Name | Number of supported studies | Average coverage | |
---|---|---|---|
endothelial cell | 13 studies | 30% ± 12% | |
macrophage | 12 studies | 28% ± 9% | |
adipocyte | 11 studies | 79% ± 19% | |
alveolar macrophage | 8 studies | 60% ± 18% | |
endothelial cell of lymphatic vessel | 8 studies | 36% ± 14% | |
pericyte | 7 studies | 31% ± 21% | |
epithelial cell | 7 studies | 25% ± 6% | |
microglial cell | 6 studies | 23% ± 8% | |
GABAergic neuron | 5 studies | 37% ± 14% | |
monocyte | 5 studies | 44% ± 28% | |
myeloid cell | 4 studies | 24% ± 5% | |
endothelial cell of vascular tree | 4 studies | 37% ± 18% | |
glutamatergic neuron | 4 studies | 38% ± 7% | |
interneuron | 4 studies | 34% ± 6% | |
extravillous trophoblast | 3 studies | 39% ± 13% | |
smooth muscle cell | 3 studies | 27% ± 8% |
Tissue | GTEx Coverage | GTEx Average TPM | GTEx Number of samples | TCGA Coverage | TCGA Average TPM | TCGA Number of samples |
---|---|---|---|---|---|---|
kidney | 100% | 1108.53 | 89 / 89 | 98% | 18.54 | 886 / 901 |
bladder | 95% | 2269.76 | 20 / 21 | 91% | 76.11 | 460 / 504 |
stomach | 88% | 1121.28 | 316 / 359 | 96% | 35.23 | 275 / 286 |
intestine | 86% | 1508.13 | 831 / 966 | 98% | 42.69 | 514 / 527 |
lung | 99% | 1601.59 | 572 / 578 | 78% | 13.00 | 901 / 1155 |
breast | 100% | 7183.42 | 459 / 459 | 59% | 6.46 | 655 / 1118 |
thymus | 100% | 1355.95 | 651 / 653 | 50% | 6.38 | 303 / 605 |
liver | 62% | 346.70 | 139 / 226 | 85% | 12.04 | 346 / 406 |
uterus | 91% | 688.99 | 155 / 170 | 39% | 11.74 | 177 / 459 |
esophagus | 53% | 311.38 | 773 / 1445 | 63% | 15.39 | 115 / 183 |
ovary | 99% | 1257.66 | 178 / 180 | 11% | 0.99 | 47 / 430 |
adipose | 100% | 9779.57 | 1204 / 1204 | 0% | 0 | 0 / 0 |
ureter | 0% | 0 | 0 / 0 | 100% | 107.21 | 1 / 1 |
spleen | 100% | 947.99 | 240 / 241 | 0% | 0 | 0 / 0 |
pancreas | 3% | 16.14 | 10 / 328 | 95% | 43.64 | 169 / 178 |
prostate | 64% | 459.46 | 158 / 245 | 29% | 2.68 | 144 / 502 |
skin | 72% | 867.41 | 1302 / 1809 | 21% | 1.59 | 98 / 472 |
heart | 90% | 661.92 | 773 / 861 | 0% | 0 | 0 / 0 |
adrenal gland | 33% | 182.74 | 86 / 258 | 30% | 2.58 | 69 / 230 |
blood vessel | 51% | 553.21 | 677 / 1335 | 0% | 0 | 0 / 0 |
eye | 0% | 0 | 0 / 0 | 48% | 7.62 | 38 / 80 |
muscle | 24% | 123.19 | 193 / 803 | 0% | 0 | 0 / 0 |
peripheral blood | 20% | 109.03 | 188 / 929 | 0% | 0 | 0 / 0 |
brain | 10% | 43.80 | 254 / 2642 | 10% | 0.62 | 69 / 705 |
tonsil | 0% | 0 | 0 / 0 | 18% | 1.26 | 8 / 45 |
lymph node | 0% | 0 | 0 / 0 | 7% | 0.30 | 2 / 29 |
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_0007584 | Biological process | response to nutrient |
GO_0010742 | Biological process | macrophage derived foam cell differentiation |
GO_1905563 | Biological process | negative regulation of vascular endothelial cell proliferation |
GO_1903845 | Biological process | negative regulation of cellular response to transforming growth factor beta stimulus |
GO_0030514 | Biological process | negative regulation of BMP signaling pathway |
GO_0043537 | Biological process | negative regulation of blood vessel endothelial cell migration |
GO_0030509 | Biological process | BMP signaling pathway |
GO_0050728 | Biological process | negative regulation of inflammatory response |
GO_1902895 | Biological process | positive regulation of miRNA transcription |
GO_0042789 | Biological process | mRNA transcription by RNA polymerase II |
GO_0043407 | Biological process | negative regulation of MAP kinase activity |
GO_0055088 | Biological process | lipid homeostasis |
GO_0048384 | Biological process | retinoic acid receptor signaling pathway |
GO_0048511 | Biological process | rhythmic process |
GO_0030224 | Biological process | monocyte differentiation |
GO_0050872 | Biological process | white fat cell differentiation |
GO_0035357 | Biological process | peroxisome proliferator activated receptor signaling pathway |
GO_0006919 | Biological process | activation of cysteine-type endopeptidase activity involved in apoptotic process |
GO_0010629 | Biological process | negative regulation of gene expression |
GO_0030855 | Biological process | epithelial cell differentiation |
GO_0045087 | Biological process | innate immune response |
GO_0006357 | Biological process | regulation of transcription by RNA polymerase II |
GO_0007165 | Biological process | signal transduction |
GO_0008217 | Biological process | regulation of blood pressure |
GO_0010628 | Biological process | positive regulation of gene expression |
GO_1902894 | Biological process | negative regulation of miRNA transcription |
GO_1901202 | Biological process | negative regulation of extracellular matrix assembly |
GO_0006631 | Biological process | fatty acid metabolic process |
GO_0042752 | Biological process | regulation of circadian rhythm |
GO_0007186 | Biological process | G protein-coupled receptor signaling pathway |
GO_1904893 | Biological process | negative regulation of receptor signaling pathway via STAT |
GO_0033993 | Biological process | response to lipid |
GO_0045165 | Biological process | cell fate commitment |
GO_0042953 | Biological process | lipoprotein transport |
GO_0090258 | Biological process | negative regulation of mitochondrial fission |
GO_0006629 | Biological process | lipid metabolic process |
GO_1904179 | Biological process | positive regulation of adipose tissue development |
GO_0060392 | Biological process | negative regulation of SMAD protein signal transduction |
GO_0032869 | Biological process | cellular response to insulin stimulus |
GO_0051091 | Biological process | positive regulation of DNA-binding transcription factor activity |
GO_2000272 | Biological process | negative regulation of signaling receptor activity |
GO_0045923 | Biological process | positive regulation of fatty acid metabolic process |
GO_0015909 | Biological process | long-chain fatty acid transport |
GO_0060336 | Biological process | negative regulation of type II interferon-mediated signaling pathway |
GO_0010891 | Biological process | negative regulation of sequestering of triglyceride |
GO_0070165 | Biological process | positive regulation of adiponectin secretion |
GO_0010745 | Biological process | negative regulation of macrophage derived foam cell differentiation |
GO_0045893 | Biological process | positive regulation of DNA-templated transcription |
GO_0045668 | Biological process | negative regulation of osteoblast differentiation |
GO_0010888 | Biological process | negative regulation of lipid storage |
GO_1900076 | Biological process | regulation of cellular response to insulin stimulus |
GO_0048469 | Biological process | cell maturation |
GO_0045892 | Biological process | negative regulation of DNA-templated transcription |
GO_1905599 | Biological process | positive regulation of low-density lipoprotein receptor activity |
GO_0045944 | Biological process | positive regulation of transcription by RNA polymerase II |
GO_1905461 | Biological process | positive regulation of vascular associated smooth muscle cell apoptotic process |
GO_1903243 | Biological process | negative regulation of cardiac muscle hypertrophy in response to stress |
GO_0030512 | Biological process | negative regulation of transforming growth factor beta receptor signaling pathway |
GO_0010887 | Biological process | negative regulation of cholesterol storage |
GO_1904706 | Biological process | negative regulation of vascular associated smooth muscle cell proliferation |
GO_0060694 | Biological process | regulation of cholesterol transporter activity |
GO_0000122 | Biological process | negative regulation of transcription by RNA polymerase II |
GO_1904597 | Biological process | negative regulation of connective tissue replacement involved in inflammatory response wound healing |
GO_0001890 | Biological process | placenta development |
GO_0016525 | Biological process | negative regulation of angiogenesis |
GO_0071404 | Biological process | cellular response to low-density lipoprotein particle stimulus |
GO_0030154 | Biological process | cell differentiation |
GO_0045600 | Biological process | positive regulation of fat cell differentiation |
GO_0048662 | Biological process | negative regulation of smooth muscle cell proliferation |
GO_0010875 | Biological process | positive regulation of cholesterol efflux |
GO_0009755 | Biological process | hormone-mediated signaling pathway |
GO_0042593 | Biological process | glucose homeostasis |
GO_0071456 | Biological process | cellular response to hypoxia |
GO_0005634 | Cellular component | nucleus |
GO_0005654 | Cellular component | nucleoplasm |
GO_0043231 | Cellular component | intracellular membrane-bounded organelle |
GO_0043235 | Cellular component | receptor complex |
GO_0090575 | Cellular component | RNA polymerase II transcription regulator complex |
GO_0000785 | Cellular component | chromatin |
GO_0005829 | Cellular component | cytosol |
GO_0140297 | Molecular function | DNA-binding transcription factor binding |
GO_0001228 | Molecular function | DNA-binding transcription activator activity, RNA polymerase II-specific |
GO_0042802 | Molecular function | identical protein binding |
GO_0008270 | Molecular function | zinc ion binding |
GO_0070888 | Molecular function | E-box binding |
GO_0000978 | Molecular function | RNA polymerase II cis-regulatory region sequence-specific DNA binding |
GO_0043565 | Molecular function | sequence-specific DNA binding |
GO_0003682 | Molecular function | chromatin binding |
GO_0003690 | Molecular function | double-stranded DNA binding |
GO_0050544 | Molecular function | arachidonic acid binding |
GO_0019899 | Molecular function | enzyme binding |
GO_0050693 | Molecular function | LBD domain binding |
GO_0000976 | Molecular function | transcription cis-regulatory region binding |
GO_0042277 | Molecular function | peptide binding |
GO_0004879 | Molecular function | nuclear receptor activity |
GO_0001221 | Molecular function | transcription coregulator binding |
GO_0050692 | Molecular function | DNA binding domain binding |
GO_0051393 | Molecular function | alpha-actinin binding |
GO_0003700 | Molecular function | DNA-binding transcription factor activity |
GO_0005515 | Molecular function | protein binding |
GO_0003677 | Molecular function | DNA binding |
GO_0070412 | Molecular function | R-SMAD binding |
GO_0001227 | Molecular function | DNA-binding transcription repressor activity, RNA polymerase II-specific |
GO_0000981 | Molecular function | DNA-binding transcription factor activity, RNA polymerase II-specific |
GO_0003676 | Molecular function | nucleic acid binding |
GO_0097677 | Molecular function | STAT family protein binding |
GO_0046965 | Molecular function | nuclear retinoid X receptor binding |
GO_0004955 | Molecular function | prostaglandin receptor activity |
Gene name | PPARG |
Protein name | Peroxisome proliferator-activated receptor gamma (PPAR-gamma) (Nuclear receptor subfamily 1 group C member 3) Peroxisome proliferator activated receptor gamma |
Synonyms | PPARG3D5 gamma PPARG5 PPARG1D5 NR1C3 hCG_26772 PPAR PPARG2D5 |
Description | FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. . FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. ARF6 acts as a key regulator of the tissue-specific adipocyte P2 (aP2) enhancer. Acts as a critical regulator of gut homeostasis by suppressing NF-kappa-B-mediated pro-inflammatory responses. Plays a role in the regulation of cardiovascular circadian rhythms by regulating the transcription of BMAL1 in the blood vessels (By similarity). .; FUNCTION: (Microbial infection) Upon treatment with M.tuberculosis or its lipoprotein LpqH, phosphorylation of MAPK p38 and IL-6 production are modulated, probably via this protein. . FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. . FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. . FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. . FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. . FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. . FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. . FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. . FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. . FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. . FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. . FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. . FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. . FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. . FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. . FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. . FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. . FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. . FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. . FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. . FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. . FUNCTION: Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. . |
Accessions | A0A494C0D9 A0A804HJN2 A0A804HIG1 ENST00000397026.7 ENST00000396999.3 A0A804HLH1 ENST00000455517.6 B6ZGS2 Q4W4C7 A0A494C0T3 ENST00000397029.8 E9PFV3 Q53EW1 ENST00000682446.1 ENST00000652098.1 ENST00000643888.2 A0A804HL89 P37231 ENST00000684065.1 ENST00000287820.10 [P37231-1] ENST00000683699.1 D2KUA6 ENST00000309576.11 ENST00000681966.1 E7EU07 ENST00000397015.7 ENST00000683749.1 Q6L9M1 ENST00000397010.7 A0A494C1F9 ENST00000438682.6 Q4W4C6 E7EUD1 ENST00000652431.1 E9PFX5 E9PFV2 ENST00000643197.2 ENST00000683586.1 ENST00000651735.1 A0A499FIV4 ENST00000397023.5 ENST00000683700.1 Q86WD1 ENST00000397000.6 A0A494C012 A0A0S2Z4K5 ENST00000681982.1 ENST00000652522.1 ENST00000644622.2 A0A3P3ZKM0 |