Name | Number of supported studies | Average coverage | |
---|---|---|---|
macrophage | 37 studies | 46% ± 18% | |
non-classical monocyte | 23 studies | 60% ± 15% | |
classical monocyte | 22 studies | 34% ± 14% | |
monocyte | 17 studies | 29% ± 10% | |
conventional dendritic cell | 15 studies | 27% ± 12% | |
myeloid cell | 12 studies | 34% ± 12% | |
dendritic cell | 11 studies | 28% ± 11% | |
fibroblast | 7 studies | 27% ± 9% | |
alveolar macrophage | 6 studies | 31% ± 8% | |
endothelial cell of vascular tree | 5 studies | 51% ± 17% | |
leukocyte | 4 studies | 22% ± 5% | |
endothelial cell | 4 studies | 26% ± 14% | |
microglial cell | 4 studies | 25% ± 5% | |
mononuclear phagocyte | 4 studies | 37% ± 11% | |
inflammatory macrophage | 4 studies | 37% ± 10% | |
intermediate monocyte | 4 studies | 53% ± 16% | |
squamous epithelial cell | 3 studies | 40% ± 11% | |
epithelial cell of proximal tubule | 3 studies | 24% ± 9% | |
epithelial cell | 3 studies | 27% ± 1% | |
tissue-resident macrophage | 3 studies | 45% ± 6% | |
monocyte-derived dendritic cell | 3 studies | 21% ± 3% |
Tissue | GTEx Coverage | GTEx Average TPM | GTEx Number of samples | TCGA Coverage | TCGA Average TPM | TCGA Number of samples |
---|---|---|---|---|---|---|
skin | 98% | 6228.12 | 1764 / 1809 | 92% | 114.35 | 433 / 472 |
lung | 96% | 9949.40 | 554 / 578 | 91% | 95.98 | 1046 / 1155 |
kidney | 90% | 6790.48 | 80 / 89 | 93% | 344.23 | 842 / 901 |
ovary | 96% | 7241.84 | 172 / 180 | 70% | 37.12 | 302 / 430 |
adrenal gland | 88% | 3950.90 | 226 / 258 | 73% | 100.92 | 169 / 230 |
liver | 79% | 4523.79 | 179 / 226 | 82% | 79.18 | 332 / 406 |
breast | 59% | 1537.75 | 271 / 459 | 94% | 80.28 | 1051 / 1118 |
bladder | 62% | 1705.67 | 13 / 21 | 81% | 80.78 | 407 / 504 |
intestine | 65% | 1901.20 | 627 / 966 | 72% | 38.88 | 379 / 527 |
uterus | 34% | 648.61 | 57 / 170 | 84% | 76.00 | 386 / 459 |
brain | 27% | 537.37 | 716 / 2642 | 88% | 118.90 | 623 / 705 |
thymus | 38% | 721.03 | 245 / 653 | 77% | 48.51 | 468 / 605 |
esophagus | 52% | 1514.49 | 752 / 1445 | 59% | 28.10 | 108 / 183 |
stomach | 32% | 1176.42 | 115 / 359 | 76% | 41.80 | 218 / 286 |
lymph node | 0% | 0 | 0 / 0 | 100% | 193.80 | 29 / 29 |
spleen | 100% | 49307.53 | 241 / 241 | 0% | 0 | 0 / 0 |
ureter | 0% | 0 | 0 / 0 | 100% | 25.47 | 1 / 1 |
peripheral blood | 97% | 7506.44 | 898 / 929 | 0% | 0 | 0 / 0 |
tonsil | 0% | 0 | 0 / 0 | 96% | 50.66 | 43 / 45 |
pancreas | 5% | 97.77 | 18 / 328 | 86% | 59.30 | 153 / 178 |
adipose | 91% | 6100.12 | 1091 / 1204 | 0% | 0 | 0 / 0 |
muscle | 67% | 4818.94 | 542 / 803 | 0% | 0 | 0 / 0 |
eye | 0% | 0 | 0 / 0 | 57% | 32.53 | 46 / 80 |
blood vessel | 51% | 1527.90 | 687 / 1335 | 0% | 0 | 0 / 0 |
prostate | 15% | 302.53 | 37 / 245 | 12% | 4.66 | 60 / 502 |
heart | 21% | 598.28 | 180 / 861 | 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 |
GO_0042542 | Biological process | response to hydrogen peroxide |
GO_0032722 | Biological process | positive regulation of chemokine production |
GO_0001525 | Biological process | angiogenesis |
GO_0002686 | Biological process | negative regulation of leukocyte migration |
GO_0016242 | Biological process | negative regulation of macroautophagy |
GO_0034605 | Biological process | cellular response to heat |
GO_0045766 | Biological process | positive regulation of angiogenesis |
GO_0006357 | Biological process | regulation of transcription by RNA polymerase II |
GO_0048661 | Biological process | positive regulation of smooth muscle cell proliferation |
GO_0110076 | Biological process | negative regulation of ferroptosis |
GO_0071276 | Biological process | cellular response to cadmium ion |
GO_0016236 | Biological process | macroautophagy |
GO_0060586 | Biological process | multicellular organismal-level iron ion homeostasis |
GO_0042167 | Biological process | heme catabolic process |
GO_1904037 | Biological process | positive regulation of epithelial cell apoptotic process |
GO_0045765 | Biological process | regulation of angiogenesis |
GO_0090050 | Biological process | positive regulation of cell migration involved in sprouting angiogenesis |
GO_0034101 | Biological process | erythrocyte homeostasis |
GO_0014806 | Biological process | smooth muscle hyperplasia |
GO_0035556 | Biological process | intracellular signal transduction |
GO_0006879 | Biological process | intracellular iron ion homeostasis |
GO_0006788 | Biological process | heme oxidation |
GO_0034383 | Biological process | low-density lipoprotein particle clearance |
GO_0001935 | Biological process | endothelial cell proliferation |
GO_0016239 | Biological process | positive regulation of macroautophagy |
GO_0035094 | Biological process | response to nicotine |
GO_0043123 | Biological process | positive regulation of canonical NF-kappaB signal transduction |
GO_0048662 | Biological process | negative regulation of smooth muscle cell proliferation |
GO_1904019 | Biological process | epithelial cell apoptotic process |
GO_0002246 | Biological process | wound healing involved in inflammatory response |
GO_1902042 | Biological process | negative regulation of extrinsic apoptotic signaling pathway via death domain receptors |
GO_0006979 | Biological process | response to oxidative stress |
GO_1903589 | Biological process | positive regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis |
GO_0071243 | Biological process | cellular response to arsenic-containing substance |
GO_0072719 | Biological process | cellular response to cisplatin |
GO_0005615 | Cellular component | extracellular space |
GO_0048471 | Cellular component | perinuclear region of cytoplasm |
GO_0016020 | Cellular component | membrane |
GO_0005789 | Cellular component | endoplasmic reticulum membrane |
GO_0005654 | Cellular component | nucleoplasm |
GO_0005783 | Cellular component | endoplasmic reticulum |
GO_0005829 | Cellular component | cytosol |
GO_0005741 | Cellular component | mitochondrial outer membrane |
GO_0005634 | Cellular component | nucleus |
GO_0019899 | Molecular function | enzyme binding |
GO_0042803 | Molecular function | protein homodimerization activity |
GO_0004392 | Molecular function | heme oxygenase (decyclizing) activity |
GO_0042802 | Molecular function | identical protein binding |
GO_0005198 | Molecular function | structural molecule activity |
GO_0020037 | Molecular function | heme binding |
GO_0046872 | Molecular function | metal ion binding |
GO_0005515 | Molecular function | protein binding |
Gene name | HMOX1 |
Protein name | Heme oxygenase (EC 1.14.14.18) Heme oxygenase 1 (EC 1.14.14.18) Heme oxygenase 1 (HO-1) (EC 1.14.14.18) [Cleaved into: Heme oxygenase 1 soluble form] Heme oxygenase 1 |
Synonyms | HO1 HO hCG_40033 |
Description | FUNCTION: [Heme oxygenase 1]: Catalyzes the oxidative cleavage of heme at the alpha-methene bridge carbon, released as carbon monoxide (CO), to generate biliverdin IXalpha, while releasing the central heme iron chelate as ferrous iron . Affords protection against programmed cell death and this cytoprotective effect relies on its ability to catabolize free heme and prevent it from sensitizing cells to undergo apoptosis . .; FUNCTION: [Heme oxygenase 1]: (Microbial infection) During SARS-COV-2 infection, promotes SARS-CoV-2 ORF3A-mediated autophagy but is unlikely to be required for ORF3A-mediated induction of reticulophagy. .; FUNCTION: [Heme oxygenase 1 soluble form]: Catalyzes the oxidative cleavage of heme at the alpha-methene bridge carbon, released as carbon monoxide (CO), to generate biliverdin IXalpha, while releasing the central heme iron chelate as ferrous iron. . FUNCTION: Catalyzes the oxidative cleavage of heme at the alpha-methene bridge carbon, released as carbon monoxide (CO), to generate biliverdin IXalpha, while releasing the central heme iron chelate as ferrous iron. . FUNCTION: Catalyzes the oxidative cleavage of heme at the alpha-methene bridge carbon, released as carbon monoxide (CO), to generate biliverdin IXalpha, while releasing the central heme iron chelate as ferrous iron. . FUNCTION: Catalyzes the oxidative cleavage of heme at the alpha-methene bridge carbon, released as carbon monoxide (CO), to generate biliverdin IXalpha, while releasing the central heme iron chelate as ferrous iron. . FUNCTION: Catalyzes the oxidative cleavage of heme at the alpha-methene bridge carbon, released as carbon monoxide (CO), to generate biliverdin IXalpha, while releasing the central heme iron chelate as ferrous iron. . FUNCTION: Catalyzes the oxidative cleavage of heme at the alpha-methene bridge carbon, released as carbon monoxide (CO), to generate biliverdin IXalpha, while releasing the central heme iron chelate as ferrous iron. . FUNCTION: Catalyzes the oxidative cleavage of heme at the alpha-methene bridge carbon, released as carbon monoxide (CO), to generate biliverdin IXalpha, while releasing the central heme iron chelate as ferrous iron. . FUNCTION: Catalyzes the oxidative cleavage of heme at the alpha-methene bridge carbon, released as carbon monoxide (CO), to generate biliverdin IXalpha, while releasing the central heme iron chelate as ferrous iron. . FUNCTION: Catalyzes the oxidative cleavage of heme at the alpha-methene bridge carbon, released as carbon monoxide (CO), to generate biliverdin IXalpha, while releasing the central heme iron chelate as ferrous iron. . |
Accessions | A0A7I2YQL9 Q6FH11 ENST00000678411.1 P09601 A0A7I2V3M0 ENST00000481190.2 D2K7W4 F2YMD9 A0A7I2V3I1 ENST00000412893.5 ENST00000677931.1 B1AHA8 ENST00000679074.1 Q96DI8 ENST00000216117.9 A0A7I2V277 |