increased carbon dioxide production Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increase in the rate at which carbon dioxide leaves the blood and enters the alveolar gas (Mammalian Phenotype Ontology, MP_0008963)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008963
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Genes

44 gene mutations causing the increased carbon dioxide production phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACER1 alkaline ceramidase 1
ADIPOQ adiponectin, C1Q and collagen domain containing
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
AKAP9 A kinase (PRKA) anchor protein 9
AKT1 v-akt murine thymoma viral oncogene homolog 1
BAZ1B bromodomain adjacent to zinc finger domain, 1B
C1QBP complement component 1, q subcomponent binding protein
CBX1 chromobox homolog 1
CDH23 cadherin-related 23
CHD7 chromodomain helicase DNA binding protein 7
DBN1 drebrin 1
DLG2 discs, large homolog 2 (Drosophila)
DLG4 discs, large homolog 4 (Drosophila)
DNASE1L2 deoxyribonuclease I-like 2
FAM134C family with sequence similarity 134, member C
FAM63A family with sequence similarity 63, member A
FOXA2 forkhead box A2
FTO fat mass and obesity associated
GNAS GNAS complex locus
GPR50 G protein-coupled receptor 50
HBA1 hemoglobin, alpha 1
HIF1AN hypoxia inducible factor 1, alpha subunit inhibitor
INS insulin
KDM8 lysine (K)-specific demethylase 8
LEPROT leptin receptor overlapping transcript
MARK4 MAP/microtubule affinity-regulating kinase 4
MB21D1 Mab-21 domain containing 1
MYO6 myosin VI
MYO7A myosin VIIA
MYSM1 Myb-like, SWIRM and MPN domains 1
NCOA3 nuclear receptor coactivator 3
NR2C2 nuclear receptor subfamily 2, group C, member 2
NSUN2 NOP2/Sun RNA methyltransferase family, member 2
RAD18 RAD18 E3 ubiquitin protein ligase
SAMD4A sterile alpha motif domain containing 4A
SLC13A5 solute carrier family 13 (sodium-dependent citrate transporter), member 5
SLC16A1 solute carrier family 16 (monocarboxylate transporter), member 1
SLC25A21 solute carrier family 25 (mitochondrial oxoadipate carrier), member 21
SPNS1 spinster homolog 1 (Drosophila)
SUV420H1 suppressor of variegation 4-20 homolog 1 (Drosophila)
USH1C Usher syndrome 1C (autosomal recessive, severe)
WDR47 WD repeat domain 47
YDJC YdjC homolog (bacterial)
ZC3HC1 zinc finger, C3HC-type containing 1