Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
123036
Gene name Gene Name - the full gene name approved by the HGNC.
Tandem C2 domains, nuclear
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TC2N
Synonyms (NCBI Gene) Gene synonyms aliases
C14orf47, C2CD1, MTAC2D1, TAC2N, Tac2-N
Chromosome Chromosome number
14
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
14q32.12
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT021482 hsa-miR-9-5p Sequencing 20371350
MIRT1415372 hsa-miR-106a CLIP-seq
MIRT1415373 hsa-miR-106b CLIP-seq
MIRT1415374 hsa-miR-1263 CLIP-seq
MIRT1415375 hsa-miR-1264 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003674 Function Molecular_function ND
GO:0005575 Component Cellular_component ND
GO:0005634 Component Nucleus IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
619305 19859 ENSG00000165929
Protein
UniProt ID Q8N9U0
Protein name Tandem C2 domains nuclear protein (Membrane targeting tandem C2 domain-containing protein 1) (Tandem C2 protein in nucleus) (Tac2-N)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00168 C2 238 342 C2 domain Domain
PF00168 C2 366 473 C2 domain Domain
Sequence
MATEFIKSCCGGCFYGETEKHNFSVERDFKAAVPNSQNATISVPPLTSVSVKPQLGCTED
YLLSKLPSDGKEVPFVVPKFKLSYIQPRTQETPSHLEELEGSARASFGDRKVELSSSSQH
GPSYDVYNPFYMYQHISPDLSRRFPPRSEVKRLYGSVCDLRTNKLPGSPGLSKSMFDLTN
SSQRFIQRHDSLSSVPSSSSSRKNSQGSNRSLDTITLSGDERDFGRLNVKLFYNSSVEQI
WITVLQCRDLSWPSSYGDTPTVSIKGILTLPKPVHFKSSAKEGSNAIEFMETFVFAIKLQ
NLQTVRLVFKIQTQTPRKKTIGECSMSLRTLSTQEMDYSLDI
TPPSKISVCHAELELGTC
FQAVNSRIQLQILEARYLPSSSTPLTLSFFVKVGMFSSGELIYKKKTRLLKASNGRVKWG
ETMIFPLIQSEKEIVFLIKLYSRSSVRRKHFVGQIWISEDSNNIEAVNQWKET
VINPEKV
VIRWHKLNPS
Sequence length 490
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Leukemia Leukemia, Myelocytic, Acute rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297 27903959
Unknown
Disease term Disease name Evidence References Source
Inflammatory Bowel Disease Inflammatory Bowel Disease GWAS
Alzheimer disease Alzheimer disease GWAS
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma Stimulate 33247676
Brain Diseases Associate 33247676
Breast Neoplasms Inhibit 33247676
Carcinogenesis Associate 30254375, 33247676
Carcinoma Hepatocellular Associate 37839635
Carcinoma Renal Cell Associate 33247676
Carcinosarcoma Inhibit 33247676
Cholangiocarcinoma Stimulate 33247676
Glioma Associate 33247676
Lung Neoplasms Stimulate 30254375, 33247676