ID   GM05093
AC   CVCL_AB47
DR   CLO; CLO_0025310
DR   Coriell; GM05093
DR   Wikidata; Q54838851
RX   CelloPub=CLPUB00447;
CC   Population: Indian.
CC   Sequence variation: Mutation; HGNC; 4422; GNS; Simple; p.Arg355Ter (c.1063C>T); ClinVar=VCV000002932; Zygosity=Homozygous (Coriell=GM05093).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C84900; Mucopolysaccharidosis type IIID
DI   ORDO; Orphanet_79272; Sanfilippo syndrome type D
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   7Y
CA   Finite cell line
DT   Created: 23-02-16; Last updated: 30-01-24; Version: 12
//
RX   CelloPub=CLPUB00447;
RA   Mulivor R.A., Suchy S.F.;
RT   "1992/1993 catalog of cell lines. NIGMS human genetic mutant cell
RT   repository. 16th edition. October 1992.";
RL   (In) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992).
//