Name | Number of supported studies | Average coverage | |
---|---|---|---|
glutamatergic neuron | 8 studies | 44% ± 25% | |
endothelial cell | 5 studies | 21% ± 4% | |
epithelial cell | 5 studies | 30% ± 16% | |
retinal rod cell | 5 studies | 28% ± 12% | |
cardiac muscle cell | 4 studies | 19% ± 2% | |
GABAergic neuron | 4 studies | 60% ± 12% | |
astrocyte | 4 studies | 28% ± 16% | |
interneuron | 4 studies | 47% ± 20% | |
neuron | 3 studies | 19% ± 2% | |
retinal cone cell | 3 studies | 24% ± 10% | |
retinal pigment epithelial cell | 3 studies | 28% ± 6% |
Tissue | GTEx Coverage | GTEx Average TPM | GTEx Number of samples | TCGA Coverage | TCGA Average TPM | TCGA Number of samples |
---|---|---|---|---|---|---|
ovary | 100% | 1488.08 | 180 / 180 | 99% | 14.99 | 427 / 430 |
lung | 99% | 775.48 | 575 / 578 | 100% | 15.09 | 1152 / 1155 |
bladder | 100% | 720.29 | 21 / 21 | 98% | 15.08 | 493 / 504 |
uterus | 100% | 659.14 | 170 / 170 | 98% | 18.03 | 448 / 459 |
intestine | 98% | 505.52 | 947 / 966 | 99% | 14.37 | 524 / 527 |
esophagus | 97% | 906.74 | 1403 / 1445 | 100% | 25.28 | 183 / 183 |
breast | 100% | 649.61 | 458 / 459 | 97% | 13.69 | 1081 / 1118 |
stomach | 97% | 423.84 | 347 / 359 | 99% | 14.22 | 283 / 286 |
prostate | 99% | 533.34 | 243 / 245 | 94% | 8.98 | 474 / 502 |
kidney | 100% | 557.34 | 89 / 89 | 92% | 7.87 | 831 / 901 |
thymus | 100% | 626.62 | 652 / 653 | 92% | 6.64 | 557 / 605 |
skin | 100% | 2003.99 | 1809 / 1809 | 90% | 9.95 | 427 / 472 |
pancreas | 93% | 317.33 | 306 / 328 | 96% | 9.29 | 171 / 178 |
liver | 96% | 362.57 | 216 / 226 | 55% | 3.33 | 224 / 406 |
adrenal gland | 100% | 785.19 | 258 / 258 | 41% | 2.69 | 94 / 230 |
brain | 69% | 190.24 | 1821 / 2642 | 53% | 2.64 | 377 / 705 |
spleen | 100% | 822.49 | 241 / 241 | 0% | 0 | 0 / 0 |
tonsil | 0% | 0 | 0 / 0 | 100% | 20.54 | 45 / 45 |
ureter | 0% | 0 | 0 / 0 | 100% | 7.72 | 1 / 1 |
adipose | 100% | 792.93 | 1202 / 1204 | 0% | 0 | 0 / 0 |
blood vessel | 93% | 333.14 | 1246 / 1335 | 0% | 0 | 0 / 0 |
lymph node | 0% | 0 | 0 / 0 | 76% | 5.73 | 22 / 29 |
peripheral blood | 67% | 489.95 | 623 / 929 | 0% | 0 | 0 / 0 |
muscle | 64% | 169.08 | 513 / 803 | 0% | 0 | 0 / 0 |
heart | 49% | 133.57 | 418 / 861 | 0% | 0 | 0 / 0 |
eye | 0% | 0 | 0 / 0 | 24% | 1.33 | 19 / 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_0008150 | Biological process | biological_process |
GO_0005654 | Cellular component | nucleoplasm |
GO_0005739 | Cellular component | mitochondrion |
GO_0005634 | Cellular component | nucleus |
GO_0005515 | Molecular function | protein binding |
Gene name | AMMECR1 |
Protein name | AMMECR nuclear protein 1 Nuclear protein AMMECR1 (AMME syndrome candidate gene 1 protein) Alport syndrome mental retardation midface hypoplasia and elliptocytosis chromosomal region protein 1 isoform 1 Alport syndrome mental retardation midface hypoplasia and elliptocytosis chromosomal region protein 1 isoform 2 (Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region, gene 1) |
Synonyms | hCG_20302 |
Description | |
Accessions | ENST00000372059.6 [Q9Y4X0-3] Q9Y4X0 ENST00000686065.1 ENST00000372057.1 [Q9Y4X0-4] A0A0S2Z4V0 A0A8I5KSJ4 A0A0S2Z4X0 ENST00000262844.10 [Q9Y4X0-1] |