智鼠故事 
C57BL/6NCya-Fgf7em1/Cya 基因敲除小鼠
基本信息
品系名称
C57BL/6NCya-Fgf7em1/Cya
品系编号
KOCMP-14178-Fgf7-B6N-VA
产品编号
S-KO-02046
基因名
Fgf7
小鼠表型
基因别称
Kgf，Fgf5b
品系背景
C57BL/6NCya
修饰方式
全身性基因敲除
品系描述
Fgf7位于小鼠的2号染色体，采用基因编辑技术，通过应用高通量电转受精卵方式，获得Fgf7基因敲除小鼠，性成熟后取精子冻存。
相关疾病：
Mucositis
Apert Syndrome
Short Bowel Syndrome
Gingival Overgrowth
Acanthoma
Adult Respiratory Distress Syndrome
Cholesteatoma of Middle Ear
Hypophosphatasia
Pfeiffer Syndrome
Hypophosphatemia
Bronchopulmonary Dysplasia
Osteomalacia
Hyperphosphatemia
Pulmonary Emphysema
Pulmonary Edema
Teratocarcinoma
Pulmonary Fibrosis
Stomatitis
Telogen Effluvium
Androgenic Alopecia
Hematologic Cancer
Diaphragmatic Hernia, Congenital
Decubitus Ulcer
Prostatic Hyperplasia, Benign
Bowel Dysfunction
Lung Disease
Lacrimoauriculodentodigital Syndrome 1
Interstitial Lung Disease 2
Alveolar Periostitis
Prostate Cancer
Colitis
Craniosynostosis
Psoriasis
Chronic Ulcer of Skin
Inflammatory Bowel Disease
Gastric Cancer
Gingival Recession
Phosphorus Metabolism Disease
Crouzon Syndrome
Developmental and Epileptic Encephalopathy 47
Corneal Ulcer
Limb Ischemia
Endometrial Cancer
Hypophosphatemic Rickets, X-Linked Dominant
Pancreatic Cancer
Skin Disease
Jackson-Weiss Syndrome
Ovarian Cancer
Macular Degeneration, Age-Related, 1
Acquired Hemangioma
Hair Disease
Kidney Disease
Colorectal Cancer
Cerebellar Vermis Medulloblastoma
Corneal Disease
Lipoprotein Quantitative Trait Locus
Exudative Vitreoretinopathy 1
Conjunctival Vascular Disease
Allergic Cutaneous Vasculitis
Exudative Vitreoretinopathy 7
Epilepsy, Idiopathic Generalized 4
Osteochondrodysplasia
Orofacial Cleft
Hypertension, Essential
Blood Group, Globoside System
Kallmann Syndrome
Brittle Bone Disorder
Tooth Agenesis
Connective Tissue Disease
Eye Disease
Rasopathy
Peripheral Nervous System Disease
Nervous System Disease
Retinitis Pigmentosa
质控标准
精子检测
① 冷冻前验证精子活力观察
② 冷冻验证每批次进行复苏验证
品系状态
活体
环境标准
SPF
供应地区
全球范围
