Biology:DEL17P13.1

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Short description: Protein-coding gene in humans


A representation of the 3D structure of the protein myoglobin showing turquoise α-helices.
Generic protein structure example

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

References

  1. ↑ "Entrez Gene: Chromosome 17p13.1 deletion syndrome". https://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=retrieve&list_uids=100653374. 
  2. ↑ "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. November 2014. doi:10.1016/j.ajhg.2014.10.006. PMID 25439725. 



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