abnormal reproductive system development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description developmental anomaly of any of the organs involved in the reproductive system (Mammalian Phenotype Ontology, MP_0003936)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003936
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Genes

66 gene mutations causing the abnormal reproductive system development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACVR2A activin A receptor, type IIA
AKAP9 A kinase (PRKA) anchor protein 9
ATM ATM serine/threonine kinase
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CLCN2 chloride channel, voltage-sensitive 2
CPEB1 cytoplasmic polyadenylation element binding protein 1
CSF1 colony stimulating factor 1 (macrophage)
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
CYP26A1 cytochrome P450, family 26, subfamily A, polypeptide 1
CYP7B1 cytochrome P450, family 7, subfamily B, polypeptide 1
DACT1 dishevelled-binding antagonist of beta-catenin 1
DHH desert hedgehog
DMRT1 doublesex and mab-3 related transcription factor 1
DMRT3 doublesex and mab-3 related transcription factor 3
DMRTC2 DMRT-like family C2
EFNB2 ephrin-B2
ESR1 estrogen receptor 1
FGF9 fibroblast growth factor 9
FGFR2 fibroblast growth factor receptor 2
FOXP3 forkhead box P3
FSHR follicle stimulating hormone receptor
GADD45G growth arrest and DNA-damage-inducible, gamma
GDF7 growth differentiation factor 7
GGT1 gamma-glutamyltransferase 1
HOXA10 homeobox A10
HOXA13 homeobox A13
INSL3 insulin-like 3 (Leydig cell)
KIF18A kinesin family member 18A
KIF7 kinesin family member 7
KISS1 KiSS-1 metastasis-suppressor
KPNA1 karyopherin alpha 1 (importin alpha 5)
LACTB2 lactamase, beta 2
LHCGR luteinizing hormone/choriogonadotropin receptor
LHFPL2 lipoma HMGIC fusion partner-like 2
LHX3 LIM homeobox 3
LRP2 low density lipoprotein receptor-related protein 2
MAP3K4 mitogen-activated protein kinase kinase kinase 4
MKS1 Meckel syndrome, type 1
NR0B1 nuclear receptor subfamily 0, group B, member 1
NR5A1 nuclear receptor subfamily 5, group A, member 1
PAX8 paired box 8
PBX1 pre-B-cell leukemia homeobox 1
PGR progesterone receptor
PLEKHA1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1
PSMC3IP PSMC3 interacting protein
RDH10 retinol dehydrogenase 10 (all-trans)
ROR2 receptor tyrosine kinase-like orphan receptor 2
RSPO1 R-spondin 1
SAFB scaffold attachment factor B
SALL4 spalt-like transcription factor 4
SCRIB scribbled planar cell polarity protein
SESTD1 SEC14 and spectrin domains 1
SGPL1 sphingosine-1-phosphate lyase 1
SH2B1 SH2B adaptor protein 1
SIRT1 sirtuin 1
SLC14A1 solute carrier family 14 (urea transporter), member 1 (Kidd blood group)
SMAD1 SMAD family member 1
SPO11 SPO11 meiotic protein covalently bound to DSB
SRY sex determining region Y
TCF21 transcription factor 21
TIMP1 TIMP metallopeptidase inhibitor 1
TMPRSS6 transmembrane protease, serine 6
WNT4 wingless-type MMTV integration site family, member 4
WNT5A wingless-type MMTV integration site family, member 5A
WNT7A wingless-type MMTV integration site family, member 7A
WT1 Wilms tumor 1