anencephaly Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001890
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Genes

19 gene mutations causing the anencephaly phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALX1 ALX homeobox 1
CARD10 caspase recruitment domain family, member 10
DLX5 distal-less homeobox 5
DLX6 distal-less homeobox 6
EFNA5 ephrin-A5
EPHA7 EPH receptor A7
GRHL3 grainyhead-like 3 (Drosophila)
HES1 hes family bHLH transcription factor 1
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
LMO4 LIM domain only 4
LUZP1 leucine zipper protein 1
NDST1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1
OTX2 orthodenticle homeobox 2
RAPGEF2 Rap guanine nucleotide exchange factor (GEF) 2
RPL38 ribosomal protein L38
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TIAM1 T-cell lymphoma invasion and metastasis 1
ZIC2 Zic family member 2
ZIC3 Zic family member 3