Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6775
Gene name Gene Name - the full gene name approved by the HGNC.
Signal transducer and activator of transcription 4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
STAT4
Synonyms (NCBI Gene) Gene synonyms aliases
DPMC, SLEB11
Disease Acronyms (UniProt) Disease acronyms from UniProt database
DPMC, SLEB11
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q32.2-q32.3
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a member of the STAT family of transcription factors. In response to cytokines and growth factors, STAT family members are phosphorylated by the receptor associated kinases, and then form homo- or heterodimers that tran
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs7574865 T>A,G Risk-factor Intron variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT052905 hsa-miR-141-3p Luciferase reporter assay, qRT-PCR, Western blot 24732377
MIRT052905 hsa-miR-141-3p Immunohistochemistry, Luciferase reporter assay, qRT-PCR, Western blot 24732377
MIRT052905 hsa-miR-141-3p Immunohistochemistry, Luciferase reporter assay, qRT-PCR, Western blot 24732377
MIRT736510 hsa-miR-200a-3p Luciferase reporter assay, Western blotting, qRT-PCR 33552256
MIRT052905 hsa-miR-141-3p Luciferase reporter assay, Western blotting, qRT-PCR 33552256
Transcription factors
Transcription factor Regulation Reference
GATA3 Repression 21632975
NFKB1 Unknown 17046972
RELA Unknown 17046972
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
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 21873635
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA 21873635
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific ISA
GO:0003700 Function DNA-binding transcription factor activity TAS 9284918
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
600558 11365 ENSG00000138378
Protein
UniProt ID Q14765
Protein name Signal transducer and activator of transcription 4
Protein function Transcriptional regulator mainly expressed in hematopoietic cells that plays a critical role in cellular growth, differentiation and immune response (PubMed:10961885, PubMed:37256972, PubMed:8943379). Plays a key role in the differentiation of T
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02865 STAT_int 2 120 STAT protein, protein interaction domain Domain
PF01017 STAT_alpha 140 308 STAT protein, all-alpha domain Family
PF02864 STAT_bind 320 454 STAT protein, DNA binding domain Domain
PF00017 SH2 569 645 SH2 domain Domain
Sequence
Sequence length 748
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Necroptosis
JAK-STAT signaling pathway
Th1 and Th2 cell differentiation
Hepatitis B
Pathways in cancer
Inflammatory bowel disease
  Interleukin-20 family signaling
Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation
Interleukin-35 Signalling
Interleukin-12 signaling
Interleukin-23 signaling
Interleukin-21 signaling
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Apraxia Apraxias rs121908377, rs121908378, rs1135401820, rs1178491246, rs1584969672
Arthritis Arthritis, Systemic onset juvenile chronic arthritis, Juvenile arthritis rs1594890601, rs1594882933, rs184370809, rs776489319, rs1594883470 23603761
Autoimmune diseases Autoimmune Diseases, AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1, AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 rs869025224 21383967, 30595370
Behcet syndrome Behcet Syndrome, Behçet disease rs886040969, rs886039866, rs746055479, rs752615209, rs774164456, rs751454741 26097239, 23001997, 23291587
Unknown
Disease term Disease name Evidence References Source
Celiac disease Celiac Disease, Celiac disease 23143596, 26546613, 25920553, 22057235 ClinVar, GWAS
Crohn disease Crohn Disease 26192919 ClinVar
Myocardial infarction Myocardial Infarction ClinVar
Pancreatitis Pancreatitis ClinVar
Associations from Text Mining
Disease Name Relationship Type References
Acute Disease Associate 25076205
Addison Disease Associate 24614117
Antiphospholipid Syndrome Associate 19644876
Aortic Aneurysm Abdominal Associate 40775512
Arthritis Associate 16096332, 22937072
Arthritis Juvenile Associate 19565500, 19674979, 20722033, 25781893, 29848367
Arthritis Rheumatoid Associate 16096332, 16760256, 17223651, 17804842, 17932559, 18434327, 18576330, 18576336, 18759272, 19109131, 19445664, 19714582, 19741008, 20353580, 20454450
View all (15 more)
Arthropathy progressive pseudorheumatoid of childhood Associate 39597056
Asthma Associate 17532201, 26399222, 35528611
Autoimmune Diseases Associate 18204446, 18576330, 19109131, 19565500, 19796918, 20131239, 22968431, 23990947, 24312163, 24614117, 25019342, 25781893, 26569609, 29276866, 29523850
View all (1 more)