VCX3B - variable charge X-linked 3B-BMKCloudï½ç¾è¿å®¢äº

例如："NBL1", "4681", "drought"

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425054 VCX3B

基因描述

Type	Description
Definition	variable charge X-linked 3B

名称对应

Type	IDs
Synonymous	VCX-C, VCXC
Gene	UniProtKB-ID: VCX3B_HUMAN UniprotKB: Q9H321 UniParc: UPI000156D0F8, UPI000057A469 EMBL: AC006062, BC098143, AF167080 Ensembl: ENSG00000205642 KO: hsa:425054
Nucleutide sequences	EMBL-CDS: AAH98143.1, AAG41766.2 Ensembl_TRS: ENST00000381032
Protein sequencees	Ensembl_PRO: ENSP00000370420 RefSeq: NP_001001888.3
Others	UniRef100: UniRef100_Q9H321 UniRef90: UniRef90_Q9H321 UniRef50: UniRef50_Q9H320 UniGene: Hs.279737, Hs.534814 CCDS: CCDS48077.2

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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
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	-
19734545	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. Hum. Mol. Genet. Anna C Need , Deborah K Attix , Jill M McEvoy , Elizabeth T Cirulli , Kristen L Linney , Priscilla Hunt , Dongliang Ge , Erin L Heinzen , Jessica M Maia , Kevin V Shianna , Michael E Weale , Lynn F Cherkas , Gail Clement , Tim D Spector , Greg Gibson , David B Goldstein	2009-12-01	LINC01135, MIR2054, LOC100505530, LOC100506497, LOC101060400, LOC101928387, KCCAT211, CORO2B, ARPP21, PAPD7, BTBD11, CCDC167, FAM91A1, EHHADH, FLT1, PLCB1, GABRB3, SLC24A2, GORASP2, VPS41, GRIN2B, DNAJC15, HCCS, FAM131C, JUN, LMO2, FAM177B, MDM4, VCX3B, MID1, MOBP, UNC13C, MTHFD1, C11orf73, FBXO40, CPVL, VANGL2, TSHZ3, KLHL1, JAM2, RIT2, SEC14L1, SH3GL2, SLC6A6, CAPN5, LOC730100, UCHL1, FAT4, GRIP2, NRIP1, IMMP2L, API5, DSEL, PXYLP1, BICDL1, NRXN1, NCOR2, TOX
19812318	Modulation of neuritogenesis by a protein implicated in X-linked mental retardation. J. Neurosci. Xinfu Jiao , Hongxin Chen , Jianmin Chen , Karl Herrup , Bonnie L Firestein , Megerditch Kiledjian	2009-10-07	-
18076704	Analysis of the VCX3A, VCX2 and VCX3B genes shows that VCX3A gene deletion is not sufficient to result in mental retardation in X-linked ichthyosis. Br. J. Dermatol. S A Cuevas-Covarrubias , L M GonzÃ¡lez-Huerta	2008-03-01	VCX3B, VCX2, VCX3A
17342728	A shared promoter region suggests a common ancestor for the human VCX/Y, SPANX, and CSAG gene families and the murine CYPT family. Mol. Reprod. Dev. Martin A Hansen , John E Nielsen , Dorota Retelska , Niels Larsen , Henrik Leffers	2008-02-01	Cypt14, Cypt2, Cypt13, Cypt11, Cypt8, Cypt7, Cypt1, Cypt3, Cypt15, CSAG2, CSAG1, VCX, VCX3B, SPANXB1, VCY
16470742	Molecular cytogenetic analysis of a familial interstitial deletion Xp22.2-22.3 with a highly variable phenotype in female carriers. Am J Med Genet A Sylwia Chocholska , Eva Rossier , Gotthold Barbi , Hildegard Kehrer-Sawatzki	2006-03-15	-
15888481	Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis. Hum. Mol. Genet. Hilde Van Esch , Karen Hollanders , Liesbeth Badisco , Cindy Melotte , Paul Van Hummelen , Joris Robert Vermeesch , Koen Devriendt , Jean-Pierre Fryns , Peter Marynen , Guy Froyen	2005-07-01	VCX3B
12862317	Expression and localization of VCX/Y proteins and their possible involvement in regulation of ribosome assembly during spermatogenesis. Cell Res. Sheng Wei Zou , Jian Chao Zhang , Xiao Dong Zhang , Shi Ying Miao , Shu Dong Zong , Qi Sheng , Lin Fang Wang	2003-06-01	VCX, VCX3B
15008409	Evolutionary dynamics of duplicated microsatellites shared by sex chromosomes. J. Mol. Evol. Patricia Balaresque , Bruno Toupance , Evelyne Heyer , Brigitte Crouau-Roy	2003-01-01	-
12477932	Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Proc. Natl. Acad. Sci. U.S.A. Robert L Strausberg , Elise A Feingold , Lynette H Grouse , Jeffery G Derge , Richard D Klausner , Francis S Collins , Lukas Wagner , Carolyn M Shenmen , Gregory D Schuler , Stephen F Altschul , Barry Zeeberg , Kenneth H Buetow , Carl F Schaefer , Narayan K Bhat , Ralph F Hopkins , Heather Jordan , Troy Moore , Steve I Max , Jun Wang , Florence Hsieh , Luda Diatchenko , Kate Marusina , Andrew A Farmer , Gerald M Rubin , Ling Hong , Mark Stapleton , M Bento Soares , Maria F Bonaldo , Tom L Casavant , Todd E Scheetz , Michael J Brownstein , Ted B Usdin , Shiraki Toshiyuki , Piero Carninci , Christa Prange , Sam S Raha , Naomi A Loquellano , Garrick J Peters , Rick D Abramson , Sara J Mullahy , Stephanie A Bosak , Paul J McEwan , Kevin J McKernan , Joel A Malek , Preethi H Gunaratne , Stephen Richards , Kim C Worley , Sarah Hale , Angela M Garcia , Laura J Gay , Stephen W Hulyk , Debbie K Villalon , Donna M Muzny , Erica J Sodergren , Xiuhua Lu , Richard A Gibbs , Jessica Fahey , Erin Helton , Mark Ketteman , Anuradha Madan , Stephanie Rodrigues , Amy Sanchez , Michelle Whiting , Anup Madan , Alice C Young , Yuriy Shevchenko , Gerard G Bouffard , Robert W Blakesley , Jeffrey W Touchman , Eric D Green , Mark C Dickson , Alex C Rodriguez , Jane Grimwood , Jeremy Schmutz , Richard M Myers , Yaron S N Butterfield , Martin I Krzywinski , Ursula Skalska , Duane E Smailus , Angelique Schnerch , Jacqueline E Schein , Steven J M Jones , Marco A Marra , Mammalian Gene Collection Program Team	2002-12-24	-

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