ENSG00000197614


Homo sapiens

Features
Gene ID: ENSG00000197614
  
Biological name :MFAP5
  
Synonyms : MFAP5 / microfibril associated protein 5 / Q13361
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 12
Strand: -1
Band: p13.31
Gene start: 8637346
Gene end: 8662888
  
Corresponding Affymetrix probe sets: 209758_s_at (Human Genome U133 Plus 2.0 Array)   213764_s_at (Human Genome U133 Plus 2.0 Array)   213765_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000444531
Ensembl peptide - ENSP00000443839
Ensembl peptide - ENSP00000445799
Ensembl peptide - ENSP00000352455
Ensembl peptide - ENSP00000440496
Ensembl peptide - ENSP00000439289
Ensembl peptide - ENSP00000438525
Ensembl peptide - ENSP00000411997
Ensembl peptide - ENSP00000379798
Ensembl peptide - ENSP00000441185
Ensembl peptide - ENSP00000441492
NCBI entrez gene - 8076     See in Manteia.
OMIM - 601103
RefSeq - NM_001297710
RefSeq - NM_001297712
RefSeq - NM_003480
RefSeq - NM_001297709
RefSeq - NM_001297711
RefSeq Peptide - NP_001284640
RefSeq Peptide - NP_001284639
RefSeq Peptide - NP_001284638
RefSeq Peptide - NP_003471
RefSeq Peptide - NP_001284641
swissprot - Q13361
swissprot - B3KW70
swissprot - F5GYX4
swissprot - F5H1C0
swissprot - F5H2W4
swissprot - F5H413
swissprot - F5H7Z2
swissprot - H0YG03
swissprot - H0YGS3
Ensembl - ENSG00000197614
  
Related genetic diseases (OMIM): 616166 - Aortic aneurysm, familial thoracic 9, 616166
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
 mfap5ENSDARG00000090560Danio rerio
 MFAP5ENSGALG00000027471Gallus gallus
 Mfap5ENSMUSG00000030116Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
MFAP2 / P55001 / microfibril associated protein 2ENSG0000011712227


Protein motifs (from Interpro)
Interpro ID Name
 IPR008673  Microfibril-associated glycoprotein


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0030198 extracellular matrix organization TAS
 biological_processGO:0060216 definitive hemopoiesis ISS
 biological_processGO:0097435 supramolecular fiber organization IEA
 cellular_componentGO:0001527 microfibril ISS
 cellular_componentGO:0005576 extracellular region TAS
 cellular_componentGO:0005615 extracellular space IEA
 cellular_componentGO:0031012 extracellular matrix IDA
 molecular_functionGO:0005201 extracellular matrix structural constituent TAS


Pathways (from Reactome)
Pathway description
Elastic fibre formation
Molecules associated with elastic fibres


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:0000023 Inguinal hernia 
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 HP:0000098 Increased body height 
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 HP:0000218 High palate "Height of the palate more than 2 SD above the mean (objective) or palatal height at the level of the first permanent molar more than twice the height of the teeth (subjective)." [pmid:19125428]
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 HP:0000278 Retrognathia 
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 HP:0000316 Hypertelorism 
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 HP:0000525 Abnormality of the iris "An abnormality of the iris, which is the pigmented muscular tissue between the cornea and the lens, that is perforated by an opening called the pupil." [HPO:curators]
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 HP:0000766 Abnormality of the sternum 
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 HP:0000767 Pectus excavatum "A defect of the chest wall characterized by a depression of the sternum, giving the chest ("pectus") a caved-in ("excavatum") appearance." [HPO:curators]
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 HP:0000768 Pectus carinatum "A deformity of the chest caused by overgrowth of the ribs and characterized by protrusion of the sternum." [HPO:curators]
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 HP:0000822 Hypertension "High blood pressure." [HPO:curators]
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 HP:0000965 Cutis marmorata 
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 HP:0000978 Ecchymoses 
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 HP:0001166 Arachnodactyly "Abnormally long and slender fingers ("spider fingers")." [HPO:curators]
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 HP:0001634 Mitral valve prolapse 
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 HP:0001640 Cardiomegaly 
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 HP:0001643 Patent ductus arteriosus 
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 HP:0001647 Bicuspid aortic valve "The presence of a bicuspid `aortic valve` (FMA:7236)." [HPO:probinson]
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 HP:0001659 Aortic insufficiency "An insufficiency of the aortic valve, leading to regurgitation (backward flow) of blood from the aorta into the left ventricle." [HPO:curators]
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 HP:0001677 Coronary artery disease 
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 HP:0001763 Pes planus "A condition in which the arch of the foot is flat, with the entire sole of the foot being in near-complete contact with the ground." [HPO:curators]
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 HP:0002105 Hemoptysis "Coughing up (expectoration) of blood or blood-streaked sputum from the larynx, trachea, bronchi, or lungs." [HPO:curators]
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 HP:0002107 Pneumothorax 
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 HP:0002138 Subarachnoid hemorrhage 
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 HP:0002140 Ischemic stroke 
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 HP:0002326 Transient ischemic attack 
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 HP:0002616 Aortic root dilatation 
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 HP:0002650 Scoliosis "The presence of an abnormal lateral curvature of the spine." [HPO:curators]
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 HP:0002686 Prenatal maternal abnormality 
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 HP:0002705 High, narrow palate "The presence of a high and narrow palate." [HPO:curators]
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 HP:0002875 Exertional dyspnea 
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 HP:0004933 ascending aortic dissection 
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 HP:0004944 Cerebral aneurysm "The presence of a localized dilatation or ballooning of a cerebral artery." [HPO:curators]
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 HP:0004950 Peripheral arterial disease 
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 HP:0004959 Dilatation of the descending thoracic aorta 
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 HP:0005110 Atrial fibrillation 
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 HP:0005112 Dilatation of the abdominal aorta 
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 HP:0005162 Impaired left ventricular function 
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 HP:0011106 Hypovolemia "An decrease in the amount of intravascular fluid, particularly in the volume of the circulating blood." [HPO:probinson]
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 HP:0012163 Carotid artery aneurysm "A aneurysm (balooning or bulging out of the vessel wall) of a carotid artery." [HPO:probinson]
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 HP:0012499 Descending aortic dissection "A separation of the layers within the wall of the `descending aorta` (FMA:3784). Tears in the intimal layer result in the propagation of dissection (proximally or distally) secondary to blood entering the intima-media space." [HPO:probinson]
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 HP:0012727 Thoracic aortic aneurysm "A bulging, weakened area in the wall of the thoracic aorta." [HPO:probinson]
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 HP:0012763 Paroxysmal dyspnea "A sudden attack of dyspnea that occurs while the affected person is at rest." [HPO:probinson]
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 HP:0100749 Chest pain 
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 HP:0100775 Dural ectasia "A widening or ballooning of the dural sac surrounding the spinal cord usually at the lumbosacral level." [HPO:sdoelken]
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 HP:0200146 Cystic medial necrosis of the aorta 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000113083 LOX / P28300 / lysyl oxidase  / reaction
 ENSG00000138829 FBN2 / P35556 / fibrillin 2  / complex / reaction
 ENSG00000129038 LOXL1 / Q08397 / lysyl oxidase like 1  / reaction
 ENSG00000140092 FBLN5 / Q9UBX5 / fibulin 5  / complex
 ENSG00000166147 FBN1 / P35555 / fibrillin 1  / complex / reaction
 ENSG00000049540 ELN / P15502 / elastin  / complex
 ENSG00000140259 MFAP1 / P55081 / microfibril associated protein 1  / complex / reaction
 ENSG00000037749 MFAP3 / P55082 / microfibril associated protein 3  / complex / reaction
 ENSG00000109072 VTN / P04004 / vitronectin  / reaction / complex
 ENSG00000166482 MFAP4 / P55083 / microfibril associated protein 4  / complex / reaction
 ENSG00000138080 Q9Y6C2 / EMILIN1 / elastin microfibril interfacer 1  / complex / reaction






 

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