Process View
The series of events required for an organism to receive an orientational stimulus, convert it to a molecular signal, and recognize and characterize the signal. Equilibrioception refers to a combination of processes by which an organism can perceive its orientation with respect to gravity. In animals, stimuli come from labyrinth system of the inner ears, monitoring the direction of motion; visual stimuli, with information on orientation and motion; pressure receptors, which tell the organism which body surfaces are in contact with the ground; and proprioceptive cues, which report which parts of the body are in motion.
In addition to gene-name show these genes:
Click on a gene's description to view its network relationships with genes known to be involved in "equilibrioception"
Name | Description | Probability | Func Analog Organism | |
---|---|---|---|---|
cdh23 | cadherin-like 23 | 0.526 | ||
col4a5 | collagen, type IV, alpha 5 (Alport syndrome) | 0.480 | ||
synj1 | synaptojanin 1 | 0.447 | ||
pcdh15a | protocadherin 15a | 0.292 | Mouse | |
ush1c | Usher syndrome 1C (autosomal recessive, severe) | 0.261 | ||
cacna1da | calcium channel, voltage-dependent, L type, alpha 1D subunit, a | 0.217 | ||
slc17a7 | solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 | 0.195 | Zebrafish | |
slc17a8 | solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8 | 0.166 | ||
sox3 | SRY-box containing gene 3 | 0.143 | ||
rc3 | rabconnectin 3 | 0.116 | ||
myo7aa | myosin VIIAa | 0.114 | ||
sox21a | SRY-box containing gene 21a | 0.083 | ||
gfi1.2 | growth factor independent 1.2 | 0.058 | ||
scn1bb | sodium channel, voltage-gated, type I, beta b | 0.058 | ||
foxa2 | forkhead box A2 | 0.046 | ||
pcsk5a | proprotein convertase subtilisin/kexin type 5a | 0.045 | ||
fgf3 | fibroblast growth factor 3 | 0.039 | ||
kal1b | Kallmann syndrome 1b sequence | 0.038 | ||
atoh1a | atonal homolog 1a | 0.037 | ||
s100s | S100 calcium binding protein S | 0.032 | ||
pdzd7a | PDZ domain containing 7a | 0.031 | ||
rorb | RAR-related orphan receptor B | 0.027 | ||
ctbp2l | C-terminal binding protein 2, like | 0.025 | ||
aldh1a3 | aldehyde dehydrogenase 1 family, member A3 | 0.025 | ||
cyfip2 | cytoplasmic FMR1 interacting protein 2 | 0.023 | ||
atoh1c | atonal homolog 1c | 0.023 | ||
kal1a | Kallmann syndrome 1a sequence | 0.022 | ||
gpr98 | G protein-coupled receptor 98 | 0.022 | ||
olig1 | oligodendrocyte lineage transcription factor 1 | 0.021 | ||
LOC559616 | calcium-binding protein 1-like | 0.020 | ||
bdnf | brain-derived neurotrophic factor | 0.020 | ||
dmd | dystrophin | 0.020 | ||
mtp | microsomal triglyceride transfer protein | 0.018 | ||
mpz | myelin protein zero | 0.018 | ||
slc17a6b | solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6b | 0.017 | Zebrafish | |
dlb | deltaB | 0.016 | ||
atoh1b | atonal homolog 1b | 0.016 | ||
lamb2l | laminin, beta 2-like | 0.016 | ||
slc12a2 | solute carrier family 12 (potassium/chloride transporters), member 2 | 0.016 | ||
pou4f1 | POU domain, class 4, transcription factor 1 | 0.014 | ||
prnprs3 | prion protein, related sequence 3 | 0.013 | ||
otof | otoferlin | 0.013 | ||
efnb2a | ephrin B2a | 0.013 | ||
slc26a5 | solute carrier family 26, member 5 | 0.012 | ||
gpx1b | glutathione peroxidase 1b | 0.011 | ||
notch3 | notch homolog 3 | 0.011 | ||
lmx1b.1 | LIM homeobox transcription factor 1, beta 1 | 0.011 | ||
msi1 | musashi homolog 1 (Drosophila) | 0.010 | ||
ptgds | prostaglandin D2 synthase | 0.010 | ||
tcf7l2 | transcription factor 7-like 2 (T-cell specific, HMG-box) | 0.010 | ||
ift88 | intraflagellar transport 88 homolog | 0.010 |