Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
51527
Gene name Gene Name - the full gene name approved by the HGNC.
GSK3B interacting protein
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
GSKIP
Synonyms (NCBI Gene) Gene synonyms aliases
C14orf129, HSPC210
Chromosome Chromosome number
14
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
14q32.2
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
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, 25920809, 27484798
GO:0005634 Component Nucleus IDA 20007971
GO:0005737 Component Cytoplasm IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
616605 20343 ENSG00000100744
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Myeloproliferative disorder Myeloproliferative disease rs267606708, rs77375493 26280900
Associations from Text Mining
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