abnormal hippocampus development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description improper differentiation of the hippocampus (Mammalian Phenotype Ontology, MP_0000808)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000808
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19 gene mutations causing the abnormal hippocampus development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARX aristaless related homeobox
CHD7 chromodomain helicase DNA binding protein 7
CHN2 chimerin 2
ID4 inhibitor of DNA binding 4, dominant negative helix-loop-helix protein
LEF1 lymphoid enhancer-binding factor 1
LHX5 LIM homeobox 5
LMX1A LIM homeobox transcription factor 1, alpha
MBD1 methyl-CpG binding domain protein 1
MDK midkine (neurite growth-promoting factor 2)
NEUROD1 neuronal differentiation 1
NFIB nuclear factor I/B
NR4A3 nuclear receptor subfamily 4, group A, member 3
PSEN1 presenilin 1
PTPN6 protein tyrosine phosphatase, non-receptor type 6
SEMA3F sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F
TLR3 toll-like receptor 3
TP73 tumor protein p73
ZBTB20 zinc finger and BTB domain containing 20
ZIC5 Zic family member 5