LHX8 (LIM homeobox 8)

2014-11-01  

Identity

HGNC
LOCATION
1p31.1
LOCUSID
ALIAS
LHX7

Other Information

Locus ID:

NCBI: 431707
MIM: 604425
HGNC: 28838
Ensembl: ENSG00000162624

Variants:

dbSNP: 431707
ClinVar: 431707
TCGA: ENSG00000162624
COSMIC: LHX8

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000162624ENST00000294638Q68G74
ENSG00000162624ENST00000356261Q68G74

Expression (GTEx)

0
1
2
3
4

References

Pubmed IDYearTitleCitations
163278842005Medical sequencing of candidate genes for nonsyndromic cleft lip and palate.70
189786782008Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts.21
206348912010Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia.18
206723502010Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate.13
205728542010MTHFR and MSX1 contribute to the risk of nonsyndromic cleft lip/palate.7
224356492012Evaluation of the LIM homeobox genes LHX6 and LHX8 as candidates for Tourette syndrome.4
243164042014Upregulation of Lhx8 increase VAChT expression and ACh release in neuronal cell line SHSY5Y.2
166907452006Oogenesis requires germ cell-specific transcriptional regulators Sohlh1 and Lhx8.0
176243442008Analysis of LHX8 mutation in premature ovarian failure.0
176243442008Analysis of LHX8 mutation in premature ovarian failure.0

Citation

Dessen P

LHX8 (LIM homeobox 8)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/65257/lhx8