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LHFPL3 (LHFPL tetraspan subfamily member 3)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
375612
Gene nameGene Name - the full gene name approved by the HGNC.
LHFPL tetraspan subfamily member 3
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
LHFPL3
SynonymsGene synonyms aliases
LHFPL4
ChromosomeChromosome number
7
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7q22.2-q22.3
SummarySummary 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
miRNAmiRNA 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 21873635
GO:0007605 Process Sensory perception of sound IBA 21873635
GO:0016020 Component Membrane IBA 21873635
GO:0016021 Component Integral component of membrane IEA
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
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
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Leukemia Leukemia, Myelocytic, Acute rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297, rs11978267, rs4132601 27903959
Obesity Obesity rs34911341, rs74315349, rs1474810899, rs2282440, rs2491132, rs121918111, rs796065034, rs753856820, rs796065035, rs121918112, rs104894023, rs137852821, rs1580764441, rs137852822, rs137852823, rs137852824, rs13447324, rs121913562, rs121913564, rs74315393, rs121913556, rs2989924, rs193922650, rs193922685, rs193922687, rs751160202, rs1421085, rs747681609, rs1553400259, rs13447339, rs370479598, rs1554394014, rs1553174844, rs756232889, rs369841551, rs1557670950, rs1571321748, rs148538980, rs1572820988, rs1591461970, rs1419374563, rs745921568, rs144159890, rs1570714352, rs779783209, rs1573250294, rs1573254045, rs1580744791, rs1580746829, rs6548238, rs7138803, rs7754840 21552555
Unknown
Disease name Disease term dbSNP ID References
Bipolar disorder Bipolar Disorder 26806518
Coronary heart disease Coronary heart disease rs9289231, rs281864746 21971053
Gout Gout 22179738
Gouty arthritis Arthritis, Gouty 22179738

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