Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
117283
Gene name Gene Name - the full gene name approved by the HGNC.
Inositol hexakisphosphate kinase 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
IP6K3
Synonyms (NCBI Gene) Gene synonyms aliases
IHPK3, INSP6K3
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p21.31
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a protein that belongs to the inositol phosphokinase (IPK) family. This protein is likely responsible for the conversion of inositol hexakisphosphate (InsP6) to diphosphoinositol pentakisphosphate (InsP7/PP-InsP5). It may also convert 1,
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT038242 hsa-miR-330-5p CLASH 23622248
MIRT727440 hsa-miR-30a-5p HITS-CLIP 22473208
MIRT727439 hsa-miR-30b-5p HITS-CLIP 22473208
MIRT727438 hsa-miR-30c-5p HITS-CLIP 22473208
MIRT727436 hsa-miR-30d-5p HITS-CLIP 22473208
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0000827 Function Inositol-1,3,4,5,6-pentakisphosphate kinase activity IEA
GO:0000827 Function Inositol-1,3,4,5,6-pentakisphosphate kinase activity TAS
GO:0000828 Function Inositol hexakisphosphate kinase activity IBA
GO:0000828 Function Inositol hexakisphosphate kinase activity IDA 11502751
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
606993 17269 ENSG00000161896
Protein
UniProt ID Q96PC2
Protein name Inositol hexakisphosphate kinase 3 (InsP6 kinase 3) (EC 2.7.4.21) (Inositol hexaphosphate kinase 3)
Protein function Converts inositol hexakisphosphate (InsP6) to diphosphoinositol pentakisphosphate (InsP7/PP-InsP5). Converts 1,3,4,5,6-pentakisphosphate (InsP5) to PP-InsP4.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03770 IPK 198 404 Inositol polyphosphate kinase Family
Tissue specificity TISSUE SPECIFICITY: Detected in brain.
Sequence
MVVQNSADAGDMRAGVQLEPFLHQVGGHMSVMKYDEHTVCKPLVSREQRFYESLPLAMKR
FTPQYKGTVTVHLWKDSTGHLSLVANPVKESQEPFKVSTESAAVAIWQTLQQTTGSNGSD
CTLAQWPHAQLARSPKESPAKALLRSEPHLNTPAFSLVEDTNGNQVERKSFNPWGLQCHQ
AHLTRLCSEYPENKRHRFLLLENVVSQYTHPCVLDLKMGTRQHGDDASEEKKARHMRKCA
QSTSACLGVRICGMQVYQTDKKYFLCKDKYYGRKLSVEGFRQALYQFLHNGSHLRRELLE
PILHQLRALLSVIRSQSSYRFYSSSLLVIYDGQEPPERAPGSPHPHEAPQAAHGSSPGGL
TKVDIRMIDFAHTTYKGYWNEHTTYDGPDPGYIFGLENLIRILQ
DIQEGE
Sequence length 410
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Phosphatidylinositol signaling system   Synthesis of pyrophosphates in the cytosol
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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
Asthma Asthma in any disease N/A N/A GWAS
Hypothyroidism Hypothyroidism N/A N/A GWAS
Insomnia Insomnia N/A N/A GWAS
Metabolic Syndrome Metabolic syndrome N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Associate 27345265
Inflammatory Bowel Diseases Associate 31185018