Name | Number of supported studies | Average coverage | |
---|---|---|---|
peripheral blood | 20 studies | 62% ± 13% | |
lung | 10 studies | 33% ± 11% | |
bone marrow | 5 studies | 42% ± 24% | |
intestine | 4 studies | 25% ± 8% | |
lymph node | 4 studies | 33% ± 8% | |
kidney | 3 studies | 48% ± 22% | |
brain | 3 studies | 43% ± 19% | |
liver | 3 studies | 55% ± 19% |
Tissue | GTEx Coverage | GTEx Average TPM | GTEx Number of samples | TCGA Coverage | TCGA Average TPM | TCGA Number of samples |
---|---|---|---|---|---|---|
lung | 100% | 215.46 | 578 / 578 | 76% | 5.23 | 874 / 1155 |
intestine | 94% | 77.34 | 907 / 966 | 62% | 5.71 | 327 / 527 |
breast | 90% | 75.37 | 414 / 459 | 64% | 3.88 | 718 / 1118 |
uterus | 86% | 43.78 | 147 / 170 | 68% | 4.82 | 311 / 459 |
ovary | 52% | 23.41 | 93 / 180 | 99% | 16.81 | 425 / 430 |
stomach | 75% | 39.92 | 271 / 359 | 74% | 9.94 | 211 / 286 |
kidney | 72% | 52.62 | 64 / 89 | 71% | 4.64 | 644 / 901 |
esophagus | 61% | 28.32 | 880 / 1445 | 80% | 6.55 | 147 / 183 |
bladder | 81% | 68.05 | 17 / 21 | 56% | 4.79 | 281 / 504 |
thymus | 79% | 45.88 | 513 / 653 | 57% | 7.05 | 347 / 605 |
brain | 65% | 41.74 | 1710 / 2642 | 63% | 4.45 | 443 / 705 |
prostate | 88% | 54.69 | 215 / 245 | 38% | 1.62 | 191 / 502 |
adrenal gland | 86% | 48.07 | 221 / 258 | 38% | 1.70 | 88 / 230 |
liver | 70% | 34.40 | 159 / 226 | 50% | 3.36 | 202 / 406 |
skin | 46% | 20.98 | 835 / 1809 | 68% | 5.67 | 321 / 472 |
pancreas | 25% | 10.65 | 81 / 328 | 83% | 5.31 | 148 / 178 |
lymph node | 0% | 0 | 0 / 0 | 100% | 67.76 | 29 / 29 |
peripheral blood | 100% | 944.41 | 929 / 929 | 0% | 0 | 0 / 0 |
spleen | 100% | 591.39 | 241 / 241 | 0% | 0 | 0 / 0 |
adipose | 99% | 141.08 | 1186 / 1204 | 0% | 0 | 0 / 0 |
blood vessel | 84% | 74.56 | 1128 / 1335 | 0% | 0 | 0 / 0 |
tonsil | 0% | 0 | 0 / 0 | 76% | 5.71 | 34 / 45 |
heart | 44% | 19.39 | 382 / 861 | 0% | 0 | 0 / 0 |
eye | 0% | 0 | 0 / 0 | 31% | 1.46 | 25 / 80 |
muscle | 9% | 2.83 | 70 / 803 | 0% | 0 | 0 / 0 |
abdomen | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
bone marrow | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
diaphragm | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
gingiva | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
nasal cavity | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
nasopharynx | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
nose | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
placenta | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
spinal column | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
ureter | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 1 |
GO_0051897 | Biological process | positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction |
GO_0006468 | Biological process | protein phosphorylation |
GO_0050776 | Biological process | regulation of immune response |
GO_0042267 | Biological process | natural killer cell mediated cytotoxicity |
GO_0009986 | Cellular component | cell surface |
GO_0005886 | Cellular component | plasma membrane |
GO_0030674 | Molecular function | protein-macromolecule adaptor activity |
GO_0043548 | Molecular function | phosphatidylinositol 3-kinase binding |
GO_0005102 | Molecular function | signaling receptor binding |
GO_0005515 | Molecular function | protein binding |
Gene name | HCST |
Protein name | Hematopoietic cell signal transducer (DNAX-activation protein 10) (Membrane protein DAP10) (Transmembrane adapter protein KAP10) |
Synonyms | DAP10 PIK3AP UNQ587/PRO1157 KAP10 |
Description | FUNCTION: Transmembrane adapter protein which associates with KLRK1 to form an activation receptor KLRK1-HCST in lymphoid and myeloid cells; this receptor plays a major role in triggering cytotoxicity against target cells expressing cell surface ligands such as MHC class I chain-related MICA and MICB, and UL16-binding proteins (ULBPs); these ligands are up-regulated by stress conditions and pathological state such as viral infection and tumor transformation. Functions as a docking site for PI3-kinase PIK3R1 and GRB2. Interaction of ULBPs with KLRK1-HCST triggers calcium mobilization and activation of the PIK3R1, MAP2K/ERK, and JAK2/STAT5 signaling pathways. Both PIK3R1 and GRB2 are required for full KLRK1-HCST-mediated activation and ultimate killing of target cells. In NK cells, KLRK1-HCST signaling directly induces cytotoxicity and enhances cytokine production initiated via DAP12/TYROBP-associated receptors. In T-cells, it provides primarily costimulation for TCR-induced signals. KLRK1-HCST receptor plays a role in immune surveillance against tumors and is required for cytolysis of tumors cells; indeed, melanoma cells that do not express KLRK1 ligands escape from immune surveillance mediated by NK cells. . |
Accessions | ENST00000246551.9 [Q9UBK5-1] Q9UBK5 ENST00000437550.2 [Q9UBK5-2] |