Title : Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family.

Pub. Date : 2002 Jun

PMID : 12032568






4 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 The TRPM6 protein is a new member of the long transient receptor potential channel (TRPM) family and is highly similar to TRPM7 (also known as TRP-PLIK), a bifunctional protein that combines calcium- and magnesium-permeable cation channel properties with protein kinase activity. Calcium transient receptor potential cation channel subfamily M member 7 Homo sapiens
2 The TRPM6 protein is a new member of the long transient receptor potential channel (TRPM) family and is highly similar to TRPM7 (also known as TRP-PLIK), a bifunctional protein that combines calcium- and magnesium-permeable cation channel properties with protein kinase activity. Calcium transient receptor potential cation channel subfamily M member 7 Homo sapiens
3 The TRPM6 protein is a new member of the long transient receptor potential channel (TRPM) family and is highly similar to TRPM7 (also known as TRP-PLIK), a bifunctional protein that combines calcium- and magnesium-permeable cation channel properties with protein kinase activity. Magnesium transient receptor potential cation channel subfamily M member 7 Homo sapiens
4 The TRPM6 protein is a new member of the long transient receptor potential channel (TRPM) family and is highly similar to TRPM7 (also known as TRP-PLIK), a bifunctional protein that combines calcium- and magnesium-permeable cation channel properties with protein kinase activity. Magnesium transient receptor potential cation channel subfamily M member 7 Homo sapiens