FOXC2

protein-coding gene in the species Homo sapiens

DBpedia resource is: http://dbpedia.org/resource/FOXC2

Abstract is: Forkhead box protein C2 (FOXC2) also known as forkhead-related protein FKHL14 (FKHL14), transcription factor FKH-14, or mesenchyme fork head protein 1 (MFH1) is a protein that in humans is encoded by the FOXC2 gene. FOXC2 is a member of the fork head box (FOX) family of transcription factors.

FOXC2 is …
instance of (P31):
geneQ7187

sublass of (P279):
protein-coding geneQ20747295

External links are
P11277CIViC gene ID1920
P594Ensembl gene IDENSG00000176692
P704Ensembl transcript IDENST00000649859
P351Entrez Gene ID2303
P2888exact matchhttp://identifiers.org/ncbigene/2303
P646Freebase ID/m/0gds0m
P353HGNC gene symbolFOXC2
P354HGNC ID3801
P593HomoloGene ID21091
P6366Microsoft Academic ID2775980229
P492OMIM ID602402
602402
P639RefSeq RNA IDNM_005251
P2892UMLS CUIC1414669

P1057chromosomehuman chromosome 16Q742870
P4196cytogenetic location16q24.1
P688encodesForkhead box C2Q5426937
P5572expressed inurethraQ9386
vena cavaQ372409
popliteal arteryQ707468
trigeminal ganglionQ776972
spinal gangliaQ1395415
palpebral conjunctivaQ30348886
cardiac muscle tissue of right atriumQ66502871
Descending thoracic aortaQ66592966
ascending aortaQ2349469
tibial arteriesQ7800442
P703found in taxonHomo sapiensQ15978631
P2293genetic associationLymphedema–distichiasis syndromeQ3508768
P645genomic end86569728
86602539
P644genomic start86566829
86600857
P684orthologFoxc2Q14905607
Foxc2Q24407683
P2548strand orientationforward strandQ22809680

Reverse relations

has part(s) (P527)
Q6713107622q11.2 copy number variation syndrome
Q30231044Adipogenesis
Q30225528BMP signaling in eyelid development
Q54989421Epithelial to mesenchymal transition in colorectal cancer
Q87828511GDNF/RET signaling axis
Q102749494Genes controlling nephrogenesis
Q30102315Heart development
Q30151256Mesodermal commitment pathway

ortholog (P684)
Q14905607Foxc2
Q24407683Foxc2

has marker (P8872)
Q101404926human endothelial cell (aorta)
Q101405083human meningeal cell
Q101405039human podocyte

Q3508768Lymphedema–distichiasis syndromegenetic associationP2293
Q5426937Forkhead box C2encoded byP702