aplasia/hypoplasia of the breasts Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence or underdevelopment of the breasts. (Human Phenotype Ontology, HP_0010311)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010311
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Genes

33 genes associated with the aplasia/hypoplasia of the breasts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ANOS1 anosmin 1
ANTXR1 anthrax toxin receptor 1
CDC6 cell division cycle 6
CDT1 chromatin licensing and DNA replication factor 1
CHD7 chromodomain helicase DNA binding protein 7
DUSP6 dual specificity phosphatase 6
EFNB1 ephrin-B1
FEZF1 FEZ family zinc finger 1
FGF17 fibroblast growth factor 17
FGF8 fibroblast growth factor 8 (androgen-induced)
FGFR1 fibroblast growth factor receptor 1
FLRT3 fibronectin leucine rich transmembrane protein 3
HESX1 HESX homeobox 1
HS6ST1 heparan sulfate 6-O-sulfotransferase 1
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
IL17RD interleukin 17 receptor D
KCTD1 potassium channel tetramerization domain containing 1
KISS1R KISS1 receptor
LMNA lamin A/C
NSMF NMDA receptor synaptonuclear signaling and neuronal migration factor
ORC1 origin recognition complex, subunit 1
ORC4 origin recognition complex, subunit 4
ORC6 origin recognition complex, subunit 6
POC1A POC1 centriolar protein A
PROK2 prokineticin 2
PROKR2 prokineticin receptor 2
SEMA3A sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A
SOX10 SRY (sex determining region Y)-box 10
SPRY4 sprouty homolog 4 (Drosophila)
TACR3 tachykinin receptor 3
TBX3 T-box 3
TP63 tumor protein p63
WDR11 WD repeat domain 11