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. This gene is fused to a high-mobility group gene in a translocation-associated lipoma. Mutations in another LHFP-like gene result in deafness in humans and mice. Alternatively spliced transcript variants have been found; however, their full-length nature is not known. [provided by RefSeq, Jul 2008]
Similarity:
Belongs to the LHFP family.
SWISS:
Q9Y693
Gene ID:
10186
Database links:
Entrez Gene: 10186 Human
Entrez Gene: 108927 Mouse
Entrez Gene: 499615 Rat
Omim: 606710 Human
SwissProt: Q9Y693 Human
SwissProt: Q8BM86 Mouse
SwissProt: Q5BJS2 Rat
Unigene: 507798 Human
Unigene: 118617 Mouse
Unigene: 6635 Rat
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