Gene Gene information from NCBI Gene database.
Entrez ID 3654
Gene name Interleukin 1 receptor associated kinase 1
Gene symbol IRAK1
Synonyms (NCBI Gene)
IRAKpelle
Chromosome X
Chromosome location Xq28
Summary This gene encodes the interleukin-1 receptor-associated kinase 1, one of two putative serine/threonine kinases that become associated with the interleukin-1 receptor (IL1R) upon stimulation. This gene is partially responsible for IL1-induced upregulation
miRNA miRNA information provided by mirtarbase database.
349
miRTarBase ID miRNA Experiments Reference
MIRT000712 hsa-miR-146a-5p Western blotNorthern blot 18504431
MIRT000712 hsa-miR-146a-5p Luciferase reporter assayWestern blot 20061417
MIRT000712 hsa-miR-146a-5p qRT-PCR 18759964
MIRT000712 hsa-miR-146a-5p qRT-PCRWestern blotImmunofluorescence 19918258
MIRT005395 hsa-miR-146b-5p Luciferase reporter assayMicroarrayNorthern blotqRT-PCR 16885212
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
86
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0001959 Process Regulation of cytokine-mediated signaling pathway IMP 10383454
GO:0002224 Process Toll-like receptor signaling pathway TAS
GO:0002376 Process Immune system process IEA
GO:0002755 Process MyD88-dependent toll-like receptor signaling pathway TAS 10383454
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
300283 6112 ENSG00000184216
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P51617
Protein name Interleukin-1 receptor-associated kinase 1 (IRAK-1) (EC 2.7.11.1)
Protein function Serine/threonine-protein kinase that plays a critical role in initiating innate immune response against foreign pathogens. Involved in Toll-like receptor (TLR) and IL-1R signaling pathways. Is rapidly recruited by MYD88 to the receptor-signaling
PDB 6BFN
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00531 Death 27 103 Death domain Domain
PF00069 Pkinase 212 517 Protein kinase domain Domain
Tissue specificity TISSUE SPECIFICITY: Isoform 1 and isoform 2 are ubiquitously expressed in all tissues examined, with isoform 1 being more strongly expressed than isoform 2. {ECO:0000269|PubMed:11397809}.
Sequence
MAGGPGPGEPAAPGAQHFLYEVPPWVMCRFYKVMDALEPADWCQFAALIVRDQTELRLCE
RSGQRTASVLWPWINRNARVADLVHILTHLQLLRARDIITAWH
PPAPLPSPGTTAPRPSS
IPAPAEAEAWSPRKLPSSASTFLSPAFPGSQTHSGPELGLVPSPASLWPPPPSPAPSSTK
PGPESSVSLLQGARPFPFCWPLCEISRGTHNFSEELKIGEGGFGCVYRAVMRNTVYAVKR
LKENADLEWTAVKQSFLTEVEQLSRFRHPNIVDFAGYCAQNGFYCLVYGFLPNGSLEDRL
HCQTQACPPLSWPQRLDILLGTARAIQFLHQDSPSLIHGDIKSSNVLLDERLTPKLGDFG
LARFSRFAGSSPSQSSMVARTQTVRGTLAYLPEEYIKTGRLAVDTDTFSFGVVVLETLAG
QRAVKTHGARTKYLKDLVEEEAEEAGVALRSTQSTLQAGLAADAWAAPIAMQIYKKHLDP
RPGPCPPELGLGLGQLACCCLHRRAKRRPPMTQVYER
LEKLQAVVAGVPGHSEAASCIPP
SPQENSYVSSTGRAHSGAAPWQPLAAPSGASAQAAEQLQRGPNQPVESDESLGGLSAALR
SWHLTPSCPLDPAPLREAGCPQGDTAGESSWGSGPGSRPTAVEGLALGSSASSSSEPPQI
IINPARQKMVQKLALYEDGALDSLQLLSSSSLPGLGLEQDRQGPEESDEFQS
Sequence length 712
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
22
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Chronic lymphocytic leukemia/small lymphocytic lymphoma Benign rs10127175 RCV005911862
Colon adenocarcinoma Benign rs10127175 RCV005911858
Gastric cancer Benign rs10127175 RCV005911859
IRAK1-related disorder Uncertain significance; Likely benign; Benign rs145414165, rs34112487, rs202203227, rs1229790473, rs782106693, rs143993525, rs782263874, rs782393640, rs368268634, rs11465829, rs782636633, rs149520139, rs2065752119, rs2521947003, rs11556424
View all (1 more)
RCV003946362
RCV003929196
RCV003939042
RCV003896804
RCV003896319
RCV003912321
RCV003899781
RCV003914103
RCV003949527
RCV003957143
RCV003922085
RCV003926845
RCV003969440
RCV003966875
RCV003960608
RCV003916260
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Aggressive Periodontitis Associate 28883894
AIDS Associated Nephropathy Associate 32276639
Alzheimer Disease Associate 20937840, 23300433
Antiphospholipid Syndrome Associate 22288586
Arthritis Psoriatic Stimulate 19166933
Arthritis Psoriatic Associate 20500689
Arthritis Rheumatoid Associate 18759964, 23233309, 28271077, 29734142
Atherosclerosis Associate 17382928
Autistic Disorder Associate 28302064
Autoimmune Diseases Associate 25550857