TRPV6
protein-coding gene in the species Homo sapiens
Facts
18 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Altered regulation leads to
- Dent disease, oculocerebrorenal syndrome, nephrolithiasis, nephrolithiasis, nephrolithiasis, Pendred syndrome, pre-eclampsia[33][34][35][36][37]
- Chromosome
- human chromosome 7[11]
- Cytogenetic location
- 7q34[40]
- Decreased expression in
- esophageal cancer[12]
- Expressed in
- body of pancreas, duodenum, placenta, prostate, islet of Langerhans, gallbladder, skin of abdomen, primary visual cortex, salivary gland, skin of leg[41]
- Found in taxon
- Homo sapiens[10]
- Gene deletion association with
- male infertility[26]
- Gene substitution association with
- transient neonatal hyperparathyroidism, chronic pancreatitis, colorectal cancer, male infertility, nephrolithiasis, osteochondrodysplasia[27][28][29][30][31][32]
- Genetic association
- transient neonatal hyperparathyroidism[38]
- HomoloGene ID
- 56812[3]
- Increased expression in
- breast cancer, breast cancer, colorectal cancer, endometrial cancer, stomach cancer, Gitelman syndrome, Gitelman syndrome, Gordon syndrome, hypocalcemic rickets, lung cancer, lung cancer, osteoporosis, osteoporosis, ovarian cancer, pancreatic cancer, pancreatic cancer, prostate cancer, prostate cancer, thyroid cancer[13][14][15][16][17][18][19][20][21][22][23][24][25]
- Strand orientation
- reverse strand[39]
🏷️ Also known as
en ABP/ZF
en CAT1
en CATL
en ECAC2
en HRPTTN
en HSA277909
en LP6728
en transient receptor potential cation channel subfamily V member 6
en TRPV6
en ZFAB
🔖 Identifiers · 12
- OpenAlex ID
- C155520015
- Ensembl gene ID
- ENSG00000276971, ENSG00000165125
- Ensembl transcript ID
- ENST00000359396, ENST00000431833, ENST00000436401, ENST00000474388, ENST00000485138, ENST00000489123, ENST00000633318, ENST00000632330, ENST00000633826, ENST00000632381, ENST00000619250, ENST00000611485, ENST00000615386, ENST00000632455, ENST00000632149, ENST00000631384, ENST00000634074
- Entrez Gene ID
- 55503
- Exact match
- identifiers.org
- Freebase ID
- /m/0cbmj_
- HGNC ID
- 14006
- HGNC gene symbol
- TRPV6
- Microsoft Academic ID (discontinued)
- 155520015
- OMIM ID
- 606680
- UMLS CUI
- C1422342
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Summary
TRPV6 is a gene[1].