absent startle reflex Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description failure to respond to variable stimuli, often auditory; usually measured by amplitude of whole body flinch (Mammalian Phenotype Ontology, MP_0006359)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006359
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22 gene mutations causing the absent 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
CASP3 caspase 3, apoptosis-related cysteine peptidase
CDH23 cadherin-related 23
CLDN9 claudin 9
ELMOD1 ELMO/CED-12 domain containing 1
FOS FBJ murine osteosarcoma viral oncogene homolog
FZD4 frizzled class receptor 4
GFI1 growth factor independent 1 transcription repressor
GRXCR1 glutaredoxin, cysteine rich 1
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
LOC102723475 putative uncharacterized protein LOC388820
LRRC4 leucine rich repeat containing 4
LRTOMT leucine rich transmembrane and O-methyltransferase domain containing
MYO7A myosin VIIA
NTNG2 netrin G2
OTOG otogelin
PCDH15 protocadherin-related 15
S1PR2 sphingosine-1-phosphate receptor 2
SCARB2 scavenger receptor class B, member 2
SLC12A2 solute carrier family 12 (sodium/potassium/chloride transporter), member 2
SLC17A8 solute carrier family 17 (vesicular glutamate transporter), member 8