abnormal brain interneuron morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of neurons that exclusively interact with other neurons in the brain; this includes most brain neuronal cell types (Mammalian Phenotype Ontology, MP_0004101)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004101
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Genes

24 gene mutations causing the abnormal brain interneuron morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARX aristaless related homeobox
BDNF brain-derived neurotrophic factor
CADPS2 Ca++-dependent secretion activator 2
CHRNA7 cholinergic receptor, nicotinic, alpha 7 (neuronal)
CNTNAP2 contactin associated protein-like 2
DCX doublecortin
DGCR8 DGCR8 microprocessor complex subunit
GAD1 glutamate decarboxylase 1 (brain, 67kDa)
GSX2 GS homeobox 2
IL6 interleukin 6
KLK8 kallikrein-related peptidase 8
LHX6 LIM homeobox 6
LRPAP1 low density lipoprotein receptor-related protein associated protein 1
MYCBP2 MYC binding protein 2, E3 ubiquitin protein ligase
NHLRC1 NHL repeat containing E3 ubiquitin protein ligase 1
PDYN prodynorphin
PHOX2B paired-like homeobox 2b
PLAUR plasminogen activator, urokinase receptor
ROBO2 roundabout, axon guidance receptor, homolog 2 (Drosophila)
RORA RAR-related orphan receptor A
SATB1 SATB homeobox 1
SLC12A5 solute carrier family 12 (potassium/chloride transporter), member 5
TUBB2B tubulin, beta 2B class IIb
ZNF365 zinc finger protein 365