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TRPV4

transient receptor potential cation channel subfamily V member 4

HCNC Approved Symbol
TRPV4 (HGNC:18083)
Genomic Coordinates
12:109,783,087 - 109,833,398 (12q24.11)
Synonyms
OTRPC4, TRP12, VROAC, VRL-2, VR-OAC, CMT2C
Disease Associations
This gene is associated with the following 11 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Avascular necrosis of femoral head, primary, 2
617383AD
[Sodium serum level QTL 1]
613508-
Brachyolmia type 3
113500AD
Digital arthropathy-brachydactyly, familial
606835AD
Hereditary motor and sensory neuropathy, type IIc
606071AD
Metatropic dysplasia
156530AD
Neuronopathy, distal hereditary motor, autosomal dominant 8
600175AD
Parastremmatic dwarfism
168400AD
Scapuloperoneal spinal muscular atrophy
181405AD
SED, Maroteaux type
184095AD
Spondylometaphyseal dysplasia, Kozlowski type
184252AD

Diagnosed Cases

14Patients

In total, 14 patients were diagnosed with a variant in the TRPV4 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

Bilateral clubfoot
 
2 (14.3%)
Exaggerated lumbar lordosis
 
2 (14.3%)
Kyphoscoliosis
 
2 (14.3%)
Short-trunked dwarfism
 
2 (14.3%)
Scoliosis
 
2 (14.3%)