inositol polyphosphate-5-phosphatase K

Summary
Gene Symbol
  • INPP5K
Aliases
  • SKIP
  • skeletal muscle and kidney enriched inositol phosphatase
Organism
Homo sapiens (human)
External Links
NCBI Gene
51763
HGNC
33882
KEGG Gene ID
hsa:51763
PubChem
51763
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Cataract
  • Congenital muscular dystrophy
  • Cytoplasm
  • Disease variant
  • Endoplasmic reticulum
  • Hydrolase
  • Intellectual disability
  • Lipid metabolism
  • Reference proteome
Proteins
Displaying 1 entry
UniProt Protein Name
Q9BT40
  • Phosphatidylinositol-3,4,5-trisphosphate 5-phosphatase
  • Phosphatidylinositol-4,5-bisphosphate 5-phosphatase
  • Skeletal muscle and kidney-enriched inositol phosphatase
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
KEGG BRITE Database
Orthology
K24222
Name
inositol polyphosphate 5-phosphatase INPP5J/K [EC:3.1.3.56]
References
Disease
Disease Ontology
Displaying entries 61 - 70 of 183 in total
DO ID Disease Name Source
DOID:0110263 cataract 19 multiple types
DOID:0110264 cataract 33
DOID:0110265 cataract 31 multiple types
DOID:0110266 cataract 9 multiple types
DOID:0110267 cataract 44
DOID:0110268 cataract 22 multiple types
DOID:0110269 cataract 3 multiple types
DOID:0110270 cataract 17 multiple types
DOID:0110271 cataract 23
DOID:0110272 cataract 40
The Human Phenotype Ontology
Displaying entries 21 - 30 of 62 in total
HPO ID HPO Term
HP:0001284 Areflexia
HP:0001288 Gait disturbance
HP:0001321 Cerebellar hypoplasia
HP:0001328 Specific learning disability
HP:0001385 Hip dysplasia
HP:0001460 Aplasia/Hypoplasia involving the skeletal musculature
HP:0001618 Dysphonia
HP:0002061 Lower limb spasticity
HP:0002063 Rigidity
HP:0002093 Respiratory insufficiency
Displaying all 2 entries
Disease ID Disease Name
OMIM:617404
  • congenital muscular dystrophy with cataracts and intellectual disability
ORPHA:559
  • Marinesco-Sjogren syndrome
LIPID MAPS Gene / Proteome Database
LMPD ID
LMP002367
Gene Name
inositol polyphosphate-5-phosphatase K

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024