CVCL_2657 - Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Cell Line : CVCL_2657 (NH17) Homo sapiens

Symbol: CVCL_2657
Name: NH17
RGD ID: 21148354
Cell Line Type: cancer cell line
Origin: Derived from sampling site: Peripheral blood.
Gender: Male
Genomic Alteration: Sequence variation: Heterozygous for NOTCH1 p.Leu1600Pro (c.4799T>C) (from parent cell line); Sequence variation: Heterozygous for NOTCH1 p.Pro2514Argfs*4 (c.7541_7542delCT) (ClinVar=VCV000581973) (from parent cell line); Sequence variation: Heterozygous for NRAS p.Gly12Cys (c.34G>T) (ClinVar=VCV000040468) (from parent cell line); Sequence variation: Homozygous for PTEN p.Lys267Argfs*9 (c.800delA) (p.Leu265fs; c.795delA) (ClinVar=VCV000092828) (from parent cell line); Sequence variation: Heterozygous for STK11 p.Gln214Ter (c.640C>T) (ClinVar=VCV000428759) (from parent cell line); Sequence variation: Heterozygous for TP53 p.Arg306Ter (c.916C>T) (ClinVar=VCV000142144) (from parent cell line)
Derived From Cell Lines: CVCL_0013 (MOLT-4)
Disease(s): T-cell adult acute lymphocytic leukemia (DOID:5602) [NCI:C9142]

References
Additional References at PubMed
PMID:11892817  


Additional Information

Database Acc Id Source(s)
Cell Line Ontology CLO_0008169 CELLOSAURUS
Cellosaurus CVCL_2657 CELLOSAURUS
ECACC 92111101 CELLOSAURUS
NCIt C9142 CELLOSAURUS
Orphanet 99861 CELLOSAURUS
Wikidata Q54930508 CELLOSAURUS