WT1 WT1 transcription factor

Information
Symbol
WT1
Type
protein-coding
Description
WT1 transcription factor
Entrez Gene ID
7490
Genome
hg19
Position
chr11:32,409,321-32,457,085
Genome
hg38
Position
chr11:32,387,775-32,435,539
MIM
607102 OMIM
HGNC
HGNC:12796 HGNC
Ensembl
ENSG00000184937 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 15 152
Likely pathogenic 1 88
Benign 9 136
Likely benign 3 1,080
Conflicting classifications of pathogenicity 0 124
not provided 379 2
Uncertain significance 12 1,650
Ranking
ClinVar
0
0
634
2,378
44
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM AWT1
SYNONYM GUD
SYNONYM NPHS4
SYNONYM WAGR
SYNONYM WIT-2
SYNONYM WT-1
SYNONYM WT33
MIM 607102 OMIM
HGNC HGNC:12796 HGNC
Ensembl ENSG00000184937 Ensembl
AllianceGenome HGNC:12796
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000332351.9 hg38 chr11 32,387,784 32,435,564 47,781
ENST00000640146.2 hg38 chr11 32,388,130 32,434,168 46,039
ENST00000527882.6 hg38 chr11 32,389,042 32,430,813 41,772
ENST00000452863.10 hg38 chr11 32,387,775 32,435,539 47,765
ENST00000639563.3 hg38 chr11 32,389,058 32,435,360 46,303
ENST00000379079.8 hg38 chr11 32,387,775 32,430,813 43,039
ENST00000530998.5 hg38 chr11 32,387,778 32,430,813 43,036
ENST00000448076.9 hg38 chr11 32,388,679 32,435,535 46,857
ENST00000379079.8 hg19 chr11 32,409,321 32,452,359 43,039
ENST00000452863.10 hg19 chr11 32,409,321 32,457,085 47,765
ENST00000332351.9 hg19 chr11 32,409,330 32,457,110 47,781
ENST00000448076.9 hg19 chr11 32,410,225 32,457,081 46,857
ENST00000527882.6 hg19 chr11 32,410,588 32,452,359 41,772
ENST00000530998.5 hg19 chr11 32,409,324 32,452,359 43,036
ENST00000639563.3 hg19 chr11 32,410,604 32,456,906 46,303
ENST00000640146.2 hg19 chr11 32,409,676 32,455,714 46,039
KeyValue
strand-
UniProtTSG
start32,409,321
VogelsteinTSG
Gene SymbolWT1
Entrez GeneId7,490
Chr Band11p13
end32,457,080
chrchr11
NameWilms tumour 1 gene
Genome browser