abnormal pulmonary ventilation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly of the respiratory minute volume, or the total volume of gas per minute inspired or expired expressed in liters per minute; refers to the exchange of air between the total respiratory space and the environment (Mammalian Phenotype Ontology, MP_0002338)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002338
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20 gene mutations causing the abnormal pulmonary ventilation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACHE acetylcholinesterase (Yt blood group)
CHRNB2 cholinergic receptor, nicotinic, beta 2 (neuronal)
DRD2 dopamine receptor D2
EDNRA endothelin receptor type A
EGLN1 egl-9 family hypoxia-inducible factor 1
EPO erythropoietin
FUT8 fucosyltransferase 8 (alpha (1,6) fucosyltransferase)
LEPR leptin receptor
MUC5B mucin 5B, oligomeric mucus/gel-forming
NDN necdin, melanoma antigen (MAGE) family member
NDUFS4 NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase)
NIPAL3 NIPA-like domain containing 3
NOS1 nitric oxide synthase 1 (neuronal)
P2RX2 purinergic receptor P2X, ligand gated ion channel, 2
PASK PAS domain containing serine/threonine kinase
PBX3 pre-B-cell leukemia homeobox 3
PHOX2A paired-like homeobox 2a
PHOX2B paired-like homeobox 2b
PKDCC protein kinase domain containing, cytoplasmic
SLC5A3 solute carrier family 5 (sodium/myo-inositol cotransporter), member 3