DCC
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Homo sapiens |
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DCC is differentially expressed in 153 experiments: 99 organism parts: lung, ovary, ... (97 more);, 115 disease states: normal, myeloma, ... (113 more);, 41 cell types 173 cell lines 9 compound treatments and 67 other conditions. |
| Synonyms |
IGDCC1 |
| Orthologs |
DCC (2 of 2)
(Danio rerio)
Dcc
(Mus musculus)
Dcc
(Rattus norvegicus)
fra
(Drosophila melanogaster)
DCC (1 of 2)
(Danio rerio)
ENSCING00000009804
(Ciona intestinalis)
DCC
(Xenopus laevis)
DCC
(Canis familiaris)
(Compare orthologs)
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| InterPro ID |
IPR003961, IPR010560, IPR007110, IPR013151, IPR013106, IPR003598, IPR003599, IPR013098 |
| InterPro Term |
Ig_V-set, Ig_sub, Immunoglobulin, Ig-like, Ig_sub2, Neogenin_C, Ig_I-set, Fibronectin_type3 |
| Gene Ontology Term |
cytosol, plasma membrane, protein binding, apoptosis, membrane raft, identical protein binding, induction of apoptosis, netrin receptor activity, axon guidance, multicellular organismal development, transcription coactivator activity, receptor activity, axonogenesis, integral to membrane, regulation of apoptosis, positive regulation of neuron projection development, negative regulation of neuron projection development, positive regulation of ERK1 and ERK2 cascade, growth cone membrane, negative regulation of collateral sprouting, response to amphetamine, negative regulation of dendrite development, transmembrane signaling receptor activity |
| Gene Ontology ID |
GO:0016021, GO:0003713, GO:0007275, GO:0007411, GO:0007409, GO:0042802, GO:0005515, GO:0004872, GO:0004888, GO:0006915, GO:0006917, GO:0005886, GO:0005829, GO:0042981, GO:0005042, GO:0045121, GO:0048671, GO:0032584, GO:0001975, GO:0070374, GO:0010977, GO:0010976, GO:2000171 |
| Ensembl Family Description |
PRECURSOR |
| Ensembl Family |
ENSFM00260000050557 |
| Description |
deleted in colorectal carcinoma [Source:HGNC Symbol;Acc:2701] |
| EMBL-Bank ID |
AC016383, AC116002, AC100777, AC110591, AC090660, AC078999, M63718, M63702, M63700, M63698, M63696, AC011155, X76132, AC019239, AC103949, AC027248, M32290, M32292, M32288, M32286, AC021486 |
| RefSeq ID |
NM_005215, NP_005206 |
| UniGene ID |
Hs.162025, Hs.600047 |
| Gene-Disease Assocation |
MIRROR MOVEMENTS, CONGENITAL |
| Ensembl Gene ID |
ENSG00000187323 |
| Entrez Gene ID |
1630 |
| UniProt Accession |
P43146, E7EQM8 |
| Ensembl Protein ID |
ENSP00000397322, ENSP00000389140, ENSP00000304146 |
| HGNC Symbol |
DCC |
| Ensembl Transcript ID |
ENST00000442544, ENST00000304775, ENST00000412726 |
| Design Element |
Hs.162025.0.A1_3p_at, 42075_at, ENST00000304775, ENST00000442544, 238914_at, 206939_at, 84017_at, g4885174_3p_at, X76132_at, 32890_at, ENST00000412726 |
| Search EB-eye |
ENSG00000187323
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