ID   Amdur II
AC   CVCL_3643
AS   CVCL_AW71
SY   AmdurII; AMDURII; GM00050; GM0050; GM-50
DR   CLO; CLO_0001713
DR   CLO; CLO_0025172
DR   CLDB; cl270
DR   CLDB; cl271
DR   ATCC; CCL-124
DR   BioSample; SAMN03151822
DR   BioSample; SAMN03472704
DR   Coriell; GM00050
DR   ECACC; 90112605
DR   IZSLER; BS CL 2
DR   KCLB; 10124
DR   Wikidata; Q54749775
RX   CelloPub=CLPUB00447;
RX   CelloPub=CLPUB00720;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=5788784;
RX   PubMed=14505435;
RX   PubMed=20143388;
WW   Info; ICLAC; -; https://iclac.org/wp-content/uploads/Cross-Contaminations_v13_distribution.xlsx
CC   Problematic cell line: Partially contaminated. Some stocks were contaminated by pig LLC-PK1 (PubMed=14505435; PubMed=20143388).
CC   Registration: International Cell Line Authentication Committee, Register of Misidentified Cell Lines; ICLAC-00289.
CC   Population: Caucasian.
CC   Senescence: Senesces at ~40 PDL (ATCC=CCL-124).
CC   Discontinued: ECACC; 90112605; true.
CC   Discontinued: KCLB; 10124; probable.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): ATCC=CCL-124; IZSLER=BS CL 2
ST   Amelogenin: X,Y
ST   CSF1PO: 10,11
ST   D13S317: 10,11
ST   D16S539: 9,12
ST   D18S51: 12,17
ST   D19S433: 14,16
ST   D21S11: 28,30
ST   D2S1338: 19,25
ST   D3S1358: 14,17
ST   D5S818: 9,13
ST   D7S820: 9,12
ST   D8S1179: 11,14
ST   FGA: 20,23
ST   Penta D: 11,13
ST   Penta E: 10
ST   TH01: 6,9
ST   TPOX: 8,11
ST   vWA: 16
DI   NCIt; C148366; Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
DI   ORDO; Orphanet_27; Vitamin B12-unresponsive methylmalonic acidemia
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   1Y
CA   Finite cell line
DT   Created: 04-04-12; Last updated: 10-04-25; Version: 29
//
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 misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992).
//
RX   CelloPub=CLPUB00720;
RA   Greene A.E., Mulivor R.A.;
RT   "1986/1987 catalog of cell lines. NIGMS human genetic mutant cell
RT   repository. 13th edition. October 1986.";
RL   (In misc. document) Institute for Medical Research (Camden, N.J.) NIH 87-2011; pp.1-549; National Institutes of Health; Bethesda; USA (1986).
//
RX   DOI=10.5962/bhl.title.4090;
RA   Coriell L.L., Greene A.E.;
RT   "The human genetic mutant cell repository: list of genetic variants,
RT   chromosomal aberrations and normal cell cultures submitted to the
RT   repository. 4th edition. October 1977.";
RL   (In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977).
//
RX   PubMed=5788784; DOI=10.1203/00006450-196905000-00005;
RA   Morrow G. 3rd, Mellman W.J., Barness L.A., Dimitrov N.V.;
RT   "Propionate metabolism in cells cultured from a patient with
RT   methylmalonic acidemia.";
RL   Pediatr. Res. 3:217-219(1969).
//
RX   PubMed=14505435; DOI=10.1007/s11626-003-0006-z;
RA   Milanesi E., Ajmone-Marsan P., Bignotti E., Losio M.N., Bernardi J.,
RA   Chegdani F., Soncini M., Ferrari M.;
RT   "Molecular detection of cell line cross-contaminations using amplified
RT   fragment length polymorphism DNA fingerprinting technology.";
RL   In Vitro Cell. Dev. Biol. Anim. 39:124-130(2003).
//
RX   PubMed=20143388; DOI=10.1002/ijc.25242;
RA   Capes-Davis A., Theodosopoulos G., Atkin I., Drexler H.G., Kohara A.,
RA   MacLeod R.A.F., Masters J.R.W., Nakamura Y., Reid Y.A., Reddel R.R.,
RA   Freshney R.I.;
RT   "Check your cultures! A list of cross-contaminated or misidentified
RT   cell lines.";
RL   Int. J. Cancer 127:1-8(2010).
//