TRPV6
protein-coding gene in the species Homo sapiens
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Summary
TRPV6 is a gene[1].
Key Facts
- Subclass of: protein-coding gene[2]
- HomoloGene ID: 56812[3]
- Genomic start: 142568956[4], 142871208[5]
- Genomic end: 142583507[6], 142885745[7]
- Ortholog: Trpv6[8]
- Encodes: Transient receptor potential cation channel subfamily V member 6[9]
- Found in taxon: Homo sapiens[10]
- Chromosome: human chromosome 7[11]
- Decreased expression in: esophageal cancer[12]
- Increased expression in: breast cancer[13], colorectal cancer[14], endometrial cancer[15], stomach cancer[16], Gitelman syndrome[17], Gordon syndrome[18], hypocalcemic rickets[19], lung cancer[20], osteoporosis[21], ovarian cancer[22], pancreatic cancer[23], prostate cancer[24], thyroid cancer[25]
- Gene deletion association with: male infertility[26]
- Gene substitution association with: transient neonatal hyperparathyroidism[27], chronic pancreatitis[28], colorectal cancer[29], male infertility[30], nephrolithiasis[31], osteochondrodysplasia[32]
- Altered regulation leads to: Dent disease[33], oculocerebrorenal syndrome[34], nephrolithiasis[35], Pendred syndrome[36], pre-eclampsia[37]
- Genetic association: transient neonatal hyperparathyroidism[38]
- Strand orientation: reverse strand[39]
- Cytogenetic location: 7q34[40]
- Expressed in: body of pancreas[41]