Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
60494
Gene name Gene Name - the full gene name approved by the HGNC.
Coiled-coil domain containing 81
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CCDC81
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q14.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT526066 hsa-miR-548c-3p PAR-CLIP 22012620
MIRT526065 hsa-miR-4705 PAR-CLIP 22012620
MIRT526064 hsa-miR-513b-5p PAR-CLIP 22012620
MIRT526063 hsa-miR-6802-3p PAR-CLIP 22012620
MIRT526066 hsa-miR-548c-3p PAR-CLIP 22012620
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 21930792
GO:0005737 Component Cytoplasm IEA
GO:0005813 Component Centrosome IDA 25074808
GO:0005813 Component Centrosome IEA
GO:0005815 Component Microtubule organizing center IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID Q6ZN84
Protein name Coiled-coil domain-containing protein 81
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14908 HU-CCDC81_euk_1 6 93 CCDC81 eukaryotic HU domain 1 Domain
PF18289 HU-CCDC81_euk_2 103 177 CCDC81 eukaryotic HU domain 2 Domain
Sequence
MLDTIARALQDLGRQVLPTLPSLSQEEVSIIWGNVSEFVRRQLTLHKGVQIPAFGTFTFI
RQKLEVGNNKFILIQRPVFIMVEKLVQIHGLKQ
NKVYTPGEIPIVPLNFVMISLEGPFNR
DVVEGCVKETLLFLSRSISMKQNVEFTFKGIGVLMIRDSKVKMRFYKDFLCTMDGSG
ALA
KALANRPGTVDSVLSSREALRKWPSSVLAFPRIELKEMENKLPMETLVEECGENRERKCK
LKDQSDKEEGTRDISSPKRLRDRQALFPAKVTNVSLLEKFERSESGGKIMTPESLSYPSC
LKHDSEMKPQTSPACQDHNKAGQEMCYVCLQRAQRNSLLYYSEERRREIEDERLIQQYQM
LKDQEALFRHQMKSLATREQNQKNAAYNLGVAEAIRNHKNEKPEFYKSFLFDKRPLSPAL
NALKQEEYSRSLLKQMDNRQENEIKQRQYRELMDRLEQVQLTEELAAQRAKFLKDKMEET
QCYKRALDAQIKNKPSRLPPFEPDSSEPIFGKNEGELMVEKQKREQNYMKHQLEAAANHK
RKAILHQLVDQRRDLQMLQRTQREHLADRTAELERVNRVNQCLQEDWERSAAMKKQRDLE
DKAFERASDKLFLLDQCEKYRRCKQCQRRTSNVGESNLWPLNKFLPGSRLLV
Sequence length 652
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Eosinophilia Eosinophilic esophagitis N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Nasopharyngeal Carcinoma Associate 31770211