increased oxygen consumption Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater than the normal rate at which oxygen enters the blood from alveolar gas; this is equal in the steady state to the consumption of oxygen by tissue metabolism throughout the body (Mammalian Phenotype Ontology, MP_0005289)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005289
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Genes

93 gene mutations causing the increased oxygen consumption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCG1 ATP-binding cassette, sub-family G (WHITE), member 1
ACACB acetyl-CoA carboxylase beta
ACER1 alkaline ceramidase 1
ACOT11 acyl-CoA thioesterase 11
ACTB actin, beta
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
ARRDC3 arrestin domain containing 3
BAZ1B bromodomain adjacent to zinc finger domain, 1B
BLOC1S1 biogenesis of lysosomal organelles complex-1, subunit 1
BTK Bruton agammaglobulinemia tyrosine kinase
C1QBP complement component 1, q subcomponent binding protein
CAV1 caveolin 1, caveolae protein, 22kDa
CBL Cbl proto-oncogene, E3 ubiquitin protein ligase
CBX1 chromobox homolog 1
CCDC7 coiled-coil domain containing 7
CDH23 cadherin-related 23
CENPJ centromere protein J
CES1 carboxylesterase 1
CHD7 chromodomain helicase DNA binding protein 7
CIDEB cell death-inducing DFFA-like effector b
CIDEC cell death-inducing DFFA-like effector c
CNOT3 CCR4-NOT transcription complex, subunit 3
CREBBP CREB binding protein
CRTC3 CREB regulated transcription coactivator 3
DBN1 drebrin 1
DFNB31 deafness, autosomal recessive 31
DGAT1 diacylglycerol O-acyltransferase 1
DLG2 discs, large homolog 2 (Drosophila)
DLG4 discs, large homolog 4 (Drosophila)
DNASE1L2 deoxyribonuclease I-like 2
DOK1 docking protein 1, 62kDa (downstream of tyrosine kinase 1)
EIF4EBP1 eukaryotic translation initiation factor 4E binding protein 1
EPM2A epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
FABP3 fatty acid binding protein 3, muscle and heart
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
IFITM1 interferon induced transmembrane protein 1
INS insulin
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11
KLF3 Kruppel-like factor 3 (basic)
LCLAT1 lysocardiolipin acyltransferase 1
LEP leptin
LGALS12 lectin, galactoside-binding, soluble, 12
LIPE lipase, hormone-sensitive
MARK4 MAP/microtubule affinity-regulating kinase 4
MGLL monoglyceride lipase
MIR378A microRNA 378a
MOGAT2 monoacylglycerol O-acyltransferase 2
MYO6 myosin VI
MYO7A myosin VIIA
MYSM1 Myb-like, SWIRM and MPN domains 1
NCOA3 nuclear receptor coactivator 3
NCOR1 nuclear receptor corepressor 1
NOS1 nitric oxide synthase 1 (neuronal)
NR2C2 nuclear receptor subfamily 2, group C, member 2
NSUN2 NOP2/Sun RNA methyltransferase family, member 2
PASK PAS domain containing serine/threonine kinase
PLIN1 perilipin 1
PLIN5 perilipin 5
PMCH pro-melanin-concentrating hormone
PNRC2 proline-rich nuclear receptor coactivator 2
PPARGC1A peroxisome proliferator-activated receptor gamma, coactivator 1 alpha
RAD18 RAD18 E3 ubiquitin protein ligase
RBL1 retinoblastoma-like 1
SAMD4A sterile alpha motif domain containing 4A
SCD stearoyl-CoA desaturase (delta-9-desaturase)
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
SERTAD2 SERTA domain containing 2
SIK3 SIK family kinase 3
SIRT1 sirtuin 1
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
SLC25A25 solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 25
SLC27A5 solute carrier family 27 (fatty acid transporter), member 5
SLC38A10 solute carrier family 38, member 10
SUV420H1 suppressor of variegation 4-20 homolog 1 (Drosophila)
TLR4 toll-like receptor 4
TMPRSS15 transmembrane protease, serine 15
TNKS tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase
USH1C Usher syndrome 1C (autosomal recessive, severe)
VGF VGF nerve growth factor inducible
WDR47 WD repeat domain 47
ZC3HC1 zinc finger, C3HC-type containing 1