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
Method
Confidence
Comments
SSD Ortholog
Ortholog supports species divergence
Not yet available
SSD Ortholog
Ortholog supports species divergence
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