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GM20016 Fibroblast from Skin, Unspecified

Description:

FARBER LIPOGRANULOMATOSIS
N-ACYLSPHINGOSINE AMIDOHYDROLASE 1; ASAH1

Affected:

Yes

Sex:

Female

Age:

No Data

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

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Lysosomal Storage Diseases
Class Disorders of Lipid Metabolism
Biopsy Source Unspecified
Cell Type Fibroblast
Tissue Type Skin
Transformant Untransformed
Sample Source Fibroblast from Skin, Unspecified
Race Other
Ethnicity TURKISH
Relation to Proband proband
Confirmation Molecular characterization before cell line submission to CCR
Species Homo sapiens
Common Name Human
Remarks Clinically affected; combined Farber and Sandhoff disease (Farber disease subtype 6); consanguineous parents; died at 2.5 years; donor subject is homozygous for a A>G transition at nucleotide 958 in exon 12 of the ASAH gene [958A>G] resulting in a substitution of aspartic acid for asparagine at codon 320 [Asn320Asp (N320D)] in the AC beta subunit.

Characterizations

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Gene ASAH
Chromosomal Location 8p22
Allelic Variant 1 613468.0004; FARBER LIPOGRANULOMATOSIS
Identified Mutation ASN320ASP; In a patient with Farber lipogranulomatosis Bar et al. (2001) described an asn320-to-asp (N320D) substitution caused by a 958A-G change in the beta subunit of acid ceramidase in homozygous state.
 
Gene ASAH
Chromosomal Location 8p22
Allelic Variant 2 613468.0004; FARBER LIPOGRANULOMATOSIS
Identified Mutation ASN320ASP; In a patient with Farber lipogranulomatosis Bar et al. (2001) described an asn320-to-asp (N320D) substitution caused by a 958A-G change in the beta subunit of acid ceramidase in homozygous state.

Phenotypic Data

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Remarks Clinically affected; combined Farber and Sandhoff disease (Farber disease subtype 6); consanguineous parents; died at 2.5 years; donor subject is homozygous for a A>G transition at nucleotide 958 in exon 12 of the ASAH gene [958A>G] resulting in a substitution of aspartic acid for asparagine at codon 320 [Asn320Asp (N320D)] in the AC beta subunit.

Publications

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Bar J, Linke T, Ferlinz K, Neumann U, Schuchman EH, Sandhoff K, Molecular analysis of acid ceramidase deficiency in patients with Farber disease. Hum Mutat17(3):199-209 2001
PubMed ID: 11241842

External Links

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dbSNP dbSNP ID: 13636
Gene Cards ASAH
ASAH1
Gene Ontology GO:0005764 lysosome
GO:0006631 fatty acid metabolism
GO:0006672 ceramide metabolism
GO:0016787 hydrolase activity
GO:0017040 ceramidase activity
NCBI Gene Gene ID:427
NCBI GTR 228000 FARBER LIPOGRANULOMATOSIS; FRBRL
613468 N-ACYLSPHINGOSINE AMIDOHYDROLASE 1; ASAH1
OMIM 228000 FARBER LIPOGRANULOMATOSIS; FRBRL
613468 N-ACYLSPHINGOSINE AMIDOHYDROLASE 1; ASAH1
Omim Description AC DEFICIENCY
  ACID CERAMIDASE DEFICIENCY
  CERAMIDASE DEFICIENCY
  FARBER LIPOGRANULOMATOSIS
  N-LAURYLSPHINGOSINE DEACYLASE DEFICIENCYN-ACYLSPHINGOSINE AMIDOHYDROLASE, INCLUDED; ASAH, INCLUDED

Culture Protocols

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Split Ratio 1:2
Temperature 37 C
Percent CO2 8%
Medium Dulbecco Modified Eagles Medium (high glucose) with 2mM L-glutamine or equivalent
Serum 10% fetal bovine serum Not inactivated
Substrate None specified
Subcultivation Method trypsin-EDTA
Supplement Sodium Pyruvate 100mM
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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