TPM3 - tropomyosin 3 Gene

Also Known as TM3; TM5; TRK; CFTD; NEM1; TM-5; TM30; CAPM1; TM30nm; TPM3nu; TPMsk3; hscp30; HEL-189; HEL-S-82p; OK/SW-cl.5

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 7170

About TPM3

Cytogenetic location: 1q21.3 Genomic coordinates (GRCh38): 1:154,155,308-154,192,100 (from NCBI)

This gene has 27 transcripts (splice variants), 119 orthologues, 3 paralogues and is associated with 83 phenotypes. Ubiquitous expression in bone marrow (RPKM 43.6), appendix (RPKM 31.3) and 25 other tissues.

Summary

This gene encodes a member of the tropomyosin family of actin-binding proteins. Tropomyosins are dimers of coiled-coil proteins that provide stability to actin filaments and regulate access of Other actin-binding proteins. Mutations in this gene result in autosomal dominant nemaline myopathy and Other muscle disorders. This locus is involved in translocations with Other loci, including anaplastic lymphoma receptor tyrosine kinase (ALK) and neurotrophic tyrosine kinase receptor type 1 (NTRK1), which result in the formation of fusion proteins that act as oncogenes. There are numerous pseudogenes for this gene on different chromosomes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]

TPM3 Products (15)

mRNA Protein Name
NM_001043351.2 NP_001036816.1 tropomyosin alpha-3 chain isoform Tpm3.2cy
NM_001043352.2 NP_001036817.1 tropomyosin alpha-3 chain isoform Tpm3.7cy
NM_001043353.2 NP_001036818.1 tropomyosin alpha-3 chain isoform Tpm3.4cy
NM_001278188.2 NP_001265117.1 tropomyosin alpha-3 chain isoform 6
NM_001278189.2 NP_001265118.1 tropomyosin alpha-3 chain isoform Tpm3.5cy
NM_001278190.2 NP_001265119.1 tropomyosin alpha-3 chain isoform 8
NM_001278191.2 NP_001265120.1 tropomyosin alpha-3 chain isoform 9
NM_001349679.2 NP_001336608.1 tropomyosin alpha-3 chain isoform Tpm3.3cy
NM_001364679.2 NP_001351608.1 tropomyosin alpha-3 chain isoform 10
NM_001364680.2 NP_001351609.1 tropomyosin alpha-3 chain isoform 11
NM_001364681.2 NP_001351610.1 tropomyosin alpha-3 chain isoform 12
NM_001364682.1 NP_001351611.1 tropomyosin alpha-3 chain isoform 13
NM_001364683.1 NP_001351612.1 tropomyosin alpha-3 chain isoform Tpm3.5cy
NM_152263.4 NP_689476.2 tropomyosin alpha-3 chain isoform Tpm3.12st
NM_153649.4 NP_705935.1 tropomyosin alpha-3 chain isoform Tpm3.1cy
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
Cellular Component GO Annotation Evidence References Source
located in stress fiber IDA
IDA: Inferred from direct assay
16236705 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

TPM3 Protein Structure

Tropomyosin

Tropomyosin: Tropomyosin (49 - 284)

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

tropomyosin alpha-3 chain

  • alpha-tropomyosin, slow skeletal

TPM3 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
TPM3 P06753 CCHCR1 Homo sapiens Q8TD31-3 32296183
Intra
TPM3 P06753 CCHCR1 Homo sapiens Q8TD31-3 25910212
Intra
TPM3 P06753 CCHCR1 Homo sapiens Q8TD31-3
SLC
25910212
Intra
TPM3 P06753 CCHCR1 Homo sapiens Q8TD31-3 25910212
Intra
TPM3 P06753 CCHCR1 Homo sapiens Q8TD31-3 25416956
Intra
TPM3 P06753 CCHCR1 Homo sapiens Q8TD31-3 25910212
Intra
TPM3 P06753 CCHCR1 Homo sapiens Q8TD31-3 32296183
Intra
TPM3 P06753 CCHCR1 Homo sapiens Q8TD31-3 32296183
Intra
TPM3 P06753 CCHCR1 Homo sapiens Q8TD31-3 25416956
Intra
TPM3 P06753 TFPT Homo sapiens P0C1Z6-2 25416956
Intra
TPM3 P06753 TFPT Homo sapiens P0C1Z6-2 25416956
Intra
TPM3 P06753 PHLDB3 Homo sapiens Q6NSJ2-2 32296183
Intra
TPM3 P06753 PHLDB3 Homo sapiens Q6NSJ2-2 32296183
Intra
TPM3 P06753 PHLDB3 Homo sapiens Q6NSJ2-2 32296183
Intra
TPM3 P06753 HSF4 Homo sapiens Q9ULV5-2 32296183
Intra
TPM3 P06753 HSF4 Homo sapiens Q9ULV5-2 32296183
Intra
TPM3 P06753 HSF4 Homo sapiens Q9ULV5-2 32296183
Intra
TPM3 P06753 TNNT1 Homo sapiens P13805-3 25910212
Intra
TPM3 P06753 TNNT1 Homo sapiens P13805-3 25910212
Intra
TPM3 P06753 TNNT1 Homo sapiens P13805-3 25910212
Intra
TPM3 P06753 TFPT Homo sapiens P0C1Z6 25910212
Intra
TPM3 P06753 TFPT Homo sapiens P0C1Z6
SLC
25910212
Intra
TPM3 P06753 TFPT Homo sapiens P0C1Z6 32296183
Intra
TPM3 P06753 TFPT Homo sapiens P0C1Z6 25910212
Intra
TPM3 P06753 TFPT Homo sapiens P0C1Z6 32296183
Intra
TPM3 P06753 TFPT Homo sapiens P0C1Z6 25910212
Intra
TPM3 P06753 TFPT Homo sapiens P0C1Z6 27107012
Intra
TPM3 P06753 TFPT Homo sapiens P0C1Z6 32296183
Intra
TPM3 P06753 TPM4 Homo sapiens P67936 32296183
Intra
TPM3 P06753 HSF2 Homo sapiens Q03933 25910212
Intra
TPM3 P06753 HSF2 Homo sapiens Q03933 31515488
Intra
TPM3 P06753 HSF2 Homo sapiens Q03933 25910212
Intra
TPM3 P06753 HSF2 Homo sapiens Q03933 25416956
Intra
TPM3 P06753 HSF2 Homo sapiens Q03933 32296183
Intra
TPM3 P06753 HSF2 Homo sapiens Q03933 32296183
Intra
TPM3 P06753 HSF2 Homo sapiens Q03933 25416956
Intra
TPM3 P06753 HSF2 Homo sapiens Q03933 25910212
Intra
TPM3 P06753 HSF2 Homo sapiens Q03933 32296183
Intra
TPM3 P06753 VPS52 Homo sapiens Q8N1B4 25416956
Intra
TPM3 P06753 FAM9C Homo sapiens Q8IZT9 32296183
Intra
TPM3 P06753 FAM9C Homo sapiens Q8IZT9 32296183
Intra
TPM3 P06753 FAM9C Homo sapiens Q8IZT9 32296183
Intra
TPM3 P06753 SNAPIN Homo sapiens O95295 32296183
Intra
TPM3 P06753 SNAPIN Homo sapiens O95295 32296183
Intra
TPM3 P06753 PSMC5 Homo sapiens P62195 32296183
Intra
TPM3 P06753 PSMC5 Homo sapiens P62195 32296183
Intra
TPM3 P06753 PSMC5 Homo sapiens P62195 32296183
Intra
TPM3 P06753 TAB2 Homo sapiens Q9NYJ8 32296183
Intra
TPM3 P06753 CAVIN3 Homo sapiens Q969G5 33961781
Intra
TPM3 P06753 CAVIN3 Homo sapiens Q969G5 32296183
Intra
TPM3 P06753 OIP5 Homo sapiens O43482 25910212
Intra
TPM3 P06753 OIP5 Homo sapiens O43482 25910212
Intra
TPM3 P06753 OIP5 Homo sapiens O43482 31515488
Intra
TPM3 P06753 OIP5 Homo sapiens O43482 25416956
Intra
TPM3 P06753 OIP5 Homo sapiens O43482 25910212
Intra
TPM3 P06753 OIP5 Homo sapiens O43482 25416956
Intra
TPM3 P06753 OIP5 Homo sapiens O43482 32296183
Intra
TPM3 P06753 OIP5 Homo sapiens O43482 25416956
Intra
TPM3 P06753 OIP5 Homo sapiens O43482 32296183
Intra
TPM3 P06753 SYCE1 Homo sapiens Q8N0S2 25910212
Intra
TPM3 P06753 SYCE1 Homo sapiens Q8N0S2
SLC
25910212
Intra
TPM3 P06753 SYCE1 Homo sapiens Q8N0S2 25910212
Intra
TPM3 P06753 SYCE1 Homo sapiens Q8N0S2 25910212
Intra
TPM3 P06753 SYCE1 Homo sapiens Q8N0S2 25416956
Intra
TPM3 P06753 KXD1 Homo sapiens Q9BQD3 32296183
Intra
TPM3 P06753 KXD1 Homo sapiens Q9BQD3 25910212
Intra
TPM3 P06753 KXD1 Homo sapiens Q9BQD3 25416956
Intra
TPM3 P06753 KXD1 Homo sapiens Q9BQD3 32296183
Intra
TPM3 P06753 KXD1 Homo sapiens Q9BQD3 16189514
Intra
TPM3 P06753 KXD1 Homo sapiens Q9BQD3 25910212
Intra
TPM3 P06753 KXD1 Homo sapiens Q9BQD3
SLC
25910212
Intra
TPM3 P06753 KXD1 Homo sapiens Q9BQD3 32296183
Intra
TPM3 P06753 KXD1 Homo sapiens Q9BQD3 25910212
Intra
TPM3 P06753 NUP54 Homo sapiens Q7Z3B4 32296183
Intra
TPM3 P06753 NUP54 Homo sapiens Q7Z3B4 32296183
Intra
TPM3 P06753 NUP54 Homo sapiens Q7Z3B4 32296183
Intra
TPM3 P06753 THAP7 Homo sapiens Q9BT49 32296183
Intra
TPM3 P06753 LURAP1 Homo sapiens Q96LR2 31515488
Intra
TPM3 P06753 LURAP1 Homo sapiens Q96LR2 25416956
Intra
TPM3 P06753 THAP1 Homo sapiens Q9NVV9 32296183
Intra
TPM3 P06753 THAP1 Homo sapiens Q9NVV9 32296183
Intra
TPM3 P06753 THAP1 Homo sapiens Q9NVV9 32296183
Intra
TPM3 P06753 MAD1L1 Homo sapiens Q9Y6D9 25416956
Intra
TPM3 P06753 MAD1L1 Homo sapiens Q9Y6D9 32296183
Intra
TPM3 P06753 MAD1L1 Homo sapiens Q9Y6D9
Y2H
21516116
Intra
TPM3 P06753 MAD1L1 Homo sapiens Q9Y6D9 25910212
Intra
TPM3 P06753 MAD1L1 Homo sapiens Q9Y6D9 25910212
Intra
TPM3 P06753 MAD1L1 Homo sapiens Q9Y6D9 25910212
Intra
TPM3 P06753 MAD1L1 Homo sapiens Q9Y6D9 25416956
Intra
TPM3 P06753 MAD1L1 Homo sapiens Q9Y6D9 32296183
Intra
TPM3 P06753 MAD1L1 Homo sapiens Q9Y6D9 32296183
Intra
TPM3 P06753 IFIT3 Homo sapiens O14879 25910212
Intra
TPM3 P06753 IFIT3 Homo sapiens O14879 25910212
Intra
TPM3 P06753 IFIT3 Homo sapiens O14879
SLC
25910212
Intra
TPM3 P06753 IFIT3 Homo sapiens O14879 25910212
Intra
TPM3 P06753 TNNI1 Homo sapiens P19237 32296183
Intra
TPM3 P06753 TNNI1 Homo sapiens P19237 32296183
Intra
TPM3 P06753 TNNI1 Homo sapiens P19237 32296183
Intra
TPM3 P06753 C1orf216 Homo sapiens Q8TAB5 32296183
Intra
TPM3 P06753 LCA5L Homo sapiens O95447 31515488
Intra
TPM3 P06753 LCA5L Homo sapiens O95447 25416956
Intra
TPM3 P06753 TSKS Homo sapiens Q9UJT2 32296183
Intra
TPM3 P06753 ATXN1 Homo sapiens P54253 32814053
Intra
TPM3 P06753 ATXN1 Homo sapiens P54253 32814053
Intra
TPM3 P06753 ATXN1 Homo sapiens P54253 32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant TPM3 Proteins

Cat. No. Product Name Accession Purity
HY-P71083 TPM3 Protein, Human P06753-2 (M1-M248) ≥ 90%, as determined by reducing SDS-PAGE.

TPM3 Antibodies

Cat. No. Product Name Application Reactivity
HY-P810812 Tropomyosin 3 Antibody (YA10055) WB Human, Mouse

Related Diseases

Diseases Alias
Nemaline Myopathy 1
  • Cap Myopathy 1

  • NEM1

  • Nemaline Myopathy 1, Autosomal Dominant Or Recessive

  • Nemaline Myopathy, Type 1

  • CAPM1

  • Cap Disease

  • Cap Myopathy Tpm3-Related

  • Nemaline Myopathy 1 Autosomal Dominant Or Recessive

  • Myopathy, Nemaline, Type 1

  • Cap Myopathy

Myopathy, Congenital, With Fiber-Type Disproportion
  • CFTD

  • Fiber-Type Disproportion Myopathy, Congenital

  • Cftdm

  • Myopathy, Congenital, With Fiber-Type Disproportion 1

  • Congenital Fiber-Type Disproportion Myopathy

  • Myopathy, Congenital, With Fiber Type Disproportion

Congenital Fiber-Type Disproportion
  • Congenital Fiber Type Disproportion

  • Cftdm

  • Congenital Myopathy With Fiber Type Disproportion

  • Cftd

  • Congenital Fiber-Type Disproportion Myopathy

  • Fiber-Type Disproportion Myopathy, Congenital

  • Myopathy, Congenital With Fiber-Type Disproportion

Cap Myopathy
  • Cap Disease

  • Congenital Myopathy With Caps

Congenital Generalized Hypercontractile Muscle Stiffness Syndrome
Inflammatory Myofibroblastic Tumor
  • Inflammatory Fibrosarcoma

Intermediate Congenital Nemaline Myopathy
  • Intermediate Nemaline Myopathy

  • Intermediate Congenital Nm

Childhood-Onset Nemaline Myopathy
  • Mild Nemaline Myopathy

  • Nemaline Myopathy, Childhood Onset

Myopathy
  • Muscular Diseases

  • Myopathies

Lipofibromatosis-Like Neural Tumor
Congenital Fibrosarcoma
  • Infantile Fibrosarcoma

Childhood Fibrosarcoma
  • Pediatric Fibrosarcoma

Epithelioid Inflammatory Myofibroblastic Sarcoma
Congenital Structural Myopathy
Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome
  • Jacobs Syndrome

  • Arthropathy-Camptodactyly Syndrome

  • Pericarditis-Arthropathy-Camptodactyly Syndrome

  • Xyy Syndrome

  • Pac Syndrome

  • Cacp Syndrome

  • CACP

  • Fibrosing Serositis, Familial

  • Camptodactyly-Arthropathy-Pericarditis Syndrome

  • Cap Syndrome

  • 47, Xyy Syndrome

  • 47,Xyy Syndrome

  • Double Y Syndrome

  • Camptodactyly-Arthropathy-Coxa-Vara-Pericarditis Syndrome

  • Hypertrophic Synovitis, Congenital Familial

  • Congenital Familial Hypertrophic Synovitis

  • Xyy Karyotype

  • Y Disomy

  • Yy Syndrome

  • Familial Fibrosing Serositis

  • Disomy Y

  • Double Y

  • Camptodactyly Arthropathy Coxa Vara Pericarditis Syndrome

  • Arthropathy Camptodactyly Syndrome

  • Camptodactyly Arthropathy Pericarditis Syndrome

  • Pericarditis Arthropathy Camptodactyly Syndrome

  • Jacob'S Syndrome

  • 47,Xyy

  • Cdags Syndrome

Congenital Mesoblastic Nephroma
  • Mesoblastic Nephroma

  • Nephroma, Mesoblastic

Spitzoid Melanoma
  • Atypical Spitz Nevus

Mesenchymal Cell Neoplasm
  • Benign Miscellaneous Mesenchymal Tumor

  • Mesenchymal Tumor

  • Mesenchymal Tumors

Infantile Myofibromatosis
  • Lipofibromatosis

  • Myofibromatosis

Pulmonary Plasma Cell Granuloma
  • Plasma Cell Granuloma, Pulmonary

  • Granuloma, Plasma Cell, Pulmonary

  • Lymphocytic Pseudotumor Of Lung

  • Sclerosing Hemangiocytoma Of Lung

Childhood Kidney Cell Carcinoma
  • Pediatric Renal Cell Carcinoma

  • Childhood Renal Cell Carcinoma

Nemaline Myopathy 2
  • NEM2

  • Nemaline Myopathy 2, Autosomal Recessive

  • Nemaline Myopathy, Type 2

  • Neb-Related Nemaline Myopathy

  • Myopathy, Nemaline, Type 2

Hypotonia
Batten-Turner Congenital Myopathy
  • Congenital Myopathy

  • Batten Turner Congenital Myopathy

  • Myopathy Congenital

  • Myopathy, Congenital

  • Myotonia Congenita

  • Benign Congenital Myopathy

Mammary Analogue Secretory Carcinoma
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

Distal Arthrogryposis
  • Arthrogryposis Multiplex Congenita

  • Arthrogryposis

  • Congenital Multiple Arthrogryposis

  • Congenital Arthromyodysplasia

  • Fibrous Ankylosis Of Multiple Joints

  • Guerin-Stern Syndrome

  • Guérin-Stern Syndrome

  • Myodystrophia Fetalis Deformans

  • Otto Syndrome

  • Rocher-Sheldon Syndrome

  • Rossi Syndrome

  • Amc

  • Multiple Congenital Arthrogryposis

  • Arthrogryposis Syndrome

  • Arthrogryposis, Distal

  • Distal Arthrogryposis Syndrome

  • Freeman-Sheldon Syndrome

  • Arthrogryposis, Distal, Type 2b

  • Congenital Multiplex Arthrogryposis

  • Amyoplasia Congenita

  • Congenital Amyoplasia

  • Amc - [Arthrogryposis Multiplex Congenita]

Kidney Cortex Disease
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

Retinitis Pigmentosa
  • RP

  • Rod-Cone Dystrophy

  • Autosomal Recessive Retinitis Pigmentosa

  • Non-Syndromic Retinitis Pigmentosa

  • Pericentral Pigmentary Retinopathy

  • Pigmentary Retinopathy

  • Tapetoretinal Degeneration

  • Rcd

  • Retinitis Pigmentosa Autosomal Recessive

  • ARRP

  • Retinitis Pigmentosa, Autosomal Recessive

  • Retinitis Pigmentosa 1

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
Canis familiaris TPM3 VGNC VGNC:47743
Rattus norvegicus TPM3 RGD RGD:621546
Mus musculus TPM3 MGD MGI:1890149
Bos taurus TPM3 VGNC VGNC:36253
Felis catus TPM3 VGNC VGNC:107956
Macaca mulatta TPM3 VGNC VGNC:78635
Others TPM3 NCBI