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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
C9J6Z6 DAG1 Dystroglycan 1 Homo sapiens (Human) 88 aa

Protein Details: C9J6Z6 (DAG1)

Protein Information
Accession C9J6Z6
Protein Names Dystroglycan 1
Gene Symbol DAG1
Organism Homo sapiens (Human)
Length 88 aa
Isoforms No isoforms
Related PMIDs 22496122 32944167
Database Sources No database sources
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.750
Bubble Size: Positive Samples Count Color Intensity: Positive Ratio
3
PC3 cells
Specificity: 0.750
3/4 (75.0%)
1
Endothelial cells
Specificity: 0.250
1/2 (50.0%)
0
Jurkat T cells
Specificity: 0.000
0/25 (0.0%)
0
U937 cells
Specificity: 0.000
0/1 (0.0%)
0
DU145 cells
Specificity: 0.000
0/2 (0.0%)
0
HeLa cells
Specificity: 0.000
0/1 (0.0%)
0
LNCaP cells
Specificity: 0.000
0/46 (0.0%)
0
T cells
Specificity: 0.000
0/4 (0.0%)
0
HAP1 cells
Specificity: 0.000
0/10 (0.0%)
0
293T cells
Specificity: 0.000
0/10 (0.0%)
0
CEMx174 cells
Specificity: 0.000
0/3 (0.0%)
0
Prefrontal cortex
Specificity: 0.000
0/1 (0.0%)
0
Cerebral cortex
Specificity: 0.000
0/4 (0.0%)
0
Liver membrane
Specificity: 0.000
0/1 (0.0%)
Palmitoylation Distribution by Study and Tissue/Cell Line
Chart Explanation: Each bar represents a study (PMID). The colored bottom segment shows palmitoylated samples, while the gray top segment shows non-palmitoylated samples. Bars are grouped by tissue/cell line for easy comparison.
Protein Sequence
Single Types:
Experimental Database High Prediction Medium Prediction Low Prediction
Combined Types:
All Three Exp + DB Exp + High Pred Exp + Med Pred Exp + Low Pred DB + High Pred DB + Med Pred DB + Low Pred Cysteine
1-501MRMSVGLSLL11LPLSGRTFLL21LLSVVMAQSH31WPSEPSEAVR41DWENQLEASM
51-8851HSVLSDLHEA61VPTVVGIPDG71TAVVGRSFRV81TIPTDLIA
Palmitoylation Sites Details

No known palmitoylation sites

TCGA Cysteine Mutation Information

Note: Mutations indicate amino acid changes that may create potential palmitoylation sites.

Position Amino Acid Change Frequency Type Function Cancer Type
76 R → C 0.002506 SNP Missense Mutation COAD
562 Y → C 0.002288 SNP Missense Mutation STAD
711 G → C 0.002033 SNP Missense Mutation LUSC
796 V → Cfs*47 0.001887 DEL Frame Shift Del UCEC
831 Y → C 0.002141 SNP Missense Mutation SKCM