widely spaced teeth Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Increased spaces (diastemata) between most of the teeth in the same dental arch. (Human Phenotype Ontology, HP_0000687)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000687
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Genes

27 genes associated with the widely spaced teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACVR1 activin A receptor, type I
CDH3 cadherin 3, type 1, P-cadherin (placental)
CDKL5 cyclin-dependent kinase-like 5
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
DLX3 distal-less homeobox 3
FGF3 fibroblast growth factor 3
GALNS galactosamine (N-acetyl)-6-sulfatase
GLB1 galactosidase, beta 1
HDAC8 histone deacetylase 8
IDS iduronate 2-sulfatase
IFT122 intraflagellar transport 122
IFT43 intraflagellar transport 43
KANSL1 KAT8 regulatory NSL complex subunit 1
MAN2B1 mannosidase, alpha, class 2B, member 1
MBD5 methyl-CpG binding domain protein 5
MECP2 methyl CpG binding protein 2
NIPBL Nipped-B homolog (Drosophila)
PIGA phosphatidylinositol glycan anchor biosynthesis, class A
PIGL phosphatidylinositol glycan anchor biosynthesis, class L
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
SMARCA2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2
TCF4 transcription factor 4
TP63 tumor protein p63
UBE3A ubiquitin protein ligase E3A
VSX1 visual system homeobox 1
WDR35 WD repeat domain 35
ZEB2 zinc finger E-box binding homeobox 2