1. Gene
  2. CALM3 - calmodulin 3 Gene

CALM3 - calmodulin 3 Gene

Homo sapiens

Also known as CaM; CALM; CAM1; CAM2; CAMB; PHKD; CPVT6; LQT16; PHKD3; CaMIII; HEL-S-72

Gene ID: 808 | Gene type: protein coding

About CALM3

Cytogenetic location: 19q13.32 Genomic coordinates (GRCh38): 19:46,601,074-46,610,782 (from NCBI)

This gene has 13 transcripts (splice variants), 195 orthologues, 20 paralogues and is associated with 5 phenotypes. Ubiquitous expression in brain (RPKM 470.4), testis (RPKM 108.1) and 23 other tissues.

Summary

This gene encodes a member of a family of proteins that binds calcium and functions as a enzymatic co-factor. Activity of this protein is important in the regulation of the cell cycle and cytokinesis. Multiple alternatively spliced transcript variants have been observed at this gene. [provided by RefSeq, Aug 2016]

CALM3 Products(7)

mRNA Protein Name
NM_001329921.1 NP_001316850.1 calmodulin-3 isoform 2
NM_001329922.1 NP_001316851.1 calmodulin-3 isoform 1
NM_001329923.1 NP_001316852.1 calmodulin-3 isoform 2
NM_001329924.2 NP_001316853.1 calmodulin-3 isoform 2
NM_001329925.2 NP_001316854.1 calmodulin-3 isoform 2
NM_001329926.2 NP_001316855.1 calmodulin-3 isoform 2
NM_005184.4 NP_005175.2 calmodulin-3 isoform 1
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables adenylate cyclase activator activity IDA
IDA: Inferred from direct assay
11807546 GOA
enables adenylate cyclase binding IPI
IPI: Inferred from physical interaction
11807546 GOA
enables calcium ion binding IDA
IDA: Inferred from direct assay
7607248 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
3111527 GOA
enables protein kinase binding IPI
IPI: Inferred from physical interaction
20668654 GOA
enables protein phosphatase activator activity IDA
IDA: Inferred from direct assay
8631777 GOA
enables protein serine/threonine kinase activator activity IDA
IDA: Inferred from direct assay
35568036 GOA
enables titin binding IPI
IPI: Inferred from physical interaction
7607248 GOA
enables transmembrane transporter binding IPI
IPI: Inferred from physical interaction
21167176 GOA
Biological Process GO Annotation Evidence Reference Source
involved in detection of calcium ion IMP
IMP: Inferred from mutant phenotype
23040497 GOA
involved in negative regulation of high voltage-gated calcium channel activity IMP
IMP: Inferred from mutant phenotype
31454269 GOA
involved in positive regulation of cyclic-nucleotide phosphodiesterase activity IDA
IDA: Inferred from direct assay
8631777 GOA
involved in positive regulation of ryanodine-sensitive calcium-release channel activity IDA
IDA: Inferred from direct assay
20226167 GOA
involved in regulation of cardiac muscle cell action potential IMP
IMP: Inferred from mutant phenotype
31454269 GOA
involved in regulation of cardiac muscle contraction IMP
IMP: Inferred from mutant phenotype
23040497 GOA
involved in regulation of cytokinesis IMP
IMP: Inferred from mutant phenotype
16760425 GOA
involved in regulation of heart rate IMP
IMP: Inferred from mutant phenotype
23040497 GOA
involved in regulation of release of sequestered calcium ion into cytosol by sarcoplasmic reticulum IDA
IDA: Inferred from direct assay
20226167 GOA
involved in response to calcium ion IDA
IDA: Inferred from direct assay
7607248 GOA
Cellular Component GO Annotation Evidence Reference Source
part of calcium channel complex IDA
IDA: Inferred from direct assay
23040497 GOA
part of catalytic complex IDA
IDA: Inferred from direct assay
11807546 GOA
located in centrosome IDA
IDA: Inferred from direct assay
16760425 GOA
part of protein-containing complex IDA
IDA: Inferred from direct assay
19855925 GOA
located in sarcomere IDA
IDA: Inferred from direct assay
20226167 GOA
located in spindle microtubule IDA
IDA: Inferred from direct assay
16760425 GOA
located in spindle pole IDA
IDA: Inferred from direct assay
16760425 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

CALM3 Protein Structure

EF-hand_7

EF-hand_7: EF-hand domain pair (14 - 73)

EF-hand_7

EF-hand_7: EF-hand domain pair (86 - 146)

  • 0
  • 100
  • 149 a.a.
Protein Preferred Names Protein Names

calmodulin-3

Calmodulin-1

Recombinant CALM3 Proteins

Cat. No. Product Name Accession Purity
HY-P7710 Calmodulin Protein, Human P0DP23 (M1-K149) ≥95%
HY-P75461 CALM2 Protein, Human (His) P0DP24 (M1-K149) ≥95%

CALM3 Antibodies

Cat. No. Product Name Application Reactivity
HY-P82082 Calmodulin Antibody (YA1827) WB, IHC-P, ICC/IF, IP, FC Human, Mouse, Rat

Related Diseases

Diseases Alias
Long Qt Syndrome 16

Ventricular Tachycardia, Catecholaminergic Polymorphic, 6

LQT16

Ventricular Tachycardia, Catecholaminergic Polymorphic 6

CPVT6

Long Qt Syndrome 1

Romano-Ward Syndrome

LQT1

Ward-Romano Syndrome

Rws

Ventricular Fibrillation With Prolonged Qt Interval

Wrs

Long Qt Syndrome 1, Acquired, Susceptibility To

Long Qt Syndrome 1, Acquired

Romano-Ward Long Qt Syndrome

Long Qt Syndrome Type 1

Long Qt Syndrome-1

Acquired Susceptibility To Long Qt Syndrome 1

Qt Syndrome, Long, Type 1

Catecholaminergic Polymorphic Ventricular Tachycardia

Cpvt

Catecholamine-Induced Polymorphic Ventricular Tachycardia

Familial Polymorphic Ventricular Tachycardia

Malignant Paroxysmal Ventricular Tachycardia

Multifocal Ventricular Premature Beats

Stress-Induced Polymorphic Ventricular Tachycardia

Bidirectional Tachycardia Induced By Catecholamine

Double Tachycardia Induced By Catecholamines

Polymorphic Catecholergic Ventricular Tachycardia

Syncopal Paroxysmal Tachycardia

Bidirectional Tachycardia Induced By Catecholamines

Fpvt

Bidirectional Ventricular Tachycardia Induced By Catecholamine

Polymorphic Ventricular Tachycardia Induced By Catecholamines

Ventricular Tachycardia, Catecholaminergic Polymorphic

Ventricular Tachycardia, Catecholaminergic Polymorphic, 1

Familial Ventricular Tachycardia

Multifocal Pvcs

Multifocal Premature Ventricular Beats

Long Qt Syndrome

Romano-Ward Syndrome

Long Q-T Syndrome

Lqt

Qt Syndrome, Long

Congenital Long Qt Syndrome

Familial Long Qt Syndrome

Long Qt Syndrome 14

LQT14

Long Qt Syndrome, Type 14

Long Qt Syndrome 15

LQT15

Long Qt Syndrome, Type 15

Cardiac Arrest

Cardiopulmonary Arrest

Circulatory Arrest

Heart Arrest

Flying Phobia

Aerophobia

Medulloblastoma Shh Activated And Tp53 Mutant
Diamond-Blackfan Anemia 3

DBA3

Anemia, Diamond-Blackfan, 3

Rps24-Related Diamond-Blackfan Anemia

Anemia Diamond-Blackfan 3

Anemia, Diamond-Blackfan, Type 3

Medulloblastoma Non-Wnt/Non-Shh
Long Qt Syndrome 2

LQT2

Long Qt Syndrome, Acquired, Reduced Susceptibility To

Long Qt Syndrome 1/2

Long Qt Syndrome 2/3

Long Qt Syndrome 2/5

Long Qt Syndrome 2, Acquired, Susceptibility To

Long Qt Syndrome, Acquired, Reduced

Long Qt Syndrome Type 2

Long Qt Syndrome 2/9

Lqt1/2

Lqt2/3

Lqt2/5

Lqt2/9

Susceptibility To Acquired Long Qt Syndrome 2

Long Qt Syndrome-2

Qt Syndrome, Long, Type 2

Long Qt Syndrome 1-2

Long Qt Syndrome 2-3

Long Qt Syndrome 2-5

Long Qt Syndrome 9

Vascular Disease

Vascular Diseases

Aneurysm

Spinal Cord Ischemia

Vascular Anomaly

Spinal Cord Vascular Diseases

Vascular Tissue Disease

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]

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

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
Mus musculus CALM3 MGD MGI:103249
Rattus norvegicus CALM3 RGD RGD:2259