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Cellosaurus GM00629 (CVCL_0L92)

[Text version]
Cell line name GM00629
Synonyms GM-629
Accession CVCL_0L92
Resource Identification Initiative To cite this cell line use: GM00629 (RRID:CVCL_0L92)
Comments Cell type: Fibroblast; CL=CL_0000057.
Sequence variations
  • Mutation; HGNC; HGNC:10818; SGSH; Simple; p.Ser66Trp (c.197C>G); ClinVar=VCV000005111; Zygosity=Heterozygous (Coriell=GM00629).
Disease Mucopolysaccharidosis type IIIA (NCIt: C84897)
Sanfilippo syndrome type A (ORDO: Orphanet_79269)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 10Y
Category Finite cell line
Publications

DOI=10.5962/bhl.title.4090
Coriell L.L., Greene A.E.
The human genetic mutant cell repository: list of genetic variants, chromosomal aberrations and normal cell cultures submitted to the repository. 4th edition. October 1977.
(In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977)

CLPUB00447
Mulivor R.A., Suchy S.F.
1992/1993 catalog of cell lines. NIGMS human genetic mutant cell repository. 16th edition. October 1992.
(In misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992)

Cross-references
Cell line collections (Providers) Coriell; GM00629
Cell line databases/resources CLO; CLO_0028870
Encyclopedic resources Wikidata; Q54836354
Entry history
Entry creation10-Apr-2015
Last entry update19-Dec-2024
Version number15