bifid uvula Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Uvula separated into two parts most easily seen at the tip. (Human Phenotype Ontology, HP_0000193)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000193
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Genes

29 genes associated with the bifid uvula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALG3 ALG3, alpha-1,3- mannosyltransferase
AMER1 APC membrane recruitment protein 1
B4GALT7 xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7
BCOR BCL6 corepressor
BMP4 bone morphogenetic protein 4
COL11A1 collagen, type XI, alpha 1
DDX59 DEAD (Asp-Glu-Ala-Asp) box polypeptide 59
EDN1 endothelin 1
EIF4A3 eukaryotic translation initiation factor 4A3
EYA1 EYA transcriptional coactivator and phosphatase 1
FGFR2 fibroblast growth factor receptor 2
FTO fat mass and obesity associated
HYAL1 hyaluronoglucosaminidase 1
IRF6 interferon regulatory factor 6
PGM1 phosphoglucomutase 1
PIEZO2 piezo-type mechanosensitive ion channel component 2
RECQL4 RecQ protein-like 4
SEC23A Sec23 homolog A (S. cerevisiae)
SIX3 SIX homeobox 3
SLC39A13 solute carrier family 39 (zinc transporter), member 13
SMS spermine synthase
TBCE tubulin folding cofactor E
TBX1 T-box 1
TBX22 T-box 22
TGFB3 transforming growth factor, beta 3
TGFBR1 transforming growth factor, beta receptor 1
TGFBR2 transforming growth factor, beta receptor II (70/80kDa)
TP63 tumor protein p63
TTC37 tetratricopeptide repeat domain 37