Exph5基因
WebAntibodies that detect EXPH5 can be used in several scientific applications, including Western Blot and Immunohistochemistry. These antibodies target EXPH5 in Human samples. Our EXPH5 polyclonal antibodies are developed in Rabbit. Find the EXPH5 antibody that fits your needs. Choose from 1 of 3 EXPH5 antibodies, which have been … WebJan 22, 2013 · McGrath et al. (2012) studied an Iraqi family in which 3 of 8 sibs born to first-cousin parents had inherited skin fragility and mutation in the EXPH5 gene. The clinical features were apparent from early childhood and consisted primarily of trauma-induced scale crusts and intermittent skin blistering that was mostly secondary to trauma, such as …
Exph5基因
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WebExophilin 5, also known as EXPH5, is a human gene. Interactions. EXPH5 has been shown to interact with RAB27A. References ^ a b c GRCh38: Ensembl release 89: ENSG00000110723 - Ensembl, May 2024 ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000034584 - Ensembl, May 2024 ^ "Human PubMed Reference:". WebOct 1, 2016 · Importance: Epidermolysis bullosa simplex (EBS) is a group of clinically and genetically diverse mechanobullous genodermatoses characterized by the fragility of skin and mucous membranes. Recently, mutations in EXPH5 encoding exophilin-5 (also known as Slac2-b, an effector protein involved in intracellular vesicle trafficking and exosome …
Web图5. 单细胞转录组数据集中exph5基因的表达分析 总结. 这篇文章的创新点就是基于疾病的分组进行了分析，再利用机器学习算法筛选诊断基因，并分析了免疫细胞浸润，最后还利 … WebGene summary (Entrez)i. Useful information about the gene from Entrez. The protein encoded by this gene is a member of the synaptotagmin-like protein (Slp) family lacking …
WebPigors et al. (2014) sequenced the EXPH5 gene in a cohort of 35 patients with clinically suspected epidermolysis bullosa simplex (EBS) who were negative for mutation in the … WebEXPH5 (Exophilin 5) is a Protein Coding gene. Diseases associated with EXPH5 include Epidermolysis Bullosa Simplex 4, Localized Or Generalized Intermediate, Autosomal …
WebAntibodies that detect EXPH5 can be used in several scientific applications, including Western Blot and Immunohistochemistry. These antibodies target EXPH5 in Human …
Web1.4 EXPH5 多个病例报道证实EXPH5基因纯合突变导致皮肤脆性增加和大疱形成[13]。EXPH5编码的Exophilin-5蛋白参与细胞内蛋白运输和外泌体分泌，在细胞内囊泡转运中起重要作用[14]。 1.5 JUP EBS的致病基因中，有许多罕见的常染色体隐性遗传基因，JUP就是其 … cal west attorneycal west arroyo grande caWebBioVector NTCC Inc. 订购电话TEL:400-800-2947 工作QQ/微信:1843439339 Email:[email protected] cal west auto in san marcosWebSummary. Predicted to enable small GTPase binding activity. Predicted to be involved in keratinocyte development; multivesicular body sorting pathway; and positive regulation of secretion by cell. Predicted to be active in endosome. Orthologous to human EXPH5 (exophilin 5). [provided by Alliance of Genome Resources, Apr 2024] cal west attorney servicesWebMar 21, 2024 · ACKR1 (Atypical Chemokine Receptor 1 (Duffy Blood Group)) is a Protein Coding gene. Diseases associated with ACKR1 include White Blood Cell Count Quantitative Trait Locus 1 and Malaria.Among its related pathways are Class A/1 (Rhodopsin-like receptors) and GPCR downstream signalling.Gene Ontology (GO) … cal west bankWeb遗传病、罕见病基因检测导读：大疱性表皮松解症(eb)基因检测是对一种罕见的遗传病所进行的基因测序分析，并对发现的基因突变进行致病性确定。大疱性表皮松解症临床表现差异很大，难以建立起基因型和表型之间的清晰的关系。 calwest bank mergerhttp://www.labome.cn/gene/human/EXPH5-gene-knockdown.html cal west atty service