Detailed information for RetinalMD_04581

Basic information
| location | chr4:6302765-6302767 (hg19) |
| gene symbol | WFS1 (Reference) |
}
?>
| band | 4p16.1 |
| reference | GTC |
| observed | - |
| disease | Wolfram syndrome |
| PubMed ID | 21538838 | |
| ethnicity | Caucasian Americann |
| description | WFS1,NM_006005,exon8,c.1243_1245del,p.415_415del;WFS1,NM_001145853,exon8,c.1243_1245del,p.415_415del (Reference) |

MGI
| MGI ID | 1328355 |
| MGI phenotype | integument phenotype |

OMIM
| OMIM ID | 606201 |
| OMIM phenotype | Diabetes mellitus, noninsulin-dependent, association with |

Genome feature annotation
| segmental duplication | conserved TFBS | Encode TFBS | DNase I hypersensitivity sites |
| - | - | |

wgEncodeBroadHmm feature annotation
| Gm12878 | H1hesc | Hepg2 | Hmec | Hsmm | Huvec | K562 | Nhek | Nhlf |
| 11_Weak_Txn | | | | | | | | |

ESP and CG annotation
| ESP5400 | ESP5400_aa | ESP5400_ea | ESP6500 | ESP6500_aa | ESP6500_ea | ESP6500si | ESP6500si_aa | ESP6500si_ea | CG46 | CG69 |
| | | | | | | | | | |

dbSNP annotation
| snp137 | snp135 | snp132 | snp131 | snp130 | snp129 | snp137_NonFlagged | snp135_NonFlagged | snp132_NonFlagged | snp131_NonFlagged | snp130_NonFlagged |
| | | | | | | | | | |

1000 genomes annotation
| 2012apr | 2012apr_eur | 2012apr_amr | 2012apr_asn | 2012apr_afr | 2012feb | 2011may | 2010nov |
| | | | | | | |

Functional prediction
| SIFT | SIFT predict | PolyPhen2 | PolyPhen2 predict | phyloP | phyloP predict | LRT | LRT predict | MT | MT predict | GERP++ | GERP++ predict | GERP++elem | GERP++gt2 |
| - | - | - | - | - | - | - | - | - | - | | | | 5351.2 |

Conserved and constrained region annotation
| multiz46way | |
| phastcons46way | |
| phylop46way | Score=1;Name=chr4.1694496 |

RNA function annotation