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GM10272 LCL from B-Lymphocyte

Description:

ANIRIDIA 1; AN1
TRANSLOCATED CHROMOSOME

Affected:

Yes

Sex:

Male

Age:

No Data

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

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Chromosome Abnormalities
Class Ophthalmologic Disorders
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 2
Relation to Proband half-brother
Confirmation Clinical summary/Case history
ISCN 46,XY,t(11;22)(11qter>11p13::22q11.2 or 12.2>22qter;22pter>22q11.2 or 12.2:: 11p13>11pter)pat
Species Homo sapiens
Common Name Human
Remarks Clinically affected; aniridia, cataracts, hyperopia, and nystagmus first noted at 3 months of age; at age 12 years there was pendular nystagmus, bilateral total aniridia, bilateral posterior subcapsular cataractous changes, and absent foveae; normal ocular pressure; visual acuity 20/400 corrected; no genitourinary tract abnormalities; IQ=67; familial chromosome translocation; father (GM10274), paternal half-sister (GM10273), and paternal grandmother also affected with aniridia and familial chromosome translocation; seven family members in 4 generations affected with aniridia but karyotype unknown.

Characterizations

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IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis and by Chromosome Analysis
 
Cytogenetics Chromosome 11: TRANSLOCATION Breakpoint 11p13 t(11;22)11p13
Chromosome 22: TRANSLOCATION Breakpoint 22q11 t(11;22)22q11
Chromosome 22: TRANSLOCATION Breakpoint 22q12 t(11;22)22q12

Phenotypic Data

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Remarks Clinically affected; aniridia, cataracts, hyperopia, and nystagmus first noted at 3 months of age; at age 12 years there was pendular nystagmus, bilateral total aniridia, bilateral posterior subcapsular cataractous changes, and absent foveae; normal ocular pressure; visual acuity 20/400 corrected; no genitourinary tract abnormalities; IQ=67; familial chromosome translocation; father (GM10274), paternal half-sister (GM10273), and paternal grandmother also affected with aniridia and familial chromosome translocation; seven family members in 4 generations affected with aniridia but karyotype unknown.

Publications

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Moore JW, Hyman S, Antonarakis SE, Mules EH, Thomas GH, Familial isolated aniridia associated with a translocation involving chromosomes 11 and 22 [t(11;22)(p13;q12.2)]. Hum Genet72:297-302 1986
PubMed ID: 3754537

External Links

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dbSNP dbSNP ID: 17098
NCBI GTR 106210 ANIRIDIA 1; AN1
OMIM 106210 ANIRIDIA 1; AN1
Omim Description PAIRED BOX HOMEOTIC GENE 6; PAX6ANIRIDIA, TYPE II, INCLUDED; AN2, INCLUDED

Culture Protocols

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Split Ratio 1:2
Temperature 37 C
Percent CO2 5%
Medium Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent
Serum 20% fetal bovine serum Not Inactivated
Substrate None specified
Subcultivation Method dilution - add fresh medium
Supplement -
Pricing
Commercial/For-profit:
$373.00USD
Academic/Non-profit/Government:
$216.00USD
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