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27 records found for search term Trpv4
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RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
69337Trpv4transient receptor potential cation channel, subfamily V, member 4ENCODES a protein that exhibits actin binding; actin filament binding; alpha-tubulin binding; INVOLVED IN actin cytoskeleton organization; actin filament organization; calcium ion import; ASSOCIATED WITH pulmonary hypertension; amyotrophic lateral sclerosis type 5 (ortholog); Auditory Neuropathy (or124759916147638143Rat409symbol , PhenoGengene, protein-coding, PROVISIONAL [RefSeq]
735797Trpv4transient receptor potential cation channel, subfamily V, member 4Enables several functions, including SH2 domain binding activity; calcium channel activity; and osmosensor activity. Involved in several processes, including cellular response to osmotic stress; positive regulation of MAPK cascade; and positive regulation of cytokine production. Acts upstream of or 5114760213114796497Mouse424symbol , old_gene_name , PhenoGen , descriptiongene, protein-coding, VALIDATED [RefSeq]
1604803TRPV4transient receptor potential cation channel subfamily V member 4This gene encodes a member of the OSM9-like transient receptor potential channel (OTRPC) subfamily in the transient receptor potential (TRP) superfamily of ion channels. The encoded protein is a Ca2+-permeable, nonselective cation channel that is thought to be involved in the regulation of systemic 12109783087109833398Human1062symbol , COSMIC , Human Proteome Mapgene, protein-coding, REVIEWED [RefSeq]
8959460Trpv4transient receptor potential cation channel subfamily V member 4ENCODES a protein that exhibits actin binding (ortholog); actin filament binding (ortholog); alpha-tubulin binding (ortholog); INVOLVED IN actin cytoskeleton organization (ortholog); actin filament organization (ortholog); ATP export (ortholog); ASSOCIATED WITH amyotrophic lateral sclerosis type 5 (NW_00495545587448658781644Chinchilla194symbolgene, protein-coding, MODEL [RefSeq]
11705898TRPV4transient receptor potential cation channel subfamily V member 4ENCODES a protein that exhibits actin binding (ortholog); actin filament binding (ortholog); alpha-tubulin binding (ortholog); INVOLVED IN actin cytoskeleton organization (ortholog); ATP export (ortholog); ATP transport (ortholog); ASSOCIATED WITH amyotrophic lateral sclerosis type 5 (ortholog); Aud12107359005107409359Bonobo193symbolgene, protein-coding, MODEL [RefSeq]
12381920TRPV4transient receptor potential cation channel subfamily V member 4ENCODES a protein that exhibits actin binding (ortholog); actin filament binding (ortholog); alpha-tubulin binding (ortholog); INVOLVED IN positive regulation of vascular permeability; actin cytoskeleton organization (ortholog); ATP export (ortholog); ASSOCIATED WITH amyotrophic lateral sclerosis ty261729333417330156Dog195symbolgene, protein-coding, PROVISIONAL [RefSeq]
12486978Trpv4transient receptor potential cation channel subfamily V member 4ENCODES a protein that exhibits actin binding (ortholog); actin filament binding (ortholog); alpha-tubulin binding (ortholog); INVOLVED IN actin cytoskeleton organization (ortholog); ATP export (ortholog); ATP transport (ortholog); ASSOCIATED WITH amyotrophic lateral sclerosis type 5 (ortholog); AudNW_00493676914245261447547Squirrel192symbolgene, protein-coding, MODEL [RefSeq]
18908921Trpv4transient receptor potential cation channel subfamily V member 4ENCODES a protein that exhibits actin binding (ortholog); actin filament binding (ortholog); alpha-tubulin binding (ortholog); INVOLVED IN actin cytoskeleton organization (ortholog); ATP export (ortholog); ATP transport (ortholog); ASSOCIATED WITH amyotrophic lateral sclerosis type 5 (ortholog); AudNaked Mole-Rat191symbolgene, protein-coding, MODEL [RefSeq]
18382097TRPV4transient receptor potential cation channel subfamily V member 4ENCODES a protein that exhibits actin binding (ortholog); actin filament binding (ortholog); alpha-tubulin binding (ortholog); INVOLVED IN actin cytoskeleton organization (ortholog); ATP export (ortholog); ATP transport (ortholog); ASSOCIATED WITH amyotrophic lateral sclerosis type 5 (ortholog); AudGreen Monkey192symbolgene, protein-coding, MODEL [RefSeq]
155251148trpv4Tropical Clawed Frogsymbolgene, null
20865855TRPV4transient receptor potential cation channel subfamily V member 4Green Monkeysymbolgene, protein-coding
13967072TRPV4transient receptor potential cation channel subfamily V member 4ENCODES a protein that exhibits calcium channel activity; actin binding (ortholog); actin filament binding (ortholog); INVOLVED IN actin filament organization; ATP export; ATP transport; ASSOCIATED WITH amyotrophic lateral sclerosis type 5 (ortholog); Auditory Neuropathy (ortholog); autosomal dominaPig188symbolgene, protein-coding, PROVISIONAL [RefSeq]
625938596Trpv4transient receptor potential cation channel subfamily V member 4ENCODES a protein that exhibits actin binding (ortholog); actin filament binding (ortholog); alpha-tubulin binding (ortholog); INVOLVED IN actin cytoskeleton organization (ortholog); actin filament organization (ortholog); ATP export (ortholog); ASSOCIATED WITH amyotrophic lateral sclerosis type 5 (Black Rat184symbolgene, protein-coding, MODEL [RefSeq]
155245096trpv4.LAfrican Clawed Frogsymbolgene, null
155249719trpv4.SAfrican Clawed Frogsymbolgene, null
39456109Trpv4em1Sagetransient receptor potential cation channel, subfamily V, member 4; ZFN induced mutant1, SageThis Trpv4 allele has a 899-bp deletion which completely removes exon 13, plus parts of intron 12-13 and intron 13-14 .Ratsymbol , descriptiongene, allele
11553851Trpv4em4Mcwitransient receptor potential cation channel, subfamily V, member 4; CRISPR/Cas9 induced mutant 4, Medical College of WisconsinThis allele was made by CRISPR/Cas9 system. The resulting mutation is a 4-bp deletion in Exon 4 of the Trpv4 geneRatsymbol , description , old_gene_symbolgene, allele
11553847Trpv4em5Mcwitransient receptor potential cation channel, subfamily V, member 4; CRISPR/Cas9 induced mutant5, Medical College of WisconsinThis allele was made by CRISPR/Cas9 system. The resulting mutation is a 5-bp deletion in Exon 4 of the Trpv4 geneRatsymbol , description , old_gene_symbolgene, allele
286225616trpv4l.1Tropical Clawed Frogsymbolgene, null
329329059trpv4l.2Tropical Clawed Frogsymbolgene, null
598153485trpv4l.3Tropical Clawed Frogsymbolgene, null
598151927trpv4l.3Tropical Clawed Frogsymbolgene, null
598152976trpv4l.3Tropical Clawed Frogsymbolgene, null
598153270trpv4l.3Tropical Clawed Frogsymbolgene, null
286225909trpv4l.1.LAfrican Clawed Frogsymbolgene, null
329329058trpv4l.2.LAfrican Clawed Frogsymbolgene, null
12270253GLTPglycolipid transfer proteinENCODES a protein that exhibits ATP binding (inferred); calcium channel activity (inferred); calmodulin binding (inferred); INVOLVED IN response to immobilization stress (ortholog); FOUND IN cytoplasm (inferred); cytosol (inferred); membrane (inferred)261726200817283735Dog39ensembl_gene_symbolgene, protein-coding, MODEL [RefSeq]