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GM00013 Fibroblast from Skin, Arm

Description:

LESCH-NYHAN SYNDROME; LNS

Affected:

No

Sex:

Female

Age:

34 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • Publications
  • External Links
  • Images
  • Culture Protocols

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Class Disorders of Nucleotide and Nucleic Acid Metabolism
Biopsy Source Arm
Cell Type Fibroblast
Tissue Type Skin
Transformant Untransformed
Sample Source Fibroblast from Skin, Arm
Race White
Family Member 2
Relation to Proband mother
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks 46,XX; 55% of normal HPRT activity in fibroblasts; clinically unaffected mother of GM00377A

Characterizations

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Passage Frozen 10
 
hypoxanthine phosphoribosyltransferase According to the submitter, biochemical test results for this subject showed decreased enzyme activity. EC Number: 2.4.2.8; 55% activity.
 

Phenotypic Data

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Remarks 46,XX; 55% of normal HPRT activity in fibroblasts; clinically unaffected mother of GM00377A

Publications

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Gao X, Nowak-Imialek M, Chen X, Chen D, Herrmann D, Ruan D, Chen ACH, Eckersley-Maslin MA, Ahmad S, Lee YL, Kobayashi T, Ryan D, Zhong J, Zhu J, Wu J, Lan G, Petkov S, Yang J, Antunes L, Campos LS, Fu B, Wang S, Yong Y, Wang X, Xue SG, Ge L, Liu Z, Huang Y, Nie T, Li P, Wu D, Pei D, Zhang Y, Lu L, Yang F, Kimber SJ, Reik W, Zou X, Shang Z, Lai L, Surani A, Tam PPL, Ahmed A, Yeung WSB, Teichmann SA, Niemann H, Liu P, Establishment of porcine and human expanded potential stem cells Nature cell biology21:687-699 2018
PubMed ID: 31160711
 
Park IH, Arora N, Huo H, Maherali N, Ahfeldt T, Shimamura A, Lensch MW, Cowan C, Hochedlinger K, Daley GQ, Disease-Specific Induced Pluripotent Stem Cells Cell134(5):877-86 2008
PubMed ID: 18691744
 
Nussbaum RL, Crowder WE, Nyhan WL, Caskey CT, A three-allele restriction-fragment-length polymorphism at the hypoxanthine phosphoribosyltransferase locus in man. Proc Natl Acad Sci U S A80:4035-9 1983
PubMed ID: 6306659

External Links

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dbSNP dbSNP ID: 22945
NCBI GTR 300322 LESCH-NYHAN SYNDROME; LNS
OMIM 300322 LESCH-NYHAN SYNDROME; LNS
Omim Description LESCH-NYHAN SYNDROME; LNS

Images

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View pedigree 

Culture Protocols

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Passage Frozen 10
Split Ratio 1:3
Temperature 37 C
Percent CO2 5%
Medium Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Not inactivated
Substrate None specified
Subcultivation Method trypsin-EDTA
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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