ENSG00000128655


Homo sapiens

Features
Gene ID: ENSG00000128655
  
Biological name :PDE11A
  
Synonyms : PDE11A / phosphodiesterase 11A / Q9HCR9
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 2
Strand: -1
Band: q31.2
Gene start: 177623252
Gene end: 178072755
  
Corresponding Affymetrix probe sets: 221110_x_at (Human Genome U133 Plus 2.0 Array)   224223_s_at (Human Genome U133 Plus 2.0 Array)   224224_s_at (Human Genome U133 Plus 2.0 Array)   237248_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000416884
Ensembl peptide - ENSP00000374333
Ensembl peptide - ENSP00000286063
Ensembl peptide - ENSP00000389777
Ensembl peptide - ENSP00000406922
Ensembl peptide - ENSP00000386539
NCBI entrez gene - 50940     See in Manteia.
OMIM - 604961
RefSeq - NM_016953
RefSeq - NM_001077196
RefSeq - NM_001077358
RefSeq Peptide - NP_001070664
RefSeq Peptide - NP_058649
RefSeq Peptide - NP_001070826
swissprot - Q9HCR9
swissprot - F8WDQ4
swissprot - H0Y6P9
swissprot - H7C4D0
Ensembl - ENSG00000128655
  
Related genetic diseases (OMIM): 610475 - Pigmented nodular adrenocortical disease, primary, 2, 610475
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 pde11aENSDARG00000063732Danio rerio
 ENSGALG00000042374Gallus gallus
 P0C1Q2ENSMUSG00000075270Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
PDE11A / phosphodiesterase 11AENSG0000028474169
PDE5A / O76074 / phosphodiesterase 5AENSG0000013873538
PDE6B / P35913 / phosphodiesterase 6BENSG0000013325628
PDE6A / P16499 / phosphodiesterase 6AENSG0000013291528
PDE6C / P51160 / phosphodiesterase 6CENSG0000009546428
PDE2A / O00408 / phosphodiesterase 2AENSG0000018664226
PDE10A / Q9Y233 / phosphodiesterase 10AENSG0000011254124
PDE3B / Q13370 / phosphodiesterase 3BENSG0000015227014
PDE3A / Q14432 / phosphodiesterase 3AENSG0000017257214
PDE9A / O76083 / phosphodiesterase 9AENSG0000016019113


Protein motifs (from Interpro)
Interpro ID Name
 IPR002073  3"5"-cyclic nucleotide phosphodiesterase, catalytic domain
 IPR003018  GAF domain
 IPR003607  HD/PDEase domain
 IPR023088  3"5"-cyclic nucleotide phosphodiesterase
 IPR023174  3"5"-cyclic nucleotide phosphodiesterase, conserved site
 IPR029016  GAF-like domain superfamily
 IPR036971  3"5"-cyclic nucleotide phosphodiesterase, catalytic domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0007165 signal transduction IEA
 biological_processGO:0007186 G-protein coupled receptor signaling pathway TAS
 biological_processGO:0008152 metabolic process IEA
 cellular_componentGO:0005575 cellular_component ND
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005829 cytosol TAS
 molecular_functionGO:0003824 catalytic activity IEA
 molecular_functionGO:0004112 cyclic-nucleotide phosphodiesterase activity NAS
 molecular_functionGO:0004114 3",5"-cyclic-nucleotide phosphodiesterase activity IEA
 molecular_functionGO:0004115 3",5"-cyclic-AMP phosphodiesterase activity TAS
 molecular_functionGO:0004118 cGMP-stimulated cyclic-nucleotide phosphodiesterase activity IDA
 molecular_functionGO:0005515 protein binding IEA
 molecular_functionGO:0008081 phosphoric diester hydrolase activity IEA
 molecular_functionGO:0016787 hydrolase activity IEA
 molecular_functionGO:0030553 cGMP binding IDA
 molecular_functionGO:0046872 metal ion binding IEA
 molecular_functionGO:0047555 3",5"-cyclic-GMP phosphodiesterase activity IEA


Pathways (from Reactome)
Pathway description
cGMP effects
G alpha (s) signalling events


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000006 Autosomal dominant inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele." [HPO:curators]
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 HP:0000135 Hypogonadism "Reduced function of the gonads (testes in males or ovaries in females)." [HPO:curators]
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 HP:0000311 Round face "An unusually round appearance of the face." [HPO:curators]
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 HP:0000709 Psychosis "A condition characterized by changes of personality and thought patterns often accompanied by hallucinations and delusional beliefs." [HPO:curators]
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 HP:0000713 Agitation 
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 HP:0000716 Depression "A condition characterized by pervasive dysphoric mood, loss of interests, and inability to experience pleasure." [HPO:curators]
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 HP:0000739 Anxiety 
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 HP:0000819 Diabetes mellitus 
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 HP:0000822 Hypertension "High blood pressure." [HPO:curators]
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 HP:0000938 Osteopenia "Osteopenia refers to a reduction in bone mineral density (BMD) below normal peak BMD but not low enough to be classified as osteoporosis. According to the WHO, osteopenia is characterized by a value of BMD more than 1 standard deviation below the young adult mean, but less than 2 standard deviations below this value." [HPO:curators]
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 HP:0000939 Osteoporosis "Osteoporosis is a systemic skeletal disease characterized by low bone density and microarchitectural deterioration of bone tissue with a consequent increase in bone fragility. According to the WHO, osteoporosis is characterized by a value of BMD 2.5 standard deviations or more below the young adult mean." [HPO:curators]
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 HP:0000963 Thin skin 
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 HP:0000978 Ecchymoses 
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 HP:0001065 Striae distensae "Thinned, erythematous, depressed bands of atrophic skin. Initially, striae appear as flattened and thinned, pinkish linear regions of the skin. Striae tend to enlarge in length and become reddish or purplish. Later, striae tend to appear as white, depressed bands that are parallel to the lines of skin tension. Striae distensae occur most often in areas that have been subject to distension such as the lower back, buttocks, thighs, breast, abdomen, and shoulders." [HPO:curators]
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 HP:0001268 Mental deterioration 
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 HP:0001324 Muscle weakness "Reduced strength of muscles." [HPO:curators]
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 HP:0001533 Asthenic habitus "Asthenic habitus refers to a slender build with long limbs, an angular profile, and prominent muscles or bones." [HPO:curators]
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 HP:0001575 Mood changes 
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 HP:0001579 ACTH-independent hypercortisolemia 
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 HP:0001580 Pigmented micronodular adrenocortical disease 
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 HP:0001956 Truncal obesity "Obesity located preferentially in the trunk of the body as opposed to the extremities." [HPO:curators]
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 HP:0002659 Increased susceptibility to fractures "An abnormally increased tendency to fractures of bones caused by an abnormal reduction in bone strength that is generally associated with an increased risk of fracture." [HPO:sdoelken]
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 HP:0002808 Kyphosis 
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 HP:0002920 Decreased serum ACTH 
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 HP:0003198 Myopathy 
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 HP:0003202 Amyotrophy "The presence of muscular atrophy (which is also known as amyotrophy)." [HPO:curators]
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 HP:0003466 Paradoxical increased cortisol secretion on dexamethasone suppression test 
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 HP:0003674 Age of onset 
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 HP:0004322 Decreased body height "A height below that which is expected according to age and gender norms. Although there is no universally accepted definition of short stature, many refer to "short stature" as height more than 2 standard deviations below the mean for age and gender (or below the 3rd percentile for age and gender dependent norms)." [HPO:curators]
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 HP:0008221 Enlarged adrenal glands 
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 HP:0012378 Fatigue "A subjective feeling of tiredness characterized by a lack of energy and motivation." [HPO:probinson]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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