decreased follicle stimulating hormone level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description less than expected concentration of the hormone that, in females, stimulates the graafian follicles of the ovary and assists in follicular maturation and the secretion of estradiol; in the male it stimulates the epithelium of the seminiferous tubules and is partly responsible for spermatogenesis (Mammalian Phenotype Ontology, MP_0005130)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005130
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Genes

31 gene mutations causing the decreased follicle stimulating hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACVR2A activin A receptor, type IIA
AMH anti-Mullerian hormone
AR androgen receptor
CDK4 cyclin-dependent kinase 4
CGA glycoprotein hormones, alpha polypeptide
FOXN1 forkhead box N1
FSHB follicle stimulating hormone, beta polypeptide
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone)
GNRHR gonadotropin-releasing hormone receptor
INHA inhibin, alpha
INSM1 insulinoma-associated 1
JUND jun D proto-oncogene
KISS1 KiSS-1 metastasis-suppressor
KISS1R KISS1 receptor
LEPR leptin receptor
LHCGR luteinizing hormone/choriogonadotropin receptor
LHX3 LIM homeobox 3
LIN28A lin-28 homolog A (C. elegans)
NHLH2 nescient helix loop helix 2
NOS1 nitric oxide synthase 1 (neuronal)
NPEPPS aminopeptidase puromycin sensitive
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
PITX2 paired-like homeodomain 2
PRL prolactin
PROKR2 prokineticin receptor 2
PROP1 PROP paired-like homeobox 1
SIRT1 sirtuin 1
SOD1 superoxide dismutase 1, soluble
SOX3 SRY (sex determining region Y)-box 3
STUB1 STIP1 homology and U-box containing protein 1, E3 ubiquitin protein ligase
VIP vasoactive intestinal peptide