STAT4 - signal transducer and activator of transcription 4 Gene

Also Known as SLEB11

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 6775

About STAT4

Cytogenetic location: 2q32.2-q32.3 Genomic coordinates (GRCh38): 2:191,029,576-191,246,175 (from NCBI)

This gene has 11 transcripts (splice variants), 199 orthologues, 6 paralogues and is associated with 6 phenotypes. Broad expression in testis (RPKM 9.8), lymph node (RPKM 6.0) and 17 other tissues.

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 translocate to the cell nucleus where they act as transcription activators. This protein is essential for mediating responses to IL12 in lymphocytes, and regulating the differentiation of T helper cells. Mutations in this gene may be associated with systemic lupus erythematosus and rheumatoid arthritis. Alternate splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Aug 2011]

STAT4 Products (2)

mRNA Protein Name
NM_001243835.2 NP_001230764.1 signal transducer and activator of transcription 4
NM_003151.4 NP_003142.1 signal transducer and activator of transcription 4
Molecular Function GO Annotation Evidence References Source
enables DNA-binding transcription factor activity IDA
IDA: Inferred from direct assay
31562212 GOA
enables DNA-binding transcription factor activity IMP
IMP: Inferred from mutant phenotype
37256972 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
18591661 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
22740693 GOA
Biological Process GO Annotation Evidence References Source
involved in T-helper 1 cell differentiation IDA
IDA: Inferred from direct assay
14688310 GOA
involved in interleukin-12-mediated signaling pathway IDA
IDA: Inferred from direct assay
7638186 GOA
involved in response to interleukin-6 IMP
IMP: Inferred from mutant phenotype
37256972 GOA
Cellular Component GO Annotation Evidence References Source
part of RNA polymerase II transcription regulator complex IPI
IPI: Inferred from physical interaction
18591661 GOA
is active in nucleus IDA
IDA: Inferred from direct assay
7638186 GOA
located in nucleus IMP
IMP: Inferred from mutant phenotype
37256972 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

STAT4 Protein Structure

STAT_int

STAT_int: STAT protein, protein interaction domain (2 - 121)

STAT_alpha

STAT_alpha: STAT protein, all-alpha domain (137 - 314)

STAT_bind

STAT_bind: STAT protein, DNA binding domain (316 - 563)

SH2

SH2: SH2 domain (573 - 627)

  • 0
  • 200
  • 400
  • 600
  • 748 a.a.
Protein Preferred Names Protein Names

signal transducer and activator of transcription 4

STAT4 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
STAT4 Q14765 NUP58 Homo sapiens Q9BVL2 32814053
Intra
STAT4 Q14765 STAT1 Homo sapiens P42224 35140242
Intra
STAT4 Q14765 STAT1 Homo sapiens P42224 33961781
Intra
STAT4 Q14765 NUP58 Homo sapiens Q9BVL2 32814053
Intra
STAT4 Q14765 STAT4 Homo sapiens Q14765
GMS
18591661
Intra
STAT4 Q14765 STAT4 Homo sapiens Q14765 18591661
Intra
STAT4 Q14765 SH2D1B Homo sapiens O14796 25814554
Intra
STAT4 Q14765 NUP58 Homo sapiens Q9BVL2 32814053
Intra
STAT4 Q14765 LAMTOR5 Homo sapiens O43504 22740693
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant STAT4 Proteins

Cat. No. Product Name Accession Purity
HY-P76664 STAT4 Protein, Human (sf9, His) Q14765 (M1-E748) ≥ 90%, as determined by reducing SDS-PAGE.

STAT4 Antibodies

Cat. No. Product Name Application Reactivity
HY-P80903 STAT4 Antibody (YA055) WB, IHC-P, IP Human
HY-P80903A STAT4 Antibody (YA055)(PBS only) WB, IHC-P, ICC/IF, IP, FC Human

Related Diseases

Diseases Alias
Systemic Lupus Erythematosus 11
  • Systemic Lupus Erythematosus, Susceptibility To, 11

  • SLEB11

  • Lupus Erythematosus, Systemic, Type 11

Systemic Lupus Erythematosus
  • Lupus Nephritis

  • SLE

  • Disseminated Lupus Erythematosus

  • Systemic Lupus Erythematosus, Susceptibility To

  • Lupus Erythematosus, Systemic

  • Lupus Nephritis, Susceptibility To

  • Libman-Sacks Disease

  • Systemic Lupus Erythematosus Susceptibility To

  • Sle - Lupus Erythematosus, Systemic

  • Le Syndrome

  • Lupus

  • Lupus Erythematosus Systemic

  • Lupus Erythematosus, Systemic, Susceptibility To

  • Lupus Vulgaris

  • Lupus Erythematosus, Discoid

  • Lupus Erythematosus

  • Systemic Lupus Erythematosus Nos

  • Sle - [Systemic Lupus Erythematosus]

Arthritis
  • Inflammatory Joint Disease

  • Inflammatory Disorder Of Joint

Lupus Erythematosus
  • Lupus

  • Lupus Vulgaris

  • Lupus Erythematosus, Discoid

  • Lupus Erythematosus, Systemic

  • Subacute Cutaneous Lupus

  • Le - [Lupus Erythematosus]

Pediatric Systemic Lupus Erythematosus
  • Sle, Pediatric Onset

Rheumatoid Arthritis
  • RA

  • Arthritis, Rheumatoid

  • Rheumatoid Arthritis, Susceptibility To

  • Arthritis Or Polyarthritis, Rheumatic

  • Atrophic Arthritis

  • Rheumatism Arthritis

  • Rheumatoid Polyarthritis

Oligoarticular Juvenile Idiopathic Arthritis
  • Oligoarticular Jia

  • Pauciarticular Chronic Arthritis

  • Juvenile Pauciarticular Chronic Arthritis

Rheumatoid Factor-Negative Polyarticular Juvenile Idiopathic Arthritis
  • Juvenile Polyarthritis Without Rheumatoid Factor

  • Juvenile Rheumatoid Factor-Negative Polyarthritis

  • Rheumatoid Factor-Negative Polyarticular Jia

  • Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative

Behcet Syndrome
  • Behcet Disease

  • Behcet'S Syndrome

  • Behcet'S Disease

  • Behçet Disease

  • Bd

  • Adamantiades-Behcet Disease

  • Triple Symptom Complex

  • Behçet'S Disease

  • Behet'S Syndrome

  • Bd Syndrome

  • Behçet Syndrome

  • Behçet'S Syndrome

  • Behcet Triple Symptom Complex

  • Malignant Aphthosis

  • Old Silk Route Disease

  • Adamantiades-Behçet Disease

Inflammatory Bowel Disease
  • Inflammatory Bowel Diseases

  • Bowel Disease, Inflammatory

Autoimmune Disease
  • Autoimmune Diseases

  • Autoimmune Hypersensitivity Disease

  • Hypersensitivity Reaction Type Ii Disease

  • Type Ii Hypersensitivity Reaction Disease

Hepatitis B
  • Chronic Hepatitis B

  • Hepatitis B Infection

  • Serum Hepatitis

  • HBV

  • Hepatitis B Chronic

  • Hbv, Susceptibility To

  • Hepatitis B, Chronic

  • Chronic Hepatitis B Without Delta Agent

  • Chronic Hbv - [Hepatitis B Virus] Infection

  • Hepatitis B Nos

  • Chronic Type B Viral Hepatitis

  • Hep B Nos

Sezary'S Disease
  • Sezary Syndrome

  • Sézary Syndrome

  • Sezary'S Lymphoma

  • Sezary Disease

  • Sezary Erythroderma

  • Sezary Lymphoma

Systemic Scleroderma
  • Scleroderma

  • Progressive Systemic Sclerosis

  • Systemic Sclerosis

  • Scleroderma, Systemic

  • Scleroderma Syndrome

  • Dermatosclerosis

  • Familial Progressive Scleroderma

  • Progressive Scleroderma

  • Scleroderma Disease

  • Scleroderma, Localized

  • Diffuse Scleroderma

  • Scleroderma, Familial Progressive

Leukodystrophy, Hypomyelinating, 8, With Or Without Oligodontia And/Or Hypogonadotropic Hypogonadism
  • Hypomyelinating Leukodystrophy 8 With Or Without Oligodontia And-Or Hypogonadotropic Hypogonadism

  • HLD8

  • Cerebellar Hypoplasia With Endosteal Sclerosis

  • 4h Leukodystrophy 2

  • Endosteal Sclerosis-Cerebellar Hypoplasia Syndrome

  • Leukodystrophy, Hypomyelinating, Type 8, With/Without Oligodontia And/Or Hypogonadotropic Hypogonadism

Potocki-Shaffer Syndrome
  • Proximal 11p Deletion Syndrome

  • Chromosome 11p11.2 Deletion Syndrome

  • Pss

  • 11p11.2 Deletion

  • P11pds

  • Defect11 Syndrome

  • Deletion Of Chromosome 11p11.2

  • POSHS

Aphthous Stomatitis
  • Oral Ulcer

  • Canker Sore

  • Aphtha

  • Aphthous Ulceration

  • Oral Aphthae

  • Oral Aphthous Ulcer

  • Canker Sores

  • Stomatitis, Aphthous

  • Minor Oral Aphthous Ulceration

Autoimmune Disease Of Exocrine System
Asthma
  • Chronic Obstructive Asthma

  • Asthma, Diminished Response To Antileukotriene Treatment In

  • Bronchial Hyperreactivity

  • Asthma, Susceptibility To

  • Asthma, Bronchial

  • Asthma, Protection Against

  • Asthma, Nocturnal, Susceptibility To

  • Nocturnal Asthma

  • Asthma-Related Traits

  • Asthma-Related Traits, Susceptibility To

  • Asthma, Nocturnal

  • Chronic Obstructive Asthma With Acute Exacerbation

  • Chronic Obstructive Asthma With Status Asthmaticus

  • Exercise Induced Asthma

  • Exercise-Induced Asthma

  • Bronchial Asthma

  • Asthma, Exercise-Induced

  • Idiosyncratic Asthma

  • Unspecified Asthma With Acute Exacerbation

  • Asthma, Unspecified, With Stated Status Asthmaticus

  • Status Asthmaticus Nos

  • Acute Severe Asthma

  • Acute Severe Bronchial Asthma

  • Status Asthma

  • Status Post Asthmaticus

Limited Scleroderma
  • Limited Cutaneous Systemic Sclerosis

  • Limited Systemic Sclerosis

  • Systemic Sclerosis Sine Scleroderma

  • Crest Syndrome

  • Limited Cutaneous Systemic Scleroderma

  • Scleroderma, Limited

  • Systemic Sclerosis, Limited

  • Progressive Systemic Sclerosis Sine Scleroderma

  • Scleroderma, Sine

  • Crest - [Calcinosis, Raynaud Phenomenon, Oesophageal Dysmotility, Sclerodactyly, And Telangiectasia] Syndrome

  • Crst - [Calcinosis, Raynaud Phenomenon, Sclerodactyly And Telangiectasia] Syndrome

Immune Deficiency Disease
  • Immunodeficiency

  • Primary Immunodeficiency

  • Primary Immunodeficiency Disease

  • Immunologic Deficiency Syndromes

  • Hypoimmunity

  • Immune Deficiency Disorder

  • Immunodeficiency Syndrome

  • Immune Disorder

  • Primary Immune Deficiency Disorder

  • Immune System Diseases

  • Human Immunodeficiency Virus Infection

  • Hiv - [Human Immunodeficiency Virus Infection]

  • Hiv Positive Nos

  • Hiv Disease

  • Acquired Immune Deficiency Syndrome-Related Complex

  • Aids-Like Syndrome

  • Aids-Related Complex Nos

  • Arc - [Aids-Related Complex]

  • Immunodeficiency Due To Human Immunodeficiency Virus Infection

  • Unspecified Human Immunodeficiency Virus Disease

  • Hiv Disease Nos

  • Human Immunodeficiency Virus Positive Nos

  • Hiv Nos

  • Deficiency Of Complement Initial Pathway

  • Deficiency Of Complement Terminal Pathway

  • Cfdd - [Complement Factor D Deficiency]

  • Immunodeficiency With Nk-Cell - [Natural-Killer Cell] Deficiency

  • Nonfamilial Hypogammaglobulinaemia

  • Common Variable Immune Deficiency

  • Nonfamilial Agammaglobulinaemia

  • Common Variable Agammaglobulinaemia

  • Agammaglobulinaemia Nos

  • Agammaglobulinaemia Antibody Deficiency Syndrome

  • Hypogammaglobulinaemia Antibody Deficiency Syndrome

  • Acquired Agammaglobulinaemia Nos

  • Hypogammaglobulinaemia Nos

  • Hyper Igm

Primary Biliary Cholangitis
  • Primary Biliary Cirrhosis

  • Biliary Liver Cirrhosis

  • Chronic Nonsuppurative Destructive Cholangitis

  • Familial Primary Biliary Cirrhosis

  • Pbc

  • Hanot Syndrome

  • Cholestatic Cirrhosis

  • Biliary Cirrhosis Primary

  • Liver Cirrhosis, Biliary

  • Hanot'S Cirrhosis

  • Biliary Cirrhosis

  • Pericholangiolic Biliary Cirrhosis

  • Tannhauser-Magendantz Syndrome

  • Hanot-Rossle Syndrome

  • Hypertrophic Cirrhosis

  • Todd Cirrhosis

  • Hanot Cirrhosis

  • Charcot Cirrhosis

  • Mahon-Tannhauser Syndrome

  • Toxic Cirrhosis

  • Hypertrophic Biliary Cirrhosis

  • Monolobular Cirrhosis

  • Unilobar Cirrhosis

  • Xanthomatous Biliary Cirrhosis

Celiac Disease 1
  • Celiac Disease

  • Coeliac Disease

  • Celiac Sprue

  • Celiac Disease, Susceptibility To

  • Gluten-Sensitive Enteropathy

  • Nontropical Sprue

  • Sprue

  • CELIAC1

  • Celiac Disease, Susceptibility To, 1

  • Celiac Sprue 1

  • Celiac Sprue, Susceptibility To, 1

  • Gluten-Sensitive Enteropathy 1

  • Gluten-Sensitive Enteropathy, Susceptibility To, 1

  • Idiopathic Steatorrhea

  • Cœliac Disease

  • Gluten Intolerance

  • Gluten-Induced Enteropathy

  • Gluten Enteropathy

  • Celiac Disease, Susceptibility To, Type 1

  • Childhood Celiac Disease

  • Coeliac Rickets

  • Gee Disease

  • Gee-Herter Disease

  • Heubner-Herter Disease

  • Idiopathic Steatorrhoea

  • Thaysen'S Disease

  • Herter Gee Syndrome

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Mus musculus STAT4 MGD MGI:103062
Bos taurus STAT4 VGNC VGNC:106954
Rattus norvegicus STAT4 RGD RGD:1305747
Macaca mulatta STAT4 VGNC VGNC:77907
Canis familiaris STAT4 VGNC VGNC:103708
Felis catus STAT4 VGNC VGNC:80367
Others STAT4 NCBI