GM23857
LCL from B-Lymphocyte
Description:
PRADER-WILLI SYNDROME; PWS
Repository
|
NIGMS Human Genetic Cell Repository
|
Subcollection |
Heritable Diseases Chromosome Abnormalities |
Biopsy Source
|
Peripheral vein
|
Cell Type
|
B-Lymphocyte
|
Tissue Type
|
Blood
|
Transformant
|
Epstein-Barr Virus
|
Sample Source
|
LCL from B-Lymphocyte
|
Race
|
White
|
Ethnicity
|
Hispanic/Latino
|
Ethnicity
|
MEXICAN
|
Family History
|
N
|
Relation to Proband
|
proband
|
Confirmation
|
Karyotypic analysis before cell line submission to CCR
|
ISCN
|
46,XY.arr 15q11.1q11.2(20556429-22588019)x1,15q11.2q13.1(23641501-28527735)x1
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by LINE assay |
|
Remarks |
Clinically affected;ish del (15)(q11.2q12)(SNRPN-,D15S10-); upslanting almond shaped eyes; mild strabismus,mild hypertelorism, difficulty feeding at birth requiring a G tube; bilateral undescended testicles at birth;flattened occiput, round facies with slight bitemporal narrowing; synophyrs, flattened nasal bridge, narrow high arched palate; small hands, narrow nails with tapered fingers; deep sacral crease with hypotrichosis; generalized hypotonia; hyperlaxity; on growth hormone and Cortef |
Tang Z, Berlin DS, Toji L, Toruner GA, Beiswanger C, Kulkarni S, Martin CL, Emanuel BS, Christman M, Gerry NP, A dynamic database of microarray-characterized cell lines with various cytogenetic and genomic backgrounds G3 (Bethesda, Md)3:1143-9 2013 |
PubMed ID: 23665875 |
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 |
- |
|
|