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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
A0A1D5RMP6 DAG1 Dystroglycan 1 Homo sapiens (Human) 8 aa

Protein Details: A0A1D5RMP6 (DAG1)

Protein Information
Accession A0A1D5RMP6
Protein Names Dystroglycan 1
Gene Symbol DAG1
Organism Homo sapiens (Human)
Length 8 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
1-81MRMSVGLS
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