LHFPL5

GENE INFORMATION

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Gene name

LHFPL5 (HGNC Symbol)

Synonyms

DFNB67, dJ510O8.8, MGC33835, Tmhs

Description

Lipoma HMGIC fusion partner-like 5 (HGNC Symbol)

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 this gene result in deafness in humans, and a mutation in a similar gene in mice results in deafness and vestibular dysfunction with severe degeneration of the organ of Corti. It is proposed to function in hair bundle morphogenesis. [provided by RefSeq, Jul 2008]

Chromosome

6

Cytoband

p21.31

Chromosome location (bp)

35805293 - 35833874

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000197753 (version 78.38)

Entrez gene

222662

UniProt

Q8TAF8 (UniProt - Evidence at protein level)

neXtProt

NX_Q8TAF8

Antibodypedia

LHFPL5 antibodies
 

PROTEIN VIEW

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LHFPL5-002
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

LHFPL5-002 ENSP00000353346
ENST00000360215
Q8TAF8
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