Gjb3 - gap junction protein, beta 3-BMKCloudï½ç¾è¿å®¢äº

例如："NBL1", "4681", "drought"

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29585 Gjb3

基因描述

Type	Description
Definition	gap junction protein, beta 3

研究结论

Date	Results	Publications
2020-12-05 12:58:00	Laser microdissection-based microproteomics of the hippocampus of a rat epilepsy model reveals regional differences in protein abundances.	32157145

名称对应

Type	IDs
Gene	UniProtKB-ID: CXB3_RAT, A0A654ICZ5_RAT UniprotKB: P25305, A0A654ICZ5 UniParc: UPI00001287ED EMBL: M59936, LT990396, CH473968 Ensembl: ENSRNOG00000014372 KO: rno:29585
Nucleutide sequences	EMBL-CDS: AAA40997.1, EDL80481.1, VZP20196.1, EDL80482.1 Gene_ORFName: rCG_31443 Ensembl_TRS: ENSRNOT00000019266
Protein sequencees	Ensembl_PRO: ENSRNOP00000019266 RefSeq: XP_006238907.1, NP_062113.1
Others	UniRef100: UniRef100_P25305 UniRef90: UniRef90_P28231 UniRef50: UniRef50_O95377 UniGene: Rn.162823

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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
32157145	Laser microdissection-based microproteomics of the hippocampus of a rat epilepsy model reveals regional differences in protein abundances. Sci Rep Amanda M do Canto , AndrÃ© S Vieira , Alexandre H B Matos , Benilton S Carvalho , Barbara Henning , Braxton A Norwood , Sebastian Bauer , Felix Rosenow , Rovilson Gilioli , Fernando Cendes , Iscia Lopes-Cendes	2020-03-10	-
25556823	The novel GJB3 mutation p.Thr202Asn in the M4 transmembrane domain underlies erythrokeratodermia variabilis. Br. J. Dermatol. K Sugiura , M Arima , K Matsunaga , M Akiyama	2015-07-01	-
22681493	A missense mutation in the GJB3 gene responsible for erythrokeratodermia variabilis in a Chinese family. Clin. Exp. Dermatol. W Wang , L H Liu , G Chen , M Gao , J Zhu , F S Zhou , H Cheng , H Y Tang , B Y Wu , L D Sun , S Yang , P G Wang , X J Zhang	2012-12-01	GJB3
21873635	Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Brief. Bioinformatics Pascale Gaudet , Michael S Livstone , Suzanna E Lewis , Paul D Thomas	2011-09-01	-
21564177	Erythrokeratoderma variabilis caused by a recessive mutation in GJB3. Clin. Exp. Dermatol. D Fuchs-Telem , Y Pessach , B Mevorah , I Shirazi , O Sarig , E Sprecher	2011-06-01	-
21188847	Novel and recurrent connexin 30.3 and connexin 31 mutations associated with erythrokeratoderma variabilis. Clin. Exp. Dermatol. C A Scott , E A O'Toole , M J Mohungoo , A Messenger , D P Kelsell	2011-01-01	-
19050930	Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31. Hum Genet Xue-Zhong Liu , Yongyi Yuan , Denise Yan , Emilie Hong Ding , Xiao Mei Ouyang , Yu Fei , Wenxue Tang , Huijun Yuan , Qing Chang , Li Lin Du , Xin Zhang , Guojian Wang , Shoeb Ahmad , Dong Yang Kang , Xi Lin , Pu Dai	2009-02-01	-
16297190	Clinical and genetic heterogeneity of erythrokeratoderma variabilis. J. Invest. Dermatol. John E A Common , Edel A O'Toole , Irene M Leigh , Anna Thomas , William A D Griffiths , Vanessa Venning , Sophie Grabczynska , Zdravko Peris , Aleksej Kansky , David P Kelsell	2005-11-01	Gjb4, Gjb3, GJB4, GJB3
15895417	Cx31 and Cx43 double-deficient mice reveal independent functions in murine placental and skin development. Dev. Dyn. Mark Kibschull , Thomas M Magin , Otto Traub , Elke Winterhager	2005-07-01	Flg, Gja1, Gja4, Gja5, Gjc1, Gjb2, Gjb3, Gjb5, Itga6, Lor
15948974	A new, recurrent mutation of GJB3 (Cx31) in erythrokeratodermia variabilis. Br. J. Dermatol. S M Morley , M I White , M Rogers , D Wasserman , P Ratajczak , W H I McLean , G Richard	2005-06-01	-

研究热度

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