forkhead box C1

Summary
Gene Symbol
  • FOXC1
Organism
Homo sapiens (human)
NCBI Gene
2296
PubChem
2296
Alliance of Genome Resources
Annotation
Keyword
  • Activator
  • Angiogenesis
  • DNA-binding
  • Deafness
  • Developmental protein
  • Disease variant
  • Nucleus
  • Peters anomaly
  • Phosphoprotein
  • Reference proteome
  • Repressor
  • Transcription regulation
  • Ubl conjugation
Proteins
Displaying all 2 entries
UniProt Protein Name
Q12948
  • Forkhead-related protein FKHL7
  • Forkhead-related transcription factor 3
W6CJ52
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
forkhead box A
Functional Category
  • I: Lipid transport and metabolism
  • O: Posttranslational modification, protein turnover, chaperones
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying all 7 entries
DO ID Disease Name Source
DOID:0080608 anterior segment dysgenesis 3
DOID:0110122 Axenfeld-Rieger syndrome type 3
DOID:11211 buphthalmos
DOID:14686 Axenfeld-Rieger syndrome
DOID:1686 glaucoma
DOID:3008 invasive ductal carcinoma
DOID:6000 congestive heart failure

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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: December 9, 2024