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Gene Gene information from NCBI Gene database.
Entrez ID 442247
Gene name Ret finger protein like 4B
Gene symbol RFPL4B
Synonyms (NCBI Gene)
RNF211
Chromosome 6
Chromosome location 6q21
miRNA miRNA information provided by mirtarbase database.
26 Show/Hide all (26)
miRTarBase ID miRNA Experiments Reference
MIRT1301950 hsa-miR-140-3p CLIP-seq
MIRT1301951 hsa-miR-3136-5p CLIP-seq
MIRT1301952 hsa-miR-4439 CLIP-seq
MIRT1301953 hsa-miR-4474-3p CLIP-seq
MIRT1301954 hsa-miR-4513 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
6 Show/Hide all (6)
GO ID Ontology Definition Evidence Reference
GO:0005737 Component Cytoplasm IBA
GO:0008270 Function Zinc ion binding IEA
GO:0010468 Process Regulation of gene expression IBA
GO:0045087 Process Innate immune response IBA
GO:0046872 Function Metal ion binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6ZWI9
Protein name Ret finger protein-like 4B (RING finger protein 211)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00622 SPRY 145 → 261 SPRY domain Family
PF15227 zf-C3HC4_4 11 → 52 Domain
Sequence
Sequence length 263
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 Reference Evidence Score
OLIGODENDROGLIOMA — GWAS catalog 36810956
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations