1. Gene
  2. MYOZ1 - myozenin 1 Gene

MYOZ1 - myozenin 1 Gene

Homo sapiens

Also known as CS-2; FATZ; MYOZ

Gene ID: 58529 | Gene type: protein coding

About MYOZ1

Cytogenetic location: 10q22.2 Genomic coordinates (GRCh38): 10:73,631,612-73,641,474 (from NCBI)

This gene has 1 transcript (splice variant), 275 orthologues and 2 paralogues. Biased expression in esophagus (RPKM 24.9), prostate (RPKM 22.9) and 4 other tissues.

Summary

The protein encoded by this gene is primarily expressed in the skeletal muscle, and belongs to the myozenin family. Members of this family function as calcineurin-interacting proteins that help tether Calcineurin to the sarcomere of cardiac and skeletal muscle. They play an important role in modulation of Calcineurin signaling. [provided by RefSeq, Apr 2012]

MYOZ1 Products(1)

mRNA Protein Name
NM_021245.4 NP_067068.1 myozenin-1
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables FATZ binding IDA
IDA: Inferred from direct assay
10984498 GOA
enables actinin binding EXP
EXP: Inferred from Experiment
34049882 GOA
enables actinin binding IMP
IMP: Inferred from mutant phenotype
34049882 GOA
enables actinin binding IPI
IPI: Inferred from physical interaction
34049882 GOA
enables molecular condensate scaffold activity IDA
IDA: Inferred from direct assay
34049882 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
10427098 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

MYOZ1 Protein Structure

Calsarcin

Calsarcin: Calcineurin-binding protein (Calsarcin) (1 - 299)

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

myozenin-1

calsarcin-2

MYOZ1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
MYOZ1 Q9NP98 KRTAP12-2 Homo sapiens P59991 32296183
Intra
MYOZ1 Q9NP98 KRTAP12-2 Homo sapiens P59991 32296183
Intra
MYOZ1 Q9NP98 KRT34 Homo sapiens O76011 32296183
Intra
MYOZ1 Q9NP98 KRT34 Homo sapiens O76011 32296183
Intra
MYOZ1 Q9NP98 GOLGA6A Homo sapiens Q9NYA3 32296183
Intra
MYOZ1 Q9NP98 GOLGA6A Homo sapiens Q9NYA3 32296183
Intra
MYOZ1 Q9NP98 GOLGA6A Homo sapiens Q9NYA3 32296183
Intra
MYOZ1 Q9NP98 KRT36 Homo sapiens O76013-2 32296183
Intra
MYOZ1 Q9NP98 KRT36 Homo sapiens O76013-2 32296183
Intra
MYOZ1 Q9NP98 WWOX Homo sapiens Q9NZC7-5 32296183
Intra
MYOZ1 Q9NP98 WWOX Homo sapiens Q9NZC7-5 32296183
Intra
MYOZ1 Q9NP98 WWOX Homo sapiens Q9NZC7-5 32296183
Intra
MYOZ1 Q9NP98 VAC14 Homo sapiens Q08AM6 32296183
Intra
MYOZ1 Q9NP98 VAC14 Homo sapiens Q08AM6 32296183
Intra
MYOZ1 Q9NP98 LHX4 Homo sapiens Q969G2 32296183
Intra
MYOZ1 Q9NP98 LHX4 Homo sapiens Q969G2 32296183
Intra
MYOZ1 Q9NP98 ACTN3 Homo sapiens Q08043 32296183
Intra
MYOZ1 Q9NP98 ACTN3 Homo sapiens Q08043 32296183
Intra
MYOZ1 Q9NP98 BAG4 Homo sapiens O95429 32296183
Intra
MYOZ1 Q9NP98 BAG4 Homo sapiens O95429 32296183
Intra
MYOZ1 Q9NP98 PNMA1 Homo sapiens Q8ND90 32296183
Intra
MYOZ1 Q9NP98 PNMA1 Homo sapiens Q8ND90 32296183
Intra
MYOZ1 Q9NP98 ACTN1 Homo sapiens P12814 32296183
Intra
MYOZ1 Q9NP98 ACTN1 Homo sapiens P12814 32296183
Intra
MYOZ1 Q9NP98 PFDN5 Homo sapiens Q99471 32296183
Intra
MYOZ1 Q9NP98 PFDN5 Homo sapiens Q99471 32296183
Intra
MYOZ1 Q9NP98 VBP1 Homo sapiens P61758 32296183
Intra
MYOZ1 Q9NP98 VBP1 Homo sapiens P61758 32296183
Intra
MYOZ1 Q9NP98 AKAP8L Homo sapiens Q9ULX6 32296183
Intra
MYOZ1 Q9NP98 AKAP8L Homo sapiens Q9ULX6 32296183
Intra
MYOZ1 Q9NP98 AKAP8L Homo sapiens Q9ULX6 32296183
Intra
MYOZ1 Q9NP98 TRAF1 Homo sapiens Q13077 32296183
Intra
MYOZ1 Q9NP98 TRAF1 Homo sapiens Q13077 32296183
Intra
MYOZ1 Q9NP98 EXOSC8 Homo sapiens Q96B26 32296183
Intra
MYOZ1 Q9NP98 EXOSC8 Homo sapiens Q96B26 32296183
Intra
MYOZ1 Q9NP98 CEACAM6 Homo sapiens P40199 32296183
Intra
MYOZ1 Q9NP98 CEACAM6 Homo sapiens P40199 32296183
Intra
MYOZ1 Q9NP98 TRIM63 Homo sapiens Q969Q1 18157088
Intra
MYOZ1 Q9NP98 EIF3F Homo sapiens O00303 32296183
Intra
MYOZ1 Q9NP98 EIF3F Homo sapiens O00303 32296183
Intra
MYOZ1 Q9NP98 WASHC3 Homo sapiens Q9Y3C0 32296183
Intra
MYOZ1 Q9NP98 WASHC3 Homo sapiens Q9Y3C0 32296183
Intra
MYOZ1 Q9NP98 WASHC3 Homo sapiens Q9Y3C0 32296183
Intra
MYOZ1 Q9NP98 USHBP1 Homo sapiens Q8N6Y0 32296183
Intra
MYOZ1 Q9NP98 USHBP1 Homo sapiens Q8N6Y0 32296183
Intra
MYOZ1 Q9NP98 TRIM23 Homo sapiens P36406 32296183
Intra
MYOZ1 Q9NP98 TRIM23 Homo sapiens P36406 32296183
Intra
MYOZ1 Q9NP98 LZTS2 Homo sapiens Q9BRK4 32296183
Intra
MYOZ1 Q9NP98 LZTS2 Homo sapiens Q9BRK4 32296183
Intra
MYOZ1 Q9NP98 CEP76 Homo sapiens Q8TAP6 32296183
Intra
MYOZ1 Q9NP98 CEP76 Homo sapiens Q8TAP6 32296183
Intra
MYOZ1 Q9NP98 CRX Homo sapiens O43186 32296183
Intra
MYOZ1 Q9NP98 CRX Homo sapiens O43186 32296183
Intra
MYOZ1 Q9NP98 PLEKHG4 Homo sapiens Q58EX7 32296183
Intra
MYOZ1 Q9NP98 PLEKHG4 Homo sapiens Q58EX7 32296183
Intra
MYOZ1 Q9NP98 FLNA Homo sapiens P21333-2 32814053
Intra
MYOZ1 Q9NP98 FLNA Homo sapiens P21333-2 32296183
Intra
MYOZ1 Q9NP98 FLNA Homo sapiens P21333-2 32814053
Intra
MYOZ1 Q9NP98 FLNA Homo sapiens P21333-2 32814053
Intra
MYOZ1 Q9NP98 FLNA Homo sapiens P21333-2 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Myopathy, Myofibrillar, 4

Myofibrillar Myopathy 4

MFM4

Zaspopathy

Myopathy, Myofibrillar, Zasp-Related

Myopathy, Spheroid Body

Spheroid Body Myopathy

Autosomal Dominant Spheroid Body Myopathy

SBM

Myopathy, Myofibrillar, 3

Myotilinopathy

Myofibrillar Myopathy 3

MFM3

Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1a

Lgmd1a

Muscular Dystrophy, Limb-Girdle, Type 1a

Myopathy, Myofibrillar, Myotilin-Related

Muscular Dystrophy, Limb-Girdle, Type 1, Formerly

Lgmd1, Formerly

Muscular Dystrophy, Limb-Girdle, Type 1a, Formerly

Lgmd1a, Formerly

Qualitative Or Quantitative Defects Of Myotilin

Limb-Girdle Muscular Dystrophy Due To Myotilin Deficiency

Distal Myotilinopathy

Lgmd1

Limb-Girdle Muscular Dystrophy 1a

Mfm Myotilin-Related

Muscular Dystrophy, Limb-Girdle, Type 1

Myopathy Myofibrillar Myotylin-Related

Myopathy, Myofibrillar, Type 3

Myopathy, Myofibrillar, 5

Myofibrillar Myopathy 5

MFM5

Myopathy, Myofibrillar, Filamin C-Related

Filaminopathy, Autosomal Dominant

Filaminopathy

Muscle Filaminopathy

Autosomal Dominant Filaminopathy

Mfm Filamin C-Related

Myopathy Myofibrillar Filamin C-Related

Myopathy, Myofibrillar, Type 5

Myofibrillar Myopathy

Desmin Related Myopathy

Myotilinopathy

Myopathy, Myofibrillar

Alpha Beta Crystallinopathy

Desmin Storage Myopathy

Desminopathy

Filaminopathy

Protein Surplus Myopathy

Zaspopathy

Myofibrillar Myopathies

Myopathy, Myofibrillar, Desmin-Related

Myopathy, Desmin Storage

Mfm - [Myofibrillar Myopathy]

Cardiomyopathy, Dilated, 3b

Dilated Cardiomyopathy 3b

CMD3B

X-Linked Dilated Cardiomyopathy

Xlcm

Dmd-Associated Dilated Cardiomyopathy

Cardiomyopathy, Dilated, X-Linked

Dmd-Related Dilated Cardiomyopathy

Xldc

Cardiomyopathy, Dilated, X-Linked 3b

Cardiomyopathy, Dilated, Type 3b

Postural Orthostatic Tachycardia Syndrome

Irritable Heart

Mitral Valve Prolapse Syndrome

Neurocirculatory Asthenia

Orthostatic Intolerance Due To Net Deficiency

Familial Orthostatic Tachycardia Due To Norepinephrine Transporter Deficiency

Orhtostatic Intolerance

Postural Tachycardia Syndrome Due To Net Deficiency

Soldiers Heart

Myopathy

Muscular Diseases

Myopathies

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

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

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

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

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
Felis catus MYOZ1 VGNC VGNC:63693
Rattus norvegicus MYOZ1 RGD RGD:1561064
Bos taurus MYOZ1 VGNC VGNC:31840
Macaca mulatta MYOZ1 VGNC VGNC:74951
Mus musculus MYOZ1 MGD MGI:1929471
Canis familiaris MYOZ1 VGNC VGNC:43583