Symbol Name ID |
Trpv4
transient receptor potential cation channel, subfamily V, member 4 MGI:1926945 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Decreased fetal movement |
Fetal akinesia sequence |
Urinary incontinence |
Vocal cord paresis |
Hoarse voice |
Disease(s) Associated with TRPV4 | |||||
autosomal dominant distal hereditary motor neuronopathy 8 | |||||
Charcot-Marie-Tooth disease axonal type 2C | |||||
metatropic dysplasia | |||||
scapuloperoneal spinal muscular atrophy |
Mouse Phenotypes | behavior/neurological phenotype |
abnormal drinking behavior |
decreased fluid intake |
abnormal response to tactile stimuli |
abnormal sensory capabilities/reflexes/nociception |
increased chemical nociceptive threshold |
abnormal mechanical nociception |
abnormal nociception after inflammation |
abnormal pain threshold |
increased thermal nociceptive threshold |
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Availability | Mouse Genotype | ||||||||||
Trpv4tm1Msz/Trpv4tm1Msz | |||||||||||
Trpv4tm1Rck/Trpv4tm1Rck | * | ||||||||||
Trpv4tm1.1Ldtk/Trpv4tm1.1Ldtk Tg(KRT14-cre/ERT)20Efu/0 (conditional) |
* |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/23/2024 MGI 6.23 |
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