ANKRD35

Ankyrin repeat domain 35 also known as ANKRD35 is a protein which in humans is encoded by the ANKRD35 gene.[1]

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

Related gene problems

• TAR syndrome[2]
• 1q21.1 deletion syndrome
• 1q21.1 duplication syndrome

References

1. "Entrez Gene: ANKRD35 ankyrin repeat domain 35".
2. 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. PMC 1785342. PMID 17236129.