ID   WAe009-A-51
AC   CVCL_A7HC
SY   TPP1 c.509-1G > C, clone #42; EMe-TPint5GC42; H9 TPP1 INT5 SA#42; BROWNe010-A-51
DR   hPSCreg; WAe009-A-51
DR   Wikidata; Q107117426
RX   PubMed=33845243;
CC   From: Brown University; Providence; USA.
CC   Sequence variation: Mutation; HGNC; 2073; TPP1; Simple_edited; c.509-1G>C (IVS5-1G>C); ClinVar=VCV000002644; Zygosity=Homozygous; Note=By CRISPR/Cas9 (PubMed=33845243).
DI   NCIt; C85864; Neuronal ceroid lipofuscinosis type 2
DI   ORDO; Orphanet_228349; CLN2 disease
OX   NCBI_TaxID=9606; ! Homo sapiens
HI   CVCL_9773 ! WA09
SX   Female
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 20-05-21; Last updated: 22-09-22; Version: 3
//
RX   PubMed=33845243; DOI=10.1016/j.scr.2021.102323;
RA   Ma L., Prada A.M., Schmidt M., Morrow E.M.;
RT   "Generation of pathogenic TPP1 mutations in human stem cells as a
RT   model for neuronal ceroid lipofuscinosis type 2 disease.";
RL   Stem Cell Res. 53:102323-102323(2021).
//