TPM1 - tropomyosin 1 Gene

Also Known as CMH3; TMSA; CMD1Y; LVNC9; C15orf13; HEL-S-265; HTM-alpha

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 7168

About TPM1

Cytogenetic location: 15q22.2 Genomic coordinates (GRCh38): 15:63,042,747-63,071,915 (from NCBI)

This gene has 39 transcripts (splice variants), 248 orthologues, 3 paralogues and is associated with 6 phenotypes. Biased expression in heart (RPKM 615.8), prostate (RPKM 140.5) and 9 other tissues.

Summary

This gene is a member of the tropomyosin family of highly conserved, widely distributed actin-binding proteins involved in the contractile system of striated and smooth muscles and the Cytoskeleton of non-muscle cells. Tropomyosin is composed of two alpha-helical chains arranged as a coiled-coil. It is polymerized end to end along the two grooves of actin filaments and provides stability to the filaments. The encoded protein is one type of alpha helical chain that forms the predominant tropomyosin of striated muscle, where it also functions in association with the troponin complex to regulate the calcium-dependent interaction of actin and Myosin during muscle contraction. In smooth muscle and non-muscle cells, alternatively spliced transcript variants encoding a range of isoforms have been described. Mutations in this gene are associated with type 3 familial hypertrophic cardiomyopathy and dilated cardiomyopathy 1Y. [provided by RefSeq, Jun 2022]

TPM1 Products (40)

mRNA Protein Name
NM_000366.6 NP_000357.3 tropomyosin alpha-1 chain isoform Tpm1.5cy
NM_001018004.2 NP_001018004.1 tropomyosin alpha-1 chain isoform Tpm1.6cy
NM_001018005.2 NP_001018005.1 tropomyosin alpha-1 chain isoform Tpm1.1st
NM_001018006.2 NP_001018006.1 tropomyosin alpha-1 chain isoform Tpm1.7cy
NM_001018007.2 NP_001018007.1 tropomyosin alpha-1 chain isoform Tpm1.4sm
NM_001018008.2 NP_001018008.1 tropomyosin alpha-1 chain isoform Tpm1.12br
NM_001018020.2 NP_001018020.1 tropomyosin alpha-1 chain isoform Tpm1.3sm
NM_001301244.2 NP_001288173.1 tropomyosin alpha-1 chain isoform Tpm1.2st
NM_001301289.2 NP_001288218.1 tropomyosin alpha-1 chain isoform Tpm1.8cy
NM_001330344.2 NP_001317273.1 tropomyosin alpha-1 chain isoform Tpm1.9cy
NM_001330346.2 NP_001317275.1 tropomyosin alpha-1 chain isoform Tpm1.13
NM_001330351.2 NP_001317280.1 tropomyosin alpha-1 chain isoform 12
NM_001365776.1 NP_001352705.1 tropomyosin alpha-1 chain isoform Tpm1.10br
NM_001365777.1 NP_001352706.1 tropomyosin alpha-1 chain isoform 14
NM_001365778.1 NP_001352707.1 tropomyosin alpha-1 chain isoform 15
NM_001365779.1 NP_001352708.1 tropomyosin alpha-1 chain isoform 16
NM_001365780.1 NP_001352709.1 tropomyosin alpha-1 chain isoform Tpm1.11br
NM_001365781.2 NP_001352710.1 tropomyosin alpha-1 chain isoform 18
NM_001365782.1 NP_001352711.1 tropomyosin alpha-1 chain isoform 19
NM_001407322.1 NP_001394251.1 tropomyosin alpha-1 chain isoform 23
NM_001407323.1 NP_001394252.1 tropomyosin alpha-1 chain isoform 24
NM_001407324.1 NP_001394253.1 tropomyosin alpha-1 chain isoform 25
NM_001407325.1 NP_001394254.1 tropomyosin alpha-1 chain isoform 26
NM_001407326.1 NP_001394255.1 tropomyosin alpha-1 chain isoform 27
NM_001407327.1 NP_001394256.1 tropomyosin alpha-1 chain isoform 28
NM_001407328.1 NP_001394257.1 tropomyosin alpha-1 chain isoform 29
NM_001407329.1 NP_001394258.1 tropomyosin alpha-1 chain isoform 30
NM_001407330.1 NP_001394259.1 tropomyosin alpha-1 chain isoform Tpm1.5cy
NM_001407331.1 NP_001394260.1 tropomyosin alpha-1 chain isoform 31
NM_001407332.1 NP_001394261.1 tropomyosin alpha-1 chain isoform 32
NM_001407333.1 NP_001394262.1 tropomyosin alpha-1 chain isoform 16
NM_001407334.1 NP_001394263.1 tropomyosin alpha-1 chain isoform 33
NM_001407335.1 NP_001394264.1 tropomyosin alpha-1 chain isoform 33
NM_001407336.1 NP_001394265.1 tropomyosin alpha-1 chain isoform 35
NM_001407337.1 NP_001394266.1 tropomyosin alpha-1 chain isoform 36
NM_001407338.1 NP_001394267.1 tropomyosin alpha-1 chain isoform 37
NM_001407340.1 NP_001394269.1 tropomyosin alpha-1 chain isoform 38
NM_001407341.1 NP_001394270.1 tropomyosin alpha-1 chain isoform 39
NM_001407342.1 NP_001394271.1 tropomyosin alpha-1 chain isoform 40
NM_001407344.1 NP_001394273.1 tropomyosin alpha-1 chain isoform 41

Gene Ontology

  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence References Source
enables cytoskeletal protein binding IPI
IPI: Inferred from physical interaction
17987659 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
Biological Process GO Annotation Evidence References Source
involved in cardiac muscle contraction IMP
IMP: Inferred from mutant phenotype
11136687 GOA
involved in cellular response to reactive oxygen species IEP
IEP: Inferred from expression pattern
12686598 GOA
involved in negative regulation of vascular associated smooth muscle cell migration IMP
IMP: Inferred from mutant phenotype
21817107 GOA
involved in negative regulation of vascular associated smooth muscle cell proliferation IMP
IMP: Inferred from mutant phenotype
21817107 GOA
involved in regulation of cell shape IMP
IMP: Inferred from mutant phenotype
21817107 GOA
involved in sarcomere organization IMP
IMP: Inferred from mutant phenotype
11273725 GOA
involved in ventricular cardiac muscle tissue morphogenesis IMP
IMP: Inferred from mutant phenotype
11136687 GOA
Cellular Component GO Annotation Evidence References Source
located in bleb IMP
IMP: Inferred from mutant phenotype
12686598 GOA
located in ruffle membrane IDA
IDA: Inferred from direct assay
12686598 GOA
located in stress fiber IDA
IDA: Inferred from direct assay
12686598 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

TPM1 Protein Structure

Tropomyosin

Tropomyosin: Tropomyosin (48 - 283)

  • 0
  • 100
  • 200
  • 284 a.a.
Protein Preferred Names Protein Names

tropomyosin alpha-1 chain

  • cardiomyopathy, hypertrophic 3

TPM1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
TPM1 P09493 CAGE1 Homo sapiens Q8TC20
Validated Y2H
25416956
Intra
TPM1 P09493 CAGE1 Homo sapiens Q8TC20
Y2H Prey Pooling
25416956
Intra
TPM1 P09493 TPM2 Homo sapiens P07951
Anti Tag CoIP
33961781
Intra
TPM1 P09493 GOLGA2 Homo sapiens Q08379
Y2H Prey Pooling
25416956
Intra
TPM1 P09493 GOLGA2 Homo sapiens Q08379
Validated Y2H
25416956
Intra
TPM1 P09493 GOLGA2 Homo sapiens Q08379
Y2H Array
25416956
Intra
TPM1 P09493 SYCE1 Homo sapiens Q8N0S2
Y2H Array
25416956
Intra
TPM1 P09493 SYCE1 Homo sapiens Q8N0S2
Y2H Prey Pooling
25416956
Intra
TPM1 P09493 TNNT1 Homo sapiens P13805
Validated Y2H
25416956
Intra
TPM1 P09493 TNNT1 Homo sapiens P13805
Y2H Array
25416956
Intra
TPM1 P09493 KXD1 Homo sapiens Q9BQD3
Y2H Pooling
16189514
Intra
TPM1 P09493 KXD1 Homo sapiens Q9BQD3
Anti Tag CoIP
33961781
Intra
TPM1 P09493 KXD1 Homo sapiens Q9BQD3
Validated Y2H
25416956
Intra
TPM1 P09493 KXD1 Homo sapiens Q9BQD3
Y2H Array
25416956
Intra
TPM1 P09493 MAD1L1 Homo sapiens Q9Y6D9
Anti Tag CoIP
33961781
Intra
TPM1 P09493 MAD1L1 Homo sapiens Q9Y6D9
Y2H Prey Pooling
25416956
Intra
TPM1 P09493 MAD1L1 Homo sapiens Q9Y6D9
Y2H Prey Pooling
26871637
Intra
TPM1 P09493 MAD1L1 Homo sapiens Q9Y6D9
Validated Y2H
25416956
Intra
TPM1 P09493 MAD1L1 Homo sapiens Q9Y6D9
Validated Y2H
26871637
Intra
TPM1 P09493 MAD1L1 Homo sapiens Q9Y6D9
Y2H Array
25416956
Intra
TPM1 P09493 MAD1L1 Homo sapiens Q9Y6D9
Y2H Array
26871637
Intra
TPM1 P09493 C1orf216 Homo sapiens Q8TAB5
Validated Y2H
25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant TPM1 Proteins

Cat. No. Product Name Accession Purity
HY-P74502 TPM1 Protein, Human (His) P09493-10/NP_000357.3 (M1-M284) ≥ 90%, as determined by reducing SDS-PAGE.

TPM1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P82438 Tropomyosin alpha 1 Chain Antibody (YA2183) WB, IHC-P, ICC/IF, IP, FC Human, Mouse, Rat

Related Diseases

Diseases Alias
Cardiomyopathy, Familial Hypertrophic, 3

  • Hypertrophic Cardiomyopathy 3

  • CMH3

  • Cardiomyopathy, Hypertrophic, 3

  • Cardiomyopathy Familial Hypertrophic 3

  • Cardiomyopathy, Familial Hypertrophic 3

  • Cardiomyopathy, Hypertrophic, Familial, Type 3
Cardiomyopathy, Dilated, 1e

  • Left Ventricular Noncompaction 9

  • Left Ventricular Noncompaction 5

  • Dilated Cardiomyopathy 1e

  • Dilated Cardiomyopathy 1s

  • CMD1E

  • Cdcd2

  • Cardiomyopathy, Dilated, 1y

  • CMD1Y

  • Cardiomyopathy, Dilated, 1s

  • CMD1S

  • Dilated Cardiomyopathy 1y

  • Dilated Cardiomyopathy With Conduction Defect 2

  • Dilated Cardiomyopathy With Conduction Disorder And Arrhythmia

  • Cardiomyopathy, Dilated, With Conduction Disorder And Arrhythmia

  • Cardiomyopathy, Dilated, With Conduction Defect 2

  • Cardiomyopathy Dilated With Conduction Defect Type 2

  • Cardiomyopathy, Dilated 1e

  • Cardiomyopathy, Dilated 1s

  • Cardiomyopathy, Dilated 1y

  • Left Ventricular Non-Compaction 5

  • LVNC5

  • Left Ventricular Non-Compaction 9

  • LVNC9

  • Cardiomyopathy, Dilated, Type 1e

  • Cardiomyopathy, Dilated, Type 1s

  • Cardiomyopathy, Dilated, Type 1y
Cardiomyopathy, Familial Hypertrophic, 1

  • Asymmetric Septal Hypertrophy

  • Familial Hypertrophic Cardiomyopathy

  • Hypertrophic Cardiomyopathy 1

  • CMH1

  • Hypertrophic Cardiomyopathy 19

  • CMH

  • Ventricular Hypertrophy, Hereditary

  • Ash

  • Hypertrophic Subaortic Stenosis, Idiopathic

  • Cardiomyopathy, Familial Hypertrophic

  • Cardiomyopathy, Hypertrophic, 1, Digenic

  • Cardiomyopathy, Familial Hypertrophic 1

  • Hcm

  • Hereditary Ventricular Hypertrophy

  • Idiopathic Hypertrophic Subaortic Stenosis

  • Hypertrophic Cardiomyopathy

  • Cardiomyopathy, Hypertrophic, Familial

  • Cardiomyopathy, Hypertrophic, 1

  • Familial Asymmetric Septal Hypertrophy

  • Heritable Hypertrophic Cardiomyopathy

  • Fhc

  • Cardiomyopathy, Hypertrophic, Familial, Type 1
Dilated Cardiomyopathy

  • Familial Dilated Cardiomyopathy

  • Primary Dilated Cardiomyopathy

  • Idiopathic Dilated Cardiomyopathy

  • Congestive Cardiomyopathy

  • Idiopathic Dilation Cardiomyopathy

  • Primary Familial Dilated Cardiomyopathy

  • Cardiomyopathy, Dilated

  • DCM

  • Cardiomyopathy, Familial Dilated

  • Dilated Cardiomyopathy, Familial

  • Hypokinetic Dilated Cardiomyopathy, Familial

  • Familial Idiopathic Cardiomyopathy

  • Fdc

  • Cardiomyopathy, Familial Idiopathic

  • Idiopathic Cardiomegaly

  • Dilated Congestive Cardiomyopathy

  • Chronic Dilated Cardiomyopathy

  • Ccm - [Congestive Cardiomyopathy]

  • Cocm - [Congestive Cardiomyopathy]

  • Dcm - [Dilated Cardiomyopathy]

  • Dilated-Hypokinetic Cardiomyopathy

  • Congestive Idiopathic Cardiomyopathy

  • Primary Idiopathic Dilated Cardiomyopathy
Hypertrophic Cardiomyopathy

  • Hypertrophic Obstructive Cardiomyopathy

  • Cardiomyopathy, Hypertrophic

  • Cardiomyopathy Hypertrophic Obstructive

  • Cardiomyopathy, Hypertrophic, Familial

  • Idiopathic Myocardial Hypertrophy

  • Idiopathic Hypertrophic Cardiomyopathy

  • Obstructive Idiopathic Hypertrophic Cardiomyopathy

  • Obstructive Cardiomyopathy

  • Idiopathic Hypertrophic Subaortic Stenosis

  • Muscular Subaortic Stenosis

  • Hypertrophic Obstructive Subaortic Stenosis
Left Ventricular Noncompaction

  • Noncompaction Cardiomyopathy

  • Left Ventricular Hypertrabeculation

  • Lvnc

  • Spongy Myocardium

  • Isolated Noncompaction Of The Ventricular Myocardium

  • Left Ventricular Myocardial Noncompaction Cardiomyopathy

  • Fetal Myocardium

  • Honeycomb Myocardium

  • Hypertrabeculation Syndrome

  • Left Ventricular Non-Compaction

  • Lvht

  • Non-Compaction Of The Left Ventricular Myocardium

  • Ventricular Noncompaction, Left

  • Non-Compaction Cardiomyopathy
Familial Isolated Dilated Cardiomyopathy

  • Familial Or Idiopathic Dilated Cardiomyopathy
Pulmonary Atresia With Intact Ventricular Septum

  • Pulmonary Atresia-Intact Ventricular Septum Syndrome

  • Pulmonary Valve Atresia With Intact Ventricular Septum
Atrial Septal Defect 1

  • ASD1

  • Atrial Heart Septal Defect 1

  • Asd
Ebstein Anomaly

  • Ebstein'S Anomaly

  • Ebstein'S Anomaly Of Common Atrioventricular Valve

  • Ebstein'S Anomaly Of Right Atrioventricular Valve

  • Ebstein'S Anomaly Of Tricuspid Valve

  • Ebstein'S Malformation

  • Ebstein Malformation Of The Tricuspid Valve

  • Ebstein Anomaly Of The Tricuspid Valve

  • Ebstein Disease

  • Accessory Tricuspid Valve Tissue

  • Congenital Ebstein Deformity Of Tricuspid Valve

  • Ebstein Syndrome

  • Ebstein Cardiopathy

  • Ebstein Anomaly Of Tricuspid Valve
Tetralogy Of Fallot

  • TOF

  • Fallot Tetralogy

  • Ventricular Septal Defect With Pulmonary Stenosis Or Atresia, Dextraposition Of Aorta, And Hypertrophy Of Right Ventricle

  • Tetrad Of Fallot

  • Fallot Tetrad

  • Fallot Disease

  • Fallot Complex

  • Subpulmonic Stenosis, Ventricular Septal Defect, Overriding Aorta, And Right Ventricular Hypertrophy

  • Interventricular Septal Defect With Dextroposition Of Aorta, Pulmonary Stenosis And Hypertrophy Of Right Ventricle

  • Interventricular Septal Defect, In Tetralogy Of Fallot

  • Ventricular Septal Defect With Obstructed Right Ventricular Outflow

  • Tof - [Tetralogy Of Fallot]

  • Pulmonary Atresia With Ventricular Septal Defect [Fallot Type]

  • Pulmonary Atresia, Ventricular Septal Defect And Mapcas

  • Pulmonary Atresia With Ventricular Septal Defect And Systemic-To-Pulmonary Collateral Arteries [Fallot Type]
Arteriosclerosis Obliterans
Arthrogryposis, Distal, Type 1a

  • Distal Arthrogryposis Type 1

  • Digitotalar Dysmorphism

  • DA1A

  • Da1

  • Amcd1

  • Arthrogryposis, Distal, Type 2b4

  • Distal Arthrogryposis Type 1a

  • Arthrogryposis, Distal, Type 1

  • Arthrogryposis Multiplex Congenita Distal Type 1

  • Arthrogryposis Multiplex Congenita, Distal Type 1

  • Arthrogryposis Multiplex Congenita, Distal, Type I

  • Distal Arthrogryposis Type 1b

  • Arthrogryposis, Distal, 1a

  • Amc

  • Arthrogryposis Multiplex Congenita

  • Arthrogryposis, Distal, 2b4

  • DA2B4

  • Arthrogryposis Multiplex Congenita, Distal, Type 1

  • Arthrogryposis
Cardiomyopathy, Dilated, 1ee

  • Dilated Cardiomyopathy 1ee

  • CMD1EE

  • Cardiomyopathy, Dilated 1ee

  • Cardiomyopathy, Dilated, Type 1ee
Arthrogryposis, Distal, Type 5

  • Oculomelic Amyoplasia

  • Distal Arthrogryposis Type 5

  • Distal Arthrogryposis Type Iib

  • DA5

  • Arthrogryposis With Oculomotor Limitation And Electroretinal Abnormalities

  • Daiib

  • Distal Arthrogryposis Type 2b

  • Arthrogryposis-Oculomotor Limitation-Electroretinal Anomalies Syndrome

  • Distal Arthrogryposis With Ophthalmoplegia

  • Arthrogryposis- Oculomotor Limitation-Electroretinal Anomalies Syndrome

  • Arthrogryposis, Distal, Type Iib

  • Da2b

  • Freeman-Sheldon Syndrome Variant

  • Sheldon-Hall Syndrome

  • Arthogryposis With Oculomotor Limitation And Electroretinal Abnormalities

  • Arthrogryposis Ophthalmoplegia Retinopathy

  • Arthrogryposis, Distal, 5

  • Arthrogryposis, Distal, Type 2b
Clubfoot

  • Congenital Talipes Equinovarus

  • Congenital Clubfoot

  • Congenital Equinovarus

  • Equinovarus Deformity Of Foot

  • Club Foot
Cardiomyopathy, Familial Hypertrophic, 25

  • Hypertrophic Cardiomyopathy 25

  • CMH25

  • Cardiomyopathy, Hypertrophic, 25

  • Cardiomyopathy Familial Hypertrophic 25

  • Cardiomyopathy, Familial Hypertrophic 25

  • Cardiomyopathy, Hypertrophic, Type 25
Brugada Syndrome

  • Sudden Unexpected Nocturnal Death Syndrome

  • Sudden Unexplained Nocturnal Death Syndrome

  • Bangungut

  • Brugada Type Idiopathic Ventricular Fibrillation

  • Pokkuri Death Syndrome

  • Sunds

  • Idiopathic Ventricular Fibrillation, Brugada Type

  • Sudden Unexplained Death

  • Dream Disease

  • Right Bundle Branch Block, St Segment Elevation, And Sudden Death Syndrome

  • Sudden Unexplained Death Syndrome

  • Suds

  • Sunds - [Sudden Unexplained Nocturnal Death Syndrome]
Cardiomyopathy, Familial Hypertrophic, 4

  • Hypertrophic Cardiomyopathy 4

  • CMH4

  • Cardiomyopathy, Hypertrophic, 4

  • Cardiomyopathy, Familial Hypertrophic 4

  • Cardiomyopathy, Familial Hypertrophic, 4, Susceptibility To

  • Cardiomyopathy, Hypertrophic, Familial, Type 4
Intrinsic Cardiomyopathy
Breast Cancer

  • Breast Carcinoma

  • Male Breast Cancer

  • Breast Cancer, Familial

  • Malignant Neoplasm Of Breast

  • Breast Cancer, Susceptibility To

  • Breast Cancer, Early-Onset

  • Malignant Tumor Of Breast

  • Carcinoma Of Male Breast

  • Breast Cancer, Invasive Ductal

  • Breast Cancer, Protection Against

  • Breast Cancer, Somatic

  • Breast Cancer, Male

  • Breast Cancer, Lobular, Somatic

  • Breast Tumor

  • Mammary Cancer

  • Mammary Tumor

  • Malignant Neoplasm Of Male Breast

  • Mammary Carcinoma

  • Male Breast Carcinoma

  • Familial Cancer Of Breast

  • Invasive Ductal Breast Carcinoma

  • Breast Cancer Susceptibility

  • Breast Cancer, Male, Susceptibility To

  • Breast Cancer, Early-Onset, Susceptibility To

  • Malignant Tumor Of The Breast

  • Mammary Neoplasm

  • Primary Breast Cancer

  • Neoplasm Of Male Breast

  • Carcinoma Of Breast

  • Breast Cancer In Men

  • Familial Breast Cancer

  • Cancer Of Breast

  • BC

  • Breast Cancer Familial

  • Breast Cancer Familial Male

  • Breast Cancer, Familial Male

  • Breast Male Carcinoma

  • Breast Neoplasms

  • Breast Neoplasms, Male

  • Mammary Tumors

  • Mammary Carcinomas

  • Cancer, Breast

  • Cancer, Breast, Susceptibility

  • Invasive Breast Ductal Carcinoma

  • Breast Neoplasm

  • Susceptibility To Breast Cancer

  • Mammary Neoplasms

  • Animal Mammary Neoplasms

  • Primary Malignant Neoplasm Of Breast

  • Infiltrating Ductal Carcinoma Of Breast

  • Infiltrating Duct Carcinoma Of Unspecified Site

  • Infiltrating Ductular Carcinoma Of Unspecified Site

  • Invasive Breast Carcinoma Of No Special Type

  • Microinvasive Carcinoma Of Breast

  • Carcinoma With Apocrine Differentiation
Restrictive Cardiomyopathy

  • Familial Restrictive Cardiomyopathy

  • Cardiomyopathy, Restrictive

  • Cardiomyopathy, Constrictive

  • Primary Restrictive Cardiomyopathy

  • Rcm

  • Cardiomyopathy Restrictive
Myopathy

  • Muscular Diseases

  • Myopathies
Arrhythmogenic Right Ventricular Cardiomyopathy

  • Arrhythmogenic Right Ventricular Dysplasia

  • Arvc

  • Arvd

  • Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy

  • Arvc Cardiomyopathy

  • Arrhythmogenic Right Ventricular Cardiomyopathy-Dysplasia

  • Arvd/C

  • Right Ventricular Dysplasia, Arrhythmogenic

  • Ventricular Dysplasia, Right, Arrhythmogenic

  • Cardiomyopathy, Ventricular, Right, Arrhythmogenic

  • Dysplasia, Arrhythmogenic Right Ventricular
Rasopathy

  • Ras/Mitogen-Activated Protein Kinase 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

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (3)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS14936 TPM1 Human Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS17596 Tpm1 Mouse Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS24056 Tpm1 Rat Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Rattus norvegicus TPM1 RGD RGD:3898
Canis familiaris TPM1 VGNC VGNC:55006
Mus musculus TPM1 MGD MGI:98809
Felis catus TPM1 VGNC VGNC:80814
Bos taurus TPM1 VGNC VGNC:106994
Macaca mulatta TPM1 VGNC VGNC:78634
Others TPM1 NCBI