Insufficient scRNA-seq data for expression of BHLHE22 at single-cell level.
Insufficient scRNA-seq data for expression of BHLHE22 at tissue level.
Tissue | GTEx Coverage | GTEx Average TPM | GTEx Number of samples | TCGA Coverage | TCGA Average TPM | TCGA Number of samples |
---|---|---|---|---|---|---|
lung | 97% | 291.29 | 562 / 578 | 66% | 1.78 | 764 / 1155 |
breast | 96% | 242.15 | 441 / 459 | 60% | 1.81 | 666 / 1118 |
bladder | 90% | 184.76 | 19 / 21 | 36% | 1.00 | 183 / 504 |
brain | 95% | 978.82 | 2514 / 2642 | 31% | 1.26 | 216 / 705 |
intestine | 82% | 182.07 | 796 / 966 | 38% | 0.93 | 201 / 527 |
pancreas | 44% | 40.94 | 144 / 328 | 76% | 2.85 | 136 / 178 |
esophagus | 87% | 182.35 | 1257 / 1445 | 19% | 0.37 | 35 / 183 |
adipose | 94% | 240.06 | 1137 / 1204 | 0% | 0 | 0 / 0 |
uterus | 55% | 79.96 | 93 / 170 | 39% | 1.65 | 177 / 459 |
skin | 57% | 100.97 | 1026 / 1809 | 36% | 2.75 | 169 / 472 |
spleen | 90% | 150.42 | 216 / 241 | 0% | 0 | 0 / 0 |
thymus | 78% | 103.41 | 509 / 653 | 10% | 0.33 | 62 / 605 |
stomach | 38% | 58.16 | 137 / 359 | 50% | 1.17 | 142 / 286 |
lymph node | 0% | 0 | 0 / 0 | 66% | 1.31 | 19 / 29 |
prostate | 42% | 47.82 | 102 / 245 | 7% | 0.12 | 35 / 502 |
blood vessel | 41% | 49.47 | 545 / 1335 | 0% | 0 | 0 / 0 |
tonsil | 0% | 0 | 0 / 0 | 38% | 0.75 | 17 / 45 |
adrenal gland | 16% | 17.13 | 40 / 258 | 19% | 1.87 | 43 / 230 |
liver | 19% | 16.63 | 42 / 226 | 15% | 0.38 | 61 / 406 |
ovary | 17% | 28.68 | 30 / 180 | 15% | 0.29 | 66 / 430 |
kidney | 7% | 5.30 | 6 / 89 | 14% | 0.35 | 123 / 901 |
peripheral blood | 18% | 567.90 | 170 / 929 | 0% | 0 | 0 / 0 |
heart | 11% | 9.56 | 94 / 861 | 0% | 0 | 0 / 0 |
eye | 0% | 0 | 0 / 0 | 3% | 0.17 | 2 / 80 |
muscle | 1% | 0.69 | 7 / 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_0007423 | Biological process | sensory organ development |
GO_0061564 | Biological process | axon development |
GO_0048663 | Biological process | neuron fate commitment |
GO_0045944 | Biological process | positive regulation of transcription by RNA polymerase II |
GO_0000785 | Cellular component | chromatin |
GO_0005634 | Cellular component | nucleus |
GO_1990837 | Molecular function | sequence-specific double-stranded DNA binding |
GO_0070888 | Molecular function | E-box binding |
GO_0046983 | Molecular function | protein dimerization activity |
GO_0003700 | Molecular function | DNA-binding transcription factor activity |
GO_0000981 | Molecular function | DNA-binding transcription factor activity, RNA polymerase II-specific |
Gene name | BHLHE22 |
Protein name | Class E basic helix-loop-helix protein 22 (bHLHe22) (Class B basic helix-loop-helix protein 5) (bHLHb5) (Trinucleotide repeat-containing gene 20 protein) |
Synonyms | BHLHB5 TNRC20 |
Description | FUNCTION: Inhibits DNA binding of TCF3/E47 homodimers and TCF3 (E47)/NEUROD1 heterodimers and acts as a strong repressor of Neurod1 and Myod-responsive genes, probably by heterodimerization with class a basic helix-loop-helix factors. Despite the presence of an intact basic domain, does not bind to DNA (By similarity). In the brain, may function as an area-specific transcription factor that regulates the postmitotic acquisition of area identities and elucidate the genetic hierarchy between progenitors and postmitotic neurons driving neocortical arealization. May be required for the survival of a specific population of inhibitory neurons in the superficial laminae of the spinal cord dorsal horn that may regulate pruritis. Seems to play a crucial role in the retinogenesis, in the specification of amacrine and bipolar subtypes. Forms with PRDM8 a transcriptional repressor complex controlling genes involved in neural development and neuronal differentiation. . |
Accessions | ENST00000321870.3 Q8NFJ8 |