decreased startle reflex Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater threshold or less severe reflex response to variable stimuli, often auditory; usually measured by amplitude of whole body flinch (Mammalian Phenotype Ontology, MP_0001489)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001489
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Genes

81 gene mutations causing the decreased startle reflex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABHD12 abhydrolase domain containing 12
ABL2 ABL proto-oncogene 2, non-receptor tyrosine kinase
ADGRV1 adhesion G protein-coupled receptor V1
ADRA1D adrenoceptor alpha 1D
AEBP2 AE binding protein 2
AGTR2 angiotensin II receptor, type 2
ALDH3A2 aldehyde dehydrogenase 3 family, member A2
APOE apolipoprotein E
ATN1 atrophin 1
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
ATP8A2 ATPase, aminophospholipid transporter, class I, type 8A, member 2
BARHL1 BarH-like homeobox 1
BBS2 Bardet-Biedl syndrome 2
C1QBP complement component 1, q subcomponent binding protein
CACNA1B calcium channel, voltage-dependent, N type, alpha 1B subunit
CACNA2D3 calcium channel, voltage-dependent, alpha 2/delta subunit 3
CACNG2 calcium channel, voltage-dependent, gamma subunit 2
CDH23 cadherin-related 23
CIB2 calcium and integrin binding family member 2
CKMT1A creatine kinase, mitochondrial 1A
CLPP caseinolytic mitochondrial matrix peptidase proteolytic subunit
CLSTN1 calsyntenin 1
CSMD1 CUB and Sushi multiple domains 1
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
CYB5R2 cytochrome b5 reductase 2
DFNB59 deafness, autosomal recessive 59
DISC1 disrupted in schizophrenia 1
DLG4 discs, large homolog 4 (Drosophila)
DNAJC5 DnaJ (Hsp40) homolog, subfamily C, member 5
DRD2 dopamine receptor D2
DRD3 dopamine receptor D3
DST dystonin
DVL1 dishevelled segment polarity protein 1
ELMOD1 ELMO/CED-12 domain containing 1
FAM134C family with sequence similarity 134, member C
FBXO11 F-box protein 11
FGF3 fibroblast growth factor 3
FMR1 fragile X mental retardation 1
FOXP2 forkhead box P2
FZD4 frizzled class receptor 4
GNAS GNAS complex locus
GPR33 G protein-coupled receptor 33 (gene/pseudogene)
GRIA3 glutamate receptor, ionotropic, AMPA 3
GRIA4 glutamate receptor, ionotropic, AMPA 4
HMGN1 high mobility group nucleosome binding domain 1
HTR1B 5-hydroxytryptamine (serotonin) receptor 1B, G protein-coupled
IDUA iduronidase, alpha-L-
KALRN kalirin, RhoGEF kinase
KCNJ16 potassium channel, inwardly rectifying subfamily J, member 16
KDM8 lysine (K)-specific demethylase 8
LOC102723475 putative uncharacterized protein LOC388820
LOXHD1 lipoxygenase homology domains 1
MECOM MDS1 and EVI1 complex locus
MECP2 methyl CpG binding protein 2
MYO6 myosin VI
MYO7A myosin VIIA
NAV2 neuron navigator 2
NDUFS4 NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase)
NLGN3 neuroligin 3
NPTN neuroplastin
NTSR1 neurotensin receptor 1 (high affinity)
NTSR2 neurotensin receptor 2
OTOF otoferlin
OTUD7B OTU deubiquitinase 7B
PARK2 parkin RBR E3 ubiquitin protein ligase
PEX5L peroxisomal biogenesis factor 5-like
PIP5K1C phosphatidylinositol-4-phosphate 5-kinase, type I, gamma
PLCB1 phospholipase C, beta 1 (phosphoinositide-specific)
POU4F3 POU class 4 homeobox 3
PTPRG protein tyrosine phosphatase, receptor type, G
RNF103 ring finger protein 103
SCN8A sodium channel, voltage gated, type VIII alpha subunit
SHANK3 SH3 and multiple ankyrin repeat domains 3
SHH sonic hedgehog
SLITRK6 SLIT and NTRK-like family, member 6
STUB1 STIP1 homology and U-box containing protein 1, E3 ubiquitin protein ligase
TMOD2 tropomodulin 2 (neuronal)
TNFRSF1B tumor necrosis factor receptor superfamily, member 1B
TYROBP TYRO protein tyrosine kinase binding protein
UCN urocortin
XBP1 X-box binding protein 1