Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
160857
Gene name Gene Name - the full gene name approved by the HGNC.
Coiled-coil domain containing 122
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CCDC122
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
13
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
13q14.11
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a protein that contains a coiled-coil domain. Naturally occurring mutations in this gene are associated with leprosy. [provided by RefSeq, Apr 2017]
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT636940 hsa-miR-6499-5p HITS-CLIP 23824327
MIRT636939 hsa-miR-4284 HITS-CLIP 23824327
MIRT636938 hsa-miR-24-3p HITS-CLIP 23824327
MIRT636937 hsa-miR-3178 HITS-CLIP 23824327
MIRT636936 hsa-miR-7977 HITS-CLIP 23824327
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
613408 26478 ENSG00000151773
Protein
UniProt ID Q5T0U0
Protein name Coiled-coil domain-containing protein 122
Family and domains
Sequence
MSDNKERKSQGFPKEDNQDTSSLADAVEKVAKQQQSQASEIEKNKKVLFNLKNELHELEK
EIAAISAETKETERQIYQQDSAIENTKLHCDSLETQIKSLHSENVKLKFDIETAQEDFEE
HMIKYNAYYAKIKAHKNSLGEVESKWSFMTELHEKRDFVKKLKTMKEELMQDLQNPGGNR
ITQVQEDITNLKDKIITVKESIIEKTCFLEEEKKTHEKLRKEIEVQHKRYDAILKRLHCQ
VNKLQSNRRQWQWNIQQLEKTAAELRKCIGMQE
Sequence length 273
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
Dementia Dementia N/A N/A GWAS