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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
R4GN67 ARL15 ADP ribosylation factor like GTPase … Homo sapiens (Human) 25 aa

Protein Details: R4GN67 (ARL15)

Protein Information
Accession R4GN67
Protein Names ADP ribosylation factor like GTPase 15
Gene Symbol ARL15
Organism Homo sapiens (Human)
Length 25 aa
Isoforms No isoforms
Related PMIDs 19801377 31251020 32944167
Database Sources No database sources
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.828
Bubble Size: Positive Samples Count Color Intensity: Positive Ratio
24
LNCaP cells
Specificity: 0.828
24/46 (52.2%)
3
PC3 cells
Specificity: 0.103
3/4 (75.0%)
2
DU145 cells
Specificity: 0.069
2/2 (100.0%)
0
Jurkat T cells
Specificity: 0.000
0/25 (0.0%)
0
U937 cells
Specificity: 0.000
0/1 (0.0%)
0
HeLa cells
Specificity: 0.000
0/1 (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
Endothelial cells
Specificity: 0.000
0/2 (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
1-251MDALKDSFSQ11LINLLEEKDH21EAVRM
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
37 C → S 0.001764 SNP Missense Mutation LUAD
53 C → Sfs*26 0.006993 DEL Frame Shift Del LAML
95 R → C 0.001887 SNP Missense Mutation UCEC
133 C → Y 0.005435 SNP Missense Mutation ESCA