Homo sapiens Gene: LHX8 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Gene | IDBG-99751.6 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | LHX8 | ||||||||||||||||||
Gene Name | LIM homeobox 8 | ||||||||||||||||||
Synonyms | |||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Gene | ENSG00000162624 | ||||||||||||||||||
Encoded Proteins |
LIM homeobox 8
LIM homeobox 8
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Protein Structure | |||||||||||||||||||
Useful resources | Stemformatics EHFPI ImmGen | ||||||||||||||||||
Entrez Gene | |||||||||||||||||||
Summary |
The protein encoded by this gene is a member of the LIM homeobox family of proteins, which are involved in patterning and differentiation of various tissue types. These proteins contain two tandemly repeated cysteine-rich double-zinc finger motifs known as LIM domains, in addition to a DNA-binding homeodomain. This family member is a transcription factor that plays a role in tooth morphogenesis. It is also involved in oogenesis and in neuronal differentiation. This gene is a candidate gene for cleft palate, and it is also associated with odontoma formation. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2012] |
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Gene Information | |||||||||||||||||||
Type | Protein coding | ||||||||||||||||||
Genomic Location | Chromosome 1:75128434-75161533 | ||||||||||||||||||
Strand | Forward strand | ||||||||||||||||||
Band | p31.1 | ||||||||||||||||||
Transcripts |
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Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||||||||||||
Species
Bos taurus
Mus musculus
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Gene ID
Gene Order
Not yet available
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Cross-References | |||||||||||||||||||
SwissProt | Q68G74 | ||||||||||||||||||
TrEMBL | Q6SV70 Q9BYB7 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 431707 | ||||||||||||||||||
UniGene | Hs.403934 Hs.629356 | ||||||||||||||||||
RefSeq | NM_001001933 NM_001256114 | ||||||||||||||||||
HUGO | HGNC:28838 | ||||||||||||||||||
OMIM | 604425 | ||||||||||||||||||
CCDS | CCDS30756 CCDS58008 | ||||||||||||||||||
HPRD | |||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AB050476 AC099786 AY449522 AY449523 BC040321 | ||||||||||||||||||
GenPept | AAH40321 AAR18075 BAB40306 | ||||||||||||||||||
RNA Seq Atlas | 431707 | ||||||||||||||||||