ENSG00000157399


Homo sapiens

Features
Gene ID: ENSG00000157399
  
Biological name :ARSE
  
Synonyms : ARSE / arylsulfatase E (chondrodysplasia punctata 1) / P51690
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: X
Strand: -1
Band: p22.33
Gene start: 2934632
Gene end: 2968310
  
Corresponding Affymetrix probe sets: 205894_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000441417
Ensembl peptide - ENSP00000370526
Ensembl peptide - ENSP00000406528
Ensembl peptide - ENSP00000438198
NCBI entrez gene - 415     See in Manteia.
OMIM - 300180
RefSeq - XM_017029526
RefSeq - NM_001282628
RefSeq - NM_001282631
RefSeq - XM_005274518
RefSeq - XM_005274519
RefSeq - XM_005274521
RefSeq - XM_011545521
RefSeq - XM_017029525
RefSeq - NM_000047
RefSeq Peptide - NP_001269560
RefSeq Peptide - NP_000038
RefSeq Peptide - NP_001269557
swissprot - C9J5G7
swissprot - P51690
swissprot - F5H324
swissprot - F5GYY5
Ensembl - ENSG00000157399
  
Related genetic diseases (OMIM): 302950 - Chondrodysplasia punctata, X-linked recessive, 302950
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
No match


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
ARSD / P51689 / arylsulfatase DENSG0000000675660
ARSH / Q5FYA8 / arylsulfatase family member HENSG0000020566755
ARSF / P54793 / arylsulfatase FENSG0000006209654
STS / P08842 / steroid sulfataseENSG0000010184649
GALNS / P34059 / galactosamine (N-acetyl)-6-sulfataseENSG0000014101228
ARSA / P15289 / arylsulfatase AENSG0000010029927
ARSG / Q96EG1 / arylsulfatase GENSG0000014133726
ARSI / Q5FYB1 / arylsulfatase family member IENSG0000018387623
ARSB / P15848 / arylsulfatase BENSG0000011327322
ARSJ / Q5FYB0 / arylsulfatase family member JENSG0000018080121


Protein motifs (from Interpro)
Interpro ID Name
 IPR000917  Sulfatase, N-terminal
 IPR017849  Alkaline phosphatase-like, alpha/beta/alpha
 IPR017850  Alkaline-phosphatase-like, core domain superfamily
 IPR024607  Sulfatase, conserved site


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001501 skeletal system development TAS
 biological_processGO:0006687 glycosphingolipid metabolic process TAS
 biological_processGO:0008152 metabolic process IEA
 biological_processGO:0043687 post-translational protein modification TAS
 cellular_componentGO:0005788 endoplasmic reticulum lumen TAS
 cellular_componentGO:0005794 Golgi apparatus IDA
 cellular_componentGO:0005795 Golgi stack IEA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0070062 extracellular exosome HDA
 molecular_functionGO:0003824 catalytic activity IEA
 molecular_functionGO:0004065 arylsulfatase activity TAS
 molecular_functionGO:0008484 sulfuric ester hydrolase activity IEA
 molecular_functionGO:0016787 hydrolase activity IEA
 molecular_functionGO:0046872 metal ion binding IEA


Pathways (from Reactome)
Pathway description
Glycosphingolipid metabolism
The activation of arylsulfatases


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000135 Hypogonadism "Reduced function of the gonads (testes in males or ovaries in females)." [HPO:curators]
Show

 HP:0000252 Microcephaly "Microcephaly is a neurodevelopmental disorder in which the circumference of the head is more than two standard deviations smaller than the age- and gender-dependent norm." [HPO:curators]
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 HP:0000365 Hearing loss 
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 HP:0000420 Short nasal septum 
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 HP:0000458 Anosmia "An inability to perceive odors. This is a general term describing inability to smell arising in any part of the process of smelling from absorption of odorants into the nasal mucous overlying the olfactory epithelium, diffusion to the cilia, binding to olfactory receptor sites, generation of action potentials in olfactory neurons, and perception of a smell." [HPO:curators]
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 HP:0000518 Cataract "A cataract is an opacity or clouding that develops in the crystalline `lens` (FMA:58241) of the eye or in its `capsule` (FMA:58881)." [HPO:probinson]
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 HP:0000925 Abnormality of the vertebral column "Any abnormality of the spine (vertebral column)." [HPO:curators]
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 HP:0001263 Developmental retardation "A delay in the achievement of motor or mental milestones manifested prior to age 18 and generally associated with lifelong mental and/or physical impairments." [HPO:curators]
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 HP:0001419 X-linked recessive inheritance "A mode of inheritance that is observed for recessive traits related to a gene encoded on the X chromosome. In the context of medical genetics, X-linked recessive disorders manifest in males (who have one copy of the X chromosome and are thus hemizygotes), but generally not in female heterozygotes who have one mutant and one normal allele." [HPO:curators]
Show

 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:0005280 Depressed nasal root and bridge 
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 HP:0008064 Ichthyosiform abnormality of the skin 
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 HP:0009882 Hypoplasia of the distal phalanges of the hand 
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 HP:0010655 Stippling of the epiphyses "The presence of abnormal punctate (speckled, dot-like) calcifications in the epiphyses (FMA:24012)." [HPO:curators]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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