abnormal primordial ovarian follicle morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the ovarian follicle in which the primary oocyte is surrounded by a single layer of flattened follicular cells; primordial follicles are indiscernible to the naked eye and develop to primary, secondary, and finally mature vesicular follicles (Mammalian Phenotype Ontology, MP_0009361)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009361
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Genes

15 gene mutations causing the abnormal primordial ovarian follicle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADRM1 adhesion regulating molecule 1
AHR aryl hydrocarbon receptor
BCL2 B-cell CLL/lymphoma 2
CASP2 caspase 2, apoptosis-related cysteine peptidase
ESR1 estrogen receptor 1
FST follistatin
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
LIN28A lin-28 homolog A (C. elegans)
MCM9 minichromosome maintenance complex component 9
MEI4 meiosis-specific 4 homolog (S. cerevisiae)
RAD21L1 RAD21-like 1 (S. pombe)
RSPO1 R-spondin 1
SPO11 SPO11 meiotic protein covalently bound to DSB
TBPL2 TATA box binding protein like 2
ZC3HC1 zinc finger, C3HC-type containing 1