Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
222662
Gene name Gene Name - the full gene name approved by the HGNC.
LHFPL tetraspan subfamily member 5
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
LHFPL5
Synonyms (NCBI Gene) Gene synonyms aliases
DFNB67, TMHS, dJ510O8.8
Disease Acronyms (UniProt) Disease acronyms from UniProt database
DFNB67
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p21.31
Summary Summary of gene provided in NCBI Entrez Gene.
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
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs104893975 A>G Pathogenic Coding sequence variant, missense variant
rs104893976 C>T Pathogenic Coding sequence variant, missense variant
rs756030149 ->G Likely-pathogenic Coding sequence variant, frameshift variant
rs762876554 G>T Pathogenic Missense variant, coding sequence variant
rs779841884 C>- Pathogenic Stop gained, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT541986 hsa-miR-3146 HITS-CLIP 21572407
MIRT541985 hsa-miR-675-3p HITS-CLIP 21572407
MIRT504315 hsa-miR-5011-5p HITS-CLIP 21572407
MIRT504314 hsa-miR-511-3p HITS-CLIP 21572407
MIRT504307 hsa-miR-574-5p HITS-CLIP 21572407
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 25910212, 31515488, 32296183
GO:0005886 Component Plasma membrane IBA 21873635
GO:0006811 Process Ion transport IEA
GO:0007605 Process Sensory perception of sound IBA 21873635
GO:0016020 Component Membrane IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
609427 21253 ENSG00000197753
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

Accession ID Position in sequence Description Type
PF10242 L_HMGIC_fpl 25 202 Lipoma HMGIC fusion partner-like protein Family
Sequence
Sequence length 219
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Deafness Deafness, Autosomal Recessive 67 rs267607135, rs387906219, rs387906220, rs387906221, rs387906222, rs606231120, rs267606855, rs121918370, rs137853185, rs137853186, rs137853187, rs137853188, rs587776522, rs587776523, rs200781822
View all (1019 more)
30177809, 26437881, 28281779, 16752389, 16459341
Nonsyndromic deafness Nonsyndromic Deafness rs606231410, rs794729665, rs730880338, rs1566538321 16752389, 19102128, 15905332, 16459341, 26029705, 26437881, 19888295, 21816241, 25550511, 25467981
Associations from Text Mining
Disease Name Relationship Type References
Deafness Associate 29568747, 37930868
Deafness Autosomal Recessive Associate 29568747
Hearing Loss Associate 19888295, 28281779, 30177809
Nonsyndromic Deafness Associate 31389194
Nonsyndromic sensorineural hearing loss Associate 30177809