NTCC® NA04663 Fibroblast DNA-BioVector NTCC典型培养物保藏中心Coriell NA04663
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- 货 号:NTCC®-Coriell NA04663
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Name:NTCC® NA04663 Fibroblast DNACategory分类:DNACat#货号:NTCC®-Coriell NA04663Size/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: 2 YRGender性别: FemaleDescription描述: NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III; HSAN3 | INHIBITOR OF KAPPA LIGHT POLYPEPTIDE GENE ENHANCER IN B CELLS, KINASE-COMPLEX ASSOCIATED PROTEIN; IKBKAP | ASPARTOACYLASE; ASPARemarks: Clinically affected; diagnosed within the first year of life; born at 36 weeks and small for gestational age (BW=1.69 kg); hypotonia and poor suck in neonatal period; questionable seizure in neonatal period; absent fungiform papillae on tongue; absent deep tendon reflexes; skin blotching; hyperhidrosis; alacrima; sluggish corneal reflexes; no flare response to histamine test; good linear growth; pneumonia; air swallowing; developmental delay; tongue thrusting; corneal ulcers; acrocyanosis; weak, hoarse cry; searching nystagmus when drinking; high palate; small umbilical hernia; at 25 months, BUN normal for age (5); poor coordination; constipation; vomits mucous and bile after meals; poor head control; extraneous movements and alternating low and high tone periods; no breath holding; hospitalized for diarrhea on at least one occasion; father is GM04664; mother is GM04665; donor subject is homozygous for the 2507+6T>C mutation in the IKBKAP gene; this donor splice site mutation (IVS20+6T>C) leads to deletion of exon 20 from the mRNA; donor subject is also heterozygous for a silent polymorphism in the ASPA gene: 693C>T [Tyr231Tyr (Y231Y)]Alternate IDs其他编号: Cell Type细胞类型:
FibroblastSource组织来源: FibroblastGene: ASPA IKBKAP Disease疾病类型: Mutations突变: c.2204+6T>C (IVS20+6T>C) TYR231TYRKaryotypes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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