Description:
NIEMANN-PICK DISEASE, TYPE C2
NPC2 GENE; NPC2
Repository
|
NIGMS Human Genetic Cell Repository
|
Subcollection |
Heritable Diseases Lysosomal Storage Diseases |
Class |
Disorders of Lipid Metabolism |
Cell Type
|
Fibroblast
|
Transformant
|
Untransformed
|
Relation to Proband
|
proband
|
Confirmation
|
Molecular characterization before cell line submission to CCR
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
PDL at Freeze |
5.59 |
Passage Frozen |
5 |
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Nucleoside Phosphorylase,Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis |
|
Gene |
NPC2 |
Chromosomal Location |
14q24.3 |
Allelic Variant 1 |
; NIEMANN-PICK DISEASE, TYPE C2 |
Identified Mutation |
IVS1+2T>C |
|
Gene |
NPC2 |
Chromosomal Location |
14q24.3 |
Allelic Variant 2 |
; NIEMANN-PICK DISEASE, TYPE C2 |
Identified Mutation |
IVS1+2T>C |
Remarks |
Clinically affected; fibroblasts showed 21 pmol CE/mg protein/6 hr activity in a cholesterol esterification assay [normal mean was 1855 +/- 1327 pmol CE/mg protein/6 hr, see Park et al. Hum Mut 22:313-325 (2003)]; a complementation test showed that the cells were type 2 (see Park et al., 2003); the donor subject is homozygous at the NPC2 gene locus: both alleles carry a substitution (T>C) at nucleotide IVS1+2 (g.IVS1+2T>C) in intron 1, resulting in a splicing defect; the first nucleotide of the initiating MET codon is numbered +1. |
Liu EA, Schultz ML, Mochida C, Chung C, Paulson HL, Lieberman AP, Fbxo2 mediates clearance of damaged lysosomes and modifies neurodegeneration in the Niemann-Pick C brain JCI insight: 2020 |
PubMed ID: 32931479 |
Passage Frozen |
5 |
Split Ratio |
1:3 |
Temperature |
37 C |
Percent CO2 |
5% |
Percent O2 |
AMBIENT |
Medium |
Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent |
Serum |
15% fetal bovine serum Not inactivated |
Substrate |
None specified |
Supplement |
- |
|
|