decreased salivation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000623
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Genes

13 gene mutations causing the decreased salivation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AQP5 aquaporin 5
BBS2 Bardet-Biedl syndrome 2
BBS4 Bardet-Biedl syndrome 4
CHRM3 cholinergic receptor, muscarinic 3
CHRM5 cholinergic receptor, muscarinic 5
E2F1 E2F transcription factor 1
ID3 inhibitor of DNA binding 3, dominant negative helix-loop-helix protein
NKX3-1 NK3 homeobox 1
OPRK1 opioid receptor, kappa 1
SLC12A2 solute carrier family 12 (sodium/potassium/chloride transporter), member 2
SLC9A1 solute carrier family 9, subfamily A (NHE1, cation proton antiporter 1), member 1
TRAF3IP2 TRAF3 interacting protein 2
TRPC1 transient receptor potential cation channel, subfamily C, member 1