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GM25204 LCL from B-Lymphocyte

Description:

DEAFNESS, AUTOSOMAL RECESSIVE 1A; DFNB1A
GAP JUNCTION PROTEIN, BETA-2; GJB2 (CONNEXIN 26; CX26)

Affected:

Yes

Sex:

Female

Age:

18 MO (At Sampling)

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

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Cell Type B-Lymphocyte
Transformant Epstein-Barr Virus
Sample Source LCL from B-Lymphocyte
Race Chinese
Ethnicity Not Hispanic/Latino
Country of Origin USA
Family History Y
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Clinically affected: bilateral sensorineural hearing loss; born at 35 weeks gestation via C-section due to preeclampsia; in NICU for 9 days where she failed her newborn hearing screen and was treated for jaundice; passed her follow up newborn hearing screen at 3 weeks; at 12 months an ABR was completed due to speech delay; Also completed at 12 months: ophthalmology exam, temporal bone MRI, temporal bone CT and EKG, all with normal results; normal motor development: walked at 12 months ; speech delay (no words at 18 months); eczema; treatments: cochlear implants; therapies: speech therapy; donor subject is a compound heterozygote for c.235delC mutation(resulting in p.Leu79CysfsX3) and c.176_191del16 mutation (resulting in p.Gly59AlafsX18) in the GJB2 gene; twin brother carries same mutations and also has bilateral sensorineural hearing loss(not in repository).

Characterizations

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IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by LINE assay
 
Gene GJB2
Chromosomal Location 13q11-q12
Allelic Variant 1 stop;
Identified Mutation 235delC; Leu79CysfsX3
 
Gene GJB2
Chromosomal Location 13q11-q12
Allelic Variant 1 Stop;
Identified Mutation 176_191del16; Gly59AlafsX18

Phenotypic Data

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Remarks Clinically affected: bilateral sensorineural hearing loss; born at 35 weeks gestation via C-section due to preeclampsia; in NICU for 9 days where she failed her newborn hearing screen and was treated for jaundice; passed her follow up newborn hearing screen at 3 weeks; at 12 months an ABR was completed due to speech delay; Also completed at 12 months: ophthalmology exam, temporal bone MRI, temporal bone CT and EKG, all with normal results; normal motor development: walked at 12 months ; speech delay (no words at 18 months); eczema; treatments: cochlear implants; therapies: speech therapy; donor subject is a compound heterozygote for c.235delC mutation(resulting in p.Leu79CysfsX3) and c.176_191del16 mutation (resulting in p.Gly59AlafsX18) in the GJB2 gene; twin brother carries same mutations and also has bilateral sensorineural hearing loss(not in repository).

External Links

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Gene Cards GJB2
Gene Ontology GO:0005886 plasma membrane
GO:0005922 connexon complex
GO:0006810 transport
GO:0007267 cell-cell signaling
GO:0007605 perception of sound
GO:0015285 connexon channel activity
GO:0016021 integral to membrane
NCBI Gene Gene ID:2706
NCBI GTR 121011 GAP JUNCTION PROTEIN, BETA-2; GJB2
220290 DEAFNESS, AUTOSOMAL RECESSIVE 1A; DFNB1A
OMIM 121011 GAP JUNCTION PROTEIN, BETA-2; GJB2
220290 DEAFNESS, AUTOSOMAL RECESSIVE 1A; DFNB1A
Omim Description DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 1; DFNB1
  NEUROSENSORY NONSYNDROMIC RECESSIVE DEAFNESS 1; NSRD1

Culture Protocols

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Split Ratio 1:3
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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