LHFPL6
Sign in to saveAlso known as LHFP, lipoma HMGIC fusion partner, LHFPL tetraspan subfamily member 6
Lipoma HMGIC fusion partner is a protein that in humans is encoded by the LHFP gene.
In the Vinony graph
Within Vinony's link graph, LHFPL6 is referenced by 2 other articles, and connects out to PubMed, human chromosome 13 and Ensembl genome database project.
It is catalogued under the topic Genes on human chromosome 13.
Its subject is documented across 5 Wikipedia language editions.
Gene data
LHFPL6- Name
- LHFPL tetraspan subfamily member 6
- Type
- protein-coding
- Position
- 39,209,116–39,603,735 (−)
- Aliases
- LHFP
- Ensembl
- ENSG00000183722
- RefSeq RNA
- NM_005780.3, XM_011534861.2, XM_054373989.1
- RefSeq protein
- NP_005771.1, XP_011533163.1, XP_054229964.1
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. This gene is fused to a high-mobility group gene in a translocation-associated lipoma. Mutations in another LHFP-like gene result in deafness in humans and mice. Alternatively spliced transcript variants have been found; however, their full-length nature is not known. [provided by RefSeq, Jul 2008].
via MyGene.info
Gene · Ensembl
LHFPL tetraspan subfamily member 6
- Symbol
- LHFPL6
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 13:39,209,116-39,603,735
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 7 more facts
- HomoloGene ID
- 4223
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/10186
- cytogenetic location
- 13q13.3-q14.11
- genomic end
- 40177665
- genomic start
- 39209116
- chromosome
- human chromosome 13
Sources (4)
via Wikidata · CC0
~1 min read
Encyclopedic overview
3 sectionsContents
- References
- Further reading
- External links
Lipoma HMGIC fusion partner is a protein that in humans is encoded by the LHFP 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. This gene is fused to a high-mobility group gene in a translocation-associated lipoma. Mutations in another LHFP-like gene (LHFPL1, LHFPL2) result in deafness in humans and mice. Alternatively spliced transcript variants have been found; however, their full-length nature is not known.
Excerpted from Wikipedia’s “LHFPL6” article, available under the CC BY-SA 4.0 licence.