NTCC? NA19988 LCL DNA-BioVector NTCC典型培養物保藏中心Coriell NA19988
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- 貨 號:NTCC?-Coriell NA19988
- 產 地:北京
- BioVector NTCC典型培養物保藏中心
- 聯系人:Dr.Xu, Biovector NTCC Inc.
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Name:NTCC? NA19988 LCL DNACategory分類:DNACat#貨號:NTCC?-Coriell NA19988Size/Quantity數量: 1 VialBiosafety Level生物安全級別:1Shipping Info運輸方式: RTStorage儲存方式: 4CSpecies物種來源: Age年齡: 36 YRGender性別: FemaleDescription描述: LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM (OVARIOLEUKODYSTROPHY, INCLUDED) | EUKARYOTIC TRANSLATION INITIATION FACTOR 2B, SUBUNIT 2; EIF2B2Remarks: Clinically affected; patient #944 in Fogli et al, Am J Hum Genet 72:1544-1550, 2003; bilateral cataracts in first week of life were excised with implantation of intraocular lens; walked at age 12 mo; difficulties in school; mild developmental delay; mild thoracic dextroscoliosis; bilateral pes cavus; menarche at age 14 yr; amenorrhea at age 26 yr; atrophied ovaries; spasticity; gait instability at age 25 yr; walker used at age 30 yr; hypophonia with mild dysarthria observed; tongue weakness and hyperreflexia; sphincter disfunction at age 26 yr; optic atrophy; visual loss at age 28 yr;glaucoma with arcuate scotoma of left eye; IQ=65 at age 30 yr; MRI showed generalized volume loss of cortex and white matter; microcephaly; visual motor difficulties; poor executive function; donor subject is a compound heterozygote: one allele has a C>T transition at nucleotide 512 of the EIF2B2 gene (512C>T), resulting in a ser171-to-phe mutation [Ser171Phe (S171F)] and the second allele has a 6 bp deletion (ATGGCT)/2 bp insertion (TG) at nucleotide 607, resulting in a frameshift at met203Alternate IDs其他編號: Cell Type細胞類型:
LCLSource組織來源: LCLGene: EIF2B2 Disease疾病類型: Mutations突變: 6-BP DEL/2-BP INS, NT607 SER171PHEKaryotypes核型: Cytogenetics: Mutation description突變描述: Origin: Transformants: Alias別名: Images圖片:References參考文獻:Supplier供應商:BioVector質粒載體菌株細胞蛋白抗體基因保藏中心
NTCC典型培養物保藏中心
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