ENSG00000104331


Homo sapiens

Features
Gene ID: ENSG00000104331
  
Biological name :IMPAD1
  
Synonyms : IMPAD1 / inositol monophosphatase domain containing 1 / Q9NX62
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 8
Strand: -1
Band: q12.1
Gene start: 56957933
Gene end: 56993844
  
Corresponding Affymetrix probe sets: 218516_s_at (Human Genome U133 Plus 2.0 Array)   222654_at (Human Genome U133 Plus 2.0 Array)   222655_s_at (Human Genome U133 Plus 2.0 Array)   224743_at (Human Genome U133 Plus 2.0 Array)   224744_at (Human Genome U133 Plus 2.0 Array)   227774_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000262644
Ensembl peptide - ENSP00000430185
Ensembl peptide - ENSP00000428617
NCBI entrez gene - 54928     See in Manteia.
OMIM - 614010
RefSeq - NM_017813
RefSeq Peptide - NP_060283
swissprot - Q9NX62
swissprot - H0YBS3
swissprot - H0YB38
swissprot - A0A024R7W0
Ensembl - ENSG00000104331
  
Related genetic diseases (OMIM): 614078 - Chondrodysplasia with joint dislocations, GPAPP type, 614078
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
 impad1ENSDARG00000058114Danio rerio
 IMPAD1ENSGALG00000041573Gallus gallus
 Impad1ENSMUSG00000066324Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
BPNT1 / O95861 / 3(2), 5-bisphosphate nucleotidase 1ENSG0000016281325


Protein motifs (from Interpro)
Interpro ID Name
 IPR000760  Inositol monophosphatase-like
 IPR020550  Inositol monophosphatase, conserved site


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001501 skeletal system development IEA
 biological_processGO:0001958 endochondral ossification IEA
 biological_processGO:0002063 chondrocyte development IEA
 biological_processGO:0006021 inositol biosynthetic process IEA
 biological_processGO:0009791 post-embryonic development IEA
 biological_processGO:0016311 dephosphorylation IEA
 biological_processGO:0030204 chondroitin sulfate metabolic process IEA
 biological_processGO:0042733 embryonic digit morphogenesis IEA
 biological_processGO:0046854 phosphatidylinositol phosphorylation IEA
 biological_processGO:0050427 3"-phosphoadenosine 5"-phosphosulfate metabolic process TAS
 cellular_componentGO:0005634 nucleus IDA
 cellular_componentGO:0005794 Golgi apparatus IEA
 cellular_componentGO:0005796 Golgi lumen TAS
 cellular_componentGO:0005829 cytosol IDA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0016604 nuclear body IDA
 molecular_functionGO:0008254 3"-nucleotidase activity IEA
 molecular_functionGO:0008441 3"(2"),5"-bisphosphate nucleotidase activity TAS
 molecular_functionGO:0008934 inositol monophosphate 1-phosphatase activity IEA
 molecular_functionGO:0016787 hydrolase activity IEA
 molecular_functionGO:0046872 metal ion binding IEA
 molecular_functionGO:0052832 inositol monophosphate 3-phosphatase activity IEA
 molecular_functionGO:0052833 inositol monophosphate 4-phosphatase activity IEA
 molecular_functionGO:0052834 inositol monophosphate phosphatase activity IEA


Pathways (from Reactome)
Pathway description
Cytosolic sulfonation of small molecules


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:0000160 Microstomia "The presence of an abnormally small `mouth` (FMA:49184)." [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:0000365 Hearing loss 
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 HP:0000431 Broad nasal bridge "Increased horizontal dimension of the upper, bony part of the nose." [HPO:curators]
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 HP:0000520 Proptosis 
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 HP:0001156 Brachydactyly 
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 HP:0001773 Short, broad feet "Abnormally short and wide feet." [HPO:curators]
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 HP:0001831 Brachydactyly (feet) 
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 HP:0002857 Genu valgum 
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 HP:0002999 Dislocation of patella "The kneecap normally is located within the groove termed trochlea on the distal femur and can slide up and down in it. Patellar dislocation occurs if the patella fully dislocates out of the groove." [HPO:curators]
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 HP:0003196 Nasal hypoplasia "Underdevelopment of the `nose` (FMA:46472)." [HPO:probinson]
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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:0004440 Coronal craniosynostosis 
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 HP:0010049 Hypoplastic/short metacarpal bones 
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 HP:0012368 Flat face "Absence of concavity or convexity of the face when viewed in profile." [pmid:19125436]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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