Name | Number of supported studies | Average coverage | |
---|---|---|---|
brain | 14 studies | 41% ± 21% | |
peripheral blood | 10 studies | 24% ± 6% | |
eye | 5 studies | 30% ± 16% | |
lung | 4 studies | 20% ± 2% | |
pancreas | 3 studies | 34% ± 14% | |
heart | 3 studies | 23% ± 2% | |
liver | 3 studies | 34% ± 11% | |
intestine | 3 studies | 17% ± 1% |
Tissue | GTEx Coverage | GTEx Average TPM | GTEx Number of samples | TCGA Coverage | TCGA Average TPM | TCGA Number of samples |
---|---|---|---|---|---|---|
intestine | 100% | 4065.67 | 966 / 966 | 100% | 27.82 | 527 / 527 |
ovary | 100% | 3742.16 | 180 / 180 | 100% | 21.47 | 430 / 430 |
esophagus | 100% | 3160.52 | 1443 / 1445 | 100% | 31.17 | 183 / 183 |
brain | 100% | 4119.49 | 2641 / 2642 | 100% | 32.29 | 703 / 705 |
prostate | 100% | 3496.26 | 244 / 245 | 100% | 21.87 | 501 / 502 |
lung | 100% | 4355.25 | 577 / 578 | 99% | 24.08 | 1149 / 1155 |
stomach | 100% | 2920.21 | 359 / 359 | 99% | 30.70 | 284 / 286 |
liver | 100% | 2553.44 | 226 / 226 | 99% | 18.58 | 403 / 406 |
thymus | 100% | 3611.56 | 652 / 653 | 99% | 24.56 | 601 / 605 |
adrenal gland | 100% | 6773.45 | 258 / 258 | 99% | 23.28 | 228 / 230 |
kidney | 100% | 3352.88 | 89 / 89 | 99% | 31.89 | 891 / 901 |
breast | 100% | 3427.64 | 459 / 459 | 98% | 22.73 | 1100 / 1118 |
pancreas | 99% | 1892.33 | 324 / 328 | 99% | 23.02 | 177 / 178 |
uterus | 100% | 3323.18 | 170 / 170 | 98% | 17.59 | 449 / 459 |
bladder | 100% | 3611.24 | 21 / 21 | 97% | 18.66 | 490 / 504 |
skin | 100% | 3363.86 | 1805 / 1809 | 91% | 15.95 | 429 / 472 |
adipose | 100% | 3633.00 | 1204 / 1204 | 0% | 0 | 0 / 0 |
blood vessel | 100% | 9793.49 | 1335 / 1335 | 0% | 0 | 0 / 0 |
lymph node | 0% | 0 | 0 / 0 | 100% | 27.76 | 29 / 29 |
muscle | 100% | 4329.26 | 803 / 803 | 0% | 0 | 0 / 0 |
peripheral blood | 100% | 5703.36 | 929 / 929 | 0% | 0 | 0 / 0 |
spleen | 100% | 3049.82 | 241 / 241 | 0% | 0 | 0 / 0 |
tonsil | 0% | 0 | 0 / 0 | 100% | 20.05 | 45 / 45 |
ureter | 0% | 0 | 0 / 0 | 100% | 11.38 | 1 / 1 |
heart | 96% | 3651.27 | 826 / 861 | 0% | 0 | 0 / 0 |
eye | 0% | 0 | 0 / 0 | 56% | 6.14 | 45 / 80 |
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_0060816 | Biological process | random inactivation of X chromosome |
GO_0045944 | Biological process | positive regulation of transcription by RNA polymerase II |
GO_0006357 | Biological process | regulation of transcription by RNA polymerase II |
GO_0031519 | Cellular component | PcG protein complex |
GO_0005813 | Cellular component | centrosome |
GO_0035102 | Cellular component | PRC1 complex |
GO_0005654 | Cellular component | nucleoplasm |
GO_0005794 | Cellular component | Golgi apparatus |
GO_0000805 | Cellular component | X chromosome |
GO_0005634 | Cellular component | nucleus |
GO_0140862 | Molecular function | histone H2AK119 ubiquitin ligase activity |
GO_0005515 | Molecular function | protein binding |
GO_0046872 | Molecular function | metal ion binding |
Gene name | PCGF5 |
Protein name | Polycomb group RING finger protein 5 (RING finger protein 159) |
Synonyms | RNF159 |
Description | FUNCTION: Component of a Polycomb group (PcG) multiprotein PRC1-like complex, a complex class required to maintain the transcriptionally repressive state of many genes, including Hox genes, throughout development. PcG PRC1 complex acts via chromatin remodeling and modification of histones; it mediates monoubiquitination of histone H2A 'Lys-119', rendering chromatin heritably changed in its expressibility . Within the PRC1-like complex, regulates RNF2 ubiquitin ligase activity . Plays a redundant role with PCGF3 as part of a PRC1-like complex that mediates monoubiquitination of histone H2A 'Lys-119' on the X chromosome and is required for normal silencing of one copy of the X chromosome in XX females (By similarity). . |
Accessions | Q86SE9 ENST00000336126.6 [Q86SE9-1] ENST00000543648.5 [Q86SE9-1] ENST00000614189.4 [Q86SE9-1] |