IL36RN interleukin 36 receptor antagonist

Information
Symbol
IL36RN
Type
protein-coding
Description
interleukin 36 receptor antagonist
Entrez Gene ID
26525
Genome
hg19
Position
chr2:113,816,215-113,822,325
Genome
hg38
Position
chr2:113,058,638-113,064,748
MIM
605507 OMIM
HGNC
HGNC:15561 HGNC
Ensembl
ENSG00000136695 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 2 8
Likely pathogenic 2 8
Benign 0 38
Likely benign 0 104
Conflicting classifications of pathogenicity 0 36
Uncertain significance 0 188
Ranking
ClinVar
0
0
42
298
2
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
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Variant name Gene AA change CDS Japanese
frequency
TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence
Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM FIL1
SYNONYM FIL1(DELTA)
SYNONYM FIL1D
SYNONYM IL-36Ra
SYNONYM IL1F5
SYNONYM IL1HY1
SYNONYM IL1L1
SYNONYM IL1RP3
SYNONYM IL36RA
SYNONYM PSORP
SYNONYM PSORS14
MIM 605507 OMIM
HGNC HGNC:15561 HGNC
Ensembl ENSG00000136695 Ensembl
AllianceGenome HGNC:15561
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000437409.2 hg38 chr2 113,059,387 113,062,677 3,291
ENST00000346807.7 hg38 chr2 113,058,638 113,064,748 6,111
ENST00000393200.7 hg38 chr2 113,059,198 113,064,744 5,547
ENST00000346807.7 hg19 chr2 113,816,215 113,822,325 6,111
ENST00000393200.7 hg19 chr2 113,816,775 113,822,321 5,547
ENST00000437409.2 hg19 chr2 113,816,964 113,820,254 3,291
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