abnormal ovary weight Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the average weight of the female reproductive gland containing the germ cells (Mammalian Phenotype Ontology, MP_0004854)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004854
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Genes

30 gene mutations causing the abnormal ovary weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AHR aryl hydrocarbon receptor
AMH anti-Mullerian hormone
ASPM asp (abnormal spindle) homolog, microcephaly associated (Drosophila)
ATR ATR serine/threonine kinase
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CSF2 colony stimulating factor 2 (granulocyte-macrophage)
DDX20 DEAD (Asp-Glu-Ala-Asp) box polypeptide 20
DMC1 DNA meiotic recombinase 1
DND1 DND microRNA-mediated repression inhibitor 1
FSHR follicle stimulating hormone receptor
GALP galanin-like peptide
GNRHR gonadotropin-releasing hormone receptor
INHA inhibin, alpha
KISS1 KiSS-1 metastasis-suppressor
KISS1R KISS1 receptor
LHCGR luteinizing hormone/choriogonadotropin receptor
LIN28A lin-28 homolog A (C. elegans)
MARK2 MAP/microtubule affinity-regulating kinase 2
MCPH1 microcephalin 1
NOS1 nitric oxide synthase 1 (neuronal)
NPC1 Niemann-Pick disease, type C1
PROKR2 prokineticin receptor 2
SH2B1 SH2B adaptor protein 1
SPO11 SPO11 meiotic protein covalently bound to DSB
SYCP1 synaptonemal complex protein 1
TET1 tet methylcytosine dioxygenase 1
UBB ubiquitin B
UBE3A ubiquitin protein ligase E3A
VGF VGF nerve growth factor inducible
ZP3 zona pellucida glycoprotein 3 (sperm receptor)