FOXB1

Gene Name		forkhead box B1
Image		No pdb structure
Gene Ontology Annotations	Cellular Component	Nucleus
	Molecular Function	Sequence-specific DNA Binding RNA Polymerase II Transcription Factor Activity Sequence-specific DNA Binding
	Biological Process	Urogenital System Development Somitogenesis Regulation Of Transcription From RNA Polymerase II Promoter Transcription From RNA Polymerase II Promoter Axon Target Recognition Lactation Visual Learning Spinal Cord Development Mammillary Body Development Thalamus Development Hypothalamus Cell Migration Telencephalon Cell Migration Midbrain Development Floor Plate Development Negative Regulation Of Neuron Apoptotic Process Epithelial Cell Differentiation Involved In Mammary Gland Alveolus Development Mammillothalamic Axonal Tract Development Mammary Gland Lobule Development Inferior Colliculus Development Cell Migration In Diencephalon
Pathways
Drugs
Diseases
GWAS
Protein-protein Interactions		8 interactors: COPB1 KRT31 KRT40 KRTAP10-3 KRTAP10-8 NOTCH2NL PHF5A TRIM27
Entrez ID		27023
HPRD ID		07017
Ensembl ID		ENSG00000171956
Uniprot IDs		Q99853
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?		15q22 box commonly de deletions disability documented epilepsy familial forkhead genotype intellectual kb larger mb microdeletions narg2 narrowed neighboring neurologic neurological novo origin orphan par phenotype region rora