decreased corpora lutea number Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description fewer than normal numbers of yellow endocrine body formed in the ovary after follicle rupture in a given oestrous cycle (Mammalian Phenotype Ontology, MP_0002680)
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21 gene mutations causing the decreased corpora lutea number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AHR aryl hydrocarbon receptor
AKT2 v-akt murine thymoma viral oncogene homolog 2
CCS copper chaperone for superoxide dismutase
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CLPP caseinolytic mitochondrial matrix peptidase proteolytic subunit
CSF1 colony stimulating factor 1 (macrophage)
ESR2 estrogen receptor 2 (ER beta)
FANCL Fanconi anemia, complementation group L
GHR growth hormone receptor
GNRHR gonadotropin-releasing hormone receptor
HERC2 HECT and RLD domain containing E3 ubiquitin protein ligase 2
HFM1 HFM1, ATP-dependent DNA helicase homolog (S. cerevisiae)
LEPR leptin receptor
MARK2 MAP/microtubule affinity-regulating kinase 2
MLH1 mutL homolog 1
NOS1 nitric oxide synthase 1 (neuronal)
NOS3 nitric oxide synthase 3 (endothelial cell)
PTGER2 prostaglandin E receptor 2 (subtype EP2), 53kDa
SOD1 superoxide dismutase 1, soluble
UBB ubiquitin B
ZC3HC1 zinc finger, C3HC-type containing 1