Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
7091
Gene name Gene Name - the full gene name approved by the HGNC.
TLE family member 4, transcriptional corepressor
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TLE4
Synonyms (NCBI Gene) Gene synonyms aliases
BCE-1, BCE1, E(spI), E(spl), ESG, ESG4, GRG4, Grg-4
Chromosome Chromosome number
9
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
9q21.31
miRNA miRNA information provided by mirtarbase database.
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 information of associated ontologies with gene provided by GO database.
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605132 11840 ENSG00000106829
Protein
UniProt ID 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
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Bipolar Disorder Bipolar disorder N/A N/A GWAS
Diabetes Severe insulin-resistant type 2 diabetes N/A N/A GWAS
Metabolic Syndrome Metabolic syndrome N/A N/A GWAS
Schizophrenia Schizophrenia N/A N/A GWAS
Associations from Text Mining Disease 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