Entity Details

Primary name VIP2_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionO43314
EntryNameVIP2_HUMAN
FullNameInositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2
TaxID9606
Evidenceevidence at protein level
Length1243
SequenceStatuscomplete
DateCreated2008-01-15
DateModified2021-06-02

Ontological Relatives

GenesPPIP5K2

GO terms

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GOName
GO:0000827 inositol-1,3,4,5,6-pentakisphosphate kinase activity
GO:0000828 inositol hexakisphosphate kinase activity
GO:0000829 inositol heptakisphosphate kinase activity
GO:0000832 inositol hexakisphosphate 5-kinase activity
GO:0005524 ATP binding
GO:0005829 cytosol
GO:0006020 inositol metabolic process
GO:0007605 sensory perception of sound
GO:0032958 inositol phosphate biosynthetic process
GO:0033857 diphosphoinositol-pentakisphosphate kinase activity
GO:0043647 inositol phosphate metabolic process
GO:0052723 inositol hexakisphosphate 1-kinase activity
GO:0052724 inositol hexakisphosphate 3-kinase activity
GO:0102092 5-diphosphoinositol pentakisphosphate 3-kinase activity

Subcellular Location

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Subcellular Location
Cytoplasm

Domains

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DomainNameCategoryType
IPR000560 Histidine phosphatase superfamily, clade-2FamilyFamily
IPR029033 Histidine phosphatase superfamilyFamilyHomologous superfamily
IPR033379 Histidine acid phosphatase active siteSiteActive site
IPR037446 Histidine acid phosphatase, VIP1 familyFamilyFamily
IPR040557 VIP1, N-terminalDomainDomain

Diseases

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Disease IDSourceNameDescription
618422 OMIMDeafness, autosomal recessive, 100 (DFNB100)A form of non-syndromic, sensorineural deafness characterized by prelingual hearing impairment. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. The disease is caused by variants affecting the gene represented in this entry.