aplasia/hypoplasia of the nipples Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006709
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30 genes associated with the aplasia/hypoplasia of the nipples phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ANTXR1 anthrax toxin receptor 1
CCDC22 coiled-coil domain containing 22
CHRNG cholinergic receptor, nicotinic, gamma (muscle)
DOLK dolichol kinase
EDA ectodysplasin A
EDARADD EDAR-associated death domain
EFNB1 ephrin-B1
FIG4 FIG4 phosphoinositide 5-phosphatase
GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
HDAC8 histone deacetylase 8
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
KCTD1 potassium channel tetramerization domain containing 1
KIAA0196 KIAA0196
LETM1 leucine zipper-EF-hand containing transmembrane protein 1
MEGF8 multiple EGF-like-domains 8
NELFA negative elongation factor complex member A
NIPBL Nipped-B homolog (Drosophila)
PIGL phosphatidylinositol glycan anchor biosynthesis, class L
PORCN porcupine homolog (Drosophila)
RAB40AL RAB40A, member RAS oncogene family-like
RAD21 RAD21 homolog (S. pombe)
SETBP1 SET binding protein 1
SMC1A structural maintenance of chromosomes 1A
SMC3 structural maintenance of chromosomes 3
TBX3 T-box 3
TP63 tumor protein p63
UBR1 ubiquitin protein ligase E3 component n-recognin 1
WHSC1 Wolf-Hirschhorn syndrome candidate 1
WNT3 wingless-type MMTV integration site family, member 3
WNT7A wingless-type MMTV integration site family, member 7A