Gene Gene information from NCBI Gene database.
Entrez ID 55337
Gene name Shiftless antiviral inhibitor of ribosomal frameshifting
Gene symbol SHFL
Synonyms (NCBI Gene)
C19orf66IRAVRyDENSFL
Chromosome 19
Chromosome location 19p13.2
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
29
GO ID Ontology Definition Evidence Reference
GO:0000932 Component P-body IDA 27974568
GO:0000932 Component P-body IEA
GO:0003723 Function RNA binding IDA 26735137, 27974568
GO:0003723 Function RNA binding IEA
GO:0005515 Function Protein binding IPI 21044950, 25416956, 25814554, 26735137, 27974568, 30682371, 32296183, 32814053
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616808 25649 ENSG00000130813
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NUL5
Protein name Shiftless antiviral inhibitor of ribosomal frameshifting protein (SFL) (SHFL) (Interferon-regulated antiviral protein) (IRAV) (Repressor of yield of DENV protein) (RyDEN)
Protein function Inhibits programmed -1 ribosomal frameshifting (-1PRF) of a variety of mRNAs from viruses, such as HIV1, and cellular genes, such as PEG10. Interacts with the -1PRF signal of target mRNA and translating ribosomes and causes premature translation
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15135 UPF0515 16 272 Uncharacterised protein UPF0515 Family
Sequence
Sequence length 291
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
HEREDITARY SENSORY AND AUTONOMIC NEUROPATHY TYPE IE Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Carcinoma Hepatocellular Hepatocellular carcinoma Pubtator 32294532 Associate
★☆☆☆☆
Found in Text Mining only
Hepatitis C Hepatitis c Pubtator 32294532 Stimulate
★☆☆☆☆
Found in Text Mining only
Hepatitis C Chronic Hepatitis c Pubtator 32294532 Stimulate
★☆☆☆☆
Found in Text Mining only
Kaposi Sarcoma Kaposi Sarcoma BEFREE 30944177
★☆☆☆☆
Found in Text Mining only
Sarcoma Kaposi Sarcoma Pubtator 30944177 Associate
★☆☆☆☆
Found in Text Mining only