abnormal hippocampus ca3 region morphology 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:0008267
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15 gene mutations causing the abnormal hippocampus ca3 region morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1
AGTR2 angiotensin II receptor, type 2
ARX aristaless related homeobox
DCX doublecortin
GDI1 GDP dissociation inhibitor 1
GRIA2 glutamate receptor, ionotropic, AMPA 2
LMX1A LIM homeobox transcription factor 1, alpha
MAN2B1 mannosidase, alpha, class 2B, member 1
NCAM1 neural cell adhesion molecule 1
NFIB nuclear factor I/B
NPC1 Niemann-Pick disease, type C1
SNAP25 synaptosomal-associated protein, 25kDa
SOX11 SRY (sex determining region Y)-box 11
SS18L1 synovial sarcoma translocation gene on chromosome 18-like 1
TP73 tumor protein p73