Gene Gene information from NCBI Gene database.
Entrez ID 136259
Gene name KLF transcription factor 14
Gene symbol KLF14
Synonyms (NCBI Gene)
BTEB5
Chromosome 7
Chromosome location 7q32.2
Summary This intronless gene encodes a member of the Kruppel-like family of transcription factors. The encoded protein functions as a transcriptional co-repressor, and is induced by transforming growth factor-beta (TGF-beta) to repress TGF-beta receptor II gene e
miRNA miRNA information provided by mirtarbase database.
49
miRTarBase ID miRNA Experiments Reference
MIRT051059 hsa-miR-16-5p CLASH 23622248
MIRT047783 hsa-miR-30d-5p CLASH 23622248
MIRT043907 hsa-miR-378a-3p CLASH 23622248
MIRT735836 hsa-miR-374a-3p Luciferase reporter assayWestern blottingqRT-PCR 32799891
MIRT1096203 hsa-miR-3121-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
16
GO ID Ontology Definition Evidence Reference
GO:0000785 Component Chromatin ISA
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IBA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific ISA
GO:0003677 Function DNA binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
609393 23025 ENSG00000266265
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8TD94
Protein name Krueppel-like factor 14 (Basic transcription element-binding protein 5) (BTE-binding protein 5) (Transcription factor BTEB5)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00096 zf-C2H2 195 219 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 225 249 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 255 277 Zinc finger, C2H2 type Domain
Sequence
MSAAVACLDYFAAECLVSMSAGAVVHRRPPDPEGAGGAAGSEVGAAPPESALPGPGPPGP
ASVPQLPQVPAPSPGAGGAAPHLLAASVWADLRGSSGEGSWENSGEAPRASSGFSDPIPC
SVQTPCSELAPASGAAAVCAPESSSDAPAVPSAPAAPGAPAASGGFSGGALGAGPAPAAD
QAPRRRSVTPAAKRHQCPFPGCTKAYYKSSHLKSHQRTHTGERPFSCDWLDCDKKFTRSD
ELARHYRTH
TGEKRFSCPLCPKQFSRSDHLTKHARRHPTYHPDMIEYRGRRRTPRIDPPL
TSEVESSASGSGPGPAPSFTTCL
Sequence length 323
Interactions View interactions
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
KLF14-related disorder Likely benign rs146271852 RCV003899745
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Associate 29849909
Alzheimer disease type 1 Associate 29849909
Brain Neoplasms Associate 35577881
Carcinogenesis Associate 30745849
Carcinoma Hepatocellular Associate 37997542
Cardiovascular Diseases Associate 37351102
Colorectal Neoplasms Associate 28423541
Colorectal Neoplasms Inhibit 30745849
Cytokine Release Syndrome Associate 37868981
Diabetes Mellitus Associate 26670163