forkhead box P1

Summary
Gene Symbol
  • FOXP1
Organism
Homo sapiens (human)
NCBI Gene
27086
PubChem
27086
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Chromosomal rearrangement
  • DNA-binding
  • Disease variant
  • Intellectual disability
  • Isopeptide bond
  • Nucleus
  • Phosphoprotein
  • Proteomics identification
  • Reference proteome
  • Repressor
  • Transcription regulation
  • Ubl conjugation
  • Zinc-finger
Proteins
Displaying all 5 entries
UniProt Protein Name
A0A3B3IT66
Q8N2P0
Q548T7
Q9H334
  • Mac-1-regulated forkhead
Q8TEA2
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
Forkhead box protein
Functional Category
  • E: Amino acid transport and metabolism
  • O: Posttranslational modification, protein turnover, chaperones
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying entries 1 - 10 of 15 in total
DO ID Disease Name Source
DOID:0060038 specific developmental disorder
DOID:0090131 complex cortical dysplasia with other brain malformations
DOID:0111331 intellectual disability-severe speech delay-mild dysmorphism syndrome
DOID:1255 trichostrongyloidiasis
DOID:12858 Huntington's disease
DOID:1682 congenital heart disease
DOID:3908 lung non-small cell carcinoma
DOID:3910 lung adenocarcinoma
DOID:4914 esophagus adenocarcinoma
DOID:5419 schizophrenia

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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 9, 2024