ITK - IL2 inducible T cell kinase Gene

Also Known as EMT; LYK; LPFS1; PSCTK2

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 3702

About ITK

Cytogenetic location: 5q33.3 Genomic coordinates (GRCh38): 5:157,180,840-157,255,185 (from NCBI)

This gene has 11 transcripts (splice variants), 206 orthologues, 32 paralogues and is associated with 69 phenotypes. Biased expression in lymph node (RPKM 23.9), appendix (RPKM 14.7) and 9 other tissues.

Summary

This gene encodes an intracellular tyrosine kinase expressed in T-cells. The protein contains both SH2 and SH3 domains which are often found in intracellular kinases. It is thought to play a role in T-cell proliferation and differentiation. [provided by RefSeq, Jul 2008]

ITK Products (1)

mRNA Protein Name
NM_005546.4 NP_005537.3 tyrosine-protein kinase ITK/TSK
Molecular Function GO Annotation Evidence Verweise Source
enables non-membrane spanning protein tyrosine kinase activity IDA
IDA: Inferred from direct assay
12186560 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
8892607 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

ITK Protein Structure

PH

PH: PH domain (7 - 110)

BTK

BTK: BTK motif (118 - 148)

SH3_1

SH3_1: SH3 domain (177 - 223)

SH2

SH2: SH2 domain (239 - 323)

Pkinase_Tyr

Pkinase_Tyr: Protein tyrosine kinase (363 - 612)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 620 a.a.
Protein Preferred Names Protein Names

tyrosine-protein kinase ITK/TSK

  • IL-2-inducible T-cell kinase

  • T-cell-specific kinase

  • homolog of mouse T-cell itk/tsk

  • interleukin-2-inducible T-cell kinase

  • kinase EMT

  • tyrosine-protein kinase LYK

ITK Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Verweise
Intra
ITK Q08881 LCP2 Homo sapiens Q13094 17420479
Intra
ITK Q08881 LCP2 Homo sapiens Q13094 17420479
Intra
ITK Q08881 HSP90AB1 Homo sapiens P08238 32707033
Intra
ITK Q08881 HSP90AB1 Homo sapiens P08238 28514442
Intra
ITK Q08881 HSP90AB1 Homo sapiens P08238 22939624
Intra
ITK Q08881 SFN Homo sapiens P31947 32707033
Intra
ITK Q08881 FASLG Homo sapiens P48023 19807924
Intra
ITK Q08881 FASLG Homo sapiens P48023 19807924
Intra
ITK Q08881 ERBB2 Homo sapiens P04626 16273093
Cross
ITK Q08881 Plcg1 Rattus norvegicus P10686 18443296
Cross
ITK Q08881 Plcg1 Rattus norvegicus P10686 31585087
Cross: Cross-species interaction Intra: Intraspecies interaction

ITK Antibodies

Art. -Nr. Produktname Anwendung Reactivity
HY-P83601 ITK Antibody (YA3346) WB, IHC-P, FC Human
HY-P83601A ITK Antibody (YA3346)(PBS only) WB, IHC-P, FC Human
HY-P85135 ITK Antibody (YA4827) WB, ICC/IF, FC, ELISA Human
HY-P85135A ITK Antibody (YA4827)(PBS only) WB, ICC/IF, FC Human

Related Diseases

Diseases Alias
Hemophagocytic Lymphohistiocytosis
  • Lymphohistiocytosis, Hemophagocytic

  • Haemophagocytic Syndrome

  • Lymphohistiocytosis Hemophagocytic

  • Hemophagocytic Syndrome

  • Familial Hemophagocytic Lymphocytosis

  • Histiocytoses Of Mononuclear Phagocytes

  • Haemophagocytic Lymphohistiocytosis Nos

Lymphopenia
  • Lymphocytopenia

Conjunctival Deposit
Supine Hypotensive Syndrome
  • Maternal Hypotension Syndrome

  • Antepartum Maternal Hypotension Syndrome

  • Postpartum Maternal Hypotension Syndrome

  • Maternal Hypotension Syndrome, Antepartum Condition Or Complication

  • Maternal Hypotension Syndrome, Postpartum Condition Or Complication

  • Maternal Hypotension Syndrome, Unspecified Trimester

Coronin-1a Deficiency
Angioimmunoblastic T-Cell Lymphoma
  • Immunoblastic Lymphadenopathy

  • Lymphogranulomatosis X

  • T-Cell Lymphoma, Aild Type

  • Aitl

  • Ailt

  • Angioimmunoblastic Lymphadenopathy

  • Aild - [Angioimmunoblastic Lymphadenopathy With Dysproteinaemia]

  • Angioimmunoblastic Lymphoma

Lissencephaly 10
  • LIS10

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

Lymphoproliferative Syndrome, X-Linked, 1
  • Lymphomatoid Papulosis

  • Duncan Disease

  • Purtilo Syndrome

  • X-Linked Lymphoproliferative Syndrome

  • Xlp

  • XLP1

  • Lyp

  • X-Linked Lymphoproliferative Disease

  • Lymphoproliferative Disease, X-Linked

  • Xlpd

  • X-Linked Lymphoproliferative Disease Due To Sh2d1a Deficiency

  • Ebv Infection, Severe, Susceptibility To

  • Ebvs

  • Immunodeficiency 5

  • Imd5

  • X-Linked Lymphoproliferative Syndrome 1

  • Epstein-Barr Virus Infection, Familial Fatal

  • Ebv Infection, Severe

  • Infectious Mononucleosis, Severe

  • Infectious Mononucleosis, Severe, Susceptibility To

  • Immunodeficiency, X-Linked Progressive Combined Variable

  • Epstein Barr Virus Infection, Familial Fatal

  • X-Linked Progressive Combined Variable Immunodeficiency 5

  • Epstein-Barr Virus-Induced Lymphoproliferative Disease In Males

  • Familial Fatal Epstein-Barr Infection

  • Severe Susceptibility To Ebv Infection

  • Severe Susceptibility To Infectious Mononucleosis

  • Sap Deficiency

  • Sh2d1a/Slam-Associated Protein Deficiency

  • X-Linked Lymphoproliferative Syndrome Type 1

  • X-Linked Progressive Combined Variable Immunodeficiency

  • Lymphoproliferative Syndrome, X-Linked

  • Sap

  • X-Linked Lymphoproliferative Disorder

Combined Immunodeficiency
  • Combined T Cell And B Cell Immunodeficiency

  • Congenital Combined Immunodeficiency

  • Syndrome With Combined Immunodeficiency

  • Combined T And B Cell Immunodeficiency

  • Combined Immunity Deficiency

  • Combined Immunodeficiency Syndrome

  • Combined T-Cell And B-Cell Immunodeficiency

  • Lymphopenic Agammaglobulinaemia

Autoimmune Lymphoproliferative Syndrome
  • ALPS

  • Canale-Smith Syndrome

  • Autoimmune Lymphoproliferative Syndrome, Type Ia

  • Autoimmune Lymphoproliferative Syndrome, Type Ib

  • Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant

  • Css

  • Autoimmune Lymphoproliferative Syndrome, Type 1b

  • Autoimmune Lymphoproliferative Syndrome, Type 1a

  • Autoimmune Lymphoproliferative Syndrome, Type I, Autosomal Dominant

  • Fas Deficiency

  • Autoimmune Lymphoproliferative Syndrome 1a

  • ALPS1A

  • Autoimmune Lymphoproliferative Syndrome Type Ia

  • Autoimmune Lymphoproliferative Syndrome 1b

  • ALPS1B

  • Autoimmune Lymphoproliferative Syndrome Type Ib

Lymphoproliferative Syndrome 2
  • Cd27 Deficiency

  • LPFS2

  • Combined Immunodeficiency Due To Cd27 Deficiency

  • Autosomal Recessive Lymphoproliferative Disease Due To Cd27 Deficiency

Lymphoma
  • Lymphoid Cancer

  • Lymphomas

  • Lymphoid Cancers

  • Lymphoid Neoplasm

  • Lymphoma Nos

  • Nhl - [Non-Hodgkin Lymphoma]

  • Non-Hodgkin Lymphoma

  • Non-Hodgkin Lymphoma, Nos

  • Non-Hodgkin Malignant Lymphoma Nos

Mantle Cell Lymphoma
  • Lymphoma, Mantle Cell

  • Lcm

  • Mcl

  • Mantle Zone Lymphoma

  • Lymphoma Mantle-Cell

  • Lymphoma, Mantle-Cell

  • Malignant Lymphoma, Lymphocytic, Intermediate Differentiation, Diffuse

  • Malignant Lymphoma - Lymphocytic, Intermediate Differentiation

  • Diffuse Small Cleaved-Cell Lymphoma

  • Diffuse Small Cleaved Cell Malignant Lymphoma

  • Small Cleaved Cell Non-Hodgkin Lymphoma

  • Diffuse Non-Hodgkin Small Cleaved Cell Lymphoma

  • Malignant Lymphomatous Polyposis

  • Malignant Small Cell, Noncleaved, Diffuse Lymphoma

  • Malignant Undifferentiated Cell, Non-Burkitt Lymphoma

  • Cleaved Cell Lymphoma

  • Small Cell Mantle Cell Lymphoma

  • Small Cleaved Cell Malignant Lymphoma

Agammaglobulinemia
  • Hypogammaglobulinemia

  • Ighm

  • Mu Heavy Chain Deficiency

  • Mu-Heavy Chain Disease

  • Mu-Hcd

  • Mu-Chain Disease

Leukemia, Chronic Lymphocytic
  • Chronic Lymphocytic Leukemia

  • B-Cell Chronic Lymphocytic Leukemia

  • CLL

  • B-Cell Chronic Lymphoid Leukemia

  • Chronic Lymphatic Leukemia

  • Chronic Lymphocytic Leukaemia

  • Lymphoplasmacytic Leukemia

  • Small Lymphocytic Lymphoma

  • Leukemia, Chronic Lymphatic

  • B-Cell Chronic Lymphocytic Leukaemia

  • Chronic Lymphatic Leukaemia

  • Lymphoplasmacytic Leukaemia

  • B Cell Chronic Lymphocytic Leukemia

  • Chronic B-Cell Lymphocytic Leukemia

  • Leukemia, Lymphocytic, Chronic

  • B-Cll

  • Chronic Lymphoid Leukemia

  • Leukemia Lymphocytic Chronic

  • Lymphoma Small Lymphocytic

  • Leukemia, Lymphocytic, Chronic, B-Cell

Agammaglobulinemia, X-Linked
  • X-Linked Agammaglobulinemia

  • XLA

  • Bruton Type Agammaglobulinemia

  • Bruton'S Agammaglobulinemia

  • Bruton-Type Agammaglobulinemia

  • Agmx1

  • Imd1

  • Agammaglobulinemia, X-Linked 1

  • Btk-Deficiency

  • Agammaglobulinemia

  • Hypogammaglobulinemia

  • Agammaglobulinemia, X-Linked, Type 1

  • Immunodeficiency 1

  • Bruton Agammaglobulinemia Tyrosine Kinase Deficiency

  • Bruton'S Agammaglobulinaemia

  • Bruton'S Sex-Linked Agammaglobulinemia

  • Bruton'S Type Agammaglobulinemia

  • Btk Deficiency

  • Agammaglobulinemia, Btk

  • Agammaglobulinemia, Bruton Tyrosine Kinase

  • Congenital Agammaglobulinemia

  • Immunodeficiency Type 1

  • X-Linked Agammaglobulinemia Type 1

Lymphoproliferative Syndrome, X-Linked, 2
  • XLP2

  • Xiap Deficiency

  • X-Linked Lymphoproliferative Syndrome 2

  • X-Linked Lymphoproliferative Disease Due To Xiap Deficiency

  • Xiap-Related Lymphoproliferative Disease, X-Linked

  • X-Linked Lymphoproliferative Syndrome Type 2

  • Xiap Deficiency Syndrome

B Cell Deficiency
  • Immunoglobulin Heavy Chain Deficiency

  • B Cell Deficiencies

  • Immunoglobulin Heavy Chain Deletion

  • Humoral Immune Defect

Pancytopenia
Immunodeficiency, X-Linked, With Magnesium Defect, Epstein-Barr Virus Infection, And Neoplasia
  • XMEN

  • X-Linked Immunodeficiency With Magnesium Defect, Epstein-Barr Virus Infection And Neoplasia

  • X-Linked Immunodeficiency With Magnesium Defect, Epstein-Barr Virus Infection, And Neoplasia

  • Immunodeficiency, X-Linked, With Magnesium Defect, Epstein-Barr Virus Infection And Neoplasia

  • Cid Due To Magt1 Deficiency

  • Combined Immunodeficiency Due To Magt1 Deficiency

  • X-Linked Immunodeficiency With Magnesium Defect, Epstein-Barr Virus Infection An

  • X-Linked Magnesium Deficiency With Epstein-Barr Virus Infection And Neoplasia

Lissencephaly 7 With Cerebellar Hypoplasia
  • LIS7

  • Lissencephaly 7, With Cerebellar Hypoplasia

  • Lissencephaly, Type 7, With Cerebellar Hypoplasia

Waldenstroem'S Macroglobulinemia
  • Waldenstrom Macroglobulinemia

  • Macroglobulinemia Of Waldenstrom

  • Lymphoplasmacytic Lymphoma With Igm Gammopathy

  • Lymphoplasmacytic Lymphoma

  • Waldenstrom'S Macroglobulinaemia

  • Waldenstrom'S Syndrome

  • Waldenström Macroglobulinemia

  • Waldenstrom'S Macroglobulinemia

  • Wm

  • Waldenström'S Macroglobulinemia

  • Malignant Lymphoma - Lymphoplasmacytic

Thrombocytopenia
  • Low Platelet Count

  • Low Platelets

  • Decreased Platelets

  • Platelet Dysfunction Nos

Lymphoproliferative Syndrome
  • Lymphoproliferative Disorder

  • Lymphoproliferative Disorders

  • Lymphoproliferative Disorders, Susceptibility To

Epidermodysplasia Verruciformis 1
  • Epidermodysplasia Verruciformis

  • Epidermodysplasia Verruciformis, Susceptibility To, 1

  • Lutz-Lewandowsky Epidermodysplasia Verruciformis

  • EV1

  • Lewandowsky-Lutz Syndrome

  • Ev

Mixed Oligodendroglioma-Astrocytoma
  • Who Grade Ii Mixed Glioma

Allergic Asthma
  • Atopic Asthma

  • Extrinsic Asthma

  • Extrinsic Asthma With Acute Exacerbation

  • Extrinsic Asthma With Status Asthmaticus

  • Asthma Allergic

  • Atopic Asthma, Susceptibility To

  • Ige-Mediated Allergic Asthma

  • Allergen-Induced Asthma

  • Allergic Asthma Without Stated Status Asthmaticus

  • Predominantly Allergic Asthma Without Stated Status Asthmaticus

  • Predominantly Allergic Asthma

  • Allergic Asthma Nos

  • Catarrh With Asthma

  • Allergic Bronchitis Nos

  • Extrinsic Allergic Asthma

  • Predominantly Allergic Asthma With Stated Status Asthmaticus

Lymphoproliferative Syndrome 1
  • LPFS1

  • Lymphoproliferative Syndrome, Ebv-Associated, Autosomal, 1

  • Combined Immunodeficiency Due To Itk Deficiency

  • Autosomal Recessive Lymphoproliferative Disease Due To Itk Deficiency

  • Itk Deficiency

Immunodeficiency 17
  • IMD17

  • Cd3-Gamma Deficiency

  • Scid-Like Immunodeficiency, T Cell-Partial, B Cell-Positive, Nk Cell-Positive

  • Combined Immunodeficiency Due To Cd3gamma Deficiency

  • Immunodeficiency 17, Cd3 Gamma Deficient

  • Cd3gamma Deficiency

  • Immunodeficiency, Type 17

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
Bos taurus ITK VGNC VGNC:30338
Macaca mulatta ITK VGNC VGNC:73797
Rattus norvegicus ITK RGD RGD:1311618
Mus musculus ITK MGD MGI:96621
Canis familiaris ITK VGNC VGNC:42149
Felis catus ITK VGNC VGNC:67863
Others ITK NCBI