ANKRD35 Information & ANKRD35 Links at HealthHaven.com

ankyrin repeat domain 35
Identifiers
Symbol	ANKRD35
Entrez	148741
HUGO	26323
RefSeq	NM_144698
UniProt	Q8N283
Other data
Locus	Chr. 1 q21.1

Ankyrin repeat domain 35 also known as ANKRD35 is a protein which in humans is encoded by the ANKRD35 gene.^[1] Mutations in this gene are possibly linked to the TAR syndrome.^[2]

[edit] References

^ "Entrez Gene: ANKRD35 ankyrin repeat domain 35". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=148741.
^ Klopocki E, Schulze H, Strauss G, et al. (February 2007). "Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome". Am. J. Hum. Genet. 80 (2): 232–40. doi:10.1086/510919. PMID 17236129.

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[entrez-0] "Entrez Gene: ANKRD35 ankyrin repeat domain 35". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=148741.

[pmid17236129-1] Klopocki E, Schulze H, Strauss G, et al. (February 2007). "Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome". Am. J. Hum. Genet. 80 (2): 232–40. doi:10.1086/510919. PMID 17236129.

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