Congenital Meningocele Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1261470
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Genes

33 genes associated with the disease Congenital Meningocele in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
A1CF APOBEC1 complementation factor
ASIP agouti signaling protein
ASPA aspartoacylase
ASPM asp (abnormal spindle) homolog, microcephaly associated (Drosophila)
ATG5 autophagy related 5
B3GALNT2 beta-1,3-N-acetylgalactosaminyltransferase 2
C3 complement component 3
CEP290 centrosomal protein 290kDa
CSF2 colony stimulating factor 2 (granulocyte-macrophage)
CSPP1 centrosome and spindle pole associated protein 1
DLL3 delta-like 3 (Drosophila)
FKRP fukutin related protein
FKTN fukutin
GMPPB GDP-mannose pyrophosphorylase B
HES7 hes family bHLH transcription factor 7
KIAA0586 KIAA0586
LAMC2 laminin, gamma 2
LARGE like-glycosyltransferase
LFNG LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
MESP2 mesoderm posterior basic helix-loop-helix transcription factor 2
MNX1 motor neuron and pancreas homeobox 1
NOTCH3 notch 3
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
RIPPLY2 ripply transcriptional repressor 2
ROPN1L rhophilin associated tail protein 1-like
SC5D sterol-C5-desaturase
TMEM216 transmembrane protein 216
VANGL1 VANGL planar cell polarity protein 1
WNT7A wingless-type MMTV integration site family, member 7A
ZSWIM6 zinc finger, SWIM-type containing 6