Vacterl Association Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A syndrome that is characterized by the presence of at least three of the following: vertebral defects, anal atresia, cardiac defects, tracheo-esophageal fistula, renal anomalies, and limb abnormalities. (Human Disease Ontology, DOID_14679)
External Link https://www.disgenet.org/browser/0/1/0/C1735591
Similar Terms
Downloads & Tools

Genes

14 genes associated with the disease Vacterl Association in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AATF apoptosis antagonizing transcription factor
BPY2 basic charge, Y-linked, 2
FANCB Fanconi anemia, complementation group B
FANCI Fanconi anemia, complementation group I
FANCL Fanconi anemia, complementation group L
FGF10 fibroblast growth factor 10
FOXF1 forkhead box F1
HOXD13 homeobox D13
PCSK5 proprotein convertase subtilisin/kexin type 5
SHH sonic hedgehog
TADA2A transcriptional adaptor 2A
TRAP1 TNF receptor-associated protein 1
UBE2K ubiquitin-conjugating enzyme E2K
ZIC3 Zic family member 3