meningocele Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002435
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Genes

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

Symbol Name
B3GALNT2 beta-1,3-N-acetylgalactosaminyltransferase 2
BMPER BMP binding endothelial regulator
DLL3 delta-like 3 (Drosophila)
FKRP fukutin related protein
FKTN fukutin
FLNA filamin A, alpha
FRAS1 Fraser extracellular matrix complex subunit 1
FREM2 FRAS1 related extracellular matrix protein 2
FUZ fuzzy planar cell polarity protein
GMPPB GDP-mannose pyrophosphorylase B
GRIP1 glutamate receptor interacting protein 1
H19 H19, imprinted maternally expressed transcript (non-protein coding)
HES7 hes family bHLH transcription factor 7
IGF2 insulin-like growth factor 2
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
KCNQ1OT1 KCNQ1 opposite strand/antisense transcript 1 (non-protein coding)
LARGE like-glycosyltransferase
LFNG LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
MESP2 mesoderm posterior basic helix-loop-helix transcription factor 2
NSDHL NAD(P) dependent steroid dehydrogenase-like
OFD1 oral-facial-digital syndrome 1
PAX3 paired box 3
POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
POMT1 protein-O-mannosyltransferase 1
POMT2 protein-O-mannosyltransferase 2
PORCN porcupine homolog (Drosophila)
SC5D sterol-C5-desaturase
TMEM216 transmembrane protein 216
VANGL1 VANGL planar cell polarity protein 1
VANGL2 VANGL planar cell polarity protein 2
WNT7A wingless-type MMTV integration site family, member 7A
ZSWIM6 zinc finger, SWIM-type containing 6