Gene Gene information from NCBI Gene database.
Entrez ID 10069
Gene name RWD domain containing 2B
Gene symbol RWDD2B
Synonyms (NCBI Gene)
C21orf6GL011
Chromosome 21
Chromosome location 21q21.3
miRNA miRNA information provided by mirtarbase database.
68
miRTarBase ID miRNA Experiments Reference
MIRT1323194 hsa-miR-29a CLIP-seq
MIRT1323195 hsa-miR-29b CLIP-seq
MIRT1323196 hsa-miR-29c CLIP-seq
MIRT1323197 hsa-miR-3128 CLIP-seq
MIRT1323198 hsa-miR-3160-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
1
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 16189514, 21516116, 25416956, 31515488, 32296183
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617843 1302 ENSG00000156253
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P57060
Protein name RWD domain-containing protein 2B
PDB 2DAX
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05773 RWD 37 162 RWD domain Domain
PF06544 DUF1115 191 313 Protein of unknown function (DUF1115) Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitous.
Sequence
Sequence length 319
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
OSTEOARTHRITIS, HIP GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
OSTEOARTHRITIS, KNEE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations