decreased circulating sodium level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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27 gene mutations causing the decreased circulating sodium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACSBG2 acyl-CoA synthetase bubblegum family member 2
ALDH16A1 aldehyde dehydrogenase 16 family, member A1
BRPF1 bromodomain and PHD finger containing, 1
BSND barttin CLCNK-type chloride channel accessory beta subunit
C1ORF198 chromosome 1 open reading frame 198
CD200 CD200 molecule
DNASE2B deoxyribonuclease II beta
DUSP4 dual specificity phosphatase 4
FARSA phenylalanyl-tRNA synthetase, alpha subunit
FHL1 four and a half LIM domains 1
GAR1 GAR1 ribonucleoprotein
GNA11 guanine nucleotide binding protein (G protein), alpha 11 (Gq class)
MAP3K1 mitogen-activated protein kinase kinase kinase 1, E3 ubiquitin protein ligase
MOCS2 molybdenum cofactor synthesis 2
MTA1 metastasis associated 1
NR3C2 nuclear receptor subfamily 3, group C, member 2
PER2 period circadian clock 2
RPE65 retinal pigment epithelium-specific protein 65kDa
SCNN1B sodium channel, non voltage gated 1 beta subunit
SCNN1G sodium channel, non voltage gated 1 gamma subunit
SIRT2 sirtuin 2
SLC26A3 solute carrier family 26 (anion exchanger), member 3
SLC4A4 solute carrier family 4 (sodium bicarbonate cotransporter), member 4
SMYD2 SET and MYND domain containing 2
TXNIP thioredoxin interacting protein
WTAP Wilms tumor 1 associated protein
WWOX WW domain containing oxidoreductase