Homo sapiens Gene: LHFPL3
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
Species Homo sapiens
Ensembl Gene ENSG00000187416
Encoded Proteins
lipoma HMGIC fusion partner-like 3
lipoma HMGIC fusion partner-like 3
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]
Gene Information
Type Protein coding
Genomic Location Chromosome 7:104328656-104907232
Strand Forward strand
Band q22.2
ENST00000401970 ENSP00000385374
ENST00000424859 ENSP00000393128
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
Cellular Component
GO:0016021 integral component of membrane
No orthologs found for this gene
SwissProt Q86UP9
TrEMBL A1L384 C9JA52
UniProt Splice Variant
Entrez Gene 375612
UniGene Hs.659164
RefSeq NM_199000 XM_005250327 XM_005250329
OMIM 609719
EMBL AC000117 AC002432 AC007384 AC007558 AC079796 AC091286 AK299759 AY260763 BC129937 BC129938 BC129941 CH236947
GenPept AAI29938 AAI29939 AAI29942 AAP14954 BAG61648 EAL24407
RNA Seq Atlas 375612