abnormal carbon dioxide production Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description deviation from the normal rate at which carbon dioxide leaves the blood and enters the alveolar gas (Mammalian Phenotype Ontology, MP_0008962)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008962
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61 gene mutations causing the abnormal 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
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
C1QBP complement component 1, q subcomponent binding protein
CBX1 chromobox homolog 1
CDH23 cadherin-related 23
CEACAM1 carcinoembryonic antigen-related cell adhesion molecule 1 (biliary glycoprotein)
CHD7 chromodomain helicase DNA binding protein 7
CISD2 CDGSH iron sulfur domain 2
CSPG4 chondroitin sulfate proteoglycan 4
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
FBXO11 F-box protein 11
FGL1 fibrinogen-like 1
FOXA2 forkhead box A2
FOXO1 forkhead box O1
FTO fat mass and obesity associated
GNAS GNAS complex locus
GPR50 G protein-coupled receptor 50
GRIN2D glutamate receptor, ionotropic, N-methyl D-aspartate 2D
HBA1 hemoglobin, alpha 1
HIF1AN hypoxia inducible factor 1, alpha subunit inhibitor
HINT1 histidine triad nucleotide binding protein 1
INS insulin
KDM8 lysine (K)-specific demethylase 8
LEPR leptin receptor
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
NCOR2 nuclear receptor corepressor 2
NOS1 nitric oxide synthase 1 (neuronal)
NR2C2 nuclear receptor subfamily 2, group C, member 2
NSUN2 NOP2/Sun RNA methyltransferase family, member 2
OMA1 OMA1 zinc metallopeptidase
PRPSAP2 phosphoribosyl pyrophosphate synthetase-associated protein 2
RAD18 RAD18 E3 ubiquitin protein ligase
SAMD4A sterile alpha motif domain containing 4A
SFRP2 secreted frizzled-related protein 2
SIRT3 sirtuin 3
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)
TMEM189 transmembrane protein 189
USH1C Usher syndrome 1C (autosomal recessive, severe)
WDR47 WD repeat domain 47
YDJC YdjC homolog (bacterial)
ZC3HC1 zinc finger, C3HC-type containing 1