Ush1g - USH1 protein network component sans-BMKCloudï½ç¾è¿å®¢äº

例如："NBL1", "4681", "drought"

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287819 Ush1g

基因描述

Type	Description
Definition	USH1 protein network component sans

名称对应

Type	IDs
Gene	UniProtKB-ID: D3ZTY5_RAT UniprotKB: D3ZTY5 UniParc: UPI00001CB2AF EMBL: AC135578, CH473948 Ensembl: ENSRNOG00000028456 KO: rno:287819
Nucleutide sequences	EMBL-CDS: EDM06571.1 Gene_ORFName: rCG_34647 Ensembl_TRS: ENSRNOT00000039387
Protein sequencees	Ensembl_PRO: ENSRNOP00000032135 RefSeq: NP_001099320.1, XP_017452645.1
Others	UniRef100: UniRef100_D3ZTY5 UniRef90: UniRef90_Q495M9 UniRef50: UniRef50_Q495M9 UniGene: Rn.218468

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mRNA

Protein

UniprotKB

Description

Refseq

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Location

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Pubmed编号	文献信息	发表日期	相关基因
23704327	The giant spectrin Î²V couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking route. Hum. Mol. Genet. Samantha Papal , Matteo Cortese , Kirian Legendre , Nasrin Sorusch , Joseph Dragavon , Iman Sahly , Spencer Shorte , Uwe Wolfrum , Christine Petit , Aziz El-Amraoui	2013-09-15	Dync1i1, Gnb1, Gnb3, Ush1g, Kif3a, Lamp1, Arr3, Myo10, Myo7a, Pde6g, Sag, Sptan1, Sptbn2, Syp, Rho, Epb41, Sptbn5, Dctn2, Ush1c, Golga2, Gnb1, Rho, Sag, Sptbn5, Ush1c, Epb41, Gnb3, Sptan1, Pde6g, USH1C, DCTN2, KIF3A, USH1G, DYNC1I1, LAMP1, ARR3, MYO7A, MYO10, SPTBN5, RHO
22177415	Sensing sound: molecules that orchestrate mechanotransduction by hair cells. Trends Neurosci. Piotr Kazmierczak , Ulrich MÃ¼ller	2012-04-01	Cdh23, Myo7a, Ush1g, Ush1c, Pcdh15
20212494	Photoreceptor degeneration: genetic and mechanistic dissection of a complex trait. Nat. Rev. Genet. Alan F Wright , Christina F Chakarova , Mai M Abd El-Aziz , Shomi S Bhattacharya	2010-04-01	-
20142502	The structure of the harmonin/sans complex reveals an unexpected interaction mode of the two Usher syndrome proteins. Proc Natl Acad Sci U S A Jing Yan , Lifeng Pan , Xiuye Chen , Lin Wu , Mingjie Zhang	2010-03-02	-
18339676	A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth. Development Gaelle LefÃ¨vre , Vincent Michel , Dominique Weil , LÃ©a Lepelletier , Emilie Bizard , Uwe Wolfrum , Jean-Pierre Hardelin , Christine Petit	2008-04-01	Scrib, Pcdh15, Ctnnb1, Fzd3, Ush1g, Myo7a, Cdh23, Ush1c, Vangl2
17906286	A novel Usher protein network at the periciliary reloading point between molecular transport machineries in vertebrate photoreceptor cells. Hum. Mol. Genet. Tina Maerker , Erwin van Wijk , Nora Overlack , Ferry F J Kersten , Joann McGee , Tobias Goldmann , Elisabeth Sehn , Ronald Roepman , Edward J Walsh , Hannie Kremer , Uwe Wolfrum	2008-01-01	-
12588793	Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice. Hum. Mol. Genet. Yoshiaki Kikkawa , Hiroshi Shitara , Shigeharu Wakana , Yuki Kohara , Toyoyuki Takada , Mieko Okamoto , Choji Taya , Kazusaku Kamiya , Yasuhiro Yoshikawa , Hisashi Tokano , Ken Kitamura , Kunihiko Shimizu , Yuichi Wakabayashi , Toshihiko Shiroishi , Ryo Kominami , Hiromichi Yonekawa	2003-03-01	-
12588794	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. Dominique Weil , Aziz El-Amraoui , Saber Masmoudi , Mirna Mustapha , Yoshiaki Kikkawa , Sophie LainÃ© , Sedigheh Delmaghani , Avital Adato , Sellama Nadifi , Zeineb Ben Zina , Christian Hamel , Andreas Gal , Hammadi Ayadi , Hiromichi Yonekawa , Christine Petit	2003-03-01	-
11398101	Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F. Am. J. Hum. Genet. Z M Ahmed , S Riazuddin , S L Bernstein , Z Ahmed , S Khan , A J Griffith , R J Morell , T B Friedman , S Riazuddin , E R Wilcox	2001-07-01	-
1442008	Ultrastructural findings in the inner ear of Jackson shaker mice. Acta Otolaryngol. K Kitamura , H Kakoi , Y Yoshikawa , F Ochikubo	1992-01-01	-

研究热度

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