abnormal nitric oxide homeostasis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the processes involved in the maintenance of an internal equilibrium of nitric oxide, a free radical gas and a potent vasodilator (Mammalian Phenotype Ontology, MP_0003957)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003957
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35 gene mutations causing the abnormal nitric oxide homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADIPOQ adiponectin, C1Q and collagen domain containing
APEX1 APEX nuclease (multifunctional DNA repair enzyme) 1
ARG1 arginase 1
ARNTL aryl hydrocarbon receptor nuclear translocator-like
ASL argininosuccinate lyase
BCL3 B-cell CLL/lymphoma 3
CAV1 caveolin 1, caveolae protein, 22kDa
CCR1 chemokine (C-C motif) receptor 1
CCR6 chemokine (C-C motif) receptor 6
CD300LF CD300 molecule-like family member f
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
CYBB cytochrome b-245, beta polypeptide
DDAH1 dimethylarginine dimethylaminohydrolase 1
DUSP1 dual specificity phosphatase 1
HLA-G major histocompatibility complex, class I, G
HPRT1 hypoxanthine phosphoribosyltransferase 1
HSPA1B heat shock 70kDa protein 1B
ICAM1 intercellular adhesion molecule 1
IFNG interferon, gamma
IL10 interleukin 10
IL13RA1 interleukin 13 receptor, alpha 1
IL18 interleukin 18
KCNA5 potassium channel, voltage gated shaker related subfamily A, member 5
LBP lipopolysaccharide binding protein
MB myoglobin
P2RX4 purinergic receptor P2X, ligand gated ion channel, 4
PECAM1 platelet/endothelial cell adhesion molecule 1
PRKCE protein kinase C, epsilon
SNTA1 syntrophin, alpha 1
STAT1 signal transducer and activator of transcription 1, 91kDa
TICAM1 toll-like receptor adaptor molecule 1
TLR2 toll-like receptor 2
TYK2 tyrosine kinase 2
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor
ZFP36 ZFP36 ring finger protein