Table 3.

Characteristics of URO-D mutations

MutationExonLocation in cDNARFLPRecombinant URO-D activity
G25E G → A 74 EarI (+) INS 
A80S12 G → T 238 HinfI (+) 33.4%  
V134Q43-150 G TG → C CA 399 BsrI (+) 93.7%  
G156D G → A 467 BanI (−) 28.8% 
M165R13 T → G 494 NlaIII (−) INS  
E167K6 G → A 499 MseI (+) 93.5%  
Exon 6 splice30 /6/ G → C IVS6 PvuII (+) NT  
R193P3-150 G → C 578 SfaNI(−) INS 
Glu218insT Insert T 652 None NT 
F232L T → C 694 StuI (−) 43.0% 
L253Q9 T → A 758 HindIII (+) 75.0%  
I260T T → C 779 HphI (+) 60.5% 
MutationExonLocation in cDNARFLPRecombinant URO-D activity
G25E G → A 74 EarI (+) INS 
A80S12 G → T 238 HinfI (+) 33.4%  
V134Q43-150 G TG → C CA 399 BsrI (+) 93.7%  
G156D G → A 467 BanI (−) 28.8% 
M165R13 T → G 494 NlaIII (−) INS  
E167K6 G → A 499 MseI (+) 93.5%  
Exon 6 splice30 /6/ G → C IVS6 PvuII (+) NT  
R193P3-150 G → C 578 SfaNI(−) INS 
Glu218insT Insert T 652 None NT 
F232L T → C 694 StuI (−) 43.0% 
L253Q9 T → A 758 HindIII (+) 75.0%  
I260T T → C 779 HphI (+) 60.5% 

Superscript numbers indicate references for mutations previously reported.

Location in cDNA indicates where A of initial ATG is 1.

RFLP indicates restriction fragment length polymorphism; (+), adds the restriction site; INS, insoluble protein in inclusion bodies; (−), removes restriction site; and NT, not tested, no protein produced.

F3-150

RFLP mutation was identified in 2 unrelated patients with PCT.

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