BLK - BLK proto-oncogene, Src family tyrosine kinase Gene

Also Known as MODY11

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 640

About BLK

Cytogenetic location: 8p23.1 Genomic coordinates (GRCh38): 8:11,494,387-11,564,599 (from NCBI)

This gene has 9 transcripts (splice variants), 196 orthologues, 32 paralogues and is associated with 3 phenotypes. Biased expression in lymph node (RPKM 18.9), spleen (RPKM 13.7) and 4 other tissues.

Summary

This gene encodes a nonreceptor tyrosine-kinase of the Src family of proto-oncogenes that are typically involved in cell proliferation and differentiation. The protein has a role in B-cell receptor signaling and B-cell development. The protein also stimulates Insulin synthesis and secretion in response to glucose and enhances the expression of several pancreatic beta-cell transcription factors. [provided by RefSeq, Aug 2010]

BLK Products (2)

mRNA Protein Name
NM_001330465.2 NP_001317394.1 tyrosine-protein kinase Blk isoform 2
NM_001715.3 NP_001706.2 tyrosine-protein kinase Blk isoform 1
Molecular Function GO Annotation Evidence References Source
enables non-membrane spanning protein tyrosine kinase activity IDA
IDA: Inferred from direct assay
876631 GOA
enables non-membrane spanning protein tyrosine kinase activity IMP
IMP: Inferred from mutant phenotype
23555801 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16273093 GOA
enables protein tyrosine kinase activity IDA
IDA: Inferred from direct assay
30356214 GOA
Biological Process GO Annotation Evidence References Source
involved in B cell receptor signaling pathway IDA
IDA: Inferred from direct assay
876631 GOA
involved in B cell receptor signaling pathway IMP
IMP: Inferred from mutant phenotype
23555801 GOA
involved in peptidyl-tyrosine phosphorylation IDA
IDA: Inferred from direct assay
30356214 GOA
involved in positive regulation of insulin secretion IMP
IMP: Inferred from mutant phenotype
19667185 GOA
involved in positive regulation of protein binding IMP
IMP: Inferred from mutant phenotype
23555801 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

BLK Protein Structure

SH3_1

SH3_1: SH3 domain (64 - 110)

SH2

SH2: SH2 domain (124 - 205)

Pkinase_Tyr

Pkinase_Tyr: Protein tyrosine kinase (241 - 489)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 505 a.a.
Protein Preferred Names Protein Names

tyrosine-protein kinase Blk

  • B lymphoid tyrosine kinase

BLK Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
BLK P51451 MID2 Homo sapiens Q9UJV3-2 32296183
Intra
BLK P51451 MID2 Homo sapiens Q9UJV3-2 32296183
Intra
BLK P51451 MID2 Homo sapiens Q9UJV3-2 32296183
Intra
BLK P51451 ZBTB32 Homo sapiens A0A0C4DGF1 32296183
Intra
BLK P51451 ZBTB32 Homo sapiens A0A0C4DGF1 32296183
Intra
BLK P51451 ZNF774 Homo sapiens Q6NX45 32296183
Intra
BLK P51451 ZNF774 Homo sapiens Q6NX45 32296183
Intra
BLK P51451 ZNF774 Homo sapiens Q6NX45 32296183
Intra
BLK P51451 FXR1 Homo sapiens P51114-2 32296183
Intra
BLK P51451 EFS Homo sapiens O43281-2 32296183
Intra
BLK P51451 EFS Homo sapiens O43281-2 32296183
Intra
BLK P51451 FLACC1 Homo sapiens Q96Q35-2 32296183
Intra
BLK P51451 FLACC1 Homo sapiens Q96Q35-2 32296183
Intra
BLK P51451 FLACC1 Homo sapiens Q96Q35-2 32296183
Intra
BLK P51451 PXN Homo sapiens P49023-2 32296183
Intra
BLK P51451 PXN Homo sapiens P49023-2 32296183
Intra
BLK P51451 ZBTB42 Homo sapiens B2RXF5 32296183
Intra
BLK P51451 ZBTB42 Homo sapiens B2RXF5 32296183
Intra
BLK P51451 GRB10 Homo sapiens Q13322-4 32296183
Intra
BLK P51451 GRB10 Homo sapiens Q13322-4 32296183
Intra
BLK P51451 GRB10 Homo sapiens Q13322-4 32296183
Intra
BLK P51451 KIT Homo sapiens P10721
FPS
24728074
Intra
BLK P51451 STAP2 Homo sapiens Q9UGK3 32296183
Intra
BLK P51451 STAP2 Homo sapiens Q9UGK3 32296183
Intra
BLK P51451 STAP2 Homo sapiens Q9UGK3 32296183
Intra
BLK P51451 SLA Homo sapiens Q13239-3 32296183
Intra
BLK P51451 SLA Homo sapiens Q13239-3 32296183
Intra
BLK P51451 SLA Homo sapiens Q13239-3 32296183
Intra
BLK P51451 JAKMIP1 Homo sapiens Q96N16 32296183
Intra
BLK P51451 JAKMIP1 Homo sapiens Q96N16 32296183
Intra
BLK P51451 JAKMIP1 Homo sapiens Q96N16 32296183
Intra
BLK P51451 TDP2 Homo sapiens O95551 32296183
Intra
BLK P51451 TDP2 Homo sapiens O95551 32296183
Intra
BLK P51451 SSBP3 Homo sapiens Q9BWW4 32296183
Intra
BLK P51451 SSBP3 Homo sapiens Q9BWW4 32296183
Intra
BLK P51451 SSBP3 Homo sapiens Q9BWW4 32296183
Intra
BLK P51451 EGFR Homo sapiens P00533 24658140
Intra
BLK P51451 HSP90AB1 Homo sapiens P08238 32707033
Intra
BLK P51451 HSP90AB1 Homo sapiens P08238 31980649
Intra
BLK P51451 VIM Homo sapiens P08670 31980649
Intra
BLK P51451 SH2D1B Homo sapiens O14796 32296183
Intra
BLK P51451 SH2D1B Homo sapiens O14796 32296183
Intra
BLK P51451 BIRC2 Homo sapiens Q13490 32296183
Intra
BLK P51451 BIRC2 Homo sapiens Q13490 32296183
Intra
BLK P51451 BIRC2 Homo sapiens Q13490 32296183
Intra
BLK P51451 GAB1 Homo sapiens Q13480
FPS
24728074
Intra
BLK P51451 STAT3 Homo sapiens P40763 25416956
Intra
BLK P51451 STAT3 Homo sapiens P40763 32296183
Intra
BLK P51451 STAT3 Homo sapiens P40763 25416956
Intra
BLK P51451 STAT3 Homo sapiens P40763 32296183
Intra
BLK P51451 STAT3 Homo sapiens P40763 31515488
Intra
BLK P51451 AR Homo sapiens P10275
FPS
24728074
Intra
BLK P51451 HSF2BP Homo sapiens O75031 32296183
Intra
BLK P51451 HSF2BP Homo sapiens O75031 32296183
Intra
BLK P51451 EFS Homo sapiens O43281 25416956
Intra
BLK P51451 EFS Homo sapiens O43281 31515488
Intra
BLK P51451 EFS Homo sapiens O43281 25416956
Intra
BLK P51451 FXR2 Homo sapiens P51116 32296183
Intra
BLK P51451 FXR2 Homo sapiens P51116 32296183
Intra
BLK P51451 ZBTB8A Homo sapiens Q96BR9 32296183
Intra
BLK P51451 ZBTB8A Homo sapiens Q96BR9 32296183
Intra
BLK P51451 ZBTB8A Homo sapiens Q96BR9 32296183
Intra
BLK P51451 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
BLK P51451 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
BLK P51451 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
BLK P51451 PICK1 Homo sapiens Q9NRD5 32296183
Intra
BLK P51451 PICK1 Homo sapiens Q9NRD5 32296183
Intra
BLK P51451 PICK1 Homo sapiens Q9NRD5 32296183
Intra
BLK P51451 PIK3R3 Homo sapiens Q92569 32296183
Intra
BLK P51451 PIK3R3 Homo sapiens Q92569 32296183
Intra
BLK P51451 PIK3R3 Homo sapiens Q92569 32296183
Intra
BLK P51451 PIK3R1 Homo sapiens P27986-2 32296183
Intra
BLK P51451 PIK3R1 Homo sapiens P27986-2 32296183
Intra
BLK P51451 CRKL Homo sapiens P46109 32296183
Intra
BLK P51451 CRKL Homo sapiens P46109 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant BLK Proteins

Cat. No. Product Name Accession Purity
HY-P72853 BLK Protein, Human (sf9, GST) P51451 (M1-P505) ≥ 85%, as determined by reducing SDS-PAGE.

BLK Antibodies

Cat. No. Product Name Application Reactivity
HY-P85056 BLK Antibody (YA4748) IHC-P, ELISA Human

Related Diseases

Diseases Alias
Maturity-Onset Diabetes Of The Young, Type 11
  • Maturity-Onset Diabetes Of The Young Type 11

  • MODY11

  • Maturity-Onset Diabetes Of The Young 11

  • Mody-11

  • Mody Type 11

  • Diabetes Of The Young, Maturity-Onset, 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]

Maturity-Onset Diabetes Of The Young
  • MODY

  • Maturity Onset Diabetes Mellitus In Young

  • Mason-Type Diabetes

  • Mason Type Diabetes

  • Maturity Onset Diabetes Of The Young

  • Mody Syndrome

  • Diabetes Of The Young, Maturity-Onset

Maturity-Onset Diabetes Of The Young, Type 7
  • Maturity-Onset Diabetes Of The Young Type 7

  • MODY7

  • Maturity-Onset Diabetes Of The Young, Type Vii

  • Maturity-Onset Diabetes Of The Young 7

  • Mody-7

  • Mody Type 7

  • Diabetes Of The Young, Maturity-Onset, Type 7

Maturity-Onset Diabetes Of The Young, Type 9
  • Maturity-Onset Diabetes Of The Young Type 9

  • MODY9

  • Maturity-Onset Diabetes Of The Young, Type Ix

  • Maturity-Onset Diabetes Of The Young 9

  • Mody-9

  • Mody Type 9

  • Diabetes Of The Young, Maturity-Onset, Type 9

Maturity-Onset Diabetes Of The Young, Type 13
  • Maturity-Onset Diabetes Of The Young Type 13

  • MODY13

  • Mody Type 13

  • Mody, Type 13

  • Maturity-Onset Diabetes Of The Young 13

  • Diabetes Of The Young, Maturity-Onset, Type 13

Maturity-Onset Diabetes Of The Young, Type 8, With Exocrine Dysfunction
  • Maturity-Onset Diabetes Of The Young Type 8

  • MODY8

  • Dped

  • Maturity-Onset Diabetes Of The Young, Type Viii

  • Mody Type 8

  • Diabetes And Pancreatic Exocrine Dysfunction

  • Diabetes-Pancreatic Exocrine Dysfunction Syndrome

  • Diabetes And Pancreatic Exocrine

  • Maturity-Onset Diabetes Of The Young Type 8 With Exocrine Dysfunction

  • Maturity-Onset Diabetes Of The Young 8 With Exocrine Dysfunction

  • Diabetes And Pancreatic Exocrine Dysfunction Syndrome

  • Mody-8

  • Diabetes Of The Young, Maturity-Onset, Type 8

Maturity-Onset Diabetes Of The Young, Type 14
  • Maturity-Onset Diabetes Of The Young Type 14

  • MODY14

  • Maturity-Onset Diabetes Of The Young 14

  • Diabetes Of The Young, Maturity-Onset, Type 14

Kawasaki Disease
  • Mucocutaneous Lymph Node Syndrome

  • Acute Febrile Mucocutaneous Lymph Node Syndrome

  • Kawasaki Syndrome

  • Kd

  • Infantile Polyarteritis

  • Kawasaki Disease, Susceptibility To

  • Acute Febrile Mcls

  • Kawasaki'S Disease

  • Mlns

  • KWD

Maturity-Onset Diabetes Of The Young, Type 10
  • Maturity-Onset Diabetes Of The Young Type 10

  • MODY10

  • Maturity-Onset Diabetes Of The Young 10

  • Mody-10

  • Mody Type 10

  • Diabetes Of The Young, Maturity-Onset, Type 10

Keratolytic Winter Erythema
  • KWE

  • Oudtshoorn Skin Disease

  • Erythrokeratolysis Hiemalis Ichthyosis

  • Erythrokeratolysis Hiemalis

  • Oudtshoorn Skin

  • Oudtshoorn Disease

Maturity-Onset Diabetes Of The Young, Type 6
  • MODY6

  • Maturity-Onset Diabetes Of The Young Type 6

  • Maturity-Onset Diabetes Of The Young 6

  • Mody Type 6

  • Mody, Type 6

  • Mody-6

  • Diabetes Of The Young, Maturity-Onset, Type 6

Rheumatoid Arthritis
  • RA

  • Arthritis, Rheumatoid

  • Rheumatoid Arthritis, Susceptibility To

  • Arthritis Or Polyarthritis, Rheumatic

  • Atrophic Arthritis

  • Rheumatism Arthritis

  • Rheumatoid Polyarthritis

Heart Aneurysm
  • Cardiac Aneurysm

Coronary Aneurysm
  • Aneurysm Of Coronary Vessels

  • Aneurysmal Lesion Of Coronary Artery

  • Arteriovenous Aneurysm Of Coronary Vessels

Arthritis
  • Inflammatory Joint Disease

  • Inflammatory Disorder Of Joint

Maturity-Onset Diabetes Of The Young, Type 4
  • Maturity-Onset Diabetes Of The Young Type 4

  • MODY4

  • Mody, Type Iv

  • Mody Type 4

  • Mody, Type 4

  • Maturity-Onset Diabetes Of The Young 4

  • Mody-4

  • Diabetes Of The Young, Maturity-Onset, Type 4

  • Maturity-Onset Diabetes Of The Young, Type Iv

Maturity-Onset Diabetes Of The Young, Type 1
  • Maturity-Onset Diabetes Of The Young Type 1

  • MODY1

  • Mild Juvenile Diabetes Mellitus

  • Mody, Type I

  • Diabetes Mellitus Type 2

  • Mody Type 1

  • Mody, Type 1

  • Maturity-Onset Diabetes Of The Young 1

  • Mody-1

  • Diabetes Of The Young, Maturity-Onset, Type 1

Maturity-Onset Diabetes Of The Young, Type 2
  • Maturity-Onset Diabetes Of The Young Type 2

  • MODY2

  • Mody Glucokinase-Related

  • Mody Type 2

  • Mody, Type 2

  • Mody, Glucokinase-Related

  • Mody, Type Ii

  • Maturity-Onset Diabetes Of The Young 2

  • Mody-2

  • Diabetes Of The Young, Maturity-Onset, Type 2

  • Diabetes Mellitus Autosomal Dominant Type Ii

Co-Trimoxazole Allergy
  • Bactrim Allergy

  • Cotrimoxazol Allergy

  • Tmp/Smx Allergy

  • Trimethoprim/Sulfamethoxazole Allergy

Maturity-Onset Diabetes Of The Young, Type 3
  • Maturity-Onset Diabetes Of The Young Type 3

  • MODY3

  • Mody, Type Iii

  • Mody Type 3

  • Mody, Type 3

  • Maturity-Onset Diabetes Of The Young 3

  • Mody-3

  • Diabetes Of The Young, Maturity-Onset, Type 3

Renal Cysts And Diabetes Syndrome
  • RCAD

  • Mody5

  • Congenital Anomalies Of The Kidney And Urinary Tract With Diabetes

  • Cakut With Diabetes

  • Maturity-Onset Diabetes Of The Young Type 5

  • Tubulointerstitial Kidney Disease, Autosomal Dominant, 3

  • Adtkd3

  • Atypical Familial Juvenile Hyperuricemic Nephropathy

  • Atypical Fjhn

  • Familial Hypoplastic Glomerulocystic Kidney

  • Maturity-Onset Diabetes Of The Young, Type 5

  • Hyperuricemic Nephropathy, Familial Juvenile, Atypical

  • Fjhn, Atypical

  • Glomerulocystic Kidney Disease, Hypoplastic Type

  • Glomerulocystic Kidney, Familial Hypoplastic

  • Hypoplastic Type Glomerulocystic Kidney Disease

  • Glomerulocystic Kidney Disease Hypoplastic Type

  • Renal-Diabetes Mody5 Syndrome

Common Variable Immunodeficiency
  • Cvid

  • Common Variable Agammaglobulinemia

  • Common Variable Immune Deficiency

  • Acquired Hypogammaglobulinemia

  • Hypogamma-Globulinemia, Acquired

  • Idiopathic Immunoglobulin Deficiency

  • Primary Antibody Deficiency

  • Primary Hypogammaglobulinemia

  • Acquired Agammaglobulinemia

  • Sporadic Hypogammaglobulinemia

  • Common Variable Hypogamma-Globulinemia

  • Immunoglobulin Deficiency, Late-Onset

  • Common Variable Hypogammaglobulinemia

  • Immunodeficiency, Common Variable

Lymph Node Disease
  • Abnormality Of The Lymph Nodes

  • Disorder Of Lymph Node

Permanent Neonatal Diabetes Mellitus
  • Pndm

  • Permanent Diabetes Mellitus Of Infancy

  • Pdmi

  • Neonatal Diabetes Mellitus, Permanent

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

Thrombocytopenia
  • Low Platelet Count

  • Low Platelets

  • Decreased Platelets

  • Platelet Dysfunction Nos

Lipoprotein Quantitative Trait Locus
  • Coronary Artery Disease

  • Coronary Artery Anomaly

  • Coronary Artery Disease, Susceptibility To

  • Myocardial Ischemia

  • Congenital Anomaly Of Coronary Artery

  • Coronary Arteriosclerosis

  • Coronary Disease

  • Coronary Heart Disease

  • Coronary Artery Disorder

  • LPAQTL

  • Lpa Deficiency, Congenital

  • Coronary Artery Abnormality

  • Coronary Artery Anomaly, Congenital

  • Chd

  • Coronary Syndrome

  • Congenital Malformations Of Coronary Vessels

  • Malformation Of Coronary Vessels

  • Congenital Coronary Artery Anomaly

  • Congenital Coronary Artery Deformity

  • Congenital Coronary Artery Disorder

  • Abnormal Coronary Artery

  • Congenital Coronary Artery Malposition

  • Congenital Coronary Disease

  • Congenital Anomaly Of Coronary Arteries

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
Rattus norvegicus BLK RGD RGD:1308859
Macaca mulatta BLK VGNC VGNC:70253
Canis familiaris BLK VGNC VGNC:38464
Bos taurus BLK VGNC VGNC:26504
Mus musculus BLK MGD MGI:88169
Felis catus BLK VGNC VGNC:60121
Others BLK NCBI