Name | Number of supported studies | Average coverage | |
---|---|---|---|
intestine | 14 studies | 42% ± 23% | |
brain | 13 studies | 26% ± 12% | |
kidney | 7 studies | 31% ± 16% | |
eye | 7 studies | 33% ± 13% | |
pancreas | 4 studies | 44% ± 18% | |
placenta | 4 studies | 29% ± 15% | |
lung | 4 studies | 46% ± 15% | |
bone marrow | 4 studies | 25% ± 7% | |
lymph node | 3 studies | 19% ± 3% |
Tissue | GTEx Coverage | GTEx Average TPM | GTEx Number of samples | TCGA Coverage | TCGA Average TPM | TCGA Number of samples |
---|---|---|---|---|---|---|
brain | 97% | 47637.29 | 2550 / 2642 | 100% | 1561.89 | 703 / 705 |
intestine | 99% | 38339.52 | 960 / 966 | 86% | 523.45 | 453 / 527 |
prostate | 93% | 8891.71 | 228 / 245 | 87% | 233.77 | 437 / 502 |
kidney | 97% | 15699.43 | 86 / 89 | 68% | 168.24 | 614 / 901 |
bladder | 76% | 8990.95 | 16 / 21 | 78% | 340.88 | 391 / 504 |
ovary | 76% | 6109.73 | 136 / 180 | 68% | 270.71 | 293 / 430 |
uterus | 83% | 8222.18 | 141 / 170 | 58% | 339.93 | 268 / 459 |
stomach | 67% | 5308.74 | 242 / 359 | 71% | 310.66 | 204 / 286 |
thymus | 50% | 3050.35 | 328 / 653 | 84% | 341.92 | 506 / 605 |
pancreas | 16% | 911.42 | 54 / 328 | 94% | 267.87 | 168 / 178 |
lung | 36% | 2080.57 | 207 / 578 | 75% | 164.57 | 866 / 1155 |
skin | 24% | 1859.47 | 436 / 1809 | 85% | 326.81 | 402 / 472 |
eye | 0% | 0 | 0 / 0 | 99% | 399.85 | 79 / 80 |
esophagus | 60% | 5561.19 | 867 / 1445 | 38% | 71.44 | 69 / 183 |
spleen | 97% | 10204.44 | 233 / 241 | 0% | 0 | 0 / 0 |
adrenal gland | 18% | 1479.03 | 47 / 258 | 76% | 723.14 | 175 / 230 |
tonsil | 0% | 0 | 0 / 0 | 58% | 106.64 | 26 / 45 |
blood vessel | 47% | 4876.23 | 625 / 1335 | 0% | 0 | 0 / 0 |
breast | 16% | 1026.90 | 75 / 459 | 24% | 46.82 | 269 / 1118 |
liver | 3% | 172.25 | 7 / 226 | 22% | 38.36 | 89 / 406 |
peripheral blood | 20% | 2580.82 | 184 / 929 | 0% | 0 | 0 / 0 |
heart | 19% | 1061.82 | 165 / 861 | 0% | 0 | 0 / 0 |
adipose | 17% | 1080.39 | 209 / 1204 | 0% | 0 | 0 / 0 |
lymph node | 0% | 0 | 0 / 0 | 10% | 26.00 | 3 / 29 |
muscle | 0% | 5.36 | 1 / 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_0030182 | Biological process | neuron differentiation |
GO_2001238 | Biological process | positive regulation of extrinsic apoptotic signaling pathway |
GO_0010977 | Biological process | negative regulation of neuron projection development |
GO_0042985 | Biological process | negative regulation of amyloid precursor protein biosynthetic process |
GO_0005764 | Cellular component | lysosome |
GO_0070062 | Cellular component | extracellular exosome |
GO_0005794 | Cellular component | Golgi apparatus |
GO_0005886 | Cellular component | plasma membrane |
GO_0005765 | Cellular component | lysosomal membrane |
GO_0048471 | Cellular component | perinuclear region of cytoplasm |
GO_0001540 | Molecular function | amyloid-beta binding |
GO_0005515 | Molecular function | protein binding |
GO_0005524 | Molecular function | ATP binding |
Gene name | ITM2C |
Protein name | Cerebral protein-3 (Integral membrane protein 2C) Integral membrane protein 2C (Cerebral protein 14) (Transmembrane protein BRI3) [Cleaved into: CT-BRI3] Integral membrane protein 2 |
Synonyms | hucep-14 hCG_34338 hucep-3 PSEC0047 NPD018 BRI3 |
Description | FUNCTION: Negative regulator of amyloid-beta peptide production. May inhibit the processing of APP by blocking its access to alpha- and beta-secretase. Binding to the beta-secretase-cleaved APP C-terminal fragment is negligible, suggesting that ITM2C is a poor gamma-secretase cleavage inhibitor. May play a role in TNF-induced cell death and neuronal differentiation (By similarity). . FUNCTION: Negative regulator of amyloid-beta peptide production. May inhibit the processing of APP by blocking its access to alpha- and beta-secretase. Binding to the beta-secretase-cleaved APP C-terminal fragment is negligible, suggesting that ITM2C is a poor gamma-secretase cleavage inhibitor. May play a role in TNF-induced cell death and neuronal differentiation. . FUNCTION: Negative regulator of amyloid-beta peptide production. May inhibit the processing of APP by blocking its access to alpha- and beta-secretase. Binding to the beta-secretase-cleaved APP C-terminal fragment is negligible, suggesting that ITM2C is a poor gamma-secretase cleavage inhibitor. May play a role in TNF-induced cell death and neuronal differentiation. . FUNCTION: Negative regulator of amyloid-beta peptide production. May inhibit the processing of APP by blocking its access to alpha- and beta-secretase. Binding to the beta-secretase-cleaved APP C-terminal fragment is negligible, suggesting that ITM2C is a poor gamma-secretase cleavage inhibitor. May play a role in TNF-induced cell death and neuronal differentiation. . FUNCTION: Negative regulator of amyloid-beta peptide production. May inhibit the processing of APP by blocking its access to alpha- and beta-secretase. Binding to the beta-secretase-cleaved APP C-terminal fragment is negligible, suggesting that ITM2C is a poor gamma-secretase cleavage inhibitor. May play a role in TNF-induced cell death and neuronal differentiation. . |
Accessions | E7EUS6 ENST00000326407.10 [Q9NQX7-3] B8ZZM6 Q96JS4 Q9NQX7 ENST00000620962.1 ENST00000326427.11 [Q9NQX7-1] ENST00000543957.5 ENST00000409704.6 C9JG41 ENST00000418408.2 ENST00000541852.5 ENST00000335005.10 [Q9NQX7-2] ENST00000457215.5 F5H4I5 |