decreased circulating chloride level 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:0003020
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Genes

24 gene mutations causing the decreased circulating chloride 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
BBS5 Bardet-Biedl syndrome 5
BSND barttin CLCNK-type chloride channel accessory beta subunit
C1ORF198 chromosome 1 open reading frame 198
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
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
HSD11B2 hydroxysteroid (11-beta) dehydrogenase 2
MTA1 metastasis associated 1
OXGR1 oxoglutarate (alpha-ketoglutarate) receptor 1
RNASE10 ribonuclease, RNase A family, 10 (non-active)
SERF1A small EDRK-rich factor 1A (telomeric)
SETMAR SET domain and mariner transposase fusion gene
SIRT2 sirtuin 2
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC26A3 solute carrier family 26 (anion exchanger), member 3
SMYD2 SET and MYND domain containing 2
WNK4 WNK lysine deficient protein kinase 4
WWOX WW domain containing oxidoreductase
XYLB xylulokinase homolog (H. influenzae)