DEL17P13.1

Chromosome 17p13.1 deletion syndrome is a protein in humans that is encoded by the DEL17P13.1 gene.[2][3]

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

100653374

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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/an/a
PubMed search[1]n/a
Wikidata
View/Edit Human

References
  1. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  2. "Entrez Gene: Chromosome 17p13.1 deletion syndrome".
  3. Carvalho CM, Vasanth S, Shinawi M, Russell C, Ramocki MB, Brown CW, et al. (November 2014). "Dosage changes of a segment at 17p13.1 lead to intellectual disability and microcephaly as a result of complex genetic interaction of multiple genes". American Journal of Human Genetics. 95 (5): 565–78. doi:10.1016/j.ajhg.2014.10.006. PMC 4225592. PMID 25439725.
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