NTCC® NA16192 Fibroblast DNA-BioVector NTCC典型培养物保藏中心Coriell NA16192
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- 货 号:NTCC®-Coriell NA16192
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- BioVector NTCC典型培养物保藏中心
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Name:NTCC® NA16192 Fibroblast DNACategory分类:DNACat#货号:NTCC®-Coriell NA16192Size/Quantity数量: 1 VialBiosafety Level生物安全级别:1Shipping Info运输方式: RTStorage储存方式: 4CSpecies物种来源: Age年龄: 1 MOGender性别: MaleDescription描述: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4 (WALKER-WARBURG SYNDROME INCLUDED) | FUKUTIN; FKTNRemarks: Clinically affected; foreskin; type II lissencephaly; congenital myotonic dystrophy; hydrocephalus indicated in utero by MRI; no aqueductal stenosis by post-natal MRI/CT; vermis hypoplasia; absent septum pellucidum; CPK = 2,200 u/ml; retinal exam showed vitreous hemorrhage but no pigmentary retinopathy; hypertonia; karyotype is 46,XY.ish 17(LIS1x2,RARAx2); donor is a compound heterozygote: one allele has a 1 bp deletion at nucleotide 385 in exon 5 of the FKTN gene (c.385delA) resulting in a frameshift and creation of a stop at codon 129 (I129fsX1); the second allele has a C>A transversion at nucleotide 1176 in exon 10 (c.1176C>A) resulting in a stop at codon 392 [Tyr392Ter (Y392X)]Alternate IDs其他编号: Cell Type细胞类型:
FibroblastSource组织来源: FibroblastGene: FKTN Disease疾病类型: Mutations突变: 385delA TYR392TERKaryotypes核型: Cytogenetics: Mutation description突变描述: Origin: Transformants: Alias别名: Images图片:References参考文献:Supplier供应商:BioVector质粒载体菌株细胞蛋白抗体基因保藏中心
NTCC典型培养物保藏中心
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