POPDC2 - popeye domain containing 2 Gene

Also Known as POP2

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 64091

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

Popeye: Popeye protein conserved region (107 - 259)

  • 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

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
Others POPDC2 NCBI