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Cellosaurus GM05659 (CVCL_7434)

Cell line name GM05659
Synonyms GM5659; GM-5659; GM 5659; GM05659B; GM5659B; GM05659C; GM 5659C; GM05659D; GM5659D
Accession CVCL_7434
Resource Identification Initiative To cite this cell line use: GM05659 (RRID:CVCL_7434)
Comments Population: Caucasian.
Omics: Transcriptome analysis by microarray.
Omics: Transcriptome analysis by RNAseq.
Derived from site: In situ; Chest, skin; UBERON=UBERON_0001868.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 4177; GBA1; Simple; p.Thr408Met (c.1223C>T) (T369M); ClinVar=VCV000093447; Zygosity=Heterozygous (PubMed=30497978).
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_ZU51 (GM05659T)CVCL_A1NK (TRNDi023-A)CVCL_A1NL (TRNDi023-B)
CVCL_A1NM (TRNDi023-C)CVCL_A1NN (TRNDi023-D)CVCL_B5TU (TRNDi028-A)
CVCL_B5TV (TRNDi028-B)CVCL_B5TW (TRNDi028-C)
Sex of cell Male
Age at sampling 1Y2M
Category Finite cell line
Publications

CLPUB00720
Greene A.E., Mulivor R.A.
1986/1987 catalog of cell lines. NIGMS human genetic mutant cell repository. 13th edition. October 1986.
(In) Institute for Medical Research (Camden, N.J.) NIH 87-2011; pp.1-549; National Institutes of Health; Bethesda (1986)

PubMed=3745952; DOI=10.1111/1523-1747.ep12285424
Sephel G.C., Davidson J.M.
Elastin production in human skin fibroblast cultures and its decline with age.
J. Invest. Dermatol. 86:279-285(1986)

PubMed=2837086
Winkler J.K., Suttle D.P.
Analysis of UMP synthase gene and mRNA structure in hereditary orotic aciduria fibroblasts.
Am. J. Hum. Genet. 43:86-94(1988)

PubMed=2475503; DOI=10.1016/S0021-9258(19)84861-5
Perry M.E., Jones M.E.
Orotic aciduria fibroblasts express a labile form of UMP synthase.
J. Biol. Chem. 264:15522-15528(1989)

PubMed=2705456
Weiss M.J., Ray K., Fallon M.D., Whyte M.P., Fedde K.N., Lafferty M.A., Mulivor R.A., Harris H.
Analysis of liver/bone/kidney alkaline phosphatase mRNA, DNA, and enzymatic activity in cultured skin fibroblasts from 14 unrelated patients with severe hypophosphatasia.
Am. J. Hum. Genet. 44:686-694(1989)

PubMed=1652892
Zhong N., Martiniuk F., Tzall S., Hirschhorn R.
Identification of a missense mutation in one allele of a patient with Pompe disease, and use of endonuclease digestion of PCR-amplified RNA to demonstrate lack of mRNA expression from the second allele.
Am. J. Hum. Genet. 49:635-645(1991)

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

PubMed=8605078; DOI=10.1007/BF02789413
Vazquez F., Grider A.
The effect of the acrodermatitis enteropathica mutation on zinc uptake in human fibroblasts.
Biol. Trace Elem. Res. 50:109-117(1995)

PubMed=17668376; DOI=10.1086/519248
Prandini P., Deutsch S., Lyle R., Gagnebin M., Delucinge-Vivier C., Delorenzi M., Gehrig C., Descombes P., Sherman S.L., Dagna-Bricarelli F., Baldo C., Novelli A., Dallapiccola B., Antonarakis S.E.
Natural gene-expression variation in Down syndrome modulates the outcome of gene-dosage imbalance.
Am. J. Hum. Genet. 81:252-263(2007)

PubMed=18973801; DOI=10.1016/j.freeradbiomed.2008.09.028
Duarte T.L., Cooke M.S., Jones G.D.D.
Gene expression profiling reveals new protective roles for vitamin C in human skin cells.
Free Radic. Biol. Med. 46:78-87(2009)

PubMed=24119401; DOI=10.1016/j.molcel.2013.09.009
Chen J.-Y., Lin J.-R., Tsai F.-C., Meyer T.
Dosage of Dyrk1a shifts cells within a p21-cyclin D1 signaling map to control the decision to enter the cell cycle.
Mol. Cell 52:87-100(2013)

PubMed=25732146; DOI=10.2174/1566524015666150303110300
Kano S.-i., Yuan M., Cardarelli R.A., Maegawa G., Higurashi N., Gaval-Cruz M., Wilson A.M., Tristan C.A., Kondo M.A., Chen Y., Koga M., Obie C., Ishizuka K., Seshadri S., Srivastava R., Kato T.A., Horiuchi Y., Sedlak T.W., Lee Y., Rapoport J.L., Hirose S., Okano H., Valle D.L., O'Donnell P., Sawa A., Kai M.
Clinical utility of neuronal cells directly converted from fibroblasts of patients for neuropsychiatric disorders: studies of lysosomal storage diseases and channelopathy.
Curr. Mol. Med. 15:138-145(2015)

PubMed=27543334; DOI=10.1073/pnas.1610020113
Reid-Bayliss K.S., Arron S.T., Loeb L.A., Bezrookove V., Cleaver J.E.
Why Cockayne syndrome patients do not get cancer despite their DNA repair deficiency.
Proc. Natl. Acad. Sci. U.S.A. 113:10151-10156(2016)

PubMed=30220252; DOI=10.1186/s13023-018-0886-3
Vu M., Li R., Baskfield A., Lu B., Farkhondeh A., Gorshkov K., Motabar O., Beers J.K., Chen G.-K., Zou J.-Z., Espejo-Mojica A.J., Rodriguez-Lopez A., Almeciga-Diaz C.J., Barrera L.A., Jiang X.-T., Ory D.S., Marugan J.J., Zheng W.
Neural stem cells for disease modeling and evaluation of therapeutics for Tay-Sachs disease.
Orphanet J. Rare Dis. 13:152.1-152.15(2018)

PubMed=30497978; DOI=10.1016/j.ebiom.2018.11.037
Fog C.K., Zago P., Malini E., Solanko L.M., Peruzzo P., Bornaes C., Magnoni R., Mehmedbasic A., Petersen N.H.T., Bembi B., Aerts J.F.M.G., Dardis A., Kirkegaard T.
The heat shock protein amplifier arimoclomol improves refolding, maturation and lysosomal activity of glucocerebrosidase.
EBioMedicine 38:142-153(2018)

PubMed=30567591; DOI=10.1186/s13059-018-1599-6
Fleischer J.G., Schulte R., Tsai H.H., Tyagi S., Ibarra A., Shokhirev M.N., Huang L., Hetzer M.W., Navlakha S.
Predicting age from the transcriptome of human dermal fibroblasts.
Genome Biol. 19:221.1-221.8(2018)

PubMed=33038742; DOI=10.1016/j.scr.2020.102011
Xu X.-G., Pradhan M., Xu M., Cheng Y.-S., Beers J.K., Linask K.L., Lin Y.-S., Zheng W., Zou J.-H.
Four induced pluripotent stem cell lines (TRNDi021-C, TRNDi023-D, TRNDi024-D and TRNDi025-A) generated from fibroblasts of four healthy individuals.
Stem Cell Res. 49:102011-102011(2020)

Cross-references
Cell line collections (Providers) Coriell; GM05659
Cell line databases/resources CLO; CLO_0024626
Encyclopedic resources Wikidata; Q54841910
Experimental variables resources EFO; EFO_0006278
Gene expression databases GEO; GSE11919
GEO; GSM3124625
Entry history
Entry creation04-Apr-2012
Last entry update29-Jun-2023
Version number27