background:
CCDC73 is a 1079 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding CCDC73 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
Database links:
Entrez Gene: 493860 Human
Omim: 612328 Human
SwissProt: Q6ZRK6 Human
Unigene: 701368 Human
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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