ID   GM03136
AC   CVCL_GS60
SY   GM 3136
DR   CLO; CLO_0013522
DR   BioSample; SAMN00808266
DR   Coriell; GM03136
DR   Wikidata; Q54837896
RX   CelloPub=CLPUB00447;
RX   PubMed=1346349;
RX   PubMed=1680289;
RX   PubMed=2567118;
CC   Population: Jewish; Sephardic.
CC   Sequence variation: Mutation; HGNC; 186; ADA; Simple; p.Leu107Pro (c.320T>C); ClinVar=VCV000001965; Zygosity=Heterozygous (PubMed=1346349).
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C3962; Adenosine deaminase deficiency
DI   ORDO; Orphanet_277; Severe combined immunodeficiency due to adenosine deaminase deficiency
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   8M
CA   Finite cell line
DT   Created: 26-09-16; Last updated: 29-06-23; Version: 13
//
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).
//
RX   PubMed=1346349; DOI=10.1002/ajmg.1320420213;
RA   Hirschhorn R., Ellenbogen A., Tzall S.;
RT   "Five missense mutations at the adenosine deaminase locus (ADA)
RT   detected by altered restriction fragments and their frequency in
RT   ADA -- patients with severe combined immunodeficiency (ADA-SCID).";
RL   Am. J. Med. Genet. 42:201-207(1992).
//
RX   PubMed=1680289;
RA   Hirschhorn R., Chakravarti V., Puck J., Douglas S.D.;
RT   "Homozygosity for a newly identified missense mutation in a patient
RT   with very severe combined immunodeficiency due to adenosine deaminase
RT   deficiency (ADA-SCID).";
RL   Am. J. Hum. Genet. 49:878-885(1991).
//
RX   PubMed=2567118;
RA   Tzall S., Ellenbogen A., Eng F., Hirschhorn R.;
RT   "Identification and characterization of nine RFLPs at the adenosine
RT   deaminase (ADA) locus.";
RL   Am. J. Hum. Genet. 44:864-875(1989).
//