NTCC® NA26095 LCL DNA-BioVector NTCC典型培养物保藏中心Coriell NA26095
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- 货 号:NTCC®-Coriell NA26095
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Name:NTCC® NA26095 LCL DNACategory分类:DNACat#货号:NTCC®-Coriell NA26095Size/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: 45 YRGender性别: MaleDescription描述: INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA; IBMPFD | HEAT-SHOCK 22-KD PROTEIN 8; HSPB8 | RIMMED VACUOLAR MYOPATHYRemarks: Clinically affected; diagnosed at 38 years of age by neuromuscular specialist; autosomal dominant distal myopathy; motor neuropathy; muscle weakness; rosacea; benign prostatic hyperplasia; gout; right bundle branch block; chronic right upper quadrant pain; whole exome sequencing revealed an insertion in an intron with a region of sequence variant identity on chromosome 9 between 35,060,302 and 35,066,579 (region includes VCP gene); co-segregation analysis results and confirmation by automated Sanger sequencing revealed a maternally inherited heterozygous mutation in the HSPB8 gene: c.515dupC (p.P173Sfs*43) in exon CDS 3; positive family history: this mutation is also present in the affected mother (lymph GM26097, fibro GM26098) and affected maternal uncle (fibro GM26579); heterozygous variants of uncertain significance (VUS) that are present in the proband, mother and uncle are: CCDC78 c.986T>C (p.I329T), MUSK c.43C>A (p.L15M), and TRIM32 c.1223G>A (p.R408H); heterozygous VUS present in the proband, but absent in both the mother and uncle are: MYH14 c.1607C>T (p.P536L), and TTN c.27601G>T (p.A9201S); unaffected brother (GM26099-lymph); at-risk maternal aunt (GM26100-lymph); also see fibro GM26096; pedigree and family history in PMID 31403083.Alternate IDs其他编号: Cell Type细胞类型:
LCLSource组织来源: LCLGene: HSPB8 Disease疾病类型: Mutations突变: c.515dupC (p.P173Sfs*43)Karyotypes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
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