excessive salivation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Excessive production of saliva. (Human Phenotype Ontology, HP_0003781)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003781
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Genes

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

Symbol Name
ALS2 amyotrophic lateral sclerosis 2 (juvenile)
AP4E1 adaptor-related protein complex 4, epsilon 1 subunit
AP4M1 adaptor-related protein complex 4, mu 1 subunit
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide
ATP7B ATPase, Cu++ transporting, beta polypeptide
ATRX alpha thalassemia/mental retardation syndrome X-linked
CDKL5 cyclin-dependent kinase-like 5
DLAT dihydrolipoamide S-acetyltransferase
FOXG1 forkhead box G1
GNS glucosamine (N-acetyl)-6-sulfatase
HLA-B major histocompatibility complex, class I, B
MECP2 methyl CpG binding protein 2
NRXN1 neurexin 1
PAK3 p21 protein (Cdc42/Rac)-activated kinase 3
POLR3A polymerase (RNA) III (DNA directed) polypeptide A, 155kDa
PRPS1 phosphoribosyl pyrophosphate synthetase 1
SETD5 SET domain containing 5
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter)
SLC9A6 solute carrier family 9, subfamily A (NHE6, cation proton antiporter 6), member 6
SPG20 spastic paraplegia 20 (Troyer syndrome)
TUBB2B tubulin, beta 2B class IIb
UBE3A ubiquitin protein ligase E3A
VPS13A vacuolar protein sorting 13 homolog A (S. cerevisiae)
ZC4H2 zinc finger, C4H2 domain containing
ZEB2 zinc finger E-box binding homeobox 2