智鼠故事 
CreERT2-P2A-Trpv4 小鼠
复苏/繁育服务
产品名称：
CreERT2-P2A-Trpv4 小鼠
产品编号：
I001101
品系背景：
C57BL/6JCya
表达组织/细胞举例：
脑、呼吸系统、感觉器官等
* 使用本品系发表的文献需注明：CreERT2-P2A-Trpv4 小鼠 mice (Catalog I001101) were purchased from Cyagen.
交付类型
周龄
性别
基因型
数量
只
基本信息
产品名称
CreERT2-P2A-Trpv4 小鼠
产品编号
I001101
基因名
品系背景
C57BL/6JCya
基因别称
Trp12；VRL-2；VROAC；OTRPC4；VR-OAC；0610033B08Rik
模型分类
诱导型Cre工具鼠
NCBI ID
小鼠表型
染色体
5
更多信息
* 使用本品系发表的文献需注明：CreERT2-P2A-Trpv4 小鼠 mice (Catalog I001101) were purchased from Cyagen.
品系描述
将 Kozak-CreERT2-P2A 插入小鼠Trpv4基因ATG起始密码子上游。当该品系与含有loxP位点的小鼠杂交后，子代小鼠经他莫昔芬诱导后将在脑、呼吸系统、感觉器官中发生由Cre重组酶介导的loxP位点间的序列重组。
相关疾病：
Metatropic Dysplasia
Hereditary Motor and Sensory Neuropathy, Type Iic
Scapuloperoneal Spinal Muscular Atrophy
Spondylometaphyseal Dysplasia, Kozlowski Type
Neuronopathy, Distal Hereditary Motor, Autosomal Dominant 8
Parastremmatic Dwarfism
Digital Arthropathy-Brachydactyly, Familial
Brachyolmia Type 3
Spondyloepiphyseal Dysplasia, Maroteaux Type
Avascular Necrosis of Femoral Head, Primary, 2
Sodium Serum Level Quantitative Trait Locus 1
Trpv4-Related Bone Disorder
Skeletal Dysplasia and Progressive Central Nervous System Degeneration, Lethal
Familial Avascular Necrosis of Femoral Head
Primary Bone Dysplasia
Clubfoot
Osteochondrodysplasia
Neuromuscular Disease
Talipes Equinovarus
Clubfoot, Congenital, with or Without Deficiency of Long Bones and/or Mirror-Image Polydactyly
Charcot-Marie-Tooth Disease
Beckwith-Wiedemann Syndrome
Brachyolmia
Genetic Motor Neuron Disease
Connective Tissue Disease
