ID   NCBSi002-A
SY   AD5
DR   hPSCreg; NCBSi002-A
RX   PubMed=30605839;
CC   From: Tata Institute of Fundamental Research, National Centre for Biological Sciences; Bangalore; India.
CC   Sequence variation: Heterozygous for APOE p.Cys130Arg (c.388T>C); allele ApoE4 (PubMed=30605839).
CC   Sequence variation: GAP43 p.Ser77Gly (c.229A>G) (PubMed=30605839).
ST   Source(s): PubMed=30605839
ST   Amelogenin: X
ST   CSF1PO: 11,12
ST   D13S317: 9,12
ST   D16S539: 9,12
ST   D21S11: 30.2,31.2
ST   D5S818: 11,13
ST   D7S820: 8,9
ST   TH01: 8,9.3
ST   TPOX: 10,11
ST   vWA: 14,18
DI   NCIt; C2866; Alzheimer's disease
OX   NCBI_TaxID=9606; ! Homo sapiens
SX   Female
AG   72Y
CA   Induced pluripotent stem cell
DT   Created: 25-02-19; Last updated: 25-02-19; Version: 1
RX   PubMed=30605839; DOI=10.1016/j.scr.2018.101370;
RA   Najar A.H., Sneha K.M., Ashok A., Babu S., Subramaniam A.G.,
RA   Kannan R., Viswanath B., Purushottam M., Varghese M., Parvez S.,
RA   Panicker M.M., Mukherjee O., Jain S.;
RT   "Derivation of iPSC lines from two patients with familial Alzheimer's
RT   disease from India.";
RL   Stem Cell Res. 34:101370-101370(2019).