Homo sapiens Gene: LHFPL4
Summary
InnateDB Gene IDBG-15368.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol LHFPL4
Gene Name lipoma HMGIC fusion partner-like 4
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000156959
Encoded Proteins
lipoma HMGIC fusion partner-like 4
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. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 3:9498361-9553802
Strand Reverse strand
Band p25.3
Transcripts
ENST00000287585 ENSP00000287585
ENST00000495730
ENST00000498277
Interactions
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
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.56782
RefSeq NM_198560
HUGO
OMIM
CCDS CCDS33691
HPRD 17361
IMGT
EMBL
GenPept
RNA Seq Atlas