LHFPL5 (LHFPL tetraspan subfamily member 5)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 222662 |
| Gene name | LHFPL tetraspan subfamily member 5 |
| Gene symbol | LHFPL5 |
| Synonyms (NCBI Gene) |
DFNB67TMHSdJ510O8.8
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| Chromosome | 6 |
| Chromosome location | 6p21.31 |
| 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 m |
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SNPs
SNP information provided by dbSNP.
8
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miRNA
miRNA information provided by mirtarbase database.
242
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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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 from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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