Sec14l5-KO 基因敲除小鼠

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产品名称

Sec14l5-KO 基因敲除小鼠

产品编号

S-KO-11758

品系全称

C57BL/6JCya-Sec14l5em1/Cya

品系背景

C57BL/6JCya

品系编号

KOCMP-665119-Sec14l5-B6J-VA

品系状态

使用本品系发表的文献需注明: Sec14l5-KO 基因敲除小鼠 mice (Strain S-KO-11758) were purchased from Cyagen.
交付类型
周龄
性别
基因型
数量

基本信息

基因研究概述

质控标准

基因
基因全称
SEC14-like lipid binding 5
基因别称
-
染色体号
Chr 16 (Mouse)
转录本 ID
NCBI: NM_001127725.1 | Ensembl: ENSMUST00000165810
修饰方式
全身性基因敲除
靶向范围
Exon 3~8
敲除长度
~7578 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
Sec14l5基因,全称为SEC14-like 5,是一个在真核生物中发现的基因,其编码的蛋白质与磷脂代谢和细胞信号传导有关。Sec14l5基因的产物在细胞膜运输、脂质代谢以及细胞内信号传导等方面发挥着重要作用,是细胞内磷脂合成和代谢的关键调控因子之一。

根据检索到的参考文献,Sec14l5基因在不同类型的癌症和疾病中具有潜在的作用和意义。例如,在肺癌中,Sec14l5基因的表达水平与病理阶段密切相关[1]。在结直肠腺癌中,Sec14l5基因的表达与患者预后相关,并被纳入一个基于风险评分系统的预后预测模型中[2]。在创伤后应激障碍(PTSD)的研究中,Sec14l5基因也被认为是一个重要的候选基因[3]。此外,Sec14l5基因的表达还与心脏疾病和多种手术风险相关[4]。在胚胎小鼠脑和原代神经元中,Sec14l5基因的环状RNA(circRNA)表达水平在电离辐射暴露后持续升高,提示其可能作为长期辐射暴露的生物标志物[5]。Sec14l5基因还与川崎病和免疫球蛋白A血管炎的遗传风险相关[6]。在肺腺癌中,Sec14l5基因的转录水平升高与患者预后不良相关[7]。在前列腺癌中,Sec14l5基因的表达与碱化耐受性相关,并可能影响化疗反应[8]。

综上所述,Sec14l5基因在多种疾病中具有潜在的作用和意义。这些研究结果表明,Sec14l5基因可能是一个重要的分子标志物和治疗靶点,值得进一步研究和探索。

参考文献:
1. Zhu, Liang, Chen, Peixin, Wang, Hao, Yu, Jia, Dai, Jiawei. . Analysis of prognostic and therapeutic values of drug resistance-related genes in the lung cancer microenvironment. In Translational cancer research, 11, 339-357. doi:10.21037/tcr-21-1841. https://pubmed.ncbi.nlm.nih.gov/35281414/
2. Huang, Wei, Li, Gen, Wang, Zihang, Feng, Yajuan, Yu, Hefen. 2021. A Ten-N6-Methyladenosine (m6A)-Modified Gene Signature Based on a Risk Score System Predicts Patient Prognosis in Rectum Adenocarcinoma. In Frontiers in oncology, 10, 567931. doi:10.3389/fonc.2020.567931. https://pubmed.ncbi.nlm.nih.gov/33680913/
3. Chitrala, Kumaraswamy Naidu, Nagarkatti, Prakash, Nagarkatti, Mitzi. 2016. Prediction of Possible Biomarkers and Novel Pathways Conferring Risk to Post-Traumatic Stress Disorder. In PloS one, 11, e0168404. doi:10.1371/journal.pone.0168404. https://pubmed.ncbi.nlm.nih.gov/27997584/
4. Pathak, Gita A, Wendt, Frank R, De Lillo, Antonella, Gelernter, Joel, Polimanti, Renato. 2021. Epigenomic Profiles of African-American Transthyretin Val122Ile Carriers Reveals Putatively Dysregulated Amyloid Mechanisms. In Circulation. Genomic and precision medicine, 14, e003011. doi:10.1161/CIRCGEN.120.003011. https://pubmed.ncbi.nlm.nih.gov/33428857/
5. Mfossa, André Claude Mbouombouo, Thekkekara Puthenparampil, Helene, Inalegwu, Auchi, Huylebroeck, Danny, Quintens, Roel. 2019. Exposure to Ionizing Radiation Triggers Prolonged Changes in Circular RNA Abundance in the Embryonic Mouse Brain and Primary Neurons. In Cells, 8, . doi:10.3390/cells8080778. https://pubmed.ncbi.nlm.nih.gov/31357500/
6. Carmona, Elio G, García-Giménez, Jose A, López-Mejías, Raquel, Martín, Javier, Márquez, Ana. . Identification of a shared genetic risk locus for Kawasaki disease and immunoglobulin A vasculitis by a cross-phenotype meta-analysis. In Rheumatology (Oxford, England), 61, 1204-1210. doi:10.1093/rheumatology/keab443. https://pubmed.ncbi.nlm.nih.gov/33993232/
7. Zhang, Shuo, Thakur, Asmitananda, Liang, Yiqian, Liu, Johnson J, Chen, Mingwei. 2015. Polymorphisms in C-reactive protein and Glypican-5 are associated with lung cancer risk and Gartrokine-1 influences Cisplatin-based chemotherapy response in a Chinese Han population. In Disease markers, 2015, 824304. doi:10.1155/2015/824304. https://pubmed.ncbi.nlm.nih.gov/25999661/
8. Song, Xiaodong, Zhang, Yu, Li, Tiewen, Xie, Zhiwen, Han, Bangmin. 2025. Identification and Validation of Alkaliptosis Resistance-Associated Genes in Prostate Cancer Via Transcriptome Sequencing and Prediction of Biochemical Recurrence. In Molecular biotechnology, , . doi:10.1007/s12033-024-01322-3. https://pubmed.ncbi.nlm.nih.gov/39760809/