SWISSVAR
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1 protein found in SwissVar (45 variants)

with gene/protein name P22309

Disclaimer: The query results are intended for research purposes only, not for clinical and diagnostic use.

Accession Entry name Disease Variants 3D mapping
(variant position)
P22309 UD11_HUMAN gilbert syndrome p.Gly71Arg
p.Phe83Leu
p.Pro229Gln
p.Ile294Thr
p.Arg367Gly
p.Tyr486Asp






P22309 UD11_HUMAN transient familial neonatal hyperbilirubinemia p.Gly71Arg
p.Tyr486Asp


P22309 UD11_HUMAN crigler-najjar syndrome 1 p.Asp36Asn
p.His39Asp
p.Cys177Arg
p.Gly276Arg
p.Glu291Val
p.Ala292Val
p.Gly308Glu
p.Arg336Gln
p.Arg336Leu
p.Gln357Arg
p.Ala368Thr
p.Ser375Phe
p.His376Arg
p.Gly377Val
p.Ser381Arg
p.Pro387Ser
p.Gly395Val
p.Ala401Pro
p.Lys402Thr
p.Lys428Glu
p.Trp461Arg





















P22309 UD11_HUMAN crigler-najjar syndrome 2 p.Leu15Arg
p.Pro34Gln
p.Gly71Arg
p.Leu175Gln
p.Ser191Phe
p.Arg209Trp
p.Val225Gly
p.Pro229Gln
p.Tyr230Cys
p.Asn279Tyr
p.Ile294Thr
p.Gln331Arg
p.Arg336Trp
p.Arg336Leu
p.Trp354Arg
p.Arg367Cys
p.Ile370Val
p.His376Arg
p.Gly377Val
p.Pro387His
p.Asn400Asp
p.Arg403Cys
p.Leu443Pro
p.Trp461Arg
p.Ala478Asp
p.Tyr486Asp