WT1
protein-coding gene in the species Homo sapiens
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WT1
Summary
WT1 is a gene[1].
Key Facts
- WT1's instance of is recorded as gene[2].
- WT1 is a type of protein-coding gene[3].
- WT1's HomoloGene ID is recorded as 11536[4].
- WT1's genomic start is recorded as 32387775[5].
- WT1's genomic start is recorded as 32409321[6].
- WT1's genomic end is recorded as 32457176[7].
- WT1's genomic end is recorded as 32435564[8].
- WT1's ortholog is recorded as Wt1[9].
- WT1's ortholog is recorded as Wt1[10].
- WT1's ortholog is recorded as wt1a[11].
- WT1's encodes is recorded as WT1 transcription factor[12].
- WT1's found in taxon is recorded as Homo sapiens[13].
- WT1's chromosome is recorded as human chromosome 11[14].
- WT1's genetic association is recorded as Frasier syndrome[15].
- WT1's genetic association is recorded as Denys-Drash syndrome[16].
- WT1's genetic association is recorded as Meacham syndrome[17].
- WT1's genetic association is recorded as nephrotic syndrome, type 4[18].
- WT1's genetic association is recorded as familial idiopathic steroid-resistant nephrotic syndrome[19].
- WT1's strand orientation is recorded as reverse strand[20].
- WT1's exact match is recorded as http://identifiers.org/ncbigene/7490[21].
- WT1's cytogenetic location is recorded as 11p13[22].
- WT1's expressed in is recorded as germinal epithelium[23].
- WT1's expressed in is recorded as glomerulus[24].
- WT1's expressed in is recorded as metanephric glomerulus[25].
- WT1's expressed in is recorded as parietal pleura[26].