GediPNet logo

RIGI (RNA sensor RIG-I)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
23586
Gene nameGene Name - the full gene name approved by the HGNC.
RNA sensor RIG-I
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
RIGI
SynonymsGene synonyms aliases
DDX58, RIG-I, RIG1, RLR-1, SGMRT2
ChromosomeChromosome number
9
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
9p21.1
SNPsSNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs786204847 T>G Pathogenic Coding sequence variant, missense variant
rs786204848 C>A Pathogenic Coding sequence variant, missense variant
rs1064795754 A>G Likely-pathogenic Coding sequence variant, missense variant
rs1131691305 A>G Likely-pathogenic Coding sequence variant, missense variant
rs1587586052 T>A Likely-pathogenic Missense variant, coding sequence variant
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT437784 hsa-miR-10b-5p Luciferase reporter assay 25312779
MIRT440833 hsa-miR-218-5p HITS-CLIP 23212916
MIRT440833 hsa-miR-218-5p HITS-CLIP 23212916
MIRT734373 hsa-miR-579-3p ELISA, Luciferase reporter assay, RNA-seq, Western blotting 32209695
MIRT734374 hsa-miR-221-3p ELISA, Luciferase reporter assay, RNA-seq, Western blotting 32209695
Transcription factors
Transcription factor Regulation Reference
IRF1 Activation 22391244
TRIM25 Unknown 21292167
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0002230 Process Positive regulation of defense response to virus by host IMP 19609254
GO:0002735 Process Positive regulation of myeloid dendritic cell cytokine production ISS
GO:0003724 Function RNA helicase activity IEA
GO:0003725 Function Double-stranded RNA binding IBA 21873635
GO:0003725 Function Double-stranded RNA binding IDA 19576794
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID O95786
Protein name Antiviral innate immune response receptor RIG-I (ATP-dependent RNA helicase DDX58) (EC 3.6.4.13) (DEAD box protein 58) (RIG-I-like receptor 1) (RLR-1) (RNA sensor RIG-I) (Retinoic acid-inducible gene 1 protein) (RIG-1) (Retinoic acid-inducible gene I prot
Protein function Innate immune receptor that senses cytoplasmic viral nucleic acids and activates a downstream signaling cascade leading to the production of type I interferons and pro-inflammatory cytokines (PubMed:15208624, PubMed:15708988, PubMed:16125763, Pu
PDB 2LWD , 2LWE , 2QFB , 2QFD , 2RMJ , 2YKG , 3LRN , 3LRR , 3NCU , 3OG8 , 3ZD6 , 3ZD7 , 4AY2 , 4BPB , 4NQK , 4ON9 , 4P4H , 5E3H , 5F98 , 5F9F , 5F9H , 6GPG , 6KYV , 7BAH , 7BAI , 7JL1 , 7JL3 , 7MK1 , 7TNX , 7TNY , 7TNZ , 7TO0 , 7TO1 , 7TO2 , 8DVR , 8DVS , 8DVU , 8G7T , 8G7U , 8G7V , 8SCZ , 8SD0
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF16739 CARD_2
1 93
Caspase recruitment domain
Domain
PF16739 CARD_2
99 190
Caspase recruitment domain
Domain
PF00270 DEAD
244 420
DEAD/DEAH box helicase
Domain
PF18119 RIG-I_C
457 602
RIG-I receptor C-terminal domain
Domain
PF00271 Helicase_C
609 734
Helicase conserved C-terminal domain
Family
PF11648 RIG-I_C-RD
806 923
C-terminal domain of RIG-I
Domain
Sequence
MTTEQRRSLQAFQDYIRKTLDPTYILSYMAPWFREEEVQYIQAEKNNKGPMEAATLFLKF
LLELQEEGWFRGFLDALDHAGYSGLYEAIESWD
FKKIEKLEEYRLLLKRLQPEFKTRIIP
TDIISDLSECLINQECEEILQICSTKGMMAGAEKLVECLLRSDKENWPKTLKLALEKERN
KFSELWIVEK
GIKDVETEDLEDKMETSDIQIFYQEDPECQNLSENSCPPSEVSDTNLYSP
FKPRNYQLELALPAMKGKNTIICAPTGCGKTFVSLLICEHHLKKFPQGQKGKVVFFANQI
PVYEQQKSVFSKYFERHGYRVTGISGATAENVPVEQIVENNDIIILTPQILVNNLKKGTI
PSLSIFTLMIFDECHNTSKQHPYNMIMFNYLDQKLGGSSGPLPQVIGLTASVGVGDAKNT

DEALDYICKLCASLDASVIATVKHNLEELEQVVYKPQKFFRKVESRISDKFKYIIAQLMR
DTESLAKRICKDLENLSQIQNREFGTQKYEQWIVTVQKACMVFQMPDKDEESRICKALFL
YTSHLRKYNDALIISEHARMKDALDYLKDFFSNVRAAGFDEIEQDLTQRFEEKLQELESV
SR
DPSNENPKLEDLCFILQEEYHLNPETITILFVKTRALVDALKNWIEGNPKLSFLKPGI
LTGRGKTNQNTGMTLPAQKCILDAFKASGDHNILIATSVADEGIDIAQCNLVILYEYVGN
VIKMIQTRGRGRAR
GSKCFLLTSNAGVIEKEQINMYKEKMMNDSILRLQTWDEAVFREKI
LHIQTHEKFIRDSQEKPKPVPDKENKKLLCRKCKALACYTADVRVIEECHYTVLGDAFKE
CFVSRPHPKPKQFSSFEKRAKIFCARQNCSHDWGIHVKYKTFEIPVIKIESFVVEDIATG
VQTLYSKWKDFHFEKIPFDPAEM
SK
Sequence length 925
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
KEGG
 
Reactome
  NF-kappa B signaling pathway
RIG-I-like receptor signaling pathway
Cytosolic DNA-sensing pathway
Hepatitis C
Hepatitis B
Measles
Influenza A
Herpes simplex virus 1 infection
Epstein-Barr virus infection
Coronavirus disease - COVID-19
  ISG15 antiviral mechanism
DDX58/IFIH1-mediated induction of interferon-alpha/beta
Ub-specific processing proteases
Ovarian tumor domain proteases
OAS antiviral response
TRAF3-dependent IRF activation pathway
TRAF6 mediated IRF7 activation
TRAF6 mediated NF-kB activation
NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10
Negative regulators of DDX58/IFIH1 signaling
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Glaucoma Glaucoma rs121918355, rs1566660365, rs1566635134, rs121918356, rs1566634475, rs28936700, rs55771538, rs28936701, rs104893622, rs55989760, rs72549387, rs104893628, rs2125316417, rs104893629, rs74315328, rs121909193, rs74315330, rs74315329, rs74315332, rs74315334, rs74315336, rs74315338, rs74315341, rs121909194, rs74315331, rs1558603396, rs387907175, rs587778873, rs587778875, rs104894979, rs137854895, rs766425037, rs72549380, rs148542782, rs541217363, rs753021890, rs771076928, rs56010818, rs777678299, rs1446110883, rs1573274915, rs1587545234, rs751768343, rs944452644
Psoriasis Psoriasis rs281875215, rs587777763, rs281875213, rs281875212 25903422, 23143594, 25574825
Singleton merten syndrome Singleton Merten syndrome, SINGLETON-MERTEN SYNDROME 2, SINGLETON-MERTEN SYNDROME 1, Singleton-Merten dysplasia rs587777445, rs587777446, rs376048533, rs786204847, rs786204848, rs1587586052, rs1576226604, rs1576229572 25620203
Unknown
Disease name Disease term dbSNP ID References
Hyperkeratosis Hyperkeratosis
Palmoplantar pustules Pustulosis of Palms and Soles 23143594

| © 2021, Biomedical Informatics Centre, NIRRH |
ICMR-National Institute for Research in Reproductive Health, Jehangir Merwanji Street, Parel, Mumbai-400012
Tel: +91-22-24192104, Fax No: +91-22-24139412