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Cell Line : CVCL_0020 (U-138MG) Homo sapiens

Symbol: CVCL_0020
Name: U-138MG
Cell Line Type: cancer cell line
Gender: Male
Research Use: Omics: CNV analysis; Omics: Deep antibody staining analysis; Omics: Deep exome analysis; Omics: Deep RNAseq analysis; Omics: SNP array analysis; Omics: Transcriptome analysis
Phenotype: Doubling time: ~70 hours (DSMZ)
Genomic Alteration: Sequence variation: Has no IDH1 mutation (PubMed=19435942); Sequence variation: Homozygous for PTEN c.1026+1G>T (IVS8+1G>T); splice donor mutation (CCLE); Sequence variation: Homozygous for TP53 p.Arg213Gln (c.638G>A) (ClinVar=VCV000135359) (PubMed=10416987; CCLE)
Groups: Part of: Cancer Cell Line Encyclopedia (CCLE) project
Description: Genome ancestry: African=1.64%; Native American=0%; East Asian, North=1.56%; East Asian, South=0%; South Asian=0%; European, North=96.13%; European, South=0.67% (PubMed=30894373).
Child Cell Lines: CVCL_0633 (U-118MG)
Aliases: 138 MG; 138MG; U 138 MG; U-138 MG; U-138-MG; U138; U138-MG; U138MG
Disease(s): astrocytoma (DOID:3069) [NCI:C60781]
autosomal dominant cerebellar ataxia (DOID:1441) [ORDO:94]


References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 21113377
Created: 2020-02-27
Species: Homo sapiens
Last Modified: 2020-02-27
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.