Gene Gene information from NCBI Gene database.
Entrez ID 51527
Gene name GSK3B interacting protein
Gene symbol GSKIP
Synonyms (NCBI Gene)
C14orf129HSPC210
Chromosome 14
Chromosome location 14q32.2
Summary This gene encodes a protein that is involved as a negative regulator of GSK3-beta in the Wnt signaling pathway. The encoded protein may play a role in the retinoic acid signaling pathway by regulating the functional interactions between GSK3-beta, beta-ca
miRNA miRNA information provided by mirtarbase database.
40
miRTarBase ID miRNA Experiments Reference
MIRT559864 hsa-miR-548ac PAR-CLIP 20371350
MIRT559863 hsa-miR-548bb-3p PAR-CLIP 20371350
MIRT559862 hsa-miR-548d-3p PAR-CLIP 20371350
MIRT559861 hsa-miR-548h-3p PAR-CLIP 20371350
MIRT559860 hsa-miR-548z PAR-CLIP 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
20
GO ID Ontology Definition Evidence Reference
GO:0004860 Function Protein kinase inhibitor activity IDA 19830702
GO:0004860 Function Protein kinase inhibitor activity IMP 16981698
GO:0005515 Function Protein binding IPI 20007971, 20368287, 23602568, 25920809, 27484798, 33961781, 35271311
GO:0005634 Component Nucleus IDA 20007971
GO:0005634 Component Nucleus IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616605 20343 ENSG00000100744
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9P0R6
Protein name GSK3B-interacting protein (GSKIP) (GSK3beta interaction protein)
Protein function A-kinase anchoring protein for GSK3B and PKA that regulates or facilitates their kinase activity towards their targets (PubMed:16981698, PubMed:25920809, PubMed:27484798). The ternary complex enhances Wnt-induced signaling by facilitating the GS
PDB 1SGO
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05303 DUF727 33 133 Protein of unknown function (DUF727) Family
Tissue specificity TISSUE SPECIFICITY: Detected in heart, brain, placenta, liver, skeletal muscle, kidney, testis, lung and pancreas. {ECO:0000269|PubMed:16981698}.
Sequence
Sequence length 139
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
GSKIP-related disorder Likely benign rs34610576 RCV003906996
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Carcinogenesis Associate 36550871
Chromosome Deletion Associate 32917334
Diabetes Mellitus Type 2 Associate 27484798
Genetic Diseases Inborn Associate 32917334
Inflammation Associate 27484798
Meningioma Associate 36550871
Parkinson Disease Associate 27484798