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GM28026 LCL from B-Lymphocyte

Description:

MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO
MAF BZIP TRANSCRIPTION FACTOR; MAFB

Affected:

Yes

Sex:

Female

Age:

3 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
Ethnicity 3/4 Jewish
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 See "Phenotypic Data" tab.

Characterizations

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Gene MAFB
Chromosomal Location 20q12
Allelic Variant 1 p.Pro71Arg; MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO
Identified Mutation c.212C>G (p.P71R)

Phenotypic Data

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Demographic Data
Relation to Proband proband
Age at Sampling 3 YR
Sex Female
Age of Onset(If not a control) 18 MO
Age at Diagnosis(If not a control) 2 YR
Racial Category White
Country USA
 
Data Elements
Clinical Element Type: General NIGMS Catalog Remarks
  (Baseline)
Mutation Information
Gene, variant, consequence, and exon number:  WHOLE EXOME SEQUENCING REVEALED A LIKELY PATHOGENIC DE NOVO VARIANT IN EXON 1 OF THE MAFB GENE (NM_005461.4), CHR:POSITION 20:39317279, C.212C>G (P.P71R). READS WERE ALIGNED TO HUMAN GENOME BUILD GRCH37/UCSC HG19
Zygosity:  Heterozygous
Notes: DE NOVO MUTATION
Other variants:  COPY NUMBER VARIANT (CNV) ANALYSIS WAS PERFORMED; THERE WAS NO INDICATION OF A CLINICALLY RELEVANT DELETION OR DUPLICATION OF 3 OR MORE EXONS IN THE DATA FOR THIS PROBAND
Age of Symptom Onset and Age at Diagnosis
Age of Symptom Onset:  18 MONTHS
Age at Diagnosis:  2 YEARS, 10 MONTHS
In Utero History Information
Birth History Information
Dysmorphic Features
Additional Information:  SHORT STATURE, EPIDERMOID CYSTO OF THE TONGUE, SKIN LAXITY, EXHIBITS CRANIOFACIAL FEATURES OF DISORDER
Neurological Symptoms
Optical and Audiological Symptoms
Musculoskeletal Symptoms
Additional Information:  SKELETAL ABNORMALITIES, SMALL TALUS BONE, C5-C6 SEGMENTATION ANOMALY, HYPOPLASTIC THUMBS, INFLAMMED SWOLLEN ANKLES
Developmental Milestones
Delayed gross motor skills
Additional Information:  DID NOT WALK UNTIL 2 YEARS OF AGE; CANNOT CLIMB STEPS, HOP, JUMP OR PUT ANY PRESSURE ON WRISTS
Gastrointestinal Symptoms
Additional Information:  ANTERIOR ANUS
Genitourinary Symptoms
Respiratory and Cardiovascular Symptoms
Cognitive and Behavioral Symptoms
Additional Information
Testing Performed
Musculoskeletal and Developmental Testing:  X-RAYS SHOW IRREULAR-SHAPED AND MISSING CARPAL AND TARSAL BONE
Treatments and Assistive Devices
Orthotics
Additional Testing:  ADDITIONAL ASSISTIVE DEVICES: BRACES SURGERIES: EAR TUBE REMOVAL, ADENOID REMOVAL, CYST REMOVAL UNDER TONGUE
Medications
 ANTI-INFLAMMATORY MEDS, METHOTREXATE, ACTEMRA, LISINOPRIL (QBRELIS)
Family History
 THIS PROBAND'S PARENTS (NOT IN THE REPOSITORY) DO NOT HARBOR THE P.P71R VARIANT IN THE MAFB GENE.
Remarks See "Phenotypic Data" tab.

External Links

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Gene Cards MAFB
NCBI GTR 166300 MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO
608968 MAF bZIP TRANSCRIPTION FACTOR B; MAFB
OMIM 166300 MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO
608968 MAF bZIP TRANSCRIPTION FACTOR B; MAFB
Omim Description IDIOPATHIC MULTICENTRIC OSTEOLYSIS; IMO
  OSTEOLYSIS, HEREDITARY, OF CARPAL BONES WITH NEPHROPATHY

Culture Protocols

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Split Ratio 1:4
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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