Tbc1d10c-flox 基因敲除小鼠

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产品名称

Tbc1d10c-flox 基因敲除小鼠

产品编号

S-CKO-00729

品系全称

C57BL/6JCya-Tbc1d10cem1flox/Cya

品系背景

C57BL/6JCya

品系编号

CKOCMP-108995-Tbc1d10c-B6J-VA

品系状态

使用本品系发表的文献需注明: Tbc1d10c-flox 基因敲除小鼠 mice (Strain S-CKO-00729) were purchased from Cyagen.
交付类型
周龄
性别
基因型
数量
cKO小鼠库模型

基本信息

基因研究概述

质控标准

基因
基因全称
TBC1 domain family, member 10c
基因别称
1810062O14Rik
染色体号
Chr 19 (Mouse)
转录本 ID
NCBI: NM_178650.3 | Ensembl: ENSMUST00000235450
修饰方式
条件性基因敲除
靶向范围
Exon 7~8
敲除长度
~870 bp
品系说明
该品系是基于策略设计时的数据库信息制作而成,建议您在购买前查询最新的数据库和相关文献,以获取最准确的表型信息。
表型提示
MGI:1922072Mice homozygous for a knock-out allele exhibit spontaneous T cell activation and increased B cell response to ovalbumin, NP-LPS and Borrelia burgdorferi infection, and increased autoimmune response to CpG-DNA.
Tbc1d10c是TBC1D10亚家族中的一个基因,与黑色素细胞运输、外泌体分泌和T细胞激活等生理和病理功能相关。在斑马鱼胚胎发育过程中,Tbc1d10c在胸鳍、耳囊、咽弓组织以及脑组织和视网膜内层核层中均有表达,并且与Tbc1d10亚家族的其他成员在表达模式上存在相似性和差异性,这表明它们可能具有不同的功能[2]。此外,Tbc1d10c在乳腺癌患者中与肿瘤微环境相关,与免疫治疗反应相关,可能是一种新的免疫治疗反应的生物标志物[1]。在心脏中,Tbc1d10c的表达增加可以降低心率,增强运动能力和生存能力,可能成为心率降低和长寿的新靶点[3]。在糖尿病肾病中,Tbc1d10c的表达与DAPA治疗相关,可能成为治疗糖尿病肾病的新靶点[4]。在肾细胞癌中,Tbc1d10c与肿瘤微环境相关,与免疫治疗反应相关,可能是一种新的免疫治疗反应的生物标志物[5]。此外,Tbc1d10c在鼻咽癌和头颈鳞状细胞癌中与免疫浸润和细胞周期调节相关,可能成为预测预后的生物标志物和治疗的靶点[6,7]。Tbc1d10c在T细胞中调节受体回收和免疫突触形成,可能参与TCR运输到免疫突触[8]。

参考文献:
1. Qiao, Huiying, Lv, Rong, Pang, Yongkui, Zhu, Wei, Zhou, Wenqing. 2022. Weighted Gene Coexpression Network Analysis Identifies TBC1D10C as a New Prognostic Biomarker for Breast Cancer. In Analytical cellular pathology (Amsterdam), 2022, 5259187. doi:10.1155/2022/5259187. https://pubmed.ncbi.nlm.nih.gov/35425695/
2. Sun, Shuna, Liu, Ziyin, Jiang, Qiu, Zou, Yunzeng. 2021. Embryonic expression patterns of TBC1D10 subfamily genes in zebrafish. In Gene expression patterns : GEP, 43, 119226. doi:10.1016/j.gep.2021.119226. https://pubmed.ncbi.nlm.nih.gov/34843939/
3. Volland, Cornelia, Bremer, Sebastian, Hellenkamp, Kristian, Hasenfuß, Gerd, Seidler, Tim. 2016. Enhanced cardiac TBC1D10C expression lowers heart rate and enhances exercise capacity and survival. In Scientific reports, 6, 33853. doi:10.1038/srep33853. https://pubmed.ncbi.nlm.nih.gov/27667030/
4. Shen, Jianxiao, Ying, Liang, Wu, Jiajia, Ni, Zhaohui, Che, Xiajing. . Integrative ATAC-seq and RNA-seq analysis associated with diabetic nephropathy and identification of novel targets for treatment by dapagliflozin. In Cell biochemistry and function, 42, e3943. doi:10.1002/cbf.3943. https://pubmed.ncbi.nlm.nih.gov/38379015/
5. Yue, Youwei, Cai, Xinyi, Lu, Changhao, Solla, Paolo, Li, Shensuo. 2023. Unraveling the prognostic significance and molecular characteristics of tumor-infiltrating B lymphocytes in clear cell renal cell carcinoma through a comprehensive bioinformatics analysis. In Frontiers in immunology, 14, 1238312. doi:10.3389/fimmu.2023.1238312. https://pubmed.ncbi.nlm.nih.gov/37908350/
6. Pane, Roberto, Laib, Loubna, Formoso, Karina, Lezoualc'h, Frank, Conte, Caroline. 2023. Macromolecular Complex Including MLL3, Carabin and Calcineurin Regulates Cardiac Remodeling. In Circulation research, 134, 100-113. doi:10.1161/CIRCRESAHA.123.323458. https://pubmed.ncbi.nlm.nih.gov/38084599/
7. Ding, Tengteng, Zhang, Yuanbin, Ren, Zhixuan, Li, Xin, Lyu, Xiaoming. 2023. EBV-Associated Hub Genes as Potential Biomarkers for Predicting the Prognosis of Nasopharyngeal Carcinoma. In Viruses, 15, . doi:10.3390/v15091915. https://pubmed.ncbi.nlm.nih.gov/37766321/
8. Patino-Lopez, Genaro, Dong, Xiaoyun, Ben-Aissa, Khadija, Samelson, Lawrence E, Shaw, Stephen. 2008. Rab35 and its GAP EPI64C in T cells regulate receptor recycling and immunological synapse formation. In The Journal of biological chemistry, 283, 18323-30. doi:10.1074/jbc.M800056200. https://pubmed.ncbi.nlm.nih.gov/18450757/