DEL17P13.1
DEL17P13.1 | |||||||
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Identifiers | |||||||
Aliases | C17DELp13.1Chromosome 17p13.1 deletion syndrome | ||||||
External IDs | GeneCards: | ||||||
Orthologs | |||||||
Species | Human | Mouse | |||||
Entrez |
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Ensembl |
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UniProt |
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RefSeq (mRNA) |
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RefSeq (protein) |
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Location (UCSC) | n/a | n/a | |||||
PubMed search | [1] | n/a | |||||
Wikidata | |||||||
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Chromosome 17p13.1 deletion syndrome is a protein in humans that is encoded by the DEL17P13.1 gene. [2]
References
- ↑ "Human PubMed Reference:".
- ↑ "Entrez Gene: Chromosome 17p13.1 deletion syndrome". Retrieved 2012-12-09.
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