abnormal hippocampus neuron morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of one or more neurons residing in the hippocampal region of the brain (Mammalian Phenotype Ontology, MP_0009939)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009939
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Genes

70 gene mutations causing the abnormal hippocampus neuron 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
ABI2 abl-interactor 2
APC2 adenomatosis polyposis coli 2
ARPC3 actin related protein 2/3 complex, subunit 3, 21kDa
ARSG arylsulfatase G
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide
C1QA complement component 1, q subcomponent, A chain
CACNG2 calcium channel, voltage-dependent, gamma subunit 2
CACNG8 calcium channel, voltage-dependent, gamma subunit 8
CAV1 caveolin 1, caveolae protein, 22kDa
CD81 CD81 molecule
CDK5R1 cyclin-dependent kinase 5, regulatory subunit 1 (p35)
CLCN3 chloride channel, voltage-sensitive 3
CLCN7 chloride channel, voltage-sensitive 7
CLN3 ceroid-lipofuscinosis, neuronal 3
COMMD3-BMI1 COMMD3-BMI1 readthrough
CPEB3 cytoplasmic polyadenylation element binding protein 3
CRMP1 collapsin response mediator protein 1
CSF1 colony stimulating factor 1 (macrophage)
CST3 cystatin C
CTNNA2 catenin (cadherin-associated protein), alpha 2
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
CTNND1 catenin (cadherin-associated protein), delta 1
DAB1 Dab, reelin signal transducer, homolog 1 (Drosophila)
DCX doublecortin
DGKB diacylglycerol kinase, beta 90kDa
DLG4 discs, large homolog 4 (Drosophila)
DPYSL4 dihydropyrimidinase-like 4
EFNA3 ephrin-A3
EHMT1 euchromatic histone-lysine N-methyltransferase 1
EIF4EBP2 eukaryotic translation initiation factor 4E binding protein 2
EPG5 ectopic P-granules autophagy protein 5 homolog (C. elegans)
EPM2A epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
FMR1 fragile X mental retardation 1
FSHR follicle stimulating hormone receptor
FUS FUS RNA binding protein
FYN FYN proto-oncogene, Src family tyrosine kinase
GRIA2 glutamate receptor, ionotropic, AMPA 2
HDAC2 histone deacetylase 2
HPCA hippocalcin
INPP4A inositol polyphosphate-4-phosphatase, type I, 107kDa
ISLR2 immunoglobulin superfamily containing leucine-rich repeat 2
KALRN kalirin, RhoGEF kinase
KCNJ6 potassium channel, inwardly rectifying subfamily J, member 6
KLF7 Kruppel-like factor 7 (ubiquitous)
KLK8 kallikrein-related peptidase 8
LYST lysosomal trafficking regulator
MAPT microtubule-associated protein tau
MECP2 methyl CpG binding protein 2
NDEL1 nudE neurodevelopment protein 1-like 1
NEUROD1 neuronal differentiation 1
NR4A3 nuclear receptor subfamily 4, group A, member 3
NRP2 neuropilin 2
PARK2 parkin RBR E3 ubiquitin protein ligase
PLCB1 phospholipase C, beta 1 (phosphoinositide-specific)
POU1F1 POU class 1 homeobox 1
PPT1 palmitoyl-protein thioesterase 1
PRKAB1 protein kinase, AMP-activated, beta 1 non-catalytic subunit
RERE arginine-glutamic acid dipeptide (RE) repeats
SHANK1 SH3 and multiple ankyrin repeat domains 1
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6
SLC1A2 solute carrier family 1 (glial high affinity glutamate transporter), member 2
STAM signal transducing adaptor molecule (SH3 domain and ITAM motif) 1
STAMBP STAM binding protein
SYN1 synapsin I
SYNGAP1 synaptic Ras GTPase activating protein 1
TP73 tumor protein p73
TRIB2 tribbles pseudokinase 2
TUBA1A tubulin, alpha 1a
USP14 ubiquitin specific peptidase 14 (tRNA-guanine transglycosylase)