ENSG00000165704


Homo sapiens

Features
Gene ID: ENSG00000165704
  
Biological name :HPRT1
  
Synonyms : HPRT1 / hypoxanthine phosphoribosyltransferase 1 / P00492
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: X
Strand: 1
Band: q26.2
Gene start: 134460153
Gene end: 134520513
  
Corresponding Affymetrix probe sets: 1565446_at (Human Genome U133 Plus 2.0 Array)   202854_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000298556
NCBI entrez gene - 3251     See in Manteia.
OMIM - 308000
RefSeq - NM_000194
RefSeq Peptide - NP_000185
swissprot - A0A140VJL3
swissprot - P00492
Ensembl - ENSG00000165704
  
Related genetic diseases (OMIM): 300322 - Lesch-Nyhan syndrome, 300322
  300323 - HPRT-related gout, 300323
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
 hprt1ENSDARG00000008884Danio rerio
 HPRT1ENSGALG00000006098Gallus gallus
 HprtENSMUSG00000025630Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Q9NRG1 / PRTFDC1 / phosphoribosyl transferase domain containing 1ENSG0000009925665


Protein motifs (from Interpro)
Interpro ID Name
 IPR000836  Phosphoribosyltransferase domain
 IPR005904  Hypoxanthine phosphoribosyl transferase
 IPR029057  Phosphoribosyltransferase-like


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001975 response to amphetamine IEA
 biological_processGO:0006164 purine nucleotide biosynthetic process IMP
 biological_processGO:0006166 purine ribonucleoside salvage IMP
 biological_processGO:0006168 adenine salvage IEA
 biological_processGO:0006178 guanine salvage IDA
 biological_processGO:0007625 grooming behavior IEA
 biological_processGO:0007626 locomotory behavior IEA
 biological_processGO:0009116 nucleoside metabolic process IEA
 biological_processGO:0019835 cytolysis IEA
 biological_processGO:0021756 striatum development IEA
 biological_processGO:0021895 cerebral cortex neuron differentiation IEA
 biological_processGO:0021954 central nervous system neuron development IEA
 biological_processGO:0032264 IMP salvage IEA
 biological_processGO:0042417 dopamine metabolic process IEA
 biological_processGO:0043101 purine-containing compound salvage TAS
 biological_processGO:0043103 hypoxanthine salvage IDA
 biological_processGO:0045964 positive regulation of dopamine metabolic process IMP
 biological_processGO:0046038 GMP catabolic process IDA
 biological_processGO:0046040 IMP metabolic process IDA
 biological_processGO:0046083 adenine metabolic process IEA
 biological_processGO:0046100 hypoxanthine metabolic process IMP
 biological_processGO:0046651 lymphocyte proliferation IEA
 biological_processGO:0048813 dendrite morphogenesis IEA
 biological_processGO:0051289 protein homotetramerization IPI
 cellular_componentGO:0005737 cytoplasm IDA
 cellular_componentGO:0005829 cytosol TAS
 cellular_componentGO:0070062 extracellular exosome HDA
 molecular_functionGO:0000166 nucleotide binding IEA
 molecular_functionGO:0000287 magnesium ion binding IDA
 molecular_functionGO:0004422 hypoxanthine phosphoribosyltransferase activity EXP
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0016740 transferase activity IEA
 molecular_functionGO:0016757 transferase activity, transferring glycosyl groups IEA
 molecular_functionGO:0042802 identical protein binding IEA
 molecular_functionGO:0042803 protein homodimerization activity IPI
 molecular_functionGO:0046872 metal ion binding IEA
 molecular_functionGO:0052657 guanine phosphoribosyltransferase activity IEA


Pathways (from Reactome)
Pathway description
Purine salvage


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000029 Testicular atrophy 
Show

 HP:0000083 Renal failure 
Show

 HP:0000708 Behavioural/Psychiatric Abnormality 
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 HP:0000787 Kidney stones 
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 HP:0000790 Hematuria "The presence of blood in the urine. Hematuria may be gross hematuria (visible to the naked eye) or microscopic hematuria (detected by dipstick or microscopic examination of the urine)." [HPO:curators]
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 HP:0001249 Mental retardation 
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 HP:0001252 Muscular hypotonia "Muscular hypotonia is an abnormally low muscle tone (the amount of tension or resistance to movement in a muscle), often involving reduced muscle strength. Hypotonia is characterized by a diminished resistance to passive stretching." [HPO:curators]
Show

 HP:0001256 Mental retardation, mild "Mild mental retardation is defined as an intelligence quotient (IQ) in the range of 50-69." [HPO:curators]
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 HP:0001257 Spasticity "A motor disorder characterized by a velocity-dependent increase in tonic stretch reflexes with increased muscle tone, exaggerated (hyperexcitable) tendon reflexes." [HPO:curators]
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 HP:0001260 Dysarthria "Dysarthric speech is a general description referring to a neurological speech disorder characterized by poor articulation. Depending on the involved neurological structures, dysarthria may be further classified as spastic, flaccid, ataxic, hyperkinetic and hypokinetic, or mixed." [HPO:curators]
Show

 HP:0001266 Choreoathetosis 
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 HP:0001270 Motor retardation 
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 HP:0001290 Generalized hypotonia "Generalized muscular hypotonia (abnormally low muscle tone)." [HPO:curators]
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 HP:0001332 Dystonia "An abnormally increased muscular tone that causes fixed abnormal postures. There is a slow, intermittent twisting motion that leads to exaggerated turning and posture of the extremities and trunk." [HPO:curators]
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 HP:0001347 Hyperreflexia "The presence of overactive or overresponsive reflexes." [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]
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 HP:0001854 Gout (feet) 
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 HP:0001889 Megaloblastic anemia 
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 HP:0001903 Anemia 
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 HP:0001997 Gout 
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 HP:0002013 Vomiting 
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 HP:0002015 Dysphagia "Difficulty in swallowing." [HPO:curators]
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 HP:0002071 Extrapyramidal signs 
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 HP:0002179 Opisthotonus 
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 HP:0002342 Mental retardation, moderate "Moderate mental retardation is defined as an intelligence quotient (IQ) in the range of 35-49." [HPO:curators]
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 HP:0003149 Hyperuricosuria 
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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:0004374 Hemiplegia/hemiparesis "Loss of strength in the arm, leg, and sometimes face on one side of the body. Hemiplegia refers to a severe or complete loss of strength, whereas hemiparesis refers to a relatively mild loss of strength." [HPO:curators]
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 HP:0100022 Abnormality of movement "An abnormality of movement with a neurological basis characterized by changes in coordination and speed of voluntary movements." [HPO:probinson]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000165704 HPRT1 / P00492 / hypoxanthine phosphoribosyltransferase 1  / complex






 

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