Gene Gene information from NCBI Gene database.
Entrez ID 64925
Gene name Coiled-coil domain containing 71
Gene symbol CCDC71
Synonyms (NCBI Gene)
-
Chromosome 3
Chromosome location 3p21.31
miRNA miRNA information provided by mirtarbase database.
10
miRTarBase ID miRNA Experiments Reference
MIRT022489 hsa-miR-124-3p Microarray 18668037
MIRT052352 hsa-let-7b-5p CLASH 23622248
MIRT037673 hsa-miR-744-5p CLASH 23622248
MIRT440990 hsa-miR-218-5p HITS-CLIP 23212916
MIRT440990 hsa-miR-218-5p HITS-CLIP 23212916
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.
Q8IV32
Protein name Coiled-coil domain-containing protein 71
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15374 CCDC71L 8 334 Coiled-coil domain-containing protein 71L Coiled-coil
PF15374 CCDC71L 313 461 Coiled-coil domain-containing protein 71L Coiled-coil
Sequence
Sequence length 467
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
BEHCET'S SYNDROME GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
INSOMNIA 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
Antiphospholipid Syndrome Antiphospholipid syndrome Pubtator 37901230 Associate
★☆☆☆☆
Found in Text Mining only
Anxiety Anxiety disorder Pubtator 39681175 Associate
★☆☆☆☆
Found in Text Mining only
Hashimoto Disease Hashimoto disease Pubtator 37545519 Associate
★☆☆☆☆
Found in Text Mining only
Polycystic Ovary Syndrome Polycystic ovary syndrome Pubtator 37545519 Associate
★☆☆☆☆
Found in Text Mining only
Stroke Stroke Pubtator 39681175 Associate
★☆☆☆☆
Found in Text Mining only