IL1RAPL2

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

X-linked interleukin-1 receptor accessory protein-like 2 is a protein that in humans is encoded by the IL1RAPL2 gene.[5][6]

AliasesIL1RAPL2, IL-1R9, IL1R9, IL1RAPL-2, TIGIRR-1, interleukin 1 receptor accessory protein like 2
End105,767,829 bp[1]
Quick facts Identifiers, Aliases ...
IL1RAPL2
Identifiers
AliasesIL1RAPL2, IL-1R9, IL1R9, IL1RAPL-2, TIGIRR-1, interleukin 1 receptor accessory protein like 2
External IDsOMIM: 300277; MGI: 1913106; HomoloGene: 9681; GeneCards: IL1RAPL2; OMA:IL1RAPL2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_017416

NM_030688

RefSeq (protein)

NP_059112

NP_109613

Location (UCSC)Chr X: 104.57 – 105.77 MbChr X: 136.47 – 137.75 Mb
PubMed search[3][4]
Wikidata
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The protein encoded by this gene is a member of the interleukin 1 receptor family. This protein is similar to the interleukin 1 accessory proteins, and is most closely related to interleukin 1 receptor accessory protein-like 1 (IL1RAPL1). This gene and IL1RAPL1 are located at a region on chromosome X that is associated with X-linked non-syndromic intellectual disability.[6]

References

Further reading

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