increased circulating sodium 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:0005633
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Genes

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

Symbol Name
ACP2 acid phosphatase 2, lysosomal
AVPR2 arginine vasopressin receptor 2
BBS4 Bardet-Biedl syndrome 4
BTK Bruton agammaglobulinemia tyrosine kinase
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit
CBX6 chromobox homolog 6
DBN1 drebrin 1
DDOST dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit (non-catalytic)
DNAJC19 DnaJ (Hsp40) homolog, subfamily C, member 19
FAM53B family with sequence similarity 53, member B
GAR1 GAR1 ribonucleoprotein
GUCA2B guanylate cyclase activator 2B (uroguanylin)
HSPA4L heat shock 70kDa protein 4-like
KCNJ1 potassium channel, inwardly rectifying subfamily J, member 1
LOC102723475 putative uncharacterized protein LOC388820
MYO7A myosin VIIA
NACAD NAC alpha domain containing
NEDD4L neural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligase
RXFP2 relaxin/insulin-like family peptide receptor 2
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC5A2 solute carrier family 5 (sodium/glucose cotransporter), member 2
SLCO1B3 solute carrier organic anion transporter family, member 1B3
SYTL1 synaptotagmin-like 1
TMEM27 transmembrane protein 27
USH1C Usher syndrome 1C (autosomal recessive, severe)
WNK1 WNK lysine deficient protein kinase 1