TCF23 (transcription factor 23)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 150921 |
| Gene name | Transcription factor 23 |
| Gene symbol | TCF23 |
| Synonyms (NCBI Gene) |
OUTTCF-23bHLHa24
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| Chromosome | 2 |
| Chromosome location | 2p23.3 |
| Summary | The gene encodes a member of the basic helix-loop-helix transcription factor family. Studies of the orthologous gene in mouse have shown the encoded protein does not bind DNA but may negatively regulate other basic helix-loop-helix factors via the formati |
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miRNA
miRNA information provided by mirtarbase database.
100
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
23
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q7RTU1 | ||||||||||
| Protein name | Transcription factor 23 (TCF-23) (Class A basic helix-loop-helix protein 24) (bHLHa24) | ||||||||||
| Protein function | Inhibits E-box-mediated binding and transactivation of bHLH factors. Inhibitory effect is similar to that of ID proteins. Inhibits the formation of TCF3 and MYOD1 homodimers and heterodimers. Lacks DNA binding activity. Seems to play a role in t | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Expressed in liver, kidney and spleen. {ECO:0000269|PubMed:14516699}. | ||||||||||
| Sequence |
MSQRKARGPPAMPGVGHSQTQAKARLLPGADRKRSRLSRTRQDPWEERSWSNQRWSRATP |
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| Sequence length | 214 | ||||||||||
| Interactions | View interactions | ||||||||||
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
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Related Genes
Genes most often co-reported with TCF23 across shared curated disease and pathway associations.
0
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to TCF23 (see Related Genes above), that are NOT already directly curated for TCF23 itself -- a lead worth checking, not a confirmed association.
0
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