POPDC2 - popeye domain containing 2 Gene

Homo sapiens

Also known as POP2

Gene ID: 64091 | Gene type: protein coding

About POPDC2

Cytogenetic location: 3q13.33 Genomic coordinates (GRCh38): 3:119,642,056-119,660,883 (from NCBI)

This gene has 9 transcripts (splice variants), 210 orthologues and 2 paralogues. Biased expression in heart (RPKM 152.4), urinary bladder (RPKM 12.2) and 2 other tissues.

Summary

This gene encodes a member of the POP family of proteins which contain three putative transmembrane domains. This membrane associated protein is predominantly expressed in skeletal and cardiac muscle, and may have an important function in these tissues. [provided by RefSeq, Jul 2008]

POPDC2 Products(3)

mRNA	Protein	Name
NM_001308333.2	NP_001295262.1	popeye domain-containing protein 2 isoform 2
NM_001369919.2	NP_001356848.1	popeye domain-containing protein 2 isoform 3
NM_022135.4	NP_071418.2	popeye domain-containing protein 2 isoform 1

POPDC2 Protein Structure

Popeye

0
100
200
300
364 a.a.

Protein Preferred Names

Protein Names

popeye domain-containing protein 2

popeye protein 2

Related Diseases

Diseases

Alias

Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2x

Lgmd2x

Muscular Dystrophy, Limb-Girdle, Type 2x

Sinoatrial Node Disease

Sa Node	Sinuatrial Node
Sinus Node Dysfunction

King-Denborough Syndrome

King Denborough Syndrome	King Syndrome
Kousseff Nichols Syndrome	KDS
Noonan Like Contracture Myopathy Hyperpyrexia	Anesthetic-Induced Malignant Hyperpyrexia In Children
Koussef-Nichols Syndrome

Sick Sinus Syndrome

Sinus Node Dysfunction	Sinus Node Disease
Sinus Node Infection	Snd
Sss	Snd - [Sinus Node Dysfunction]
Sinoatrial Node Dysfunction	Sss - [Sick Sinus Syndrome]
Sick Sinus	Sick Sinus Tachycardia

Atrioventricular Block

Av Block

Chronic Atrial And Intestinal Dysrhythmia

CAID	Caid Syndrome
Cohesinopathy Affecting Heart And Gut Rhythm	Chronic Atrial Intestinal Dysrhythmia Syndrome
Chronic Atrial And Intestinal Dysrhythmia Syndrome	Chronic Atrial Dysrhythmia-Intestinal Motility Disorder
Dysrhythmia, Atrial And Intestinal, Chronic

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]

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

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS10879	POPDC2 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	POPDC2	MGD	MGI:1930150
Canis familiaris	POPDC2	VGNC	VGNC:56134
Felis catus	POPDC2	VGNC	VGNC:64300
Rattus norvegicus	POPDC2	RGD	RGD:735226
Macaca mulatta	POPDC2	VGNC	VGNC:76048
Bos taurus	POPDC2	VGNC	VGNC:33167

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