TRPV4

Summary

TRPV4 is a gene^[1]. TRPV4 ranks in the top 2% of gene entities by monthly Wikipedia readership (72 views/month).^[2]

Key Facts

• TRPV4's instance of is recorded as gene^[3].
• TRPV4 is a type of protein-coding gene^[4].
• TRPV4's HomoloGene ID is recorded as 11003^[5].
• TRPV4's genomic start is recorded as 110220890^[6].
• TRPV4's genomic start is recorded as 109783087^[7].
• TRPV4's genomic end is recorded as 110271212^[8].
• TRPV4's genomic end is recorded as 109833406^[9].
• TRPV4's ortholog is recorded as Trpv4^[10].
• TRPV4's ortholog is recorded as Trpv4^[11].
• TRPV4's ortholog is recorded as trpv4^[12].
• TRPV4's encodes is recorded as Transient receptor potential cation channel subfamily V member 4^[13].
• TRPV4's found in taxon is recorded as Homo sapiens^[14].
• TRPV4's chromosome is recorded as human chromosome 12^[15].
• TRPV4's genetic association is recorded as spondylometaphyseal dysplasia, Kozlowski type^[16].
• TRPV4's genetic association is recorded as metatropic dysplasia^[17].
• TRPV4's genetic association is recorded as Charcot-Marie-Tooth disease axonal type 2C^[18].
• TRPV4's genetic association is recorded as spondyloepiphyseal dysplasia, Maroteaux type^[19].
• TRPV4's genetic association is recorded as parastremmatic dwarfism^[20].
• TRPV4's genetic association is recorded as familial digital arthropathy-brachydactyly^[21].
• TRPV4's genetic association is recorded as neuromuscular disease^[22].
• TRPV4's genetic association is recorded as scapuloperoneal spinal muscular atrophy^[23].
• TRPV4's genetic association is recorded as autosomal dominant congenital benign spinal muscular atrophy^[24].
• TRPV4's strand orientation is recorded as reverse strand^[25].
• TRPV4's exact match is recorded as http://identifiers.org/ncbigene/59341^[26].
• TRPV4's cytogenetic location is recorded as 12q24.11^[27].

Why It Matters

TRPV4 ranks in the top 2% of gene entities by monthly Wikipedia readership (72 views/month).^[2]