ANKRD35 From Wikipedia, the free encyclopedia Mammalian protein found in Homo sapiens SymbolANKRD35NCBI gene148741HGNC26323RefSeqNM_144698ankyrin repeat domain 35IdentifiersSymbolANKRD35NCBI gene148741HGNC26323RefSeqNM_144698UniProtQ8N283Other dataLocusChr. 1 q21.1Search forStructuresSwiss-modelDomainsInterPro Ankyrin repeat domain 35 also known as ANKRD35 is a protein which in humans is encoded by the ANKRD35 gene.[1] TAR syndrome[2] 1q21.1 deletion syndrome 1q21.1 duplication syndrome References ↑ "Entrez Gene: ANKRD35 ankyrin repeat domain 35". ↑ 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. This article on a gene on human chromosome 1 is a stub. You can help Wikipedia by expanding it.vte Related Articles
