Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
100129654
Gene name Gene Name - the full gene name approved by the HGNC.
Transcription factor 24
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TCF24
Synonyms (NCBI Gene) Gene synonyms aliases
TCF-24, bHLHa25
Chromosome Chromosome number
8
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
8q13.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT640281 hsa-miR-548ac HITS-CLIP 23824327
MIRT640280 hsa-miR-548bb-3p HITS-CLIP 23824327
MIRT640279 hsa-miR-548d-3p HITS-CLIP 23824327
MIRT640278 hsa-miR-548h-3p HITS-CLIP 23824327
MIRT640277 hsa-miR-548z HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000977 Function RNA polymerase II transcription regulatory region sequence-specific DNA binding IBA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA
GO:0003677 Function DNA binding IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0005634 Component Nucleus IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID Q7RTU0
Protein name Transcription factor 24 (TCF-24)
Protein function Putative transcription factor.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00010 HLH 51 102 Helix-loop-helix DNA-binding domain Domain
Sequence
MDRGRPAGSPLSASAEPAPLAAAIRDSRPGRTGPGPAGPGGGSRSGSGRPAAANAARERS
RVQTLRHAFLELQRTLPSVPPDTKLSKLDVLLLATTYIAHLT
RSLQDDAEAPADAGLGAL
RGDGYLHPVKKWPMRSRLYIGATGQFLKHSVSGEKTNHDNTPTDSQP
Sequence length 167
Interactions View interactions
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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
Intracranial Aneurysm Intracranial aneurysm N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Intracranial Aneurysm Associate 35177760