Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
124817
Gene name Gene Name - the full gene name approved by the HGNC.
Cyclin N-terminal domain containing 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CNTD1
Synonyms (NCBI Gene) Gene synonyms aliases
CNTD, COSA1
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17q21.2-q21.31
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT901498 hsa-miR-125a-5p CLIP-seq
MIRT901499 hsa-miR-125b CLIP-seq
MIRT901500 hsa-miR-129-3p CLIP-seq
MIRT901501 hsa-miR-3134 CLIP-seq
MIRT901502 hsa-miR-3189-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005634 Component Nucleus IEA
GO:0005694 Component Chromosome IEA
GO:0005694 Component Chromosome ISS
GO:0005737 Component Cytoplasm IEA
GO:0007131 Process Reciprocal meiotic recombination IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
618166 26847 ENSG00000176563
Protein
UniProt ID Q8N815
Protein name Cyclin N-terminal domain-containing protein 1
Protein function Plays a role in the different steps of crossover formation during meiotic recombination. Participates in the crossover differentiation step of crossover-specific recombination intermediates through its interaction with PRR19. In addition, stimul
Family and domains
Sequence
MDGPMRPRSASLVDFQFGVVATETIEDALLHLAQQNEQAVREASGRLGRFREPQIVEFVF
LLSEQWCLEKSVSYQAVEILERFMVKQAENICRQATIQPRDNKRESQNWRALKQQLVNKF
TLRLVSCVQLASKLSFRNKIISNITVLNFLQALGYLHTKEELLESELDVLKSLNFRINLP
TPLAYVETLLEVLGYNGCLVPAMRLHATCLTLLDLVYLLHEPIYESLLRASIENSTPSQL
QGEKFTSVKEDFMLLAVGIIAASAFIQNHECWSQVVGHLQSITGIALASIAEFSYAILTH
GVGANTPGRQQSIPPHLAARALKTVASSNT
Sequence length 330
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
Breast Cancer Breast cancer N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Vasculitis Associate 34961976