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Gene Gene information from NCBI Gene database.
Entrez ID 79635
Gene name Coiled-coil domain containing 121
Gene symbol CCDC121
Synonyms (NCBI Gene)
-
Chromosome 2
Chromosome location 2p23.3
miRNA miRNA information provided by mirtarbase database.
78 Show/Hide all (78)
miRTarBase ID miRNA Experiments Reference
MIRT022834 hsa-miR-124-3p Microarray 18668037
MIRT024586 hsa-miR-215-5p Microarray 19074876
MIRT026670 hsa-miR-192-5p Microarray 19074876
MIRT647539 hsa-miR-4688 HITS-CLIP 23824327
MIRT647540 hsa-miR-6743-5p HITS-CLIP 23824327
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 21516116, 25416956, 31515488, 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.
Q6ZUS5
Protein name Coiled-coil domain-containing protein 121
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14988 DUF4515 35 → 240 Domain of unknown function (DUF4515) Family
Sequence
Sequence length 278
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
FAMILIAL HYPERLIPIDEMIA — GWAS catalog 34906840
★★★★★
★★☆☆☆
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
Stomach Neoplasms Stomach neoplasms Pubtator 26330360 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only