USH1G

Usher syndrome type-1G protein is a protein that in humans is encoded by the USH1G gene.[5][6]

USH1G
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 2L7T, 3K1R, 3PVL
Identifiers
Aliases	USH1G, ANKS4A, SANS, USH1 protein network component sans
External IDs	OMIM: 607696 MGI: 2450757 HomoloGene: 56113 GeneCards: USH1G
Gene location (Human) Chr. Chromosome 17 (human)[1] Band 17q25.1 Start 74,916,083 bp[1] End 74,923,256 bp[1]
Gene location (Mouse) Chr. Chromosome 11 (mouse)[2] Band 11 E2|11 80.84 cM Start 115,315,192 bp[2] End 115,322,041 bp[2]
RNA expression pattern More reference expression data
Gene ontology Molecular function • spectrin binding • GO:0001948 protein binding • protein homodimerization activity • identical protein binding Cellular component • photoreceptor inner segment • cytoplasm • ciliary basal body • cytosol • cell membrane • cytoskeleton • membrane • photoreceptor connecting cilium • actin cytoskeleton Biological process • inner ear receptor cell differentiation • photoreceptor cell maintenance • sensory perception of sound • inner ear morphogenesis • inner ear receptor stereocilium organization • sensory perception of light stimulus • equilibrioception Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	124590	16470
Ensembl	ENSG00000182040	ENSMUSG00000045288
UniProt	Q495M9	Q80T11
RefSeq (mRNA)	NM_001282489 NM_173477	NM_176847
RefSeq (protein)	NP_001269418 NP_775748	NP_789817
Location (UCSC)	Chr 17: 74.92 – 74.92 Mb	Chr 11: 115.32 – 115.32 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

This gene encodes a protein that contains three ankyrin domains, a class I PDZ-binding motif and a sterile alpha motif. The encoded protein interacts with harmonin, which is associated with Usher syndrome type 1C.

This protein plays a role in the development and maintenance of the auditory and visual systems and functions in the cohesion of hair bundles formed by inner ear sensory cells. Mutations in this gene are associated with Usher syndrome type 1G (USH1G).[6]

References

1. GRCh38: Ensembl release 89: ENSG00000182040 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000045288 - 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.
5. Weil D, El-Amraoui A, Masmoudi S, Mustapha M, Kikkawa Y, Laine S, Delmaghani S, Adato A, Nadifi S, Zina ZB, Hamel C, Gal A, Ayadi H, Yonekawa H, Petit C (Feb 2003). "Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin". Hum Mol Genet. 12 (5): 463–71. doi:10.1093/hmg/ddg051. PMID 12588794.
6. "Entrez Gene: USH1G Usher syndrome 1G (autosomal recessive)".

Further reading

• Ahmed ZM, Riazuddin S, Riazuddin S, Wilcox ER (2004). "The molecular genetics of Usher syndrome". Clin. Genet. 63 (6): 431–44. doi:10.1034/j.1399-0004.2003.00109.x. PMID 12786748.
• Ahmed ZM, Riazuddin S, Bernstein SL, et al. (2001). "Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F". Am. J. Hum. Genet. 69 (1): 25–34. doi:10.1086/321277. PMC 1226045. PMID 11398101.
• Mustapha M, Chouery E, Torchard-Pagnez D, et al. (2002). "A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25". Hum. Genet. 110 (4): 348–50. doi:10.1007/s00439-002-0690-x. PMID 11941484.
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
• Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
• Ouyang XM, Yan D, Du LL, et al. (2005). "Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population". Hum. Genet. 116 (4): 292–9. doi:10.1007/s00439-004-1227-2. PMID 15660226.
• Kalay E, de Brouwer AP, Caylan R, et al. (2006). "A novel D458V mutation in the SANS PDZ binding motif causes atypical Usher syndrome". J. Mol. Med. 83 (12): 1025–32. doi:10.1007/s00109-005-0719-4. PMID 16283141.

External links

• GeneReviews/NCBI/NIH/UW entry on Usher Syndrome Type I