Gene Gene information from NCBI Gene database.
Entrez ID 57827
Gene name Chromosome 6 open reading frame 47
Gene symbol C6orf47
Synonyms (NCBI Gene)
D6S53EG4NG34
Chromosome 6
Chromosome location 6p21.33
miRNA miRNA information provided by mirtarbase database.
78
miRTarBase ID miRNA Experiments Reference
MIRT050157 hsa-miR-26a-5p CLASH 23622248
MIRT528183 hsa-miR-200b-3p PAR-CLIP 22012620
MIRT528182 hsa-miR-200c-3p PAR-CLIP 22012620
MIRT528181 hsa-miR-429 PAR-CLIP 22012620
MIRT528180 hsa-miR-193a-3p PAR-CLIP 22012620
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 32296183
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.
O95873
Protein name Uncharacterized protein C6orf47 (Protein G4)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15576 DUF4661 16 265 Domain of unknown function (DUF4661) Family
Sequence
Sequence length 294
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
7
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
CROHN'S DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
FAMILIAL APOLIPOPROTEIN B HYPOBETALIPOPROTEINEMIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
INFLAMMATORY BOWEL DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PROSTATE CANCER GWAS catalog
★★☆☆☆
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
Celiac Disease Celiac disease BEFREE 28282431
★☆☆☆☆
Found in Text Mining only
Celiac Disease Celiac disease Pubtator 28282431 Associate
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus, Insulin-Dependent Diabetes Mellitus GWASDB_DG 17632545
★☆☆☆☆
Found in Text Mining only
Glioblastoma Glioblastoma BEFREE 29511029
★☆☆☆☆
Found in Text Mining only
Glioblastoma Multiforme Glioblastoma BEFREE 29511029
★☆☆☆☆
Found in Text Mining only
Hashimoto Disease Hashimoto Disease BEFREE 29541194
★☆☆☆☆
Found in Text Mining only
Lymphoma, Non-Hodgkin Non-Hodgkin lymphoma BEFREE 28282431
★☆☆☆☆
Found in Text Mining only
Lymphoma, Non-Hodgkin, Familial Lymphoma BEFREE 28282431
★☆☆☆☆
Found in Text Mining only
Malignant Neoplasms Malignant Neoplasm BEFREE 29511029
★☆☆☆☆
Found in Text Mining only
Papillary thyroid carcinoma Papillary thyroid carcinoma BEFREE 29541194
★☆☆☆☆
Found in Text Mining only