MYCN
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Homo sapiens |
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MYCN is differentially expressed in 262 experiments: 132 organism parts: brain, kidney, ... (130 more);, 181 disease states: normal, acute myeloid leukemia, ... (179 more);, 78 cell types 397 cell lines 24 compound treatments and 89 other conditions. |
| Synonyms |
NMYC, N-myc, bHLHe37 |
| Orthologs |
Mycs
(Mus musculus)
MYCN
(Bos taurus)
MYCN
(Gallus gallus)
mycn
(Danio rerio)
Q4H361_CIOIN
(Ciona intestinalis)
Mycn
(Mus musculus)
Mycn
(Rattus norvegicus)
Mycs
(Rattus norvegicus)
mycn
(Xenopus laevis)
MYCN
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology ID |
GO:0003677, GO:0003700, GO:0005515, GO:0005634, GO:0000785, GO:0006355, GO:0006357, GO:0006351, GO:0045944, GO:0048704, GO:0048754, GO:0042733, GO:0002053, GO:0001502, GO:0030324, GO:0010942, GO:2000378 |
| InterPro ID |
IPR002418, IPR011598, IPR012682 |
| Gene Ontology Term |
DNA binding, protein binding, regulation of transcription, DNA-dependent, transcription, DNA-dependent, positive regulation of transcription from RNA polymerase II promoter, nucleus, chromatin, regulation of transcription from RNA polymerase II promoter, positive regulation of mesenchymal cell proliferation, embryonic skeletal system morphogenesis, positive regulation of cell death, cartilage condensation, branching morphogenesis of a tube, embryonic digit morphogenesis, lung development, sequence-specific DNA binding transcription factor activity, negative regulation of reactive oxygen species metabolic process |
| InterPro Term |
Tscrpt_reg_Myc, Tscrpt_reg_Myc_N, HLH_DNA-bd |
| Ensembl Family Description |
N MYC PROTO ONCOGENE |
| Ensembl Family |
ENSFM00500000271387 |
| EMBL-Bank ID |
X03295, X03294, BT007384, M13228, M13241, CH471053, BC002712, Y00664, X02363, AJ242956, AC010145, M18090, AK299495 |
| Ensembl Protein ID |
ENSP00000281043, ENSP00000390305 |
| RefSeq ID |
NM_005378, NP_005369 |
| UniProt Accession |
Q9UMQ5, Q53XS5, P04198, Q7Z7Q9, B4DRZ1 |
| Entrez Gene ID |
4613 |
| UniGene ID |
Hs.25960 |
| Ensembl Gene ID |
ENSG00000134323 |
| Gene-Disease Assocation |
FEINGOLD SYNDROME |
| Description |
v-myc myelocytomatosis viral related oncogene, neuroblastoma derived (avian) [Source:HGNC Symbol;Acc:7559] |
| HGNC Symbol |
MYCN |
| Ensembl Transcript ID |
ENST00000426211, ENST00000281043 |
| Design Element |
2078_s_at, g12803748_3p_a_at, g11692795_3p_a_at, g11692795_3p_x_at, 35158_at, Hs.25960.1.S1_3p_a_at, 209756_s_at, 209756_3p_s_at, M13241_at, ENST00000281043, 211377_x_at, ENST00000426211, 209757_s_at |
| Search EB-eye |
ENSG00000134323
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