LHFPL3

LHFPL3
Identifiers
Aliases	LHFPL3, LHFPL4, lipoma HMGIC fusion partner-like 3, LHFPL tetraspan subfamily member 3
External IDs	OMIM: 609719; MGI: 1925076; GeneCards: LHFPL3
Gene location (Human)
Chr.	Chromosome 7 (human)
End	104,908,561 bp
Gene location (Mouse)
Chr.	Chromosome 5 (mouse)
End	23,480,595 bp
RNA expression pattern
	Top expressed in
	lateral nuclear group of thalamus; ; subthalamic nucleus; ; inferior ganglion of vagus nerve; ; ventral tegmental area; ; external globus pallidus; ; amygdala; ; corpus callosum; ; Brodmann area 46; ; hypothalamus; ; superior vestibular nucleus;
	Top expressed in
	globus pallidus; ; habenula; ; deep cerebellar nuclei; ; medial dorsal nucleus; ; dorsal tegmental nucleus; ; dorsomedial hypothalamic nucleus; ; ventromedial nucleus; ; lateral hypothalamus; ; inferior colliculi; ; superior colliculus;
	More reference expression data
	n/a
Orthologs
Databases	NCBI: entry; OMA: entry
	375612
	269629
	ENSG00000187416
	ENSMUSG00000106379
	Q86UP9
	Q9CTN8
	NM_199000; NM_001386065
	NM_001081231; NM_029990; NM_001359998
	NP_945351
	NP_001074700; NP_084266; NP_001346927
	Wikidata
View/Edit Human	View/Edit Mouse

LHFPL tetraspan subfamily member 3 is a protein that in humans is encoded by the LHFPL3 gene.

Function

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-like gene is fused to a high-mobility group gene in a translocation-associated lipoma. A partial gene fragment named LHFPL4 corresponds to a portion of the first exon of this gene. [provided by RefSeq, Jul 2008].

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000187416 – Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000106379 – Ensembl, May 2017
↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ "Entrez Gene: LHFPL tetraspan subfamily member 3". Retrieved 2018-01-30.

Longo-Guess CM, Gagnon LH, Cook SA, Wu J, Zheng QY, Johnson KR (2005). "A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice". Proc. Natl. Acad. Sci. U.S.A. 102 (22): 7894–9. Bibcode:2005PNAS..102.7894L. doi:10.1073/pnas.0500760102. PMC 1142366. PMID 15905332.
Maestrini E, Pagnamenta AT, Lamb JA, Bacchelli E, Sykes NH, Sousa I, Toma C, Barnby G, Butler H, Winchester L, Scerri TS, Minopoli F, Reichert J, Cai G, Buxbaum JD, Korvatska O, Schellenberg GD, Dawson G, de Bildt A, Minderaa RB, Mulder EJ, Morris AP, Bailey AJ, Monaco AP (2010). "High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility". Mol. Psychiatry. 15 (9): 954–68. doi:10.1038/mp.2009.34. PMC 2934739. PMID 19401682.

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

This article on a gene on human chromosome 7 is a stub. You can help Wikipedia by adding missing information.

[refGRCh38Ensembl-1] 1 2 3 GRCh38: Ensembl release 89: ENSG00000187416 – Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000106379 – Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[entrez-5] "Entrez Gene: LHFPL tetraspan subfamily member 3". Retrieved 2018-01-30.

LHFPL3

Function

References

Further reading