Gene Gene information from NCBI Gene database.
Entrez ID 84282
Gene name Ring finger protein 135
Gene symbol RNF135
Synonyms (NCBI Gene)
L13MMFDREULRiplet
Chromosome 17
Chromosome location 17q11.2
Summary The protein encoded by this gene contains a RING finger domain, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. This gene is located in a chromosomal region known to
SNPs SNP information provided by dbSNP.
1
SNP ID Visualize variation Clinical significance Consequence
rs724159978 G>- Pathogenic, uncertain-significance 3 prime UTR variant, coding sequence variant, frameshift variant, downstream transcript variant, non coding transcript variant, genic downstream transcript variant
miRNA miRNA information provided by mirtarbase database.
179
miRTarBase ID miRNA Experiments Reference
MIRT642861 hsa-miR-3174 HITS-CLIP 23824327
MIRT642860 hsa-miR-4714-3p HITS-CLIP 23824327
MIRT642859 hsa-miR-1226-3p HITS-CLIP 23824327
MIRT642858 hsa-miR-6849-3p HITS-CLIP 23824327
MIRT642857 hsa-miR-939-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
39
GO ID Ontology Definition Evidence Reference
GO:0000209 Process Protein polyubiquitination IDA 31006531
GO:0000209 Process Protein polyubiquitination IEA
GO:0002376 Process Immune system process IEA
GO:0004842 Function Ubiquitin-protein transferase activity EXP 17392790, 19017631, 19484123
GO:0004842 Function Ubiquitin-protein transferase activity IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
611358 21158 ENSG00000181481
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8IUD6
Protein name E3 ubiquitin-protein ligase RNF135 (EC 2.3.2.27) (RIG-I E3 ubiquitin ligase) (REUL) (RING finger protein 135) (RING finger protein leading to RIG-I activation) (Riplet) (RING-type E3 ubiquitin transferase RNF135)
Protein function E2-dependent E3 ubiquitin-protein ligase that functions as a RIGI coreceptor in the sensing of viral RNAs in cell cytoplasm and the activation of the antiviral innate immune response (PubMed:19017631, PubMed:19484123, PubMed:21147464, PubMed:239
PDB 7JL1 , 7JL3 , 8G7T , 8G7U , 8G7V
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15227 zf-C3HC4_4 21 62 Domain
PF00622 SPRY 312 427 SPRY domain Family
Tissue specificity TISSUE SPECIFICITY: Expressed in skeletal muscle, spleen, kidney, placenta, prostate, stomach, thyroid and tongue. Also weakly expressed in heart, thymus, liver and lung. {ECO:0000269|PubMed:19017631}.
Sequence
MAGLGLGSAVPVWLAEDDLGCIICQGLLDWPATLPCGHSFCRHCLEALWGARDARRWACP
TC
RQGAAQQPHLRKNTLLQDLADKYRRAAREIQAGSDPAHCPCPGSSSLSSAAARPRRRP
ELQRVAVEKSITEVAQELTELVEHLVDIVRSLQNQRPLSESGPDNELSILGKAFSSGVDL
SMASPKLVTSDTAAGKIRDILHDLEEIQEKLQESVTWKEAPEAQMQGELLEAPSSSSCPL
PDQSHPALRRASRFAQWAIHPTFNLKSLSCSLEVSKDSRTVTVSHRPQPYRWSCERFSTS
QVLCSQALSSGKHYWEVDTRNCSHWAVGVASWEMSRDQVLGRTMDSCCVEWKGTSQLSAW
HMVKETVLGSDRPGVVGIWLNLEEGKLAFYSVDNQEKLLYECTISASSPLYPAFWLYGLH
PGNYLII
KQVKV
Sequence length 432
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    DDX58/IFIH1-mediated induction of interferon-alpha/beta
Ovarian tumor domain proteases
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 Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
17
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Autism spectrum disorder Pathogenic rs724159978 RCV000754673
Macrocephaly, macrosomia, facial dysmorphism syndrome Pathogenic rs724159978 RCV000001028
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Chromosome 17q11.2 deletion syndrome, 1.4Mb Uncertain significance rs1907708509 RCV001335203
RNF135-related disorder Uncertain significance; Likely benign; Benign rs371982152, rs201019019, rs745775948, rs926995158, rs763339124, rs111902263, rs61749868, rs376823094, rs142836972 RCV003944088
RCV003959201
RCV003926794
RCV003934633
RCV003962294
RCV003979899
RCV004758041
RCV003905849
RCV004731073
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Autism Spectrum Disorder Associate 37108679
Carcinoma Hepatocellular Associate 37803338, 38154055, 39324668
Carcinoma Hepatocellular Inhibit 39766812
Cholangiocarcinoma Associate 39766812
Developmental Disabilities Associate 30665703
Glioma Associate 18492260
Neoplasm Metastasis Associate 36495591
Neoplasm Metastasis Inhibit 39766812
Neoplasms Inhibit 20844836, 37145209
Neoplasms Associate 36495591