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GM06119 LCL from B-Lymphocyte

Description:

OSTEOPETROSIS WITH RENAL TUBULAR ACIDOSIS

Affected:

No Data

Sex:

Female

Age:

46 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 Connective Tissue, Muscle, and Bone
Biopsy Source Peripheral vein
Cell Type B-Lymphocyte
Tissue Type Blood
Transformant Epstein-Barr Virus
Sample Source LCL from B-Lymphocyte
Race White
Family Member 9
Relation to Proband paternal aunt
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Asymptomatic; 50% of normal RBC carbonic anhydrase II activity

Characterizations

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IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase Isoenzyme Electrophoresis
 
carbonate dehydratase (carbonic anhydrase II) According to the submitter, biochemical test results for this subject showed decreased enzyme activity. EC Number: 4.2.1.1; 50% activity.
 

Phenotypic Data

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Remarks Asymptomatic; 50% of normal RBC carbonic anhydrase II activity

Publications

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Roth DE, Venta PJ, Tashian RE, Sly WS, Molecular basis of human carbonic anhydrase II deficiency. Proc Natl Acad Sci U S A89(5):1804-8 1992
PubMed ID: 1542674
 
Sly WS, Whyte MP, Sundaram V, Tashian RE, Hewett-Emmett D, Guibaud P, Vainsel M, Baluarte HJ, Gruskin A, Al-Mosawi M, et al, Carbonic anhydrase II deficiency in 12 families with the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification. N Engl J Med313:139-45 1985
PubMed ID: 3925334
 
Sly WS, Hewett-Emmett D, Whyte MP, Yu YS, Tashian RE, Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification. Proc Natl Acad Sci U S A80:2752-6 1983
PubMed ID: 6405388
 
Whyte MP, Murphy WA, Fallon MD, Sly WS, Teitelbaum SL, McAlister WH, Avioli LV, Osteopetrosis, renal tubular acidosis and basal ganglia calcification in three sisters. Am J Med69:64-74 1980
PubMed ID: 7386510
 
Sly, Recessive osteopetrosis: New clinical phenotype. Am J Hum Genet24:34a (1972):64-74 1972
PubMed ID: 7386510

External Links

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dbSNP dbSNP ID: 17855
Gene Ontology GO:0004089 carbonate dehydratase activity
GO:0005737 cytoplasm
GO:0006730 one-carbon compound metabolism
GO:0008270 zinc ion binding
GO:0016829 lyase activity
NCBI Gene Gene ID:760
NCBI GTR 259730 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3; OPTB3
OMIM 259730 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3; OPTB3
Omim Description CA II, INCLUDED
  CARBONIC ANHYDRASE B, INCLUDED
  CARBONIC ANHYDRASE II DEFICIENCY
  CARBONIC ANHYDRASE II, ERYTHROCYTE, ELECTROPHORETIC VARIANTS OF, INCLUDED
  GUIBAUD-VAINSEL SYNDROME
  MARBLE BRAIN DISEASECARBONIC ANHYDRASE II, INCLUDED; CA2, INCLUDED
  OSTEOPETROSIS WITH RENAL TUBULAR ACIDOSIS

Culture Protocols

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Split Ratio 1:4
Temperature 37 C
Percent CO2 5%
Medium Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Not Inactivated
Substrate None specified
Subcultivation Method dilution - add fresh medium
Supplement -
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$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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