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

Also Known as SLK; SYN; p59-FYN

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 2534

About FYN

Cytogenetic location: 6q21 Genomic coordinates (GRCh38): 6:111,660,332-111,873,452 (from NCBI)

This gene has 29 transcripts (splice variants), 265 orthologues and 32 paralogues. Broad expression in brain (RPKM 36.8), lymph node (RPKM 29.8) and 23 other tissues.

Summary

This gene is a member of the protein-tyrosine kinase oncogene family. It encodes a membrane-associated tyrosine kinase that has been implicated in the control of cell growth. The protein associates with the p85 subunit of phosphatidylinositol 3-kinase and interacts with the fyn-binding protein. Alternatively spliced transcript variants encoding distinct isoforms exist. [provided by RefSeq, Jul 2008]

FYN Products (4)

mRNA Protein Name
NM_001370529.1 NP_001357458.1 tyrosine-protein kinase Fyn isoform a
NM_002037.5 NP_002028.1 tyrosine-protein kinase Fyn isoform a
NM_153047.4 NP_694592.1 tyrosine-protein kinase Fyn isoform b
NM_153048.4 NP_694593.1 tyrosine-protein kinase Fyn isoform c
Molecular Function GO Annotation Evidence References Source
enables G protein-coupled receptor binding IPI
IPI: Inferred from physical interaction
23169819 GOA
enables disordered domain specific binding IPI
IPI: Inferred from physical interaction
9351809 GOA
enables enzyme binding IPI
IPI: Inferred from physical interaction
27525436 GOA
enables ephrin receptor binding IPI
IPI: Inferred from physical interaction
10498895 GOA
enables growth factor receptor binding IPI
IPI: Inferred from physical interaction
16479011 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
14993658 GOA
enables non-membrane spanning protein tyrosine kinase activity IDA
IDA: Inferred from direct assay
11606584 GOA
enables phospholipase activator activity IDA
IDA: Inferred from direct assay
11606584 GOA
enables phospholipase binding IPI
IPI: Inferred from physical interaction
11606584 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
1661130 GOA
enables protein tyrosine kinase activity EXP
EXP: Inferred from Experiment
1381360 GOA
enables protein tyrosine kinase activity IDA
IDA: Inferred from direct assay
15713798 GOA
enables protein tyrosine kinase activity IMP
IMP: Inferred from mutant phenotype
16979591 GOA
enables scaffold protein binding IPI
IPI: Inferred from physical interaction
23555801 GOA
Biological Process GO Annotation Evidence References Source
involved in G protein-coupled glutamate receptor signaling pathway IDA
IDA: Inferred from direct assay
24012003 GOA
involved in T cell receptor signaling pathway IDA
IDA: Inferred from direct assay
7722293 GOA
involved in cellular response to amyloid-beta IMP
IMP: Inferred from mutant phenotype
27520374 GOA
involved in heart process IGI
IGI: Inferred from genetic interaction
27525436 GOA
involved in intracellular signal transduction IDA
IDA: Inferred from direct assay
11606584 GOA
involved in natural killer cell activation IDA
IDA: Inferred from direct assay
15713798 GOA
involved in peptidyl-tyrosine phosphorylation IMP
IMP: Inferred from mutant phenotype
11606584 GOA
Cellular Component GO Annotation Evidence References Source
is active in dendrite IDA
IDA: Inferred from direct assay
24012003 GOA
located in endosome IDA
IDA: Inferred from direct assay
15611048 GOA
colocalizes with membrane raft IDA
IDA: Inferred from direct assay
12150984 GOA
is active in membrane raft IDA
IDA: Inferred from direct assay
12218089 GOA
located in membrane raft IMP
IMP: Inferred from mutant phenotype
23386614 GOA
located in plasma membrane IDA
IDA: Inferred from direct assay
12150984 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

FYN Protein Structure

SH3_1

SH3_1: SH3 domain (88 - 135)

SH2

SH2: SH2 domain (149 - 231)

Pkinase_Tyr

Pkinase_Tyr: Protein tyrosine kinase (269 - 517)

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

tyrosine-protein kinase Fyn

  • FYN oncogene related to SRC, FGR, YES

FYN Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
FYN P06241 ABL2 Homo sapiens P42684 17474147
Cross
FYN P06241 Slamf7 Mus musculus Q8BHK6 19151721
Intra
FYN P06241 HTR6 Homo sapiens P50406 17189269
Intra
FYN P06241 HTR6 Homo sapiens P50406 17189269
Intra
FYN P06241 HTR6 Homo sapiens P50406
Y2H
17189269
Intra
FYN P06241 ARHGAP33 Homo sapiens O14559
Y2H
16777849
Intra
FYN P06241 KHDRBS1 Homo sapiens Q07666 9045636
Intra
FYN P06241 KHDRBS1 Homo sapiens Q07666 9045636
Intra
FYN P06241 KHDRBS1 Homo sapiens Q07666 31980649
Intra
FYN P06241 KHDRBS1 Homo sapiens Q07666 7516469
Intra
FYN P06241 KHDRBS1 Homo sapiens Q07666 31413325
Intra
FYN P06241 GP6 Homo sapiens Q9HCN6-1 19940238
Intra
FYN P06241 GP6 Homo sapiens Q9HCN6-1 19940238
Intra
FYN P06241 FYB1 Homo sapiens O15117 25814554
Intra
FYN P06241 FYB1 Homo sapiens O15117 10409671
Intra
FYN P06241 FYB1 Homo sapiens O15117 17474147
Intra
FYN P06241 FYB1 Homo sapiens O15117 9207119
Intra
FYN P06241 FYB1 Homo sapiens O15117 9207119
Intra
FYN P06241 FYB1 Homo sapiens O15117 25814554
Intra
FYN P06241 MAPT Homo sapiens P10636-5 25156556
Intra
FYN P06241 APBB2 Homo sapiens Q92870-2 32814053
Intra
FYN P06241 APBB2 Homo sapiens Q92870-2 32814053
Intra
FYN P06241 APBB2 Homo sapiens Q92870-2 32814053
Cross
FYN P06241 q2ghu2_ehrcr Ehrlichia chaffeensis Q2GHU2 19273555
Intra
FYN P06241 PAG1 Homo sapiens Q9NWQ8 18056706
Intra
FYN P06241 PAG1 Homo sapiens Q9NWQ8 23866081
Intra
FYN P06241 PAG1 Homo sapiens Q9NWQ8 18056706
Intra
FYN P06241 CDC37 Homo sapiens Q16543 31980649
Intra
FYN P06241 CDC37 Homo sapiens Q16543 32707033
Intra
FYN P06241 CDC37 Homo sapiens Q16543 33961781
Intra
FYN P06241 HSP90AA1 Homo sapiens P07900 33961781
Intra
FYN P06241 HSP90AA1 Homo sapiens P07900 31980649
Intra
FYN P06241 HSP90AA1 Homo sapiens P07900 32707033
Intra
FYN P06241 CD2AP Homo sapiens Q9Y5K6 17474147
Intra
FYN P06241 PTK2B Homo sapiens Q14289 10867021
Intra
FYN P06241 PTK2B Homo sapiens Q14289 31413325
Intra
FYN P06241 ARHGAP32 Homo sapiens A7KAX9 12788081
Intra
FYN P06241 ARHGAP32 Homo sapiens A7KAX9 12788081
Intra
FYN P06241 ARHGAP32 Homo sapiens A7KAX9 12788081
Intra
FYN P06241 PDCD6IP Homo sapiens Q8WUM4
ITC
22641034
Intra
FYN P06241 PDCD6IP Homo sapiens Q8WUM4
NMR
22641034
Intra
FYN P06241 PDCD6IP Homo sapiens Q8WUM4 22641034
Intra
FYN P06241 PDCD6IP Homo sapiens Q8WUM4 22641034
Intra
FYN P06241 ASAP1 Homo sapiens Q9ULH1 17474147
Intra
FYN P06241 NELFB Homo sapiens Q8WX92 17474147
Intra
FYN P06241 HSP90AB1 Homo sapiens P08238 22939624
Intra
FYN P06241 HSP90AB1 Homo sapiens P08238 31980649
Intra
FYN P06241 HSP90AB1 Homo sapiens P08238 32707033
Intra
FYN P06241 MAPT Homo sapiens P10636 25156556
Intra
FYN P06241 MAPT Homo sapiens P10636-8 25156556
Intra
FYN P06241 MAPT Homo sapiens P10636-8 25156556
Intra
FYN P06241 PRKCQ Homo sapiens Q04759
Y2H
10383400
Intra
FYN P06241 PRKCQ Homo sapiens Q04759 10383400
Intra
FYN P06241 PRKCQ Homo sapiens Q04759 10383400
Intra
FYN P06241 FASLG Homo sapiens P48023 19807924
Intra
FYN P06241 MED28 Homo sapiens Q9H204 16964398
Intra
FYN P06241 MED28 Homo sapiens Q9H204 16899217
Intra
FYN P06241 MED28 Homo sapiens Q9H204 16899217
Intra
FYN P06241 CBL Homo sapiens P22681 7642581
Intra
FYN P06241 CBL Homo sapiens P22681 7642581
Intra
FYN P06241 CBL Homo sapiens P22681 8621719
Intra
FYN P06241 CBL Homo sapiens P22681 15556646
Intra
FYN P06241 SRC Homo sapiens P12931 33961781
Intra
FYN P06241 SRC Homo sapiens P12931 16966330
Intra
FYN P06241 SRC Homo sapiens P12931 31980649
Intra
FYN P06241 ERBB2 Homo sapiens P04626
SPR
24815698
Intra
FYN P06241 PDGFRB Homo sapiens P09619 7687537
Intra
FYN P06241 PDGFRB Homo sapiens P09619 1661130
Intra
FYN P06241 BCAR1 Homo sapiens P56945 17474147
Intra
FYN P06241 BCAR1 Homo sapiens P56945 31413325
Intra
FYN P06241 BCAR1 Homo sapiens P56945 9360983
Intra
FYN P06241 PTK2 Homo sapiens Q05397 31413325
Intra
FYN P06241 PRKCD Homo sapiens Q05655
PLA
25241761
Intra
FYN P06241 PRKCD Homo sapiens Q05655 12721299
Intra
FYN P06241 PNP Homo sapiens P00491 32814053
Intra
FYN P06241 PNP Homo sapiens P00491 32814053
Intra
FYN P06241 PNP Homo sapiens P00491 32814053
Intra
FYN P06241 FN1 Homo sapiens P02751-7
SPR
17130124
Intra
FYN P06241 FN1 Homo sapiens P02751-7 17130124
Intra
FYN P06241 WBP11 Homo sapiens Q9Y2W2 25416956
Intra
FYN P06241 EFS Homo sapiens O43281 31515488
Intra
FYN P06241 NCKIPSD Homo sapiens Q9NZQ3 25416956
Intra
FYN P06241 ADAM15 Homo sapiens Q13444 16374509
Intra
FYN P06241 MAPT Homo sapiens P10636-2 25156556
Intra
FYN P06241 MAPT Homo sapiens P10636-2
SPR
16115884
Intra
FYN P06241 MAPT Homo sapiens P10636-6
SPR
16115884
Intra
FYN P06241 MAPT Homo sapiens P10636-6 25156556
Intra
FYN P06241 CBX1 Homo sapiens P83916 32814053
Intra
FYN P06241 CBX1 Homo sapiens P83916 32814053
Intra
FYN P06241 CBX1 Homo sapiens P83916 32814053
Intra
FYN P06241 ATXN1 Homo sapiens P54253 32814053
Intra
FYN P06241 ATXN1 Homo sapiens P54253 32814053
Intra
FYN P06241 ATXN1 Homo sapiens P54253 32814053
Intra
FYN P06241 ATXN1 Homo sapiens P54253
Y2H
16713569
Intra
FYN P06241 SNCA Homo sapiens P37840 32814053
Intra
FYN P06241 SNCA Homo sapiens P37840 32814053
Intra
FYN P06241 SNCA Homo sapiens P37840 32814053
Cross
FYN P06241 polg_hcv77 Hepatitis C virus P27958 15784897
Cross
FYN P06241 polg_hcv77 Hepatitis C virus P27958 14993658
Cross
FYN P06241 polg_hcv77 Hepatitis C virus P27958 15784897
Cross
FYN P06241 polg_hcvco Hepatitis C virus Q9WMX2 15784897
Cross
FYN P06241 Grm5 Rattus norvegicus P31424-2 24012003
Cross
FYN P06241 Grm5 Rattus norvegicus P31424-2 24012003
Cross: Cross-species interaction Intra: Intraspecies interaction

FYN Antibodies

Cat. No. Product Name Application Reactivity
HY-P80681 Fyn Antibody WB Human, Mouse, Rat
HY-P85176 Fyn Antibody (YA4868) WB, IHC-P, ICC/IF, FC, ELISA Human
HY-P85545 Fyn Antibody (YA5237) WB, ICC/IF Human, Monkey, Rat, Mouse

Related Diseases

Diseases Alias
Hepatitis E
Prion Disease
  • Spongiform Encephalopathy

  • Transmissible Spongiform Encephalopathies

  • Prion Diseases

  • Prion Disease Pathway

  • Transmissible Spongiform Encephalopathy

  • Prion Induced Disorder

  • Prion Protein Disease

  • Inherited Human Transmissible Spongiform Encephalopathies

  • Prion Protein Diseases

  • Prion-Associated Disorders

  • Prion-Induced Disorders

  • Transmissible Dementias

  • Tses

  • Human Prion Disease

  • Tse

  • Encephalopathy, Transmissible Spongiform

  • Prion Disease, Susceptibility To

  • Spongiform Encephalopathies

  • Human Transmissible Spongiform Encephalopathies, Inherited

Wiskott-Aldrich Syndrome
  • WAS

  • Eczema-Thrombocytopenia-Immunodeficiency Syndrome

  • Immunodeficiency 2

  • Aldrich Syndrome

  • Imd2

  • Wiskott-Aldrich Syndrome 1

  • Was1

  • Wiskott Syndrome

  • Wiskott Aldrich Syndrome

  • Eczema Thrombocytopenia Immunodeficiency Syndrome

  • Imd 2

Cd45 Deficiency
Platelet Glycoprotein Iv Deficiency
  • Platelet-Type Bleeding Disorder 10

  • Bdplt10

  • Cd36 Deficiency

  • Bleeding Disorder, Platelet-Type, 10

  • PG4D

  • Bleeding Disorder Platelet-Type 10

  • Deficiency, Platelet Glycoprotein Iv

Alcohol Dependence
  • Alcoholism

  • Alcohol Dependence, Susceptibility To

  • Alcohol Dependence, Protection Against

  • Aerodigestive Tract Cancer, Squamous Cell, Alcohol-Related, Protection Against

  • Alcoholism, Susceptibility To

  • Alcoholic Intoxication, Chronic

  • Pharyngeal Neoplasms

  • Chronic Alcoholism

  • Dipsomania

  • Alcohol Addiction

  • Ethanol Dependence

  • Chronic Ethanolism

  • Chronic Alcoholic Disease Nos

  • Alcoholic Disease Nos

  • Alcoholic

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

Congenital Generalized Lipodystrophy
  • Berardinelli-Seip Congenital Lipodystrophy

  • Berardinelli-Seip Syndrome

  • Brunzell Syndrome

  • Bscl

  • Generalized Lipodystrophy

  • Lipodystrophy, Congenital Generalized

  • Seip Syndrome

  • Total Lipodystrophy

  • Cgl

  • Lipoatrophic Diabetes

  • Lipodystrophy, Generalized, Congenital

  • Familial Generalized Lipodystrophy

  • Congenital Generalized Lipodystrophy Type 2

  • Lipoatrophic Diabetes Mellitus

  • Familial Partial Lipodystrophy, Type 2

Fragile X Syndrome
  • FXS

  • Martin-Bell Syndrome

  • Fraxa Syndrome

  • Marker X Syndrome

  • X-Linked Mental Retardation And Macroorchidism

  • Fragile X Mental Retardation Syndrome

  • Fra Syndrome

  • Mental Retardation, X-Linked, Associated With Marxq28

  • X-Linked Intellectual Disability And Macroorchidism

  • Frax Syndrome

  • Symptomatic Form Of Fragile X Syndrome In Female Carriers

  • Fragile-X Syndrome

  • Fraxe Syndrome

Focal Segmental Glomerulosclerosis
  • Familial Idiopathic Steroid-Resistant Nephrotic Syndrome

  • Focal Glomerulosclerosis

  • Fsgs

  • Segmental Glomerulosclerosis

  • Glomerulosclerosis, Focal Segmental

  • Fgs

  • Focal Glomerular Sclerosis

  • Familial Idiopathic Nephrotic Syndrome

  • Focal Sclerosis With Hyalinosis

  • Glomerulosclerosis, Focal

  • Glomerulosclerosis Focal

  • Glomerulosclerosis, Segmental, Focal

  • Focal Segmental Glomerulosclerosis, Not Otherwise Specified

Severe Combined Immunodeficiency
  • Scid

  • Severe Combined Immunodeficiency Disease

  • Combined T And B Cell Inborn Immunodeficiency

  • Immunodeficiency, Severe Combined

  • Scid - [Severe Combined Immunodeficiencies]

Pick Disease Of Brain
  • Pick Disease

  • Pick'S Disease

  • Pick Disease Of The Brain

  • Lobar Atrophy Of Brain

  • Dementia With Lobar Atrophy And Neuronal Cytoplasmic Inclusions

  • Behavioral Variant Of Frontotemporal Dementia

  • Dementia In Pick'S Disease

  • Lobar Atrophy Of The Brain

  • Bvftd

  • Bv-Ftd

  • PIDB

  • Picks Disease

Schizophrenia
  • SCZD

  • Schizophrenia With Or Without An Affective Disorder

  • Schizophrenia 12

  • Schizophrenia, Susceptibility To

  • Schizophrenia-1

  • Dementia Praecox

  • Schizophrenia 1

Thrombocytopenia
  • Low Platelet Count

  • Low Platelets

  • Decreased Platelets

  • Platelet Dysfunction Nos

Co-Trimoxazole Allergy
  • Bactrim Allergy

  • Cotrimoxazol Allergy

  • Tmp/Smx Allergy

  • Trimethoprim/Sulfamethoxazole Allergy

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

T-Cell Acute Lymphoblastic Leukemia
  • T-Cell Leukemia

  • Acute T Cell Leukemia

  • Precursor T Lymphoblastic Leukemia

  • Precursor T-Lymphoblastic Lymphoma/Leukemia

  • T Acute Lymphoblastic Leukemia

  • T-Cell Acute Lymphocytic Leukaemia

  • T-Cell Lymphoblastic Leukemia/Lymphoma

  • Leukemia T-Cell

  • Leukemia, T-Cell

  • Leukemia, Acute, Lymphoblastic, T-Cell

  • Leukemia, T-Cell Acute Lymphoblastic

  • Leukemia, Acute T-Cell

  • Precursor T-Cell Lymphoblastic Leukemia-Lymphoma

  • Precursor T-Cell Lymphoblastic Lymphoma

  • Precursor T Cell Lymphoblastic Leukemia/Lymphoblastic Lymphoma

Colorectal Cancer
  • Colon Cancer

  • Colorectal Carcinoma

  • Colon Carcinoma

  • Colorectal Cancer, Susceptibility To

  • Carcinoma Of Colon

  • CRC

  • Colorectal Cancer With Chromosomal Instability, Somatic

  • Colon Cancer, Somatic

  • Colon Cancer, Susceptibility To

  • Colonic Neoplasms

  • Colorectal Neoplasms

  • Colorectal Cancer, Somatic

  • Colon Cancer, Advanced, Somatic

  • Colonic Carcinoma

  • Colorectal Carcinomas

  • Colon Cancers

  • Colorectal Cancers

  • Cancer, Colorectal, Somatic

  • Cancer, Colon

  • Cancer, Colorectal, Susceptibility To

  • Colorectal Neoplasm

  • Colonic Neoplasm

  • Malignant Tumor Of Colon

Alzheimer Disease, Familial, 1
  • Alzheimer Disease

  • Alzheimer'S Disease

  • Presenile And Senile Dementia

  • AD1

  • Alzheimer Disease, Susceptibility To

  • Alzheimer Disease, Late-Onset, Susceptibility To

  • Alzheimer Disease 1, Familial

  • AD

  • Familial Alzheimer Disease

  • Alzheimer Disease, Late-Onset

  • Alzheimers Dementia

  • Alzheimer Dementia

  • Alzheimer Sclerosis

  • Alzheimer Syndrome

  • Alzheimer-Type Dementia

  • Dat

  • Primary Senile Degenerative Dementia

  • Sdat

  • Alzheimer Disease 1

  • Autosomal Dominant Alzheimer Disease

  • Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy

  • Late Onset Alzheimer Disease

  • Alzheimers Disease

  • Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy

  • Late-Onset Alzheimers Disease

  • Alzheimer'S Disease Pathway Kegg

  • Dementia Due To Alzheimer'S Disease

  • Alzheimer Disease Type 1

  • Alzheimers

Supranuclear Palsy, Progressive, 1
  • Progressive Supranuclear Palsy

  • Steele-Richardson-Olszewski Syndrome

  • Supranuclear Palsy, Progressive

  • Progressive Supranuclear Ophthalmoplegia

  • Psp

  • PSNP1

  • Familial Progressive Supranuclear Palsy

  • Richardson'S Syndrome

  • Psp Syndrome

  • Progressive Supranuclear Palsy 1

  • Supranuclear Palsy Progressive

  • Ophthalmoplegia, Supranuclear, Progressive

  • Steele-Richardson-Olszewksi Syndrome

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]

Nervous System Disease
  • Abnormality Of The Nervous System

  • Nervous System Diseases

  • Nervous System Disorder

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 FYN VGNC VGNC:29163
Macaca mulatta FYN VGNC VGNC:72832
Felis catus FYN VGNC VGNC:62400
Rattus norvegicus FYN RGD RGD:2641
Canis familiaris FYN VGNC VGNC:41027
Mus musculus FYN MGD MGI:95602
Others FYN NCBI