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Cellosaurus WG0290 (CVCL_B4KY)

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Cell line name WG0290
Synonyms WG 290
Accession CVCL_B4KY
Resource Identification Initiative To cite this cell line use: WG0290 (RRID:CVCL_B4KY)
Comments From: Montreal Children's Hospital cell repository; Montreal; Canada.
Miscellaneous: Cell line no longer available.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Adenosine deaminase deficiency (NCIt: C3962)
Severe combined immunodeficiency due to adenosine deaminase deficiency (ORDO: Orphanet_277)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Category Finite cell line
Publications

PubMed=2567118; PMCID=PMC1715668
Stephanie Tzall, Amy Ellenbogen, Fay Eng, Rochelle Hirschhorn;
Identification and characterization of nine RFLPs at the adenosine deaminase (ADA) locus.
Am. J. Hum. Genet. 44:864-875(1989)

PubMed=1680289; PMCID=PMC1683191
Rochelle Hirschhorn, Vijay Chakravarti, Jennifer M. Puck, Steven D. Douglas;
Homozygosity for a newly identified missense mutation in a patient with very severe combined immunodeficiency due to adenosine deaminase deficiency (ADA-SCID).
Am. J. Hum. Genet. 49:878-885(1991)

PubMed=1346349; DOI=10.1002/ajmg.1320420213
Rochelle Hirschhorn, Amy Ellenbogen, Stephanie Tzall;
Five missense mutations at the adenosine deaminase locus (ADA) detected by altered restriction fragments and their frequency in ADA- patients with severe combined immunodeficiency (ADA- SCID).
Am. J. Med. Genet. 42:201-207(1992)

Cross-references
Encyclopedic resources Wikidata; Q110433993
Entry history
Entry creation16-Dec-2021
Last entry update29-Jun-2023
Version number4