LIX1L

Lix1 homolog (mouse)-like also known as LIX1L is a protein which in humans is encoded by the LIX1L gene.[1][2]

Lix1 homolog (mouse)-like
Identifiers
Symbol	LIX1L
NCBI gene	128077
HGNC	28715
RefSeq	NM_153713
UniProt	Q8IVB5
Other data
Locus	Chr. 1 q21.1
Search for Structures Swiss-model Domains InterPro

Related gene problems

• TAR syndrome[3]
• 1q21.1 deletion syndrome
• 1q21.1 duplication syndrome

References

1. "Entrez Gene: LIX1L Lix1 homolog (mouse)-like".
2. 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.
3. 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.