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GM07531 Fibroblast

Description:

ADRENOLEUKODYSTROPHY; ALD

Affected:

Yes

Sex:

Male

Age:

19 YR (At Sampling)

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

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Class Disorders of Steroid Metabolism
Cell Type Fibroblast
Transformant Untransformed
Race White
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Adrenomyeloneuropathy; adrenal insufficiency since age 11; unsteady gait since age 13; slt wkness & hyperreflexia since age 19; brother has mild spastic paraparesis; mother had progressive paraparesis; elevated level of C26 fatty acid in plasma & fibr

Characterizations

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PDL at Freeze 5.74
Passage Frozen 9
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis
 

Phenotypic Data

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Remarks Adrenomyeloneuropathy; adrenal insufficiency since age 11; unsteady gait since age 13; slt wkness & hyperreflexia since age 19; brother has mild spastic paraparesis; mother had progressive paraparesis; elevated level of C26 fatty acid in plasma & fibr

Publications

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Come JH, Senter TJ, Clark MP, Court JJ, Gale-Day Z, Gu W, Krueger E, Liang J, Morris M, Nanthakumar S, O'Dowd H, Maltais F, Iyer G, Andreassi J, Boucher C, Considine T, Moody CS, Taylor W, Mohanty AK, Huang Y, Zuccola H, Coll J, Bonanno KC, Gagnon KJ, Gan L, Lu F, Gao H, Chakilam A, Engtrakul J, Song B, Crawford D, Doyle E, Kramer T, Vought B, Phillips J, Kemper R, Sanders M, Swett R, Furey B, Winquist R, Bunnage ME, Jackson KL, Charifson PS, Magavi SS, Discovery and Optimization of Pyrazole Amides as Inhibitors of ELOVL1 Journal of medicinal chemistry64:17753-17776 2021
PubMed ID: 34748351
 
Singh J, Khan M, Singh I, Caffeic acid phenethyl ester induces adrenoleukodystrophy (Abcd2) gene in human X-ALD fibroblasts and inhibits the proinflammatory response in Abcd1/2 silenced mouse primary astrocytes Biochimica et biophysica acta64:17753-17776 2012
PubMed ID: 23318275
 
Pahan K, Khan M, Singh I, Therapy for X-adrenoleukodystrophy: normalization of very long chain fatty acids and inhibition of induction of cytokines by cAMP. J Lipid Res39(5):1091-100 1998
PubMed ID: 9610777
 
Moser HW, Moser AB, Kawamura N, Murphy J, Suzuki K, Schaumburg H, Kishimoto Y, Adrenoleukodystrophy: elevated C26 fatty acid in cultured skin fibroblasts. Ann Neurol7:542-9 1980
PubMed ID: 7436359

External Links

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dbSNP dbSNP ID: 21027
Gene Cards ALD
NCBI GTR 300100 ADRENOLEUKODYSTROPHY; ALD
OMIM 300100 ADRENOLEUKODYSTROPHY; ALD
Omim Description ADDISON DISEASE AND CEREBRAL SCLEROSIS
  ADRENOLEUKODYSTROPHY; ALD
  ADRENOMYELONEUROPATHY; AMN
  BRONZE SCHILDER'S DISEASE
  MELANODERMIC LEUKODYSTROPHYADRENOLEUKODYSTROPHY PROTEIN, INCLUDED; ALDP, INCLUDED
  SIEMERLING-CREUTZFELDT DISEASE

Culture Protocols

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Passage Frozen 9
Split Ratio 1:4
Temperature 37 C
Percent CO2 5%
Percent O2 AMBIENT
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
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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