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GENATLAS PHENOTYPE

last update : 13/07/2006

Symbol	JK
Location	18q12.3
Name	Kidd blood group
Corresponding gene	SLC14A1
related resource	Blood Group Antigen Mutation Database
Main clinical features	Jk-null red blood cells have reduced urea permeability, but the Jk deficiency is not associated with any obvious clinical syndrome except for a urine concentration defect
Genetic determination	autosomal dominant
Function/system disorder	hematology
Type	other

Gene product

Name	solute carrier family 14 (urea transport) member 1

Remark(s)