Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
80352
Gene name Gene Name - the full gene name approved by the HGNC.
Ring finger protein 39
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RNF39
Synonyms (NCBI Gene) Gene synonyms aliases
FAP216, HZF, HZFW, LIRF
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p22.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene lies within the major histocompatibility complex class I region on chromosome 6. Studies of a similar rat protein suggest that this gene encodes a protein that plays a role in an early phase of synaptic plasticity. Multiple transcript variants e
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1312903 hsa-miR-1257 CLIP-seq
MIRT1312904 hsa-miR-1278 CLIP-seq
MIRT1312905 hsa-miR-3918 CLIP-seq
MIRT1312906 hsa-miR-4434 CLIP-seq
MIRT1312907 hsa-miR-4481 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0002753 Process Cytoplasmic pattern recognition receptor signaling pathway IDA 23478265
GO:0005515 Function Protein binding IPI 32296183
GO:0005737 Component Cytoplasm IBA
GO:0005737 Component Cytoplasm IDA 33674311, 39255680
GO:0005737 Component Cytoplasm IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
607524 18064 ENSG00000204618
Protein
UniProt ID Q9H2S5
Protein name RING finger protein 39 (EC 2.3.2.27) (Protein HZFw)
Protein function Plays an inhibitory role in anti-RNA viral innate immunity by targeting the adapter DDX3X and promoting its 'Lys-48'-linked polyubiquitination (PubMed:33674311). Alternatively, enhances the cGAS-STING pathway activation by promoting 'Lys-63'-lin
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00097 zf-C3HC4 88 134 Zinc finger, C3HC4 type (RING finger) Domain
PF13765 PRY 230 279 SPRY-associated domain Family
Tissue specificity TISSUE SPECIFICITY: Expressed in testis. {ECO:0000269|PubMed:11130983}.
Sequence
MWWRDLTRLRLWLKREAIPGEGRKAAKVNAGVGEKGIYTASSRGGPPSARSKAVTVVAEG
AASRSWLSMDAPELGPGLVERLEQLATCPLCGGSFEDPVLLACEHSFCRACLARRWGTPP
ATGTEASPTACPCC
GLPCPRRSLRSNVRLAVEVRISRELREKLAEPGARAGRRRGGRIPT
MGCLDLPGEDMRKTWRRFEVPTSKSSNSEDDLPEDYPVVKKMLHRLTADLTLDPGTAHRR
LLISADRRSVQLAPPGTPAPPDGPKRFDQLPAVLGAQGF
GAGRHCWEVETADAASCRDSS
GEDADDEESHYAVGAAGESVQRKGCVRLCPAGAVWAVEGRGGRLWALTAPEPTLLGGVEP
PPRRIRVDLDWERGRVAFYDGRSLDLLYAFQAPGPLGERIFPLFCTCDPRAPLRIVPAES
Sequence length 420
Interactions View interactions
<
Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Cervical Cancer Cervical cancer N/A N/A GWAS
Lymphocytic Leukemia Chronic lymphocytic leukemia N/A N/A GWAS
Myasthenia Gravis Myasthenia gravis N/A N/A GWAS
Psoriasis Psoriasis N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Cardio Renal Syndrome Associate 26534935
Coronary Artery Disease Inhibit 26534935
Coronary Artery Disease Associate 26534935
Distal Myopathies Associate 38015635
Infertility Male Associate 31103287
Lesch Nyhan Syndrome Stimulate 33875724
Metabolic Diseases Associate 30782033
Multiple Sclerosis Associate 28729889
Pain Associate 38015635
Rhinitis Allergic Associate 28149331