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

Summary
Gene Symbol
  • PIK3CD
Aliases
  • p110D
  • phosphatidylinositol 3-kinase, catalytic, delta polypeptide
  • phosphoinositide-3-kinase C
Organism
Homo sapiens (human)
NCBI Gene
5293
HGNC
8977
KEGG Gene ID
hsa:5293
PubChem
5293
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • ATP-binding
  • Adaptive immunity
  • Alternative splicing
  • Chemotaxis
  • Cytoplasm
  • Differentiation
  • Direct protein sequencing
  • Disease variant
  • Inflammatory response
  • Innate immunity
  • Kinase
  • Lipid metabolism
  • Phosphoprotein
  • Proteomics identification
  • Reference proteome
Proteins
Displaying all 5 entries
UniProt Protein Name
A0A8V8TM62
O00329
  • Phosphatidylinositol 4,5-bisphosphate 3-kinase 110 kDa catalytic subunit delta
B7ZM44
  • Phosphatidylinositol 4,5-bisphosphate 3-kinase 110 kDa catalytic subunit delta
A7E2E0
  • Phosphatidylinositol 4,5-bisphosphate 3-kinase 110 kDa catalytic subunit delta
A0A2K8FKV1
  • Phosphatidylinositol 4,5-bisphosphate 3-kinase 110 kDa catalytic subunit delta
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
KEGG BRITE Database
Orthology
K00922
Name
phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha/beta/delta [EC:2.7.1.153]
References
Disease
Disease Ontology
Displaying all 4 entries
DO ID Disease Name Source
DOID:0111936 immunodeficiency 14
DOID:1380 endometrial cancer
DOID:5419 schizophrenia
DOID:9256 colorectal cancer
The Human Phenotype Ontology
Displaying entries 81 - 90 of 106 in total
HPO ID HPO Term
HP:0007678 Lacrimal duct stenosis
HP:0008348 Decreased circulating IgG2 level
HP:0009098 Chronic oral candidiasis
HP:0009650 Short distal phalanx of the thumb
HP:0009844 Broad middle phalanx of finger
HP:0009891 Underdeveloped supraorbital ridges
HP:0010049 Short metacarpal
HP:0010282 Thin lower lip vermilion
HP:0010579 Cone-shaped epiphysis
HP:0010743 Short metatarsal
Displaying all 5 entries
Disease ID Disease Name
ORPHA:397596
  • activated PI3K-delta syndrome
OMIM:615513
  • immunodeficiency 14
OMIM:613328
  • combined immunodeficiency with faciooculoskeletal anomalies
ORPHA:221139
  • combined immunodeficiency with faciooculoskeletal anomalies
OMIM:619281
  • immunodeficiency 14b, autosomal recessive
LIPID MAPS Gene / Proteome Database
LMPD ID
LMP000687
Gene Name
phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit delta

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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: December 8, 2025