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 ID | CVCL_0B81 |
---|---|
Species | Homo sapiens (Human) |
Tissue Source | Lung[UBERON:UBERON_0002048] |
Donor Information
Age Category | Unknown |
---|---|
Sex | Female |
Disease Information
Disease | Uveal melanoma |
---|---|
Lineage | Eye |
Subtype | Uveal Melanoma |
OncoTree Code | UM |
DepMap Information
Source Type | Rockland Immunochemicals, Inc. |
---|---|
Source ID | ACH-002687_source |
Known Sequence Variations
Type | Gene/Protein | Description | Zygosity | Note | Source |
---|---|---|---|---|---|
Gene deletion | CDKN2A | - | Homozygous | Possible | PubMed=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
Loading cohorts...
Full DepMap dataset with combined data across cell lines
Loading gene expression data...