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 | ||||||
| |||||||
Related gene problems
editReferences
edit- ^ "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.
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