wide nose Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Interalar distance more than two standard deviations above the mean for age, i.e., an apparently increased width of the nasal base and alae. (Human Phenotype Ontology, HP_0000445)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000445
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Genes

25 genes associated with the wide nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADAMTS18 ADAM metallopeptidase with thrombospondin type 1 motif, 18
ASPH aspartate beta-hydroxylase
AVP arginine vasopressin
BUB1B BUB1 mitotic checkpoint serine/threonine kinase B
CRLF1 cytokine receptor-like factor 1
FGFR1 fibroblast growth factor receptor 1
FRAS1 Fraser extracellular matrix complex subunit 1
FREM2 FRAS1 related extracellular matrix protein 2
FUCA1 fucosidase, alpha-L- 1, tissue
GDF5 growth differentiation factor 5
GRIP1 glutamate receptor interacting protein 1
IDUA iduronidase, alpha-L-
KAT6B K(lysine) acetyltransferase 6B
KMT2A lysine (K)-specific methyltransferase 2A
LARP7 La ribonucleoprotein domain family, member 7
MOGS mannosyl-oligosaccharide glucosidase
NOTCH2 notch 2
OFD1 oral-facial-digital syndrome 1
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
SKIV2L superkiller viralicidic activity 2-like (S. cerevisiae)
STAMBP STAM binding protein
STAT3 signal transducer and activator of transcription 3 (acute-phase response factor)
TMCO1 transmembrane and coiled-coil domains 1
TRMT10A tRNA methyltransferase 10 homolog A (S. cerevisiae)
TTC37 tetratricopeptide repeat domain 37