increased 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:0003019
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Genes

25 gene mutations causing the increased circulating chloride level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADGRB1 adhesion G protein-coupled receptor B1
ATP6V0A4 ATPase, H+ transporting, lysosomal V0 subunit a4
AVPR2 arginine vasopressin receptor 2
CBX6 chromobox homolog 6
CUL7 cullin 7
DBN1 drebrin 1
DDOST dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit (non-catalytic)
DNAJC19 DnaJ (Hsp40) homolog, subfamily C, member 19
ELMOD1 ELMO/CED-12 domain containing 1
GHR growth hormone receptor
GIMAP6 GTPase, IMAP family member 6
IFT20 intraflagellar transport 20
KCNJ16 potassium channel, inwardly rectifying subfamily J, member 16
LOC102723475 putative uncharacterized protein LOC388820
MC2R melanocortin 2 receptor (adrenocorticotropic hormone)
MYO6 myosin VI
MYSM1 Myb-like, SWIRM and MPN domains 1
SCNN1B sodium channel, non voltage gated 1 beta subunit
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
SLC5A2 solute carrier family 5 (sodium/glucose cotransporter), member 2
SLCO1B3 solute carrier organic anion transporter family, member 1B3
STARD8 StAR-related lipid transfer (START) domain containing 8
USH1C Usher syndrome 1C (autosomal recessive, severe)
WWOX WW domain containing oxidoreductase