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GM28726 LCL from B-Lymphocyte

Description:

HOMOCYSTINURIA
CYSTATHIONINE BETA-SYNTHASE; CBS

Affected:

Yes

Sex:

Male

Age:

9 YR (At Sampling)

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

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
PIGI Consented Sample
Biopsy Source Peripheral vein
Cell Type B-Lymphocyte
Tissue Type Blood
Transformant Epstein-Barr Virus
Sample Source LCL from B-Lymphocyte
Race White
Subject Type trio
Ethnicity Not Hispanic/Latino
Ethnicity European
Country of Origin USA
Family Member 1
Family History N
Relation to Proband proband
Confirmation Molecular characterization before cell line submission to CCR
Species Homo sapiens
Common Name Human
Remarks Clinically affected. See "Phenotypic Data" tab; unaffected mother is GM28728 (lymph) and unaffected father is GM28727 (lymph).

Characterizations

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Gene CBS
Chromosomal Location 21q22.3
Allelic Variant 1 Asn149Glufs; Homocystinuria, B6-responsive and nonresponsive types
Identified Mutation c.444dup (p.Asn149Glufs*39)
 
Gene CBS
Chromosomal Location 21q22.3
Allelic Variant 2 Arg121Cys; Homocystinuria, B6-responsive and nonresponsive types
Identified Mutation c.361C>T (p.Arg121Cys)

Phenotypic Data

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Demographic Data
Relation to Proband proband
Age at Sampling 9 YR
Sex Male
Age of Onset(If not a control) 8 YR
Age at Diagnosis(If not a control) 8 YR
Hispanic or Latino/Not Hispanic or Latino Not Hispanic/Latino
Racial Category White
Country USA
 
Data Elements
Clinical Element Type: General NIGMS Catalog Remarks
  (Baseline)
Mutation Information
Gene, variant, consequence, and exon number:  CBS, C.444DUP, P.(ASN149GLUFS), EXON 5. SEQUENCE ANALYSIS USING THE BLUEPRINT GENETICS CBS SINGLE GENE TEST
Zygosity:  Compound Heterozygous
Other variants:  CBS, C.361C
Age of Symptom Onset and Age at Diagnosis
Age of Symptom Onset:  8 YEARS OLD
Age at Diagnosis:  8 YEARS OLD
In Utero History Information
Birth History Information
Dysmorphic Features
Neurological Symptoms
Optical and Audiological Symptoms
Additional Information:  LENS DISLOCATION: LENSES IN BOTH EYES HAD TO BE REMOVED SEVERE MYOPIA
Musculoskeletal Symptoms
Additional Information:  FRACTURES MILD OSTEOPENIA
Developmental Milestones
Gastrointestinal Symptoms
Genitourinary Symptoms
Respiratory and Cardiovascular Symptoms
Cognitive and Behavioral Symptoms
Additional Information
Testing Performed
Metabolic, Hematologic, and Endocrinologic Testing:  ELEVATED HOMOCYSTEINE AND METHIONINE
Treatments and Assistive Devices
Surgeries  CATARACT SURGERY
Medications
 BETAINE METHIONINE/PROTEIN RESTRICTED DIET
Family History
Remarks Clinically affected. See "Phenotypic Data" tab; unaffected mother is GM28728 (lymph) and unaffected father is GM28727 (lymph).

External Links

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Gene Cards CBS
Gene Ontology GO:0004122 cystathionine beta-synthase activity
GO:0005737 cytoplasm
GO:0006520 amino acid metabolism
GO:0006535 cysteine biosynthesis from serine
GO:0016829 lyase activity
GO:0019343 cysteine biosynthesis via cystathione
NCBI Gene Gene ID:875
NCBI GTR 236200 HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY
613381 CYSTATHIONINE BETA-SYNTHASE; CBS
OMIM 236200 HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY
613381 CYSTATHIONINE BETA-SYNTHASE; CBS
Omim Description CBS DEFICIENCYCYSTATHIONINE BETA-SYNTHASE, INCLUDED; CBS, INCLUDED
  CYSTATHIONINE BETA-SYNTHASE DEFICIENCY
  HOMOCYSTINURIA
  HOMOCYSTINURIA, PYRIDOXINE-RESPONSIVE, INCLUDED

Culture Protocols

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Split Ratio 1:5
Temperature 37 C
Percent CO2 5%
Percent O2 AMBIENT
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 -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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How to Order
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