WM3772FHomo sapiens (Human)Cancer cell line

Also known as: WM3772

🤖 AI Summary0

Quick Overview

Human cell line with unknown tissue and disease origins.

Detailed Summary

WM3772F is a human cell line, though specific details about its tissue of origin, disease association, and cell type remain unknown. The available description does not provide further insights into its characteristics or research applications. Researchers interested in this cell line may need to consult additional sources for more detailed information.
Generated on 6/15/2025

Basic Information

Database IDCVCL_0B81
SpeciesHomo sapiens (Human)
Tissue SourceLung[UBERON:UBERON_0002048]

Donor Information

Age CategoryUnknown
SexFemale

Disease Information

DiseaseUveal melanoma
LineageEye
SubtypeUveal Melanoma
OncoTree CodeUM

DepMap Information

Source TypeRockland Immunochemicals, Inc.
Source IDACH-002687_source

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
Gene deletionCDKN2A-HomozygousPossiblePubMed=26870271

Haplotype Information (STR Profile)

Short Tandem Repeat (STR) profile for cell line authentication.

Amelogenin
X
CSF1PO
11,12
D13S317
8,12
D16S539
13
D18S51
13,14
D19S433
13,14
D21S11
28,31
D2S1338
20,25
D3S1358
16
D5S818
11,13
D7S820
10,13
D8S1179
10,15
FGA
20
TH01
9.3
TPOX
8,9
vWA
15,16
Gene Expression Profile
Gene expression levels and statistical distribution
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Full DepMap dataset with combined data across cell lines

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Web Resources