Annotation Detail
Information
- Associated Genes
- MECP2
- Associated Variants
-
MECP2 p.Thr170Met (p.T170M)
(
ENST00000303391.11,
ENST00000415944.4,
ENST00000407218.5,
ENST00000453960.7,
ENST00000628176.2 )
MECP2 p.Phe167Cys (p.F167C) ( ENST00000303391.11, ENST00000407218.5, ENST00000415944.4, ENST00000453960.7, ENST00000628176.2 )
MECP2 p.Phe167Ser (p.F167S) ( ENST00000303391.11, ENST00000407218.5, ENST00000415944.4, ENST00000453960.7, ENST00000628176.2 )
MECP2 p.Arg145Cys (p.R145C) ( ENST00000303391.11, ENST00000407218.5, ENST00000415944.4, ENST00000453960.7, ENST00000628176.2 )
MECP2 p.Arg145Gly (p.R145G) ( ENST00000303391.11, ENST00000407218.5, ENST00000415944.4, ENST00000453960.7, ENST00000628176.2 )
MECP2 p.Arg118Trp (p.R118W) ( ENST00000407218.5, ENST00000453960.7, ENST00000303391.11, ENST00000628176.2, ENST00000415944.4 )
MECP2 p.Arg118Gly (p.R118G) ( ENST00000303391.11, ENST00000407218.5, ENST00000415944.4, ENST00000453960.7, ENST00000628176.2 )
MECP2 p.Thr170Met (p.T170M) ( ENST00000453960.7, ENST00000303391.11, ENST00000407218.5, ENST00000415944.4, ENST00000628176.2 )
MECP2 p.Phe167Cys (p.F167C) ( ENST00000303391.11, ENST00000407218.5, ENST00000415944.4, ENST00000453960.7, ENST00000628176.2 )
MECP2 p.Phe167Ser (p.F167S) ( ENST00000303391.11, ENST00000407218.5, ENST00000415944.4, ENST00000453960.7, ENST00000628176.2 )
MECP2 p.Arg145Cys (p.R145C) ( ENST00000453960.7, ENST00000303391.11, ENST00000407218.5, ENST00000415944.4, ENST00000628176.2 )
MECP2 p.Arg145Gly (p.R145G) ( ENST00000303391.11, ENST00000407218.5, ENST00000415944.4, ENST00000453960.7, ENST00000628176.2 )
MECP2 p.Arg118Trp (p.R118W) ( ENST00000415944.4, ENST00000303391.11, ENST00000407218.5, ENST00000453960.7, ENST00000628176.2 )
MECP2 p.Arg118Gly (p.R118G) ( ENST00000303391.11, ENST00000407218.5, ENST00000415944.4, ENST00000453960.7, ENST00000628176.2 ) - Associated Disease
- Rett syndrome
- Source Database
- DisGeNET
- Description
- Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.
- Pubmed
- 10508514
- Original source reporting the Gene Disease association
- UNIPROT
- DisGENET score for the Gene Disease association
- 0.8
- Year of publication
- 1999
Drugs