Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
51447
Gene name Gene Name - the full gene name approved by the HGNC.
Inositol hexakisphosphate kinase 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
IP6K2
Synonyms (NCBI Gene) Gene synonyms aliases
IHPK2, InsP6K2, PIUS
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3p21.31
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
MIRT003850 hsa-miR-1-3p Microarray 15685193
MIRT003850 hsa-miR-1-3p Microarray;Other 15685193
MIRT003850 hsa-miR-1-3p Microarray 18668037
MIRT027801 hsa-miR-98-5p Microarray 19088304
MIRT040826 hsa-miR-18a-3p CLASH 23622248
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000828 Function Inositol hexakisphosphate kinase activity IBA 21873635
GO:0000828 Function Inositol hexakisphosphate kinase activity IDA 10574768
GO:0000832 Function Inositol hexakisphosphate 5-kinase activity IDA 30624931
GO:0001650 Component Fibrillar center IDA
GO:0005515 Function Protein binding IPI 18195352, 21078964, 21516116, 25416956, 29892012, 31515488, 32296183
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
606992 17313 ENSG00000068745
Protein
UniProt ID Q9UHH9
Protein name Inositol hexakisphosphate kinase 2 (InsP6 kinase 2) (InsP6K2) (EC 2.7.4.-) (P(i)-uptake stimulator) (PiUS)
Protein function Converts inositol hexakisphosphate (InsP6) to diphosphoinositol pentakisphosphate (InsP7/PP-InsP5).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03770 IPK 203 418 Inositol polyphosphate kinase Family
Sequence
MSPAFRAMDVEPRAKGVLLEPFVHQVGGHSCVLRFNETTLCKPLVPREHQFYETLPAEMR
KFTPQYKGVVSVRFEEDEDRNLCLIAYPLKGDHGIVDIVDNSDCEPKSKLLRWTTNKKHH
VLETEKTPKDWVRQHRKEEKMKSHKLEEEFEWLKKSEVLYYTVEKKGNISSQLKHYNPWS
MKCHQQQLQRMKENAKHRNQYKFILLENLTSRYEVPCVLDLKMGTRQHGDDASEEKAANQ
IRKCQQSTSAVIGVRVCGMQVYQAGSGQLMFMNKYHGRKLSVQGFKEALFQFFHNGRYLR
RELLGPVLKKLTELKAVLERQESYRFYSSSLLVIYDGKERPEVVLDSDAEDLEDLSEESA
DESAGAYAYKPIGASSVDVRMIDFAHTTCRLYGEDTVVHEGQDAGYIFGLQSLIDIVT
EI
SEESGE
Sequence length 426
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Phosphatidylinositol signaling system   Synthesis of IPs in the nucleus
Interferon alpha/beta signaling
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Parkinson disease Parkinson Disease rs33939927, rs35801418, rs34805604, rs35870237, rs34995376, rs74315355, rs28940284, rs74315356, rs74315357, rs28940285, rs730880302, rs750664040, rs74315359, rs74315360, rs45539432
View all (84 more)
28892059
Unknown
Disease term Disease name Evidence References Source
Huntington disease Huntington Disease, Huntington Disease, Late Onset, Juvenile Huntington Disease 21652713 ClinVar
Parkinson Disease Parkinson Disease GWAS
Asthma Asthma GWAS
Hypertension Hypertension GWAS
Associations from Text Mining
Disease Name Relationship Type References
Anorexia Nervosa Associate 39741260
Autoimmune Diseases Associate 22446964
Autonomic Nervous System Diseases Associate 34994165
Axial osteomalacia Associate 34602499
Carcinoma Hepatocellular Associate 31856847
Colorectal Neoplasms Associate 21078964
Glioblastoma Associate 32176627
Glioma Associate 35156508
Neoplasms Associate 11896621
Ovarian Neoplasms Associate 11337497, 11896621, 15634191