anencephaly Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002323
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Genes

27 genes associated with the anencephaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
B9D1 B9 protein domain 1
B9D2 B9 protein domain 2
CC2D2A coiled-coil and C2 domain containing 2A
CEP290 centrosomal protein 290kDa
CHD7 chromodomain helicase DNA binding protein 7
DACT1 dishevelled-binding antagonist of beta-catenin 1
FIG4 FIG4 phosphoinositide 5-phosphatase
FLVCR2 feline leukemia virus subgroup C cellular receptor family, member 2
FUZ fuzzy planar cell polarity protein
HOXD13 homeobox D13
HYLS1 hydrolethalus syndrome 1
KIF7 kinesin family member 7
MKS1 Meckel syndrome, type 1
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
NDE1 nudE neurodevelopment protein 1
PHGDH phosphoglycerate dehydrogenase
RPGRIP1 retinitis pigmentosa GTPase regulator interacting protein 1
RPGRIP1L RPGRIP1-like
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
TBX15 T-box 15
TCTN2 tectonic family member 2
TMEM216 transmembrane protein 216
TMEM231 transmembrane protein 231
TMEM67 transmembrane protein 67
VANGL1 VANGL planar cell polarity protein 1
VANGL2 VANGL planar cell polarity protein 2
WDPCP WD repeat containing planar cell polarity effector