Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6941
Gene name Gene Name - the full gene name approved by the HGNC.
Transcription factor 19
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TCF19
Synonyms (NCBI Gene) Gene synonyms aliases
SC1, TCF-19
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p21.33
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a protein that contains a PHD-type zinc finger domain and likely functions as a transcription factor. The encoded protein plays a role proliferation and apoptosis of pancreatic beta cells. Alternative splicing results in multiple transcr
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT048303 hsa-miR-107 CLASH 23622248
MIRT041802 hsa-miR-484 CLASH 23622248
MIRT439113 hsa-miR-10b-5p 3'LIFE 25074381
MIRT439113 hsa-miR-10b-5p 3'LIFE 25074381
MIRT1416008 hsa-miR-1182 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 21516116, 28514442, 31515488, 32296183, 33961781
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IEA
GO:0008270 Function Zinc ion binding IEA
GO:0010468 Process Regulation of gene expression IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
600912 11629 ENSG00000137310
Protein
UniProt ID Q9Y242
Protein name Transcription factor 19 (TCF-19) (Transcription factor SC1)
Protein function Potential transcription factor that may play a role in the regulation of genes involved in cell cycle G1/S transition (PubMed:1868030, PubMed:31141247). May bind to regulatory elements of genes, including the promoter of the transcription factor
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00498 FHA 31 105 FHA domain Family
Sequence
MLPCFQLLRIGGGRGGDLYTFHPPAGAGCTYRLGHRADLCDVALRPQQEPGLISGIHAEL
HAEPRGDDWRVSLEDHSSQGTLVNNVRLPRGHRLELSDGDLLTFG
PEGPPGTSPSEFYFM
FQQVRVKPQDFAAITIPRSRGEARVGAGFRPMLPSQGAPQRPLSTFSPAPKATLILNSIG
SLSKLRPQPLTFSPSWGGPKSLPVPAPPGEMGTTPSAPPQRNRRKSVHRVLAELDDESEP
PENPPPVLMEPRKKLRVDKAPLTPTGNRRGRPRKYPVSAPMAPPAVGGGEPCAAPCCCLP
QEETVAWVQCDGCDVWFHVACVGCSIQAAREADFRCPGCRAGIQT
Sequence length 345
Interactions View interactions
<
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
Diabetes Type 2 diabetes, Type 2 diabetes (adjusted for BMI), Type 2 diabetes or schizophrenia (pleiotropy) N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Carcinogenesis Associate 36233194
Carcinoma Hepatocellular Associate 24987808, 31746185
Carcinoma Non Small Cell Lung Associate 1645569, 31746185
Colorectal Neoplasms Stimulate 32016966
Diabetes Mellitus Type 1 Associate 29042441, 31746185
Diabetes Mellitus Type 2 Associate 25799151, 29042441
Hearing Loss Associate 33713422
Hepatitis B Chronic Associate 24987808
Multiple Myeloma Associate 27718532
Myasthenia Gravis Associate 23055271