Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
9314
Gene name Gene Name - the full gene name approved by the HGNC.
KLF transcription factor 4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
KLF4
Synonyms (NCBI Gene) Gene synonyms aliases
EZF, GKLF
Chromosome Chromosome number
9
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
9q31.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a protein that belongs to the Kruppel family of transcription factors. The encoded zinc finger protein is required for normal development of the barrier function of skin. The encoded protein is thought to control the G1-to-S transition o
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT003605 hsa-miR-25-3p Western blot 19541842
MIRT003216 hsa-miR-10b-5p Luciferase reporter assay, Western blot 20075075
MIRT003216 hsa-miR-10b-5p Luciferase reporter assay, Western blot 20075075
MIRT005674 hsa-miR-130a-3p Luciferase reporter assay, Microarray, qRT-PCR 20981674
MIRT005440 hsa-miR-135b-5p Luciferase reporter assay, Microarray, qRT-PCR 20981674
Transcription factors
Transcription factor Regulation Reference
APC Unknown 12387883
CDX2 Activation 11521200
CDX2 Unknown 23202735
HDAC1 Repression 15051827
HDAC2 Repression 19486889
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 IDA 20551324
GO:0000785 Component Chromatin IDA 21539536
GO:0000785 Component Chromatin ISA
GO:0000791 Component Euchromatin IEA
GO:0000976 Function Transcription regulatory region sequence-specific DNA binding ISS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602253 6348 ENSG00000136826
Protein
UniProt ID O43474
Protein name Krueppel-like factor 4 (Epithelial zinc finger protein EZF) (Gut-enriched krueppel-like factor)
Protein function Transcription factor; can act both as activator and as repressor. Binds the 5'-CACCC-3' core sequence. Binds to the promoter region of its own gene and can activate its own transcription. Regulates the expression of key transcription factors dur
PDB 6VTX
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00096 zf-C2H2 430 454 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 460 484 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 490 512 Zinc finger, C2H2 type Domain
Sequence
MRQPPGESDMAVSDALLPSFSTFASGPAGREKTLRQAGAPNNRWREELSHMKRLPPVLPG
RPYDLAAATVATDLESGGAGAACGGSNLAPLPRRETEEFNDLLDLDFILSNSLTHPPESV
AATVSSSASASSSSSPSSSGPASAPSTCSFTYPIRAGNDPGVAPGGTGGGLLYGRESAPP
PTAPFNLADINDVSPSGGFVAELLRPELDPVYIPPQQPQPPGGGLMGKFVLKASLSAPGS
EYGSPSVISVSKGSPDGSHPVVVAPYNGGPPRTCPKIKQEAVSSCTHLGAGPPLSNGHRP
AAHDFPLGRQLPSRTTPTLGLEEVLSSRDCHPALPLPPGFHPHPGPNYPSFLPDQMQPQV
PPLHYQGQSRGFVARAGEPCVCWPHFGTHGMMLTPPSSPLELMPPGSCMPEEPKPKRGRR
SWPRKRTATHTCDYAGCGKTYTKSSHLKAHLRTHTGEKPYHCDWDGCGWKFARSDELTRH
YRKH
TGHRPFQCQKCDRAFSRSDHLALHMKRHF
Sequence length 513
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Signaling pathways regulating pluripotency of stem cells
Chemical carcinogenesis - receptor activation
  Synthesis, secretion, and deacylation of Ghrelin
Transcriptional regulation of pluripotent stem cells
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Arthritis Juvenile arthritis rs1594890601, rs1594882933, rs184370809, rs776489319, rs1594883470 19565504
Congenital heart defects Congenital Heart Defects rs267607101, rs121434422, rs387906498, rs397509416, rs587777371, rs587777372, rs587777374, rs367537998, rs797044882, rs886041730, rs768027510, rs1064793873, rs1555447012, rs1554263268, rs1554263321
View all (13 more)
20439457
Meningioma Meningioma rs587776563, rs121434259, rs387906857, rs397509405, rs797045990, rs876659443, rs878854603, rs1057518166, rs1060501395, rs1554897280, rs1554898242, rs1555605347, rs587782187, rs1555605750, rs878853937
View all (3 more)
Unknown
Disease term Disease name Evidence References Source
Prostate cancer Prostate cancer Together, these results show that PRRX2 is an oncogene and might play a role in the aggressiveness of PC within the DNPC population. GWAS, CBGDA
Breast Cancer Breast Cancer Importantly, breast cancer patients bearing PRC2 LOF mutations displayed significantly worse prognosis compared with PRC2 wild-type patients GWAS, CBGDA
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma Associate 28751461
Adenocarcinoma of Lung Associate 33661044, 37287976
Adenoma Associate 35750256
Adenomatous Polyposis Coli Inhibit 11521200
Adenomatous Polyps Inhibit 11005769
Adrenoleukodystrophy Associate 29065337
Alzheimer Disease Associate 29753274, 31401456, 31698192, 37549144
Ameloblastoma Associate 37559082
Aneurysm Associate 27720318, 30792063
Anophthalmia with pulmonary hypoplasia Associate 27802195