ENSG00000169306


Homo sapiens

Features
Gene ID: ENSG00000169306
  
Biological name :IL1RAPL1
  
Synonyms : IL1RAPL1 / interleukin 1 receptor accessory protein like 1 / Q9NZN1
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: X
Strand: 1
Band: p21.3
Gene start: 28587399
Gene end: 29956723
  
Corresponding Affymetrix probe sets: 220663_at (Human Genome U133 Plus 2.0 Array)   222963_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000368278
Ensembl peptide - ENSP00000305200
NCBI entrez gene - 11141     See in Manteia.
OMIM - 300206
RefSeq - XM_017029241
RefSeq - NM_014271
RefSeq - XM_017029240
RefSeq Peptide - NP_055086
swissprot - Q9NZN1
swissprot - X5DNQ7
swissprot - A0A0A0MR17
Ensembl - ENSG00000169306
  
Related genetic diseases (OMIM): 300143 - Mental retardation, X-linked 21/34, 300143
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
 il1rapl1aENSDARG00000062045Danio rerio
 il1rapl1bENSDARG00000104853Danio rerio
 IL1RAPL1ENSGALG00000016288Gallus gallus
 Il1rapl1ENSMUSG00000052372Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Q9NP60 / IL1RAPL2 / interleukin 1 receptor accessory protein like 2ENSG0000018910861
IL1RAP / Q9NPH3 / interleukin 1 receptor accessory proteinENSG0000019608328
IL1R1 / P14778 / interleukin 1 receptor type 1ENSG0000011559421
IL18R1 / Q13478 / interleukin 18 receptor 1ENSG0000011560421
IL1RL2 / Q9HB29 / interleukin 1 receptor like 2ENSG0000011559821
O95256 / IL18RAP / interleukin 18 receptor accessory proteinENSG0000011560721
IL1RL1 / Q01638 / interleukin 1 receptor like 1ENSG0000011560219
IL1R2 / P27930 / interleukin 1 receptor type 2ENSG0000011559012


Protein motifs (from Interpro)
Interpro ID Name
 IPR000157  Toll/interleukin-1 receptor homology (TIR) domain
 IPR003598  Immunoglobulin subtype 2
 IPR003599  Immunoglobulin subtype
 IPR007110  Immunoglobulin-like domain
 IPR013151  Immunoglobulin
 IPR013783  Immunoglobulin-like fold
 IPR015621  Interleukin-1 receptor family
 IPR035897  Toll/interleukin-1 receptor homology (TIR) domain superfamily
 IPR036179  Immunoglobulin-like domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0007157 heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules ISS
 biological_processGO:0007165 signal transduction IEA
 biological_processGO:0010975 regulation of neuron projection development ISS
 biological_processGO:0030182 neuron differentiation ISS
 biological_processGO:0045920 negative regulation of exocytosis IDA
 biological_processGO:0050775 positive regulation of dendrite morphogenesis ISS
 biological_processGO:0051965 positive regulation of synapse assembly ISS
 biological_processGO:0070588 calcium ion transmembrane transport IEA
 biological_processGO:0071345 cellular response to cytokine stimulus TAS
 biological_processGO:0097105 presynaptic membrane assembly ISS
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005886 plasma membrane TAS
 cellular_componentGO:0009986 cell surface ISS
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0030424 axon IEA
 cellular_componentGO:0030425 dendrite ISS
 cellular_componentGO:0042995 cell projection IEA
 cellular_componentGO:0045211 postsynaptic membrane NAS
 molecular_functionGO:0005102 signaling receptor binding ISS
 molecular_functionGO:0005245 voltage-gated calcium channel activity ISS
 molecular_functionGO:0005515 protein binding IEA


Pathways (from Reactome)
Pathway description
Receptor-type tyrosine-protein phosphatases
Interleukin-38 signaling


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000194 Open mouth 
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 HP:0000303 Mandibular prognathia "Abnormal prominence of the chin related to an abnormally long mandible." [HPO:curators]
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 HP:0000316 Hypertelorism 
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 HP:0000582 Upslanting palpebral fissures 
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 HP:0000664 Synophrys "Fusion of the left and right `eyebrow` (FMA:54237)." [HPO:probinson]
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 HP:0000678 Dental overcrowding 
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 HP:0000717 Autism 
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 HP:0000752 Hyperactivity 
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 HP:0001249 Mental retardation 
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 HP:0001250 Seizures "Seizures are an intermittent `abnormality of the central nervous system` (FMA:HP:0002011) due to a sudden, excessive, disorderly discharge of cerebral neurons and characterized clinically by some combination of disturbance of sensation, loss of consciousness, impairment of psychic function, or convulsive movements." [HPO:probinson]
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 HP:0001382 Joint hypermobility "The ability of a joint to move beyond its normal range of motion." [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: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:0003196 Nasal hypoplasia "Underdevelopment of the `nose` (FMA:46472)." [HPO:probinson]
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 HP:0009909 Uplifted earlobes "An abnormal orientation of the earlobes such that they point out- and upward." [HPO:curators]
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 HP:0010804 Tented upper lip vermilion "Triangular appearance of the oral aperture with the apex in the midpoint of the upper vermilion and the lower vermilion forming the base." [pmid:19125428]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000136697 IL1F10 / Q8WWZ1 / interleukin 1 family member 10  / complex / reaction






 

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