Homo sapiens Gene: LHFPL1
Summary
InnateDB Gene IDBG-82864.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol LHFPL1
Gene Name lipoma HMGIC fusion partner-like 1
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000182508
Encoded Proteins
lipoma HMGIC fusion partner-like 1
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 X:112630648-112680054
Strand Reverse strand
Band q23
Transcripts
ENST00000371968 ENSP00000361036
ENST00000478229
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.297420
RefSeq NM_178175 XM_005262128
HUGO
OMIM
CCDS CCDS14562
HPRD 06610
IMGT
EMBL
GenPept
RNA Seq Atlas