Homo sapiens Gene: LHFPL3 | |||||
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Summary | |||||
InnateDB Gene | IDBG-34720.6 | ||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||
Gene Symbol | LHFPL3 | ||||
Gene Name | lipoma HMGIC fusion partner-like 3 | ||||
Synonyms | |||||
Species | Homo sapiens | ||||
Ensembl Gene | ENSG00000187416 | ||||
Encoded Proteins |
lipoma HMGIC fusion partner-like 3
lipoma HMGIC fusion partner-like 3
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Protein Structure | |||||
Useful resources | Stemformatics EHFPI ImmGen | ||||
Entrez Gene | |||||
Summary |
This gene is a member of the lipoma HMGIC fusion partner (LHFP) gene family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. Mutations in one LHFP-like gene result in deafness in humans and mice, and a second LHFP-like gene is fused to a high-mobility group gene in a translocation-associated lipoma. A partial gene fragment named LHFPL4 corresponds to a portion of the first exon of this gene. [provided by RefSeq, Jul 2008] |
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Gene Information | |||||
Type | Protein coding | ||||
Genomic Location | Chromosome 7:104328656-104907232 | ||||
Strand | Forward strand | ||||
Band | q22.2 | ||||
Transcripts |
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Interactions | |||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 0 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 | |||||
No orthologs found for this gene | |||||
Cross-References | |||||
SwissProt | Q86UP9 | ||||
TrEMBL | A1L384 C9JA52 | ||||
UniProt Splice Variant | |||||
Entrez Gene | 375612 | ||||
UniGene | Hs.659164 | ||||
RefSeq | NM_199000 XM_005250327 XM_005250329 | ||||
HUGO | HGNC:6589 | ||||
OMIM | 609719 | ||||
CCDS | |||||
HPRD | |||||
IMGT | |||||
EMBL | AC000117 AC002432 AC007384 AC007558 AC079796 AC091286 AK299759 AY260763 BC129937 BC129938 BC129941 CH236947 | ||||
GenPept | AAI29938 AAI29939 AAI29942 AAP14954 BAG61648 EAL24407 | ||||
RNA Seq Atlas | 375612 | ||||