ID   NEDCASB FiPS319-Ep6F-7
AC   CVCL_E7A8
WW   Provider; BNLC; -; https://www.isciii.es/documents/20119/880364/Caracteristicas+-+NEDCASB+FiPS319-Ep6F-7+Solicitud+de+dep%C3%B3sito.pdf
WW   Provider; BNLC; -; https://www.isciii.es/documents/20119/880377/NEDCASB%2520FiPS319-Ep6F-7%2520Anexo.pdf
CC   Part of: Spanish Stem Cell Bank (Banco Nacional de Lineas Celulares) collection.
CC   From: Institut d'Investigacio Biomedica de Bellvitge (IDIBELL); Barcelona; Spain.
CC   Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): BNLC
ST   Amelogenin: X,Y
ST   CSF1PO: 13
ST   D13S317: 12,13
ST   D16S539: 11,12
ST   D21S11: 29,30
ST   D5S818: 11,13
ST   D7S820: 8,10
ST   TH01: 9,9.3
ST   TPOX: 8,10
ST   vWA: 14,17
DI   NCIt; C215054; Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   3Y
CA   Induced pluripotent stem cell
DT   Created: 10-04-25; Last updated: 10-04-25; Version: 1
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