| |||||
RefSeq (mRNA) |
|
| |||||
RefSeq (protein) |
|
| |||||
Location (UCSC) | n/a | n/a | |||||
PubMed search | [1] | n/a | |||||
Wikidata | |||||||
|
References
- "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- "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.