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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
A0A0G2JNU9 ATP9B ATPase phospholipid transporting 9B (putative) Homo sapiens (Human) 39 aa

Protein Details: A0A0G2JNU9 (ATP9B)

Protein Information
Accession A0A0G2JNU9
Protein Names ATPase phospholipid transporting 9B (putative)
Gene Symbol ATP9B
Organism Homo sapiens (Human)
Length 39 aa
Isoforms No isoforms
Related PMIDs 19137006 31251020
Database Sources No database sources
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.900
Bubble Size: Positive Samples Count Color Intensity: Positive Ratio
36
LNCaP cells
Specificity: 0.900
36/46 (78.3%)
4
Jurkat T cells
Specificity: 0.100
4/25 (16.0%)
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
PC3 cells
Specificity: 0.000
0/4 (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
1-391MADQIPLYPV11RSAAAAAANR21KRAAYYSAAG31PRPGADRHS
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
180 Y → C 0.001969 SNP Missense Mutation HNSC
216 Y → C 0.005435 SNP Missense Mutation ESCA
229 S → C 0.019608 SNP Missense Mutation CHOL
252 F → C 0.001887 SNP Missense Mutation UCEC
321 S → C 0.002747 SNP Missense Mutation LIHC
401 F → C 0.001887 SNP Missense Mutation UCEC
425 R → C 0.003774 SNP Missense Mutation UCEC
435 Y → C 0.002288 SNP Missense Mutation STAD
461 R → C 0.002545 SNP Missense Mutation GBM
557 V → Cfs*59 0.001887 DEL Frame Shift Del UCEC
756 R → C 0.001887 SNP Missense Mutation UCEC
814 C → Y 0.003460 SNP Missense Mutation CESC
856 R → C 0.001887 SNP Missense Mutation UCEC
868 R → C 0.002506 SNP Missense Mutation COAD
870 C → C 0.001887 SNP Silent UCEC
949 F → Cfs*34 0.002747 INS Frame Shift Ins LIHC
1022 Y → C 0.002545 SNP Missense Mutation GBM
1135 R → C 0.002288 SNP Missense Mutation STAD
1135 R → C 0.001887 SNP Missense Mutation UCEC
1135 R → C 0.003460 SNP Missense Mutation CESC