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GM12123 Fibroblast from Muscle, Unspecified

Description:

ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAA
AAAS GENE; AAAS

Affected:

Yes

Sex:

Male

Age:

25 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
Biopsy Source Unspecified
Cell Type Fibroblast
Tissue Type Muscle
Transformant Untransformed
Sample Source Fibroblast from Muscle, Unspecified
Ethnicity HISPANIC
Family Member 1
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Muscle biopsy fibroblast culture; bilateral adrenal gland atrophy; esophageal achalasia; deficient tear production; mental retardation; expired at age 25; an affected sister died at age 3; product of consanguineous marriage; donor subject has a splice-site mutation in the donor site of intron 14 of the AAAS (ALADIN) gene [IVS14+1>C]; there were two different aberrantly spliced AAAS transcripts, the predicted protein products of which lacked the C-terminal, NPC-targeting domain

Characterizations

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Passage Frozen 3
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis
 
Gene AAAS
Chromosomal Location 12q13
Allelic Variant 1 ; ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME
Identified Mutation IVS14+1>C
 
Gene AAAS
Chromosomal Location 12q13
Allelic Variant 2 ; ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME
Identified Mutation IVS14+1>C

Phenotypic Data

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Remarks Muscle biopsy fibroblast culture; bilateral adrenal gland atrophy; esophageal achalasia; deficient tear production; mental retardation; expired at age 25; an affected sister died at age 3; product of consanguineous marriage; donor subject has a splice-site mutation in the donor site of intron 14 of the AAAS (ALADIN) gene [IVS14+1>C]; there were two different aberrantly spliced AAAS transcripts, the predicted protein products of which lacked the C-terminal, NPC-targeting domain

Publications

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Cronshaw JM, Matunis MJ, The nuclear pore complex protein ALADIN is mislocalized in triple A syndrome. Proc Natl Acad Sci U S A100(10):5823-7 2003
PubMed ID: 12730363

External Links

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dbSNP dbSNP ID: 23248
Gene Cards AAAS
Gene Ontology GO:0000004 biological_process unknown
GO:0005554 molecular_function unknown
GO:0008372 cellular_component unknown
NCBI Gene Gene ID:8086
NCBI GTR 231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS
605378 AAAS GENE; AAAS
OMIM 231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS
605378 AAAS GENE; AAAS
Omim Description ACHALASIA-ADDISONIANISM-ALACRIMIA SYNDROME; AAA
  ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMIA
  ADDISONIAN-ACHALASIA SYNDROME
  ALACRIMIA-ACHALASIA-ADDISONIANISM
  ALLGROVE SYNDROME
  GLUCOCORTICOID DEFICIENCY AND ACHALASIA
  HYPOADRENALISM WITH ACHALASIA
  TRIPLE-A SYNDROME

Culture Protocols

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Passage Frozen 3
Split Ratio 1:3
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
Subcultivation Method trypsin-EDTA
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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