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Gene Gene information from NCBI Gene database.
Entrez ID 414236
Gene name Chromosome 10 putative open reading frame 55
Gene symbol C10orf55
Synonyms (NCBI Gene)
-
Chromosome 10
Chromosome location 10q22.2
miRNA miRNA information provided by mirtarbase database.
93 Show/Hide all (93)
miRTarBase ID miRNA Experiments Reference
MIRT487061 hsa-miR-6873-5p PAR-CLIP 23592263
MIRT487060 hsa-miR-1321 PAR-CLIP 23592263
MIRT487059 hsa-miR-4739 PAR-CLIP 23592263
MIRT487058 hsa-miR-4756-5p PAR-CLIP 23592263
MIRT487057 hsa-miR-6784-5p PAR-CLIP 23592263
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
2
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 28514442, 32296183, 33961781
GO:0042802 Function Identical 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.
Q5SWW7
Protein name Uncharacterized protein C10orf55
Family and domains
Sequence
MFLHLDSHSSLERTKPTVVGVDTHMELDEVHCCPGRDSGGGFIKGPMLQGLQGEGKLAPI
PKPTLPSPSRLTLFVSSSQMEDHGFPARRNGLTQASFIYQMPAGWGSPGGLFLPCQPVPT
PVVLKPPLPPCPISWGESGPAVDGIRRTPAP
Sequence length 151
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
C10orf55-related disorder Likely benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Show/Hide Text Mining Associations (6)
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Carcinoma Squamous Cell Squamous cell carcinoma Pubtator 36845013 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Crohn Disease Crohn Disease GWASCAT_DG 28067908
★★★★★
★☆☆☆☆
Found in Text Mining only
Inflammatory Bowel Diseases Inflammatory Bowel Disease GWASCAT_DG 23128233
★★★★★
★☆☆☆☆
Found in Text Mining only
Inflammatory Bowel Diseases Inflammatory Bowel Disease GWASDB_DG 23128233
★★★★★
★☆☆☆☆
Found in Text Mining only
Quebec platelet disorder Quebec Platelet Disorder BEFREE 28301587
★★★★★
★☆☆☆☆
Found in Text Mining only
Venous Thrombosis Venous thrombosis Pubtator 29334895 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only