phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma

Summary
Gene Symbol
  • PIK3CG
Organism
Homo sapiens (human)
External Links
NCBI Gene
5294
HGNC
8978
KEGG Gene ID
hsa:5294
PubChem
5294
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • ATP-binding
  • Angiogenesis
  • Cell membrane
  • Chemotaxis
  • Cytoplasm
  • Disease variant
  • Endocytosis
  • Immunity
  • Inflammatory response
  • Kinase
  • Lipid metabolism
  • Phosphoprotein
  • Reference proteome
  • Serine/threonine-protein kinase
Proteins
Displaying all 2 entries
UniProt Protein Name
P48736
  • Phosphatidylinositol 4,5-bisphosphate 3-kinase 110 kDa catalytic subunit gamma
  • Phosphoinositide-3-kinase catalytic gamma polypeptide
  • Serine/threonine protein kinase PIK3CG
  • p120-PI3K
A8K9G9
Gene Ontology (GO)
Displaying entry 41 - 41 of 41 in total
GO Term Evidence Code PMID
negative regulation of fibroblast apoptotic process
GO Hierarchy
Displaying entry 11 - 11 of 11 in total
GO Term Evidence Code PMID
identical protein binding
GO Hierarchy
KEGG BRITE Database
Orthology
K21289
Name
phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma [EC:2.7.1.153]
References
Disease
Disease Ontology
Displaying entries 81 - 90 of 948 in total
DO ID Disease Name Source
DOID:0060586 Noonan syndrome 8
DOID:0060587 Noonan syndrome 9
DOID:0060588 Noonan syndrome 10
DOID:0060592 B-cell adult acute lymphocytic leukemia
DOID:0060597 atypical chronic myeloid leukemia, BCR-ABL1 negative
DOID:0060608 microcephalic osteodysplastic primordial dwarfism type I
DOID:0060609 microcephalic osteodysplastic primordial dwarfism type II
DOID:0060642 recessive dystrophic epidermolysis bullosa
DOID:0060644 chondrodysplasia-pseudohermaphroditism syndrome
DOID:0060707 lymphoproliferative syndrome 1
The Human Phenotype Ontology
Displaying entries 1 - 10 of 36 in total
HPO ID HPO Term
HP:0000007 Autosomal recessive inheritance
HP:0000010 Recurrent urinary tract infections
HP:0000403 Recurrent otitis media
HP:0000964 Eczematoid dermatitis
HP:0001252 Hypotonia
HP:0001433 Hepatosplenomegaly
HP:0001581 Recurrent skin infections
HP:0001742 Nasal congestion
HP:0001744 Splenomegaly
HP:0001873 Thrombocytopenia
Displaying 1 entry
Disease ID Disease Name
OMIM:619802
  • immunodeficiency 97 with autoinflammation
LIPID MAPS Gene / Proteome Database
LMPD ID
LMP000468
Gene Name
phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit gamma

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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