Gene Gene information from NCBI Gene database.
Entrez ID 6775
Gene name Signal transducer and activator of transcription 4
Gene symbol STAT4
Synonyms (NCBI Gene)
DPMCSLEB11
Chromosome 2
Chromosome location 2q32.2-q32.3
Summary 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.
1
SNP ID Visualize variation Clinical significance Consequence
rs7574865 T>A,G Risk-factor Intron variant
miRNA miRNA information provided by mirtarbase database.
10
miRTarBase ID miRNA Experiments Reference
MIRT052905 hsa-miR-141-3p Luciferase reporter assayqRT-PCRWestern blot 24732377
MIRT052905 hsa-miR-141-3p ImmunohistochemistryLuciferase reporter assayqRT-PCRWestern blot 24732377
MIRT052905 hsa-miR-141-3p ImmunohistochemistryLuciferase reporter assayqRT-PCRWestern blot 24732377
MIRT736510 hsa-miR-200a-3p Luciferase reporter assayWestern blottingqRT-PCR 33552256
MIRT052905 hsa-miR-141-3p Luciferase reporter assayWestern blottingqRT-PCR 33552256
Transcription factors Transcription factors information provided by TRRUST V2 database.
3
Transcription factor Regulation Reference
GATA3 Repression 21632975
NFKB1 Unknown 17046972
RELA Unknown 17046972
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
42
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
600558 11365 ENSG00000138378
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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 associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
69
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Disabling pansclerotic morphea of childhood Likely pathogenic; Pathogenic rs2470644258, rs2470644108, rs2470644386 RCV003313748
RCV003313749
RCV003313750
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ANTI-CENTROMERE-ANTIBODY-POSITIVE SYSTEMIC SCLERODERMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ARTHRITIS, PSORIATIC Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ARTHRITIS, RHEUMATOID CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ASTHMA CTD, Disgenet
CTD, Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Acne Acne HPO_DG
★☆☆☆☆
Found in Text Mining only
Addison Disease Addison`s Disease BEFREE 22537753
★☆☆☆☆
Found in Text Mining only
Adenocarcinoma of pancreas Pancreatic adenocarcinoma BEFREE 29959375
★☆☆☆☆
Found in Text Mining only
Alloimmunisation Alloimmunisation BEFREE 31168801
★☆☆☆☆
Found in Text Mining only
Alopecia Alopecia HPO_DG
★☆☆☆☆
Found in Text Mining only
Alveolitis, Fibrosing Alveolitis BEFREE 19644887
★☆☆☆☆
Found in Text Mining only
Androgen-Insensitivity Syndrome Androgen-Insensitivity Syndrome BEFREE 31465536
★☆☆☆☆
Found in Text Mining only
Ankylosing spondylitis Ankylosing Spondylitis BEFREE 23727609, 27394003
★☆☆☆☆
Found in Text Mining only
Anorexia Anorexia HPO_DG
★☆☆☆☆
Found in Text Mining only
Anterior uveitis Uveitis BEFREE 24312163
★☆☆☆☆
Found in Text Mining only