ENSG00000171551


Homo sapiens

Features
Gene ID: ENSG00000171551
  
Biological name :ECEL1
  
Synonyms : ECEL1 / endothelin converting enzyme like 1 / O95672
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 2
Strand: -1
Band: q37.1
Gene start: 232479827
Gene end: 232487828
  
Corresponding Affymetrix probe sets: 219914_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000386333
Ensembl peptide - ENSP00000302051
Ensembl peptide - ENSP00000412683
NCBI entrez gene - 9427     See in Manteia.
OMIM - 605896
RefSeq - NM_004826
RefSeq - NM_001290787
RefSeq Peptide - NP_001277716
RefSeq Peptide - NP_004817
swissprot - O95672
swissprot - H7C3M0
Ensembl - ENSG00000171551
  
Related genetic diseases (OMIM): 615065 - Arthrogryposis, distal, type 5D, 615065
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
 ecel1ENSDARG00000060549Danio rerio
 ENSGALG00000030420Gallus gallus
 ENSGALG00000007875Gallus gallus
 Ecel1ENSMUSG00000026247Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
ECE2 / O60344 / endothelin converting enzyme 2ENSG0000014519437
ECE1 / P42892 / endothelin converting enzyme 1ENSG0000011729837
O60344 / EEF1AKMT4-ECE2 / EEF1AKMT4-ECE2 readthroughENSG0000028491736
MMEL1 / Q495T6 / membrane metalloendopeptidase like 1ENSG0000014260633
MME / P08473 / membrane metalloendopeptidaseENSG0000019654932
PHEX / P78562 / phosphate regulating endopeptidase homolog X-linkedENSG0000010217429
KEL / P23276 / Kell blood group, metallo-endopeptidaseENSG0000019799325


Protein motifs (from Interpro)
Interpro ID Name
 IPR000718  Peptidase M13
 IPR008753  Peptidase M13, N-terminal domain
 IPR018497  Peptidase M13, C-terminal domain
 IPR024079  Metallopeptidase, catalytic domain superfamily
 IPR029736  Endothelin-converting enzyme-like 1


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0003016 respiratory system process ISS
 biological_processGO:0006508 proteolysis IEA
 biological_processGO:0007218 neuropeptide signaling pathway TAS
 cellular_componentGO:0005887 integral component of plasma membrane TAS
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 molecular_functionGO:0004222 metalloendopeptidase activity IEA
 molecular_functionGO:0008233 peptidase activity IEA
 molecular_functionGO:0008237 metallopeptidase activity TAS
 molecular_functionGO:0016787 hydrolase activity IEA
 molecular_functionGO:0046872 metal ion binding IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000007 Autosomal recessive 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 homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators]
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 HP:0000059 Hypoplastic labia majora 
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 HP:0000175 Cleft palate "Cleft palate is a developmental defect of the `palate` (FMA:54549) resulting from a failure of fusion of the palatine processes." [HPO:curators]
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 HP:0000221 Furrowed tongue "Accentuation of the grooves on the dorsal surface of the tongue." [pmid:19125428]
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 HP:0000311 Round face "An unusually round appearance of the face." [HPO:curators]
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 HP:0000347 Mandibular hypoplasia "Underdevelopment of the mandible." [HPO:curators]
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 HP:0000414 Bulbous nose 
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 HP:0000463 Nares, anteverted "Anteriorly-facing nostrils viewed with the head in the Frankfurt horizontal and the eyes of the observer level with the eyes of the subject." [pmid:19152422]
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 HP:0000470 Short neck 
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 HP:0001181 Adducted thumbs 
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 HP:0001762 Talipes equinovarus "Also called clubfoot typically has 4 main components: inversion and adduction of the forefoot; inversion of the heel and hindfoot; equinus (limitation of extension) of the ankle and subtalar joint; and internal rotation of the leg. Clubfoot is a complex, multifactorial deformity with genetic and intrauterine factors. One popular theory postulates that a clubfoot is a result of intrauterine maldevelopment of the talus that leads to adduction and plantarflexion of the foot. On radiographic projection a clubfoot can be noted as parallel axes of talus and calcaneus." [HPO:curators]
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 HP:0001848 Calcaneovalgus deformities 
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 HP:0002553 Arched eyebrows 
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 HP:0002650 Scoliosis "The presence of an abnormal lateral curvature of the spine." [HPO:curators]
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 HP:0002804 Arthrogryposis multiplex congenita 
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 HP:0002827 Dislocated hips 
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 HP:0002987 Elbow contractures 
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 HP:0003199 Decreased muscle mass 
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 HP:0003307 Hyperlordosis 
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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:0012385 Camptodactyly "The distal interphalangeal joint and/or the proximal interphalangeal joint of the fingers or toes cannot be extended to 180 degrees by either active or passive extension." [HPO:probinson]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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