LIX1L explained

Lix1 homolog (mouse)-like
Hgncid:	28715
Symbol:	LIX1L
Entrezgene:	128077
Refseq:	NM_153713
Uniprot:	Q8IVB5
Chromosome:	1
Arm:	q
Band:	21.1

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

Related gene problems

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

Notes and References

1. Web site: Entrez Gene: LIX1L Lix1 homolog (mouse)-like .
2. Strausberg RL, Feingold EA, Grouse LH, etal . 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 . December 2002 . 12477932 . 139241 . 10.1073/pnas.242603899 . 2002PNAS...9916899M . free .
3. Klopocki E, Schulze H, Strauss G, etal . Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome . Am. J. Hum. Genet. . 80 . 2 . 232–40 . February 2007 . 17236129 . 1785342 . 10.1086/510919 .