LHFPL5 (LHFPL tetraspan subfamily member 5)
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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222662 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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LHFPL tetraspan subfamily member 5 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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LHFPL5 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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DFNB67, TMHS, dJ510O8.8 |
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Chromosome
Chromosome number
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6 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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6p21.31 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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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 m |
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SNPs
SNP information provided by dbSNP.
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | |||||||||||
| UniProt ID | Q8TAF8 | ||||||||||
| Protein name | LHFPL tetraspan subfamily member 5 protein (Lipoma HMGIC fusion partner-like 5 protein) (Tetraspan membrane protein of hair cell stereocilia) | ||||||||||
| Protein function | Auxiliary subunit of the mechanotransducer (MET) non-specific cation channel complex located at the tips of the shorter stereocilia of cochlear hair cells and that mediates sensory transduction in the auditory system. The MET complex is composed | ||||||||||
| Family and domains |
Pfam
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| Sequence |
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| Sequence length | 219 | ||||||||||
| Interactions | View interactions | ||||||||||
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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