Gene Gene information from NCBI Gene database.
Entrez ID 1455
Gene name Casein kinase 1 gamma 2
Gene symbol CSNK1G2
Synonyms (NCBI Gene)
CK1g2
Chromosome 19
Chromosome location 19p13.3
miRNA miRNA information provided by mirtarbase database.
122
miRTarBase ID miRNA Experiments Reference
MIRT026979 hsa-miR-107 Microarray 20489155
MIRT028634 hsa-miR-30a-5p Proteomics 18668040
MIRT650076 hsa-miR-877-3p HITS-CLIP 23824327
MIRT650075 hsa-miR-627-3p HITS-CLIP 23824327
MIRT650074 hsa-miR-7111-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
25
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0004672 Function Protein kinase activity IEA
GO:0004674 Function Protein serine/threonine kinase activity IBA
GO:0004674 Function Protein serine/threonine kinase activity IDA 25500533
GO:0004674 Function Protein serine/threonine kinase activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
602214 2455 ENSG00000133275
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P78368
Protein name Casein kinase I isoform gamma-2 (CKI-gamma 2) (EC 2.7.11.1)
Protein function Serine/threonine-protein kinase. Casein kinases are operationally defined by their preferential utilization of acidic proteins such as caseins as substrates. It can phosphorylate a large number of proteins. Participates in Wnt signaling (By simi
PDB 2C47
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00069 Pkinase 46 299 Protein kinase domain Domain
PF12605 CK1gamma_C 356 385 Casein kinase 1 gamma C terminal Family
Tissue specificity TISSUE SPECIFICITY: Testis. {ECO:0000269|PubMed:9403068}.
Sequence
Sequence length 415
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Hedgehog signaling pathway   Sphingolipid de novo biosynthesis
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
4
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
CORONARY ARTERY DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
METABOLIC SYNDROME GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PERIODONTITIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
TYPE 2 DIABETES MELLITUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Adenoma Associate 17660800
★☆☆☆☆
Found in Text Mining only
Carcinoma Papillary Follicular Associate 17660800
★☆☆☆☆
Found in Text Mining only
Colonic Neoplasms Associate 37975370
★☆☆☆☆
Found in Text Mining only
Follicular Cyst Associate 17660800
★☆☆☆☆
Found in Text Mining only
Thyroid Cancer Papillary Associate 17660800
★☆☆☆☆
Found in Text Mining only