dehydration 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:0001429
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Genes

72 gene mutations causing the dehydration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCA12 ATP-binding cassette, sub-family A (ABC1), member 12
ALOX12B arachidonate 12-lipoxygenase, 12R type
ALOXE3 arachidonate lipoxygenase 3
APRT adenine phosphoribosyltransferase
AQP1 aquaporin 1 (Colton blood group)
AQP2 aquaporin 2 (collecting duct)
ARNTL aryl hydrocarbon receptor nuclear translocator-like
ARX aristaless related homeobox
ATCAY ataxia, cerebellar, Cayman type
ATP6V0A4 ATPase, H+ transporting, lysosomal V0 subunit a4
AVP arginine vasopressin
B4GALT1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1
BSND barttin CLCNK-type chloride channel accessory beta subunit
CACNA2D2 calcium channel, voltage-dependent, alpha 2/delta subunit 2
CASP14 caspase 14, apoptosis-related cysteine peptidase
CASR calcium-sensing receptor
CDKN2C cyclin-dependent kinase inhibitor 2C (p18, inhibits CDK4)
CERS3 ceramide synthase 3
CHRNG cholinergic receptor, nicotinic, gamma (muscle)
CLDN1 claudin 1
CLDN7 claudin 7
DGAT2 diacylglycerol O-acyltransferase 2
DIAPH1 diaphanous-related formin 1
E2F4 E2F transcription factor 4, p107/p130-binding
E2F5 E2F transcription factor 5, p130-binding
EGFR epidermal growth factor receptor
EPB42 erythrocyte membrane protein band 4.2
FCGR2B Fc fragment of IgG, low affinity IIb, receptor (CD32)
FERMT1 fermitin family member 1
FKBP8 FK506 binding protein 8, 38kDa
GABBR1 gamma-aminobutyric acid (GABA) B receptor, 1
GBA glucosidase, beta, acid
GLIS3 GLIS family zinc finger 3
HAP1 huntingtin-associated protein 1
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled
IGF2BP1 insulin-like growth factor 2 mRNA binding protein 1
INS insulin
ITGA3 integrin, alpha 3 (antigen CD49C, alpha 3 subunit of VLA-3 receptor)
ITGB4 integrin, beta 4
KCNJ1 potassium channel, inwardly rectifying subfamily J, member 1
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
KL klotho
KLF4 Kruppel-like factor 4 (gut)
KRT1 keratin 1, type II
LOC102723475 putative uncharacterized protein LOC388820
MAP1B microtubule-associated protein 1B
MSI1 musashi RNA-binding protein 1
MUT methylmalonyl CoA mutase
NEUROD1 neuronal differentiation 1
NEUROG3 neurogenin 3
NPR3 natriuretic peptide receptor 3
NR3C2 nuclear receptor subfamily 3, group C, member 2
NR4A2 nuclear receptor subfamily 4, group A, member 2
OPA3 optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
PCCA propionyl CoA carboxylase, alpha polypeptide
PDX1 pancreatic and duodenal homeobox 1
POU2F2 POU class 2 homeobox 2
PRSS8 protease, serine, 8
REN renin
SALL3 spalt-like transcription factor 3
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
SLC6A9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9
SNRPN small nuclear ribonucleoprotein polypeptide N
SPINK1 serine peptidase inhibitor, Kazal type 1
SPINK5 serine peptidase inhibitor, Kazal type 5
ST14 suppression of tumorigenicity 14 (colon carcinoma)
TGFB3 transforming growth factor, beta 3
TGM1 transglutaminase 1
TP63 tumor protein p63
TPP1 tripeptidyl peptidase I
TSTA3 tissue specific transplantation antigen P35B
ZNF423 zinc finger protein 423