abnormal pulmonary respiratory rate Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description deviation from the normal number of breaths per minute (Mammalian Phenotype Ontology, MP_0005572)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005572
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Genes

36 gene mutations causing the abnormal pulmonary respiratory rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARID4A AT rich interactive domain 4A (RBP1-like)
ATOH1 atonal homolog 1 (Drosophila)
BDNF brain-derived neurotrophic factor
BRAF B-Raf proto-oncogene, serine/threonine kinase
CHD2 chromodomain helicase DNA binding protein 2
DHCR7 7-dehydrocholesterol reductase
DNM1L dynamin 1-like
DRD2 dopamine receptor D2
DSCAM Down syndrome cell adhesion molecule
EGR2 early growth response 2
EPAS1 endothelial PAS domain protein 1
FOXD1 forkhead box D1
FOXP2 forkhead box P2
GLRA1 glycine receptor, alpha 1
GRIN1 glutamate receptor, ionotropic, N-methyl D-aspartate 1
HCRT hypocretin (orexin) neuropeptide precursor
HIF1AN hypoxia inducible factor 1, alpha subunit inhibitor
HMOX2 heme oxygenase 2
IGHMBP2 immunoglobulin mu binding protein 2
ILF3 interleukin enhancer binding factor 3, 90kDa
KCNN3 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 3
LMNA lamin A/C
MECP2 methyl CpG binding protein 2
NDUFS4 NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase)
NOS1 nitric oxide synthase 1 (neuronal)
PHOX2A paired-like homeobox 2a
PITX3 paired-like homeodomain 3
RYR1 ryanodine receptor 1 (skeletal)
SLC6A9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9
SOX11 SRY (sex determining region Y)-box 11
TACR1 tachykinin receptor 1
TLX3 T-cell leukemia homeobox 3
TPH2 tryptophan hydroxylase 2
TPP1 tripeptidyl peptidase I
TREX1 three prime repair exonuclease 1
UNC13A unc-13 homolog A (C. elegans)