LIX1L From Wikipedia, the free encyclopedia Protein SymbolLIX1LNCBI gene128077HGNC28715RefSeqNM_153713Lix1 homolog (mouse)-likeIdentifiersSymbolLIX1LNCBI gene128077HGNC28715RefSeqNM_153713UniProtQ8IVB5Other dataLocusChr. 1 q21.1Search forStructuresSwiss-modelDomainsInterPro Lix1 homolog (mouse)-like also known as LIX1L is a protein which in humans is encoded by the LIX1L gene.[1][2] TAR syndrome[3] 1q21.1 deletion syndrome 1q21.1 duplication syndrome References ↑ "Entrez Gene: LIX1L Lix1 homolog (mouse)-like". ↑ Strausberg RL, Feingold EA, Grouse LH, et al. (December 2002). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932. ↑ 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
