Gene Gene information from NCBI Gene database.
Entrez ID 7091
Gene name TLE family member 4, transcriptional corepressor
Gene symbol TLE4
Synonyms (NCBI Gene)
BCE-1BCE1E(spI)E(spl)ESGESG4GRG4Grg-4
Chromosome 9
Chromosome location 9q21.31
miRNA miRNA information provided by mirtarbase database.
115
miRTarBase ID miRNA Experiments Reference
MIRT005105 hsa-miR-155-5p Microarray 19193853
MIRT016236 hsa-miR-548b-3p Sequencing 20371350
MIRT017745 hsa-miR-335-5p Microarray 18185580
MIRT005105 hsa-miR-155-5p Reporter assay;Other 20584899
MIRT021114 hsa-miR-186-5p Sequencing 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
21
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IEA
GO:0000122 Process Negative regulation of transcription by RNA polymerase II ISS
GO:0003682 Function Chromatin binding IEA
GO:0003714 Function Transcription corepressor activity IBA
GO:0003714 Function Transcription corepressor activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
605132 11840 ENSG00000106829
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q04727
Protein name Transducin-like enhancer protein 4 (Grg-4) (Groucho-related protein 4)
Protein function Transcriptional corepressor that binds to a number of transcription factors. Inhibits the transcriptional activation mediated by PAX5, and by CTNNB1 and TCF family members in Wnt signaling. The effects of full-length TLE family members may be mo
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03920 TLE_N 8 138 Groucho/TLE N-terminal Q-rich domain Family
PF00400 WD40 571 605 WD domain, G-beta repeat Repeat
PF00400 WD40 609 647 WD domain, G-beta repeat Repeat
Tissue specificity TISSUE SPECIFICITY: In all tissues examined, mostly in brain, and muscle.
Sequence
MIRDLSKMYPQTRHPAPHQPAQPFKFTISESCDRIKEEFQFLQAQYHSLKLECEKLASEK
TEMQRHYVMYYEMSYGLNIEMHKQAEIVKRLNAICAQVIPFLSQEHQQQVVQAVERAKQV
TMAELNAIIGQQLQAQHL
SHGHGLPVPLTPHPSGLQPPAIPPIGSSAGLLALSSALGGQS
HLPIKDEKKHHDNDHQRDRDSIKSSSVSPSASFRGAEKHRNSADYSSESKKQKTEEKEIA
ARYDSDGEKSDDNLVVDVSNEDPSSPRGSPAHSPRENGLDKTRLLKKDAPISPASIASSS
STPSSKSKELSLNEKSTTPVSKSNTPTPRTDAPTPGSNSTPGLRPVPGKPPGVDPLASSL
RTPMAVPCPYPTPFGIVPHAGMNGELTSPGAAYAGLHNISPQMSAAAAAAAAAAAYGRSP
VVGFDPHHHMRVPAIPPNLTGIPGGKPAYSFHVSADGQMQPVPFPPDALIGPGIPRHARQ
INTLNHGEVVCAVTISNPTRHVYTGGKGCVKVWDISHPGNKSPVSQLDCLNRDNYIRSCR
LLPDGRTLIVGGEASTLSIWDLAAPTPRIKAELTSSAPACYALAISPDSKVCFSCCSDGN
IAVWD
LHNQTLVRQFQGHTDGASCIDISNDGTKLWTGGLDNTVRSWDLREGRQLQQHDFT
SQIFSLGYCPTGEWLAVGMENSNVEVLHVTKPDKYQLHLHESCVLSLKFAHCGKWFVSTG
KDNLLNAWRTPYGASIFQSKESSSVLSCDISVDDKYIVTGSGDKKATVYEVIY
Sequence length 773
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Wnt signaling pathway
Notch signaling pathway
  Formation of the beta-catenin:TCF transactivating complex
Deactivation of the beta-catenin transactivating complex
Repression of WNT target genes
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Malignant tumor of urinary bladder Benign rs181919110 RCV005904817
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Associate 34438242
Colorectal Neoplasms Associate 36171645, 38092774, 40473764
Focal Cortical Dysplasia Associate 24252438
Inflammation Associate 27486062
Leukemia Associate 27486062
Leukemia Myeloid Associate 27486062
Neoplasm Metastasis Associate 28121627
Neoplasms Inhibit 27486062
Neoplastic Syndromes Hereditary Associate 2472742