forkhead box P2

Summary
Gene Symbol
  • FOXP2
Organism
Homo sapiens (human)
NCBI Gene
93986
KEGG Gene ID
PubChem
93986
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Chromosomal rearrangement
  • Coiled coil
  • DNA-binding
  • Disease variant
  • Nucleus
  • Proteomics identification
  • Reference proteome
  • Repressor
  • Transcription regulation
  • Zinc-finger
Proteins
Displaying all 5 entries
UniProt Protein Name
X5D2H2
Q8N6B6
O15409
  • CAG repeat protein 44
  • Trinucleotide repeat-containing gene 10 protein
B7ZLK5
Q8N6B5
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
Disease
Disease Ontology
Displaying all 9 entries
DO ID Disease Name Source
DOID:93 language disorder
DOID:5419 schizophrenia
DOID:0060041 autism spectrum disorder
DOID:4186 articulation disorder
DOID:0111275 speech-language disorder-1
DOID:1094 attention deficit hyperactivity disorder
DOID:12849 autistic disorder
DOID:1470 major depressive disorder
DOID:4428 dyslexia

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: April 6, 2026