Mus musculus Gene: Tcf4 | |||||||||||||||||||||||||
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Summary | |||||||||||||||||||||||||
InnateDB Gene | IDBG-156674.6 | ||||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||||
Gene Symbol | Tcf4 | ||||||||||||||||||||||||
Gene Name | transcription factor 4 | ||||||||||||||||||||||||
Synonyms | 5730422P05Rik; ASP-I2; bHLHb19; E2-2; E2.2; ITF-2; ITF-2b; ITF2; ME2; MITF-2A; MITF-2B; SEF-2; SEF2; SEF2-1; Tcf-4; TFE | ||||||||||||||||||||||||
Species | Mus musculus | ||||||||||||||||||||||||
Ensembl Gene | ENSMUSG00000053477 | ||||||||||||||||||||||||
Encoded Proteins |
transcription factor 4
transcription factor 4
transcription factor 4
transcription factor 4
transcription factor 4
transcription factor 4
transcription factor 4
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Protein Structure |
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Useful resources | Stemformatics EHFPI ImmGen | ||||||||||||||||||||||||
InnateDB Annotation from Orthologs | |||||||||||||||||||||||||
Summary |
[Homo sapiens] Transcription Factor that is an essential and specific regulator of Plasmacytoid dendritic cell development
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Entrez Gene | |||||||||||||||||||||||||
Summary |
This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000196628:
This gene encodes transcription factor 4, a basic helix-loop-helix transcription factor. The encoded protein recognizes an Ephrussi-box ('E-box') binding site ('CANNTG') - a motif first identified in immunoglobulin enhancers. This gene is broadly expressed, and may play an important role in nervous system development. Defects in this gene are a cause of Pitt-Hopkins syndrome. Multiple alternatively spliced transcript variants that encode different proteins have been described. [provided by RefSeq, Aug 2011] This gene encodes transcription factor 4, a basic helix-loop-helix transcription factor. The encoded protein recognizes an Ephrussi-box (\'E-box\') binding site (\'CANNTG\') - a motif first identified in immunoglobulin enhancers. This gene is broadly expressed, and may play an important role in nervous system development. Defects in this gene are a cause of Pitt-Hopkins syndrome. Multiple alternatively spliced transcript variants that encode different proteins have been described. [provided by RefSeq, Aug 2011] |
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Gene Information | |||||||||||||||||||||||||
Type | Protein coding | ||||||||||||||||||||||||
Genomic Location | Chromosome 18:69344146-69687967 | ||||||||||||||||||||||||
Strand | Forward strand | ||||||||||||||||||||||||
Band | E2 | ||||||||||||||||||||||||
Transcripts | |||||||||||||||||||||||||
Interactions | |||||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 48 experimentally validated interaction(s) in this database.
They are also associated with 57 interaction(s) predicted by orthology.
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Gene Ontology | |||||||||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||||||||||||||||||
Species
Homo sapiens
Bos taurus
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Gene ID
Gene Order
Not yet available
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Pathway Predictions based on Human Orthology Data | |||||||||||||||||||||||||
NETPATH |
AndrogenReceptor pathway
ID pathway
TGF_beta_Receptor pathway
Wnt pathway
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REACTOME |
CDO in myogenesis pathway
Developmental Biology pathway
Myogenesis pathway
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KEGG | |||||||||||||||||||||||||
INOH | |||||||||||||||||||||||||
PID NCI |
Coregulation of Androgen receptor activity
Regulation of nuclear beta catenin signaling and target gene transcription
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Cross-References | |||||||||||||||||||||||||
SwissProt | Q60722 | ||||||||||||||||||||||||
TrEMBL | E9Q8G4 Q91XK1 Q91YV0 | ||||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||||
Entrez Gene | 21413 | ||||||||||||||||||||||||
UniGene | Mm.394316 Mm.4269 Mm.457828 Mm.470505 Mm.485755 | ||||||||||||||||||||||||
RefSeq | NM_001083967 NM_013685 XM_006525746 XM_006525747 XM_006525748 XM_006525749 XM_006525750 XM_006525751 XM_006525752 XM_006525753 XM_006525754 XM_006525755 XM_006525756 XM_006525757 XM_006525758 XM_006525759 XM_006525764 XM_006525765 | ||||||||||||||||||||||||
OMIM | |||||||||||||||||||||||||
CCDS | CCDS29329 CCDS50315 | ||||||||||||||||||||||||
HPRD | |||||||||||||||||||||||||
IMGT | |||||||||||||||||||||||||
MGI ID | MGI:98506 | ||||||||||||||||||||||||
MGI Symbol | Tcf4 | ||||||||||||||||||||||||
EMBL | AC109258 AC157576 AC163095 AC167546 AC169193 AK014343 AK081012 AK151433 BC014293 BC043050 CH466528 S75870 U16321 U16322 X91753 | ||||||||||||||||||||||||
GenPept | AAB32662 AAC52414 AAC52415 AAH14293 AAH43050 BAB29285 BAC38116 BAE30396 CAA62868 EDL09593 | ||||||||||||||||||||||||
RNA Seq Atlas | 21413 | ||||||||||||||||||||||||