Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
375612
Gene name Gene Name - the full gene name approved by the HGNC.
LHFPL tetraspan subfamily member 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
LHFPL3
Synonyms (NCBI Gene) Gene synonyms aliases
LHFPL4
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7q22.2-q22.3
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 one LHFP-like gene result in deafness in humans and mice, and a second LHFP-l
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT540674 hsa-miR-8485 HITS-CLIP 23824327
MIRT540673 hsa-miR-574-3p HITS-CLIP 23824327
MIRT540671 hsa-miR-342-3p HITS-CLIP 23824327
MIRT540674 hsa-miR-8485 HITS-CLIP 23824327
MIRT540673 hsa-miR-574-3p HITS-CLIP 23824327
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 32296183
GO:0005886 Component Plasma membrane IBA
GO:0007605 Process Sensory perception of sound IBA
GO:0016020 Component Membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
609719 6589 ENSG00000187416
Protein
UniProt ID Q86UP9
Protein name LHFPL tetraspan subfamily member 3 protein (Lipoma HMGIC fusion partner-like 3 protein)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10242 L_HMGIC_fpl 36 213 Lipoma HMGIC fusion partner-like protein Family
Sequence
Sequence length 236
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)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Diabetes Type 2 diabetes, Type 2 diabetes (adjusted for BMI) N/A N/A GWAS
Eosinophilia Eosinophilic esophagitis N/A N/A GWAS
Gout Gout N/A N/A GWAS
Insomnia Insomnia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma Inhibit 35435361
Adenocarcinoma of Lung Associate 35435361
Carcinogenesis Associate 35435361
Colorectal Neoplasms Associate 33431054
Glioblastoma Associate 24358143
Glioma Associate 24358143, 30314994, 32987560
Neoplasms Associate 30314994