sensory perception of mechanical stimulus Gene Set

Dataset GO Biological Process Annotations
Category structural or functional annotations
Type biological process
Description The series of events required for an organism to receive a sensory mechanical stimulus, convert it to a molecular signal, and recognize and characterize the signal. This is a neurological process. (Gene Ontology, GO_0050954)
External Link http://amigo.geneontology.org/amigo/term/GO:0050954
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Genes

132 genes participating in the sensory perception of mechanical stimulus biological process from the curated GO Biological Process Annotations dataset.

Symbol Name
ADGRV1 adhesion G protein-coupled receptor V1
ALDH7A1 aldehyde dehydrogenase 7 family, member A1
AQP4 aquaporin 4
ASIC2 acid sensing (proton gated) ion channel 2
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
ATP6V0A4 ATPase, H+ transporting, lysosomal V0 subunit a4
ATP6V1B1 ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B1
ATP8B1 ATPase, aminophospholipid transporter, class I, type 8B, member 1
AXIN1 axin 1
BARHL1 BarH-like homeobox 1
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit
CASP3 caspase 3, apoptosis-related cysteine peptidase
CDH1 cadherin 1, type 1, E-cadherin (epithelial)
CDH23 cadherin-related 23
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CDKN2D cyclin-dependent kinase inhibitor 2D (p19, inhibits CDK4)
CEACAM16 carcinoembryonic antigen-related cell adhesion molecule 16
CEMIP cell migration inducing protein, hyaluronan binding
CHD7 chromodomain helicase DNA binding protein 7
CHRNB2 cholinergic receptor, nicotinic, beta 2 (neuronal)
CLIC5 chloride intracellular channel 5
CLRN1 clarin 1
CNTN5 contactin 5
COCH cochlin
COL11A1 collagen, type XI, alpha 1
COL11A2 collagen, type XI, alpha 2
COL1A1 collagen, type I, alpha 1
COL2A1 collagen, type II, alpha 1
COL4A3 collagen, type IV, alpha 3 (Goodpasture antigen)
CRYM crystallin, mu
DFNA5 deafness, autosomal dominant 5
DFNB31 deafness, autosomal recessive 31
DFNB59 deafness, autosomal recessive 59
DIAPH1 diaphanous-related formin 1
DRGX dorsal root ganglia homeobox
EML2 echinoderm microtubule associated protein like 2
ESPN espin
EYA1 EYA transcriptional coactivator and phosphatase 1
EYA4 EYA transcriptional coactivator and phosphatase 4
FAM107B family with sequence similarity 107, member B
FAM65B family with sequence similarity 65, member B
FBXO11 F-box protein 11
FGFR1 fibroblast growth factor receptor 1
FZD4 frizzled class receptor 4
GABRA5 gamma-aminobutyric acid (GABA) A receptor, alpha 5
GABRB2 gamma-aminobutyric acid (GABA) A receptor, beta 2
GABRB3 gamma-aminobutyric acid (GABA) A receptor, beta 3
GJB2 gap junction protein, beta 2, 26kDa
GJB3 gap junction protein, beta 3, 31kDa
GJB6 gap junction protein, beta 6, 30kDa
GJC3 gap junction protein, gamma 3, 30.2kDa
GPX1 glutathione peroxidase 1
GRM7 glutamate receptor, metabotropic 7
GRXCR1 glutaredoxin, cysteine rich 1
HEXB hexosaminidase B (beta polypeptide)
HOXA1 homeobox A1
ICAM1 intercellular adhesion molecule 1
IFNG interferon, gamma
KCNE1 potassium channel, voltage gated subfamily E regulatory beta subunit 1
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
KCNQ4 potassium channel, voltage gated KQT-like subfamily Q, member 4
KPTN kaptin (actin binding protein)
LOXHD1 lipoxygenase homology domains 1
LRIG1 leucine-rich repeats and immunoglobulin-like domains 1
LRIG2 leucine-rich repeats and immunoglobulin-like domains 2
LRTOMT leucine rich transmembrane and O-methyltransferase domain containing
MAP1A microtubule-associated protein 1A
MARVELD2 MARVEL domain containing 2
MYH14 myosin, heavy chain 14, non-muscle
MYO15A myosin XVA
MYO1A myosin IA
MYO3A myosin IIIA
MYO6 myosin VI
MYO7A myosin VIIA
NAV2 neuron navigator 2
NDP Norrie disease (pseudoglioma)
NDUFB9 NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 9, 22kDa
NIPBL Nipped-B homolog (Drosophila)
OTOA otoancorin
OTOF otoferlin
OTOG otogelin
OTOR otoraplin
OTOS otospiralin
P2RX2 purinergic receptor P2X, ligand gated ion channel, 2
PAX3 paired box 3
PCDH15 protocadherin-related 15
PGAP1 post-GPI attachment to proteins 1
POU3F4 POU class 3 homeobox 4
POU4F2 POU class 4 homeobox 2
POU4F3 POU class 4 homeobox 3
RAB3A RAB3A, member RAS oncogene family
RPL38 ribosomal protein L38
SCN8A sodium channel, voltage gated, type VIII alpha subunit
SERPINB6 serpin peptidase inhibitor, clade B (ovalbumin), member 6
SIX1 SIX homeobox 1
SLC17A8 solute carrier family 17 (vesicular glutamate transporter), member 8
SLC1A3 solute carrier family 1 (glial high affinity glutamate transporter), member 3
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SLC26A5 solute carrier family 26 (anion exchanger), member 5
SLC52A3 solute carrier family 52 (riboflavin transporter), member 3
SLITRK6 SLIT and NTRK-like family, member 6
SNAI2 snail family zinc finger 2
SOBP sine oculis binding protein homolog (Drosophila)
SOD1 superoxide dismutase 1, soluble
SPRY2 sprouty homolog 2 (Drosophila)
SPTBN4 spectrin, beta, non-erythrocytic 4
SRRM4 serine/arginine repetitive matrix 4
TBL1X transducin (beta)-like 1X-linked
TBX1 T-box 1
TBX18 T-box 18
TECTA tectorin alpha
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TH tyrosine hydroxylase
THRB thyroid hormone receptor, beta
TIMM10 translocase of inner mitochondrial membrane 10 homolog (yeast)
TIMM13 translocase of inner mitochondrial membrane 13 homolog (yeast)
TIMM8B translocase of inner mitochondrial membrane 8 homolog B (yeast)
TIMM9 translocase of inner mitochondrial membrane 9 homolog (yeast)
TJP1 tight junction protein 1
TMIE transmembrane inner ear
TMPRSS3 transmembrane protease, serine 3
TPRN taperin
TSHZ3 teashirt zinc finger homeobox 3
TSPEAR thrombospondin-type laminin G domain and EAR repeats
TUB tubby bipartite transcription factor
UCN urocortin
USH1C Usher syndrome 1C (autosomal recessive, severe)
USH1G Usher syndrome 1G (autosomal recessive)
USH2A Usher syndrome 2A (autosomal recessive, mild)
WDR1 WD repeat domain 1
WFS1 Wolfram syndrome 1 (wolframin)
ZNF354A zinc finger protein 354A