PDE4D - phosphodiesterase 4D Gene

Also Known as DPDE3; PDE43; STRK1; ACRDYS2; HSPDE4D; PDE4DN2

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 5144

About PDE4D

Cytogenetic location: 5q11.2-q12.1 Genomic coordinates (GRCh38): 5:58,969,038-60,522,128 (from NCBI)

This gene has 28 transcripts (splice variants), 243 orthologues, 20 paralogues and is associated with 5 phenotypes. Broad expression in bone marrow (RPKM 7.8), lung (RPKM 3.1) and 20 other tissues.

Summary

This gene encodes one of four mammalian counterparts to the fruit fly 'dunce' gene. The encoded protein has 3',5'-cyclic-AMP phosphodiesterase activity and degrades cAMP, which acts as a signal transduction molecule in multiple cell types. This gene uses different promoters to generate multiple alternatively spliced transcript variants that encode functional proteins.[provided by RefSeq, Sep 2009]

PDE4D Products (18)

mRNA Protein Name
NM_001104631.2 NP_001098101.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform PDE4D4
NM_001165899.2 NP_001159371.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform PDE4D7
NM_001197218.2 NP_001184147.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform PDE4D5
NM_001197219.2 NP_001184148.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform PDE4D8
NM_001197220.2 NP_001184149.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform PDE4D9
NM_001197221.2 NP_001184150.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform PDE4D2
NM_001197222.2 NP_001184151.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform PDE4D1
NM_001197223.2 NP_001184152.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform PDE4D6
NM_001349241.2 NP_001336170.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform 10
NM_001349242.2 NP_001336171.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform 11
NM_001349243.2 NP_001336172.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform 12
NM_001364599.1 NP_001351528.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform PDE4D7
NM_001364600.2 NP_001351529.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform 14
NM_001364601.1 NP_001351530.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform 15
NM_001364602.2 NP_001351531.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform 16
NM_001364603.1 NP_001351532.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform PDE4D2
NM_001364604.1 NP_001351533.1 cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform 12
NM_006203.5 NP_006194.2 cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform PDE4D3
Molecular Function GO Annotation Evidence References Source
enables 3',5'-cyclic-AMP phosphodiesterase activity IDA
IDA: Inferred from direct assay
9371713 GOA
enables 3',5'-cyclic-AMP phosphodiesterase activity IGI
IGI: Inferred from genetic interaction
8413254 GOA
enables ATPase binding IPI
IPI: Inferred from physical interaction
21903937 GOA
enables cAMP binding IDA
IDA: Inferred from direct assay
9371713 GOA
enables heterocyclic compound binding IPI
IPI: Inferred from physical interaction
9371713 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
17620599 GOA
enables scaffold protein binding IPI
IPI: Inferred from physical interaction
15182229 GOA
enables transmembrane transporter binding IPI
IPI: Inferred from physical interaction
16213210 GOA
Cellular Component GO Annotation Evidence References Source
part of calcium channel complex IDA
IDA: Inferred from direct assay
16213210 GOA
located in cytosol IDA
IDA: Inferred from direct assay
9371713 GOA
NOT located in membrane IDA
IDA: Inferred from direct assay
9371713 GOA
located in membrane IDA
IDA: Inferred from direct assay
9371713 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

PDE4D Protein Structure

PDEase_I

PDEase_I: 3'5'-cyclic nucleotide phosphodiesterase (461 - 705)

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

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

  • cAMP-specific phosphodiesterase PDE4D6

PDE4D Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
PDE4D Q08499 GOLGA8F Homo sapiens Q08AF8 25416956
Intra
PDE4D Q08499 GOLGA8DP Homo sapiens Q0D2H9 25416956
Intra
PDE4D Q08499 GOLGA8DP Homo sapiens Q0D2H9 25416956
Intra
PDE4D Q08499 GOLGA8DP Homo sapiens Q0D2H9 25416956
Intra
PDE4D Q08499 MAGEA6 Homo sapiens P43360 25416956
Intra
PDE4D Q08499 PDE4B Homo sapiens Q07343 33961781
Intra
PDE4D Q08499 TRAF1 Homo sapiens Q13077 25416956
Intra
PDE4D Q08499 TRAF1 Homo sapiens Q13077 25416956
Intra
PDE4D Q08499 COIL Homo sapiens P38432 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

PDE4D Antibodies

Cat. No. Product Name Application Reactivity
HY-P81969 PDE4D Antibody (YA1714) WB Human

Related Diseases

Diseases Alias
Acrodysostosis 2 With Or Without Hormone Resistance
  • ACRDYS2

  • Acrodysostosis 2, With Or Without Hormone Resistance

  • Acrodysostosis, With/Without Hormone Resistance, Type 2

  • Acrodysostosis

Acrodysostosis With Multiple Hormone Resistance
Acrodysostosis
  • Acrodysplasia

  • Arkless-Graham Syndrome

  • Maroteaux-Malamut Syndrome

  • Nasal Hypoplasia-Peripheral Dysostosis-Intellectual Disability Syndrome

  • Peripheral Dysostosis-Nasal Hypoplasia-Intellectual Disability Syndrome

Chromosome 5q12 Deletion Syndrome
  • Pde4d Haploinsufficiency Syndrome

Pseudohypoparathyroidism
  • Familial Pseudohypoparathyroidism

  • Parathyroid Hormone Resistant Hypoparathyroidism

  • Php - [Pseudohypoparathyroidism]

  • Constitutional Chronic Hypocalcaemia

Stroke, Ischemic
  • Cerebral Infarction

  • Stroke

  • Ischemic Stroke

  • Cerebrovascular Accident

  • Cerebral Infarction, Susceptibility To

  • Stroke, Ischemic, Susceptibility To

  • Cerebral Infarct

  • Ischemic Stroke, Susceptibility To

  • Stroke, Susceptibility To

  • Cva - Cerebral Infarction

  • ISCHSTR

  • Ischemic Cerebrovascular Accident

Ocular Hypotension
  • Hypotony Of Eye

Spinal Stenosis
  • Lumbar Spinal Stenosis

  • Cervical Spinal Stenosis

  • Spinal Stenosis Of Lumbar Region

  • Spinal Stenosis In Cervical Region

  • Spinal Canal Stenosis

Brachydactyly
Hypertension And Brachydactyly Syndrome
  • Brachydactyly With Hypertension

  • Bilginturan Syndrome

  • HTNB

  • Brachydactyly-Arterial Hypertension Syndrome

  • Brachydactyly, Type E, With Short Stature And Hypertension

  • Bilginturan Brachydactyly

  • Brachydactyly Type E With Short Stature And Hypertension

  • Type E Brachydactyly With Short Stature And Hypertension

  • Brachydactyly Type E, With Short Stature And Hypertension

  • Hypertension With Brachydactyly

Hypothyroidism, Congenital, Nongoitrous, 1
  • Tsh Resistance

  • CHNG1

  • Hypothyroidism Due To Tsh Receptor Mutations

  • Thyrotropin Resistance

  • Thyroid-Stimulating Hormone

  • Rtsh

  • Hypothyroidism Due To Unresponsiveness To Thyrotropin

  • Congenital Nongoitrous Hypothyroidism 1

  • Thyroid-Stimulating Hormone, Resistance To

  • Hypothyroidism, Nonautoimmune

  • Hypothyroidism, Congenital, Due To Tsh Resistance

  • Hypothyroidism, Congenital, Non-Goitrous, 1

  • Congenital Hypothyroidism Due To Tsh Resistance

  • Non-Autoimmune Hypothyroidism

  • Thyroid-Stimulating Hormone Resistance

  • Hypothyroidism, Congenital, Nongoitrous, Type 1

  • Hypothyroidism, Congenital, Nongoitrous, 3

  • Thyroid Hormone Resistance Syndrome

Pseudohypoparathyroidism, Type Ia
  • Albright'S Hereditary Osteodystrophy

  • Albright Hereditary Osteodystrophy

  • Pseudohypoparathyroidism Type 1a

  • PHP1A

  • Albright Hereditary Osteodystrophy With Multiple Hormone Resistance

  • Pseudohypoparathyroidism Ia

  • AHO

  • Pseudohypoparathyroidism With Albright Hereditary Osteodystrophy

  • Pseudo-Pseudohypoparathyroidism

  • Pseudohypoparathyroidism Type I A

  • Php Ia

  • Pseudopseudohypoparathyroidism

  • Albright Hereditary Osteodystrophy Without Multiple Hormone Resistance

  • Pphp

  • Pseudopseudo-Hypoparathyroidism

  • Aho-Php Syndrome Ia

  • Albright Hereditary Osteodystrophy-Php Syndrome Ia

  • Pseudohypoparathyroidism 1a

  • Pseudohypoparathyroidism

Impotence
  • Erectile Dysfunction

  • Sexual Impotence

  • Erectile Dysfunction Adverse Event

Pseudopseudohypoparathyroidism
  • PPHP

  • Albright Hereditary Osteodystrophy Without Multiple Hormone Resistance

  • Normocalcemic Pseudohypoparathyroidism

  • Aho-Pphp Syndrome

  • Albright Hereditary Osteodystrophy-Pphp Syndrome

  • Pseudohypoparathyroidism

Chondrodysplasia, Blomstrand Type
  • Chondrodysplasia Blomstrand Type

  • BOCD

  • Blomstrand Lethal Chondrodysplasia

  • Blomstrand Lethal Osteochondrodysplasia

  • Blomstrand'S Lethal Chondrodysplasia

  • Blc

  • Blomstrand Chondrodysplasia

  • Blomstrand Osteochondrodysplasia

Osseous Heteroplasia, Progressive
  • Progressive Osseous Heteroplasia

  • POH

  • Osteoma Cutis

  • Familial Ectopic Ossification

  • Ectopic Ossification Familial Type

  • Ectopic Ossification

  • Heterotopic Ossification

  • Ectopic Ossification, Familial

  • Cutaneous Ossification

  • Myositis Ossificans Progressiva

  • Osteodermia

  • Osteosis Cutis

  • Ossification Heterotopic

  • Heteroplasia, Osseous, Progressive

  • Fibrodysplasia Ossificans Progressiva

Chromosome 2q37 Deletion Syndrome
  • Albright Hereditary Osteodystrophy-Like Syndrome

  • 2q37 Microdeletion Syndrome

  • Brachydactyly-Intellectual Disability Syndrome

  • Deletion 2q37

  • 2q37 Deletion Syndrome

  • Brachydactyly-Mental Retardation Syndrome

  • Bdmr

  • Albright Hereditary Osteodystrophy Type 3

  • Del(2)(Q37)

  • Monosomy 2q37qter

  • Albright'S Hereditary Osteodystrophy-Like Syndrome

  • Monosomy 2q37

  • Chromosome Deletion Syndrome 2q37

Pulmonary Disease, Chronic Obstructive
  • Chronic Obstructive Pulmonary Disease

  • COPD

  • Pulmonary Disease, Chronic Obstructive, Severe Early-Onset

  • Chronic Obstructive Lung Disease

  • Chronic Obstructive Airway Disease

  • Pulmonary Disease, Chronic Obstructive, Susceptibility To

  • Cold

  • Severe Early-Onset Chronic Obstructive Pulmonary Disease

  • Pulmonary Disease Chronic Obstructive

  • Pulmonary Disease, Obstructive, Chronic, Susceptibility To

  • Chronic Obstructive Pulmonary Disease Of Horses

  • Common Cold

  • Upper Respiratory Infections

  • Copd - [Chronic Obstructive Pulmonary Disease]

  • Coad - [Chronic Obstructive Airways Disease]

  • Cold - [Chronic Obstructive Lung Disease]

  • Chronic Airway Disease Nos

  • Chronic Airways Limitation, Unspecified

  • Chronic Obstructed Airway, Unspecified

  • Chronic Obstructive Airway Disease, Unspecified

  • Chronic Obstructive Airway, Unspecified

  • Obstructive Lung Disease Nos

  • Chronic Obstructive Lung Disease Nos

  • Chronic Obstructive Lung Nos

  • Obstructive Pulmonary Disease Nos

  • Exacerbation Copd Nos

  • Acute Exacerbation Copd

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

Pseudohypoparathyroidism, Type Ib
  • Pseudohypoparathyroidism Type 1b

  • PHP1B

  • Pseudohypoparathyroidism Ib

  • Pseudohypoparathyroidism Type Ib

  • Php Ib

  • Pseudohypoparathyroidism 1b

Myocardial Infarction
  • Heart Attack

  • Myocardial Infarction, Susceptibility To

  • Myocardial Infarction 1

  • Myocardial Infarction, Protection Against

  • Myocardial Infarction, Decreased Susceptibility To

  • Myocardial Infarction, Decreased

  • Myocardial Infarct

  • MCI1

  • Premature Myocardial Infarction

  • Myocardial Infarction, Susceptibility To, Type 1

Cerebral Palsy
  • Infantile Cerebral Palsy

  • Mixed Cerebral Palsy

  • Palsy Cerebral

  • Palsy, Cerebral

  • Cerebral Palsy, Mixed

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
Bos taurus PDE4D VGNC VGNC:32677
Felis catus PDE4D VGNC VGNC:68759
Macaca mulatta PDE4D VGNC VGNC:75917
Canis familiaris PDE4D VGNC VGNC:44355
Rattus norvegicus PDE4D RGD RGD:3281
Mus musculus PDE4D MGD MGI:99555
Others PDE4D NCBI