Name | Number of supported studies | Average coverage | |
---|---|---|---|
astrocyte | 16 studies | 39% ± 16% | |
oligodendrocyte precursor cell | 14 studies | 45% ± 17% | |
GABAergic neuron | 8 studies | 35% ± 19% | |
neuron | 6 studies | 35% ± 14% | |
interneuron | 6 studies | 34% ± 20% | |
glutamatergic neuron | 5 studies | 42% ± 15% | |
pericyte | 5 studies | 23% ± 7% | |
Mueller cell | 5 studies | 26% ± 7% | |
GABAergic interneuron | 3 studies | 22% ± 5% | |
adipocyte | 3 studies | 24% ± 5% |
Name | Number of supported studies | Average coverage | |
---|---|---|---|
brain | 12 studies | 24% ± 11% |
Tissue | GTEx Coverage | GTEx Average TPM | GTEx Number of samples | TCGA Coverage | TCGA Average TPM | TCGA Number of samples |
---|---|---|---|---|---|---|
brain | 100% | 7675.45 | 2630 / 2642 | 100% | 356.67 | 702 / 705 |
liver | 64% | 1685.10 | 145 / 226 | 89% | 87.04 | 361 / 406 |
prostate | 55% | 700.22 | 135 / 245 | 95% | 49.88 | 475 / 502 |
adrenal gland | 99% | 2570.86 | 255 / 258 | 50% | 63.65 | 114 / 230 |
breast | 79% | 2118.54 | 361 / 459 | 68% | 30.93 | 757 / 1118 |
thymus | 81% | 1164.68 | 529 / 653 | 46% | 17.51 | 277 / 605 |
uterus | 72% | 1320.86 | 122 / 170 | 49% | 30.36 | 225 / 459 |
skin | 80% | 4123.78 | 1440 / 1809 | 39% | 22.42 | 183 / 472 |
ovary | 51% | 645.78 | 92 / 180 | 61% | 34.01 | 262 / 430 |
lung | 45% | 649.35 | 261 / 578 | 59% | 25.68 | 683 / 1155 |
adipose | 87% | 2399.34 | 1053 / 1204 | 0% | 0 | 0 / 0 |
pancreas | 5% | 56.72 | 18 / 328 | 53% | 17.23 | 94 / 178 |
esophagus | 7% | 63.19 | 94 / 1445 | 50% | 28.54 | 92 / 183 |
eye | 0% | 0 | 0 / 0 | 53% | 15.33 | 42 / 80 |
tonsil | 0% | 0 | 0 / 0 | 42% | 15.92 | 19 / 45 |
bladder | 5% | 35.24 | 1 / 21 | 31% | 11.86 | 155 / 504 |
kidney | 9% | 119.62 | 8 / 89 | 22% | 8.82 | 199 / 901 |
stomach | 1% | 9.72 | 4 / 359 | 26% | 10.87 | 75 / 286 |
intestine | 7% | 72.53 | 69 / 966 | 18% | 5.37 | 97 / 527 |
heart | 16% | 189.18 | 135 / 861 | 0% | 0 | 0 / 0 |
lymph node | 0% | 0 | 0 / 0 | 7% | 1.21 | 2 / 29 |
blood vessel | 6% | 97.31 | 86 / 1335 | 0% | 0 | 0 / 0 |
muscle | 0% | 2.08 | 2 / 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 |
peripheral blood | 0% | 0 | 0 / 929 | 0% | 0 | 0 / 0 |
placenta | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
spinal column | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
spleen | 0% | 0 | 0 / 241 | 0% | 0 | 0 / 0 |
ureter | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 1 |
GO_0007165 | Biological process | signal transduction |
GO_1905174 | Biological process | regulation of vascular associated smooth muscle cell dedifferentiation |
GO_0051152 | Biological process | positive regulation of smooth muscle cell differentiation |
GO_0009306 | Biological process | protein secretion |
GO_0005615 | Cellular component | extracellular space |
GO_0005654 | Cellular component | nucleoplasm |
GO_0045202 | Cellular component | synapse |
GO_0005576 | Cellular component | extracellular region |
GO_0032281 | Cellular component | AMPA glutamate receptor complex |
GO_0005737 | Cellular component | cytoplasm |
GO_0005634 | Cellular component | nucleus |
GO_0005515 | Molecular function | protein binding |
Gene name | OLFM2 |
Protein name | Alternative protein OLFM2 Olfactomedin 2 Noelin-2 (Olfactomedin-2) |
Synonyms | NOE2 |
Description | FUNCTION: Involved in transforming growth factor beta (TGF-beta)-induced smooth muscle differentiation. TGF-beta induces expression and translocation of OLFM2 to the nucleus where it binds to SRF, causing its dissociation from the transcriptional repressor HEY2/HERP1 and facilitating binding of SRF to target genes . Plays a role in AMPAR complex organization (By similarity). Is a regulator of vascular smooth-muscle cell (SMC) phenotypic switching, that acts by promoting RUNX2 and inhibiting MYOCD binding to SRF. SMC phenotypic switching is the process through which vascular SMCs undergo transition between a quiescent contractile phenotype and a proliferative synthetic phenotype in response to pathological stimuli. SMC phenotypic plasticity is essential for vascular development and remodeling (By similarity). . |
Accessions | O95897 L8E9J3 ENST00000264833.9 ENST00000590841.5 K7EIS8 K7EKW2 ENST00000593091.2 ENST00000592448.1 K7ELC6 |