1. Gene
  2. PDE4B - phosphodiesterase 4B Gene

PDE4B - phosphodiesterase 4B Gene

Homo sapiens

Also known as DPDE4; PDEIVB

Gene ID: 5142 | Gene type: protein coding

About PDE4B

Cytogenetic location: 1p31.3 Genomic coordinates (GRCh38): 1:65,792,510-66,374,579 (from NCBI)

This gene has 18 transcripts (splice variants), 290 orthologues and 20 paralogues. Broad expression in bone marrow (RPKM 18.7), brain (RPKM 17.6) and 22 other tissues.

Summary

This gene is a member of the type IV, cyclic AMP (cAMP)-specific, cyclic nucleotide phosphodiesterase (PDE) family. The encoded protein regulates the cellular concentrations of cyclic nucleotides and thereby play a role in signal transduction. Altered activity of this protein has been associated with schizophrenia and bipolar affective disorder. Alternative splicing and the use of alternative promoters results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2014]

PDE4B Products(7)

mRNA Protein Name
NM_001037339.2 NP_001032416.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4B isoform 2
NM_001037340.3 NP_001032417.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4B isoform 3
NM_001037341.2 NP_001032418.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4B isoform 1
NM_001297440.2 NP_001284369.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4B isoform 4
NM_001297441.1 NP_001284370.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4B isoform 5
NM_001297442.2 NP_001284371.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4B isoform 6
NM_002600.4 NP_002591.2 cAMP-specific 3',5'-cyclic phosphodiesterase 4B isoform 1

PDE4B Protein Structure

PDEase_I

PDEase_I: 3'5'-cyclic nucleotide phosphodiesterase (405 - 649)

  • 0
  • 200
  • 400
  • 600
  • 736 a.a.
Protein Preferred Names Protein Names

cAMP-specific 3',5'-cyclic phosphodiesterase 4B

dunce-like phosphodiesterase E4

Recombinant PDE4B Proteins

Cat. No. Product Name Accession Purity
HY-P74646 PDE4B Protein, Human (sf9, His-GST) Q07343-2 (M1-T564) ≥95%

Related Diseases

Diseases Alias
Ocular Hypotension

Hypotony Of Eye

Schizophrenia

SCZD

Schizophrenia With Or Without An Affective Disorder

Schizophrenia 12

Schizophrenia, Susceptibility To

Schizophrenia-1

Dementia Praecox

Schizophrenia 1

Bipolar Disorder

Bipolar Depression

Manic Disorder

Depression, Bipolar

Bipolar Disorder Manic Phase

Depressive-Manic Psych.

Manic Bipolar Affective Disorder

Manic Bipolar I Disorder

Manic Depression

Manic Depressive Disorder

Mixed Bipolar Disorder

Bipolar Affective Disorder

Bipolar Affective Psychosis

Bipolar Spectrum Disorder

Manic Depressive Illness

Depression Bipolar

Bipolar Disorder, Mixed

Major Affective Disorder

Major Affective Disorder 1

Major Affective Disorder 2

Brugada Syndrome 3

BRGDA3

Brugada Syndrome, Type 3

Impotence

Erectile Dysfunction

Sexual Impotence

Erectile Dysfunction Adverse Event

Severe Congenital Neutropenia 8

Autosomal Dominant Severe Congenital Neutropenia 8 With Or Without Pancreatic Dysfunction And/Or Neurological Abnormalities

Scn8

Sdsl

Shwachman-Diamond Syndrome-Like

Acrodysostosis

Acrodysplasia

Arkless-Graham Syndrome

Maroteaux-Malamut Syndrome

Nasal Hypoplasia-Peripheral Dysostosis-Intellectual Disability Syndrome

Peripheral Dysostosis-Nasal Hypoplasia-Intellectual Disability Syndrome

Asthma

Chronic Obstructive Asthma

Asthma, Diminished Response To Antileukotriene Treatment In

Bronchial Hyperreactivity

Asthma, Susceptibility To

Asthma, Bronchial

Asthma, Protection Against

Asthma, Nocturnal, Susceptibility To

Nocturnal Asthma

Asthma-Related Traits

Asthma-Related Traits, Susceptibility To

Asthma, Nocturnal

Chronic Obstructive Asthma With Acute Exacerbation

Chronic Obstructive Asthma With Status Asthmaticus

Exercise Induced Asthma

Exercise-Induced Asthma

Bronchial Asthma

Asthma, Exercise-Induced

Idiosyncratic Asthma

Unspecified Asthma With Acute Exacerbation

Asthma, Unspecified, With Stated Status Asthmaticus

Status Asthmaticus Nos

Acute Severe Asthma

Acute Severe Bronchial Asthma

Status Asthma

Status Post Asthmaticus

Autosomal Dominant Severe Congenital Neutropenia

Severe Congenital Neutropenia Autosomal Dominant

Neutropenia, Congenital, Severe, Autosomal Dominant

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
Macaca mulatta PDE4B VGNC VGNC:75916
Rattus norvegicus PDE4B RGD RGD:3280
Bos taurus PDE4B VGNC VGNC:32676
Felis catus PDE4B VGNC VGNC:82496
Mus musculus PDE4B MGD MGI:99557
Canis familiaris PDE4B VGNC VGNC:44354