ⓘ LHFPL2

                                     

ⓘ LHFPL2

Lipoma HMGIC fusion partner-like 2 protein is a protein that in humans is encoded by the LHFPL2 gene.

This gene is a member of the lipoma HMGIC fusion partner LHFP genetic family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. Mutations in one LHFP-like gene result deafness in humans and mice, and a second LHFP-like gene is fused with high mobility group gene in a translocation associated lipomas. Alternative spliced transcript variants have been found, but their biological validity has not been determined.

                                     
  • translocation - associated lipoma. Mutations in another LHFP - like gene LHFPL 1, LHFPL2 result in deafness in humans and mice. Alternatively spliced transcript
  • fusion partner - like 1 protein is a protein that in humans is encoded by the LHFPL 1 gene. This gene is a member of the lipoma HMGIC fusion partner LHFP gene
  • LHFPL tetraspan subfamily member 3 is a protein that in humans is encoded by the LHFPL 3 gene. This gene is a member of the lipoma HMGIC fusion partner
  • implicating genes CCDC50, DIAPH1, DSPP, ESRRB, GJB3, GRHL 2 GRXCR1, HGF, LHFPL 5, LOXHD1, LRTOMT, MARVELD 2 MIR96, MYH14, MYH9, MYO1A, MYO3A, OTOA, PJVK, POU4F3
  • HGNC: 6585 P22888 8706 LHFPL 1 HGNC: 6587 Q86WI0 8707 LHFPL2 HGNC: 6588 Q6ZUX7 8708 LHFPL 3 HGNC: 6589 Q86UP9 8709 LHFPL 4 HGNC: 29568 Q7Z7J7 8710 LHFPL 5 HGNC: 21253 Q8TAF8