Homo sapiens Gene: LHFPL2
Summary
InnateDB Gene IDBG-30649.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol LHFPL2
Gene Name lipoma HMGIC fusion partner-like 2
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000145685
Encoded Proteins
lipoma HMGIC fusion partner-like 2
lipoma HMGIC fusion partner-like 2
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. Alternatively spliced transcript variants have been found, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 5:78485215-78770021
Strand Reverse strand
Band q14.1
Transcripts
ENST00000380345 ENSP00000369702
ENST00000515007 ENSP00000425906
ENST00000502722
ENST00000503686
ENST00000512759
ENST00000510949
ENST00000515349
ENST00000514587
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003674 molecular_function
Biological Process
GO:0008150 biological_process
Cellular Component
GO:0005575 cellular_component
GO:0016021 integral component of membrane
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.670094 Hs.688005 Hs.689060 Hs.79299
RefSeq NM_005779 XM_006714515
HUGO
OMIM
CCDS CCDS4042
HPRD 17272
IMGT
EMBL
GenPept
RNA Seq Atlas