LHX1
From Wikipedia, the free encyclopedia
LIM homeobox 1
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Identifiers | ||||||||||||||
Symbol(s) | LHX1; LIM-1; LIM1; MGC126723; MGC138141 | |||||||||||||
External IDs | OMIM: 601999 MGI: 99783 HomoloGene: 4068 | |||||||||||||
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RNA expression pattern | ||||||||||||||
Orthologs | ||||||||||||||
Human | Mouse | |||||||||||||
Entrez | 3975 | 16869 | ||||||||||||
Ensembl | ENSG00000132130 | ENSMUSG00000018698 | ||||||||||||
Uniprot | P48742 | Q3URX6 | ||||||||||||
Refseq | NM_005568 (mRNA) NP_005559 (protein) |
NM_008498 (mRNA) NP_032524 (protein) |
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Location | Chr 17: 32.37 - 32.37 Mb | Chr 11: 84.33 - 84.34 Mb | ||||||||||||
Pubmed search | [1] | [2] |
LIM homeobox 1, also known as LHX1, is a human gene.[1]
This gene encodes a member of a large protein family which contains the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein may function as a transcriptional regulator and be involved in control of differentiation and development of neural and lymphoid cells. A similar protein in mice is an essential regulator of the vertebrate head organizer.[1]
[edit] References
[edit] Further reading
- Shawlot W, Behringer RR (1995). "Requirement for Lim1 in head-organizer function.". Nature 374 (6521): 425-30. doi: . PMID 7700351.
- Bozzi F, Bertuzzi S, Strina D, et al. (1997). "The exon-intron structure of human LHX1 gene.". Biochem. Biophys. Res. Commun. 229 (2): 494-7. doi: . PMID 8954926.
- Dong WF, Heng HH, Lowsky R, et al. (1997). "Cloning, expression, and chromosomal localization to 11p12-13 of a human LIM/HOMEOBOX gene, hLim-1.". DNA Cell Biol. 16 (6): 671-8. PMID 9212161.
- Jurata LW, Pfaff SL, Gill GN (1998). "The nuclear LIM domain interactor NLI mediates homo- and heterodimerization of LIM domain transcription factors.". J. Biol. Chem. 273 (6): 3152-7. PMID 9452425.
- Ostendorff HP, Peirano RI, Peters MA, et al. (2002). "Ubiquitination-dependent cofactor exchange on LIM homeodomain transcription factors.". Nature 416 (6876): 99-103. doi: . PMID 11882901.
- Phillips JC (2003). "Assignment of LHX1 to human chromosome bands 17q11.2-->q12 by use of radiation hybrid mapping and somatic cell hybridization.". Cytogenet. Genome Res. 97 (1-2): 140D. doi: . PMID 12438757.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "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. doi: . PMID 12477932.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121-7. doi: . PMID 15489334.
- Zody MC, Garber M, Adams DJ, et al. (2006). "DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage.". Nature 440 (7087): 1045-9. doi: . PMID 16625196.