LHFP

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Lipoma HMGIC fusion partner
Identifiers
Symbols LHFP ; MGC22429
External IDs OMIM606710 MGI1920048 HomoloGene4223 GeneCards: LHFP Gene
EC number 3.6.5.4
RNA expression pattern
PBB GE LHFP 218656 s at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez 10186 108927
Ensembl ENSG00000183722 ENSMUSG00000048332
UniProt Q9Y693 Q8BM86
RefSeq (mRNA) NM_005780 NM_175386
RefSeq (protein) NP_005771 NP_780595
Location (UCSC) Chr 13:
39.92 – 40.18 Mb
Chr 3:
53.04 – 53.26 Mb
PubMed search [1] [2]

Lipoma HMGIC fusion partner is a protein that in humans is encoded by the LHFP gene.[1][2]

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 (LHFPL1, LHFPL2) result in deafness in humans and mice. Alternatively spliced transcript variants have been found; however, their full-length nature is not known.[2]

References[edit]

  1. ^ Petit MM, Schoenmakers EF, Huysmans C, Geurts JM, Mandahl N, Van de Ven WJ (Aug 1999). "LHFP, a novel translocation partner gene of HMGIC in a lipoma, is a member of a new family of LHFP-like genes". Genomics 57 (3): 438–41. doi:10.1006/geno.1999.5778. PMID 10329012. 
  2. ^ a b "Entrez Gene: LHFP lipoma HMGIC fusion partner". 

Further reading[edit]

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