abnormal hippocampus ca1 region morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of a cytoarchitectural subregion of the Ammon's horn region of the hippocampal formation consisting primarily of pyramidal neurons; the pyramidal neurons of CA1 receive projections from pyramidal neurons of CA3 via the Schaffer collaterals and send outputs to the entorhinal cortex and to the subiculum (Mammalian Phenotype Ontology, MP_0008263)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008263
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Genes

21 gene mutations causing the abnormal hippocampus ca1 region morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABI2 abl-interactor 2
AGTR2 angiotensin II receptor, type 2
CAV1 caveolin 1, caveolae protein, 22kDa
CD81 CD81 molecule
CLSTN3 calsyntenin 3
CTNND1 catenin (cadherin-associated protein), delta 1
DPYSL4 dihydropyrimidinase-like 4
EIF4EBP2 eukaryotic translation initiation factor 4E binding protein 2
GABBR2 gamma-aminobutyric acid (GABA) B receptor, 2
GABRA5 gamma-aminobutyric acid (GABA) A receptor, alpha 5
HDAC2 histone deacetylase 2
MAPT microtubule-associated protein tau
NFIX nuclear factor I/X (CCAAT-binding transcription factor)
PRNP prion protein
PTPN6 protein tyrosine phosphatase, non-receptor type 6
RELN reelin
RGS2 regulator of G-protein signaling 2
SLC1A2 solute carrier family 1 (glial high affinity glutamate transporter), member 2
TLR3 toll-like receptor 3
TNR tenascin R
TRIB2 tribbles pseudokinase 2