ENSG00000149257


Homo sapiens

Features
Gene ID: ENSG00000149257
  
Biological name :SERPINH1
  
Synonyms : P50454 / serpin family H member 1 / SERPINH1
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 11
Strand: 1
Band: q13.5
Gene start: 75562056
Gene end: 75572783
  
Corresponding Affymetrix probe sets: 207714_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000431384
Ensembl peptide - ENSP00000431827
Ensembl peptide - ENSP00000437108
Ensembl peptide - ENSP00000436306
Ensembl peptide - ENSP00000436305
Ensembl peptide - ENSP00000436040
Ensembl peptide - ENSP00000435936
Ensembl peptide - ENSP00000435452
Ensembl peptide - ENSP00000434964
Ensembl peptide - ENSP00000434657
Ensembl peptide - ENSP00000434482
Ensembl peptide - ENSP00000434412
Ensembl peptide - ENSP00000433532
Ensembl peptide - ENSP00000432007
Ensembl peptide - ENSP00000350894
NCBI entrez gene - 871     See in Manteia.
OMIM - 600943
RefSeq - NM_001235
RefSeq - NM_001207014
RefSeq - XM_011545327
RefSeq Peptide - NP_001193943
RefSeq Peptide - NP_001226
swissprot - E9PMI5
swissprot - E9PLA6
swissprot - E9PKH2
swissprot - E9PK86
swissprot - E9PRS3
swissprot - E9PIG2
swissprot - A0A024R5K8
swissprot - H0YEP8
swissprot - P50454
swissprot - E9PJH8
swissprot - E9PR70
swissprot - E9PQ34
swissprot - E9PPV6
swissprot - E9PNX1
Ensembl - ENSG00000149257
  
Related genetic diseases (OMIM): 610504 - {Preterm premature rupture of the membranes, susceptibility to}, 610504
  613848 - Osteogenesis imperfecta, type X, 613848
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
 serpinh1aENSDARG00000075954Danio rerio
 serpinh1bENSDARG00000019949Danio rerio
 P13731ENSGALG00000011214Gallus gallus
 P19324ENSMUSG00000070436Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Q96P63 / SERPINB12 / serpin family B member 12ENSG0000016663427
O75830 / SERPINI2 / serpin family I member 2ENSG0000011420425
Q99574 / SERPINI1 / serpin family I member 1ENSG0000016353623
O75635 / SERPINB7 / serpin family B member 7ENSG0000016639622
P07093 / SERPINE2 / serpin family E member 2ENSG0000013591922
P05121 / SERPINE1 / serpin family E member 1ENSG0000010636622
A8MV23 / SERPINE3 / serpin family E member 3ENSG0000025330921
P01008 / SERPINC1 / serpin family C member 1ENSG0000011760121
Q96P15 / SERPINB11 / serpin family B member 11 (gene/pseudogene)ENSG0000020607219


Protein motifs (from Interpro)
Interpro ID Name
 IPR000215  Serpin family
 IPR023795  Serpin, conserved site
 IPR023796  Serpin domain
 IPR033547  Serpin H1
 IPR033830  Serpin H1 inhibitory domain
 IPR036186  Serpin superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0003433 chondrocyte development involved in endochondral bone morphogenesis IEA
 biological_processGO:0006986 response to unfolded protein TAS
 biological_processGO:0010951 negative regulation of endopeptidase activity IEA
 biological_processGO:0030199 collagen fibril organization IBA
 biological_processGO:0032964 collagen biosynthetic process IEA
 biological_processGO:0051604 protein maturation IEA
 cellular_componentGO:0005581 collagen trimer IEA
 cellular_componentGO:0005615 extracellular space IEA
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005783 endoplasmic reticulum IDA
 cellular_componentGO:0005788 endoplasmic reticulum lumen TAS
 cellular_componentGO:0005793 endoplasmic reticulum-Golgi intermediate compartment IDA
 cellular_componentGO:0045121 membrane raft IDA
 cellular_componentGO:0070062 extracellular exosome HDA
 molecular_functionGO:0003723 RNA binding HDA
 molecular_functionGO:0004867 serine-type endopeptidase inhibitor activity IEA
 molecular_functionGO:0005518 collagen binding IEA
 molecular_functionGO:0051082 unfolded protein binding IEA


Pathways (from Reactome)
Pathway description
Collagen biosynthesis and modifying enzymes


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:0000023 Inguinal hernia 
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 HP:0000272 Malar hypoplasia "Underdeveloped midface region." [HPO:curators]
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 HP:0000325 Triangular facies 
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 HP:0000341 Narrow forehead "An abnormally reduced side-to-side width of the forehead." [HPO:curators]
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 HP:0000347 Mandibular hypoplasia "Underdevelopment of the mandible." [HPO:curators]
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 HP:0000348 High forehead "An abnormally increased height of the forehead." [HPO:curators]
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 HP:0000586 Shallow orbits 
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 HP:0000592 Blue sclerae 
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 HP:0000703 Dentinogenesis imperfecta 
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 HP:0000774 Narrow chest 
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 HP:0000787 Kidney stones 
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 HP:0000883 Thin ribs 
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 HP:0000885 Broad ribs 
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 HP:0000926 Platyspondyly 
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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:0001290 Generalized hypotonia "Generalized muscular hypotonia (abnormally low muscle tone)." [HPO:curators]
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 HP:0001388 Joint laxity 
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 HP:0001620 High pitched voice 
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 HP:0002021 Pyloric stenosis 
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 HP:0002650 Scoliosis "The presence of an abnormal lateral curvature of the spine." [HPO:curators]
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 HP:0002761 Generalized joint laxity "Joint hypermobility (ability of a joint to move beyond its normal range of motion) affecting many or all joints of the body." [HPO:curators]
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 HP:0002857 Genu valgum 
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 HP:0002953 Vertebral compression fractures 
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 HP:0002983 Micromelia 
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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:0004482 Relative macrocephaly "A relatively mild degree of macrocephaly in which the head circumference is not above two standard deviations from the mean, but appears dysproportionately large when other factors such as body stature are taken into account." [HPO:curators]
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 HP:0006528 Chronic lung disease 
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 HP:0011220 Prominent forehead "Forward prominence of the entire forehead, due to protrusion of the frontal bone." [pmid:19125436]
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 HP:0011800 Midface retrusion "Posterior positions and/or vertical shortening of the infraorbital and perialar regions, or increased concavity of the face and/or reduced nasolabial angle." [DDD:jclayton-smith]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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