WT1 Chromosome 11

WT1 transcription factor
244 variants 244 Health Risk

Upload your DNA to see your personal genotypes for variants in WT1.

What This Gene Does
This gene encodes a transcription factor that contains four zinc-finger motifs at the C-terminus and a proline/glutamine-rich DNA-binding domain at the N-terminus. It has an essential role in the normal development of the urogenital system, and it is mutated in a small subset of patients with Wilms tumor. This gene exhibits complex tissue-specific and polymorphic imprinting pattern, with biallelic, and monoallelic expression from the maternal and paternal alleles in different tissues. Multiple transcript variants have been described. In several variants, there is evidence for the use of a non-AUG (CUG) translation initiation codon upstream of, and in-frame with the first AUG. Authors of PMID:7926762 also provide evidence that WT1 mRNA undergoes RNA editing in human and rat, and that this process is tissue-restricted and developmentally regulated. [provided by RefSeq, Mar 2015]
Gene Info
Gene Group
Zinc fingers C2H2-type
Locus Type
gene with protein product
Location
11p13
Ensembl
ENSG00000184937
Associated Conditions (31)
Drash syndrome
Frasier syndrome
Wilms tumor 1
11p partial monosomy syndrome
Hereditary cancer-predisposing syndrome
8 conditions
Inborn genetic diseases
Nephrotic syndrome
type 4
Focal segmental glomerulosclerosis
6 conditions
Acute myeloid leukemia
WT1-related disorder
Ovarian cancer
Meacham syndrome
Hereditary cancer
Kidney disorder
Male infertility with azoospermia or oligozoospermia due to single gene mutation
Ambiguous genitalia
Disorder of sexual differentiation
+11 more conditions
Key Variants
All Variants (244)
RSID Category Clinical Significance Conditions
RS1036899554 Health Risk Conflicting classifications of pathogenicity Drash syndrome, Frasier syndrome, Wilms tumor 1
RS1037084691 Health Risk Conflicting classifications of pathogenicity Nephrotic syndrome, type 4, Focal segmental glomerulosclerosis
RS1170323988 Health Risk Conflicting classifications of pathogenicity Drash syndrome, Frasier syndrome, Wilms tumor 1
RS1189241211 Health Risk Conflicting classifications of pathogenicity Drash syndrome, Frasier syndrome, Wilms tumor 1
RS1214646426 Health Risk Conflicting classifications of pathogenicity Drash syndrome, Frasier syndrome, Wilms tumor 1
RS1298313010 Health Risk Conflicting classifications of pathogenicity Drash syndrome, Frasier syndrome, Wilms tumor 1
RS1308955642 Health Risk Conflicting classifications of pathogenicity Drash syndrome, Frasier syndrome, Wilms tumor 1
RS1309250331 Health Risk Conflicting classifications of pathogenicity Drash syndrome, Frasier syndrome, Wilms tumor 1
RS1314273962 Health Risk Conflicting classifications of pathogenicity Wilms tumor 1, Inborn genetic diseases, Wilms tumor 1
RS1327516147 Health Risk Conflicting classifications of pathogenicity Frasier syndrome, Drash syndrome, Wilms tumor 1
RS1330792627 Health Risk Conflicting classifications of pathogenicity Drash syndrome, Frasier syndrome, Wilms tumor 1
RS1341857958 Health Risk Conflicting classifications of pathogenicity Nephrotic syndrome, type 4, Wilms tumor 1
RS1351753257 Health Risk Conflicting classifications of pathogenicity Drash syndrome, Hereditary cancer-predisposing syndrome, WT1-related disorder
RS1362460137 Health Risk Conflicting classifications of pathogenicity 8 conditions, Frasier syndrome, Wilms tumor 1
RS1369099437 Health Risk Conflicting classifications of pathogenicity Drash syndrome, Frasier syndrome, Wilms tumor 1
RS1384974578 Health Risk Conflicting classifications of pathogenicity Wilms tumor 1, 11p partial monosomy syndrome, Drash syndrome
RS1392191365 Health Risk Conflicting classifications of pathogenicity Wilms tumor 1, 11p partial monosomy syndrome, Drash syndrome
RS1396104394 Health Risk Conflicting classifications of pathogenicity Wilms tumor 1, 11p partial monosomy syndrome, Frasier syndrome
RS1397886023 Health Risk Conflicting classifications of pathogenicity Drash syndrome, Frasier syndrome, Wilms tumor 1
RS142059681 Health Risk Conflicting classifications of pathogenicity Frasier syndrome, Wilms tumor 1, 11p partial monosomy syndrome
RS1438888966 Health Risk Conflicting classifications of pathogenicity Drash syndrome, Frasier syndrome, Wilms tumor 1
RS1443423967 Health Risk Conflicting classifications of pathogenicity Drash syndrome, Frasier syndrome, Wilms tumor 1
RS1447574915 Health Risk Conflicting classifications of pathogenicity Wilms tumor 1, Drash syndrome, Frasier syndrome
RS1455790542 Health Risk Conflicting classifications of pathogenicity Wilms tumor 1, 11p partial monosomy syndrome, Drash syndrome
RS1469499452 Health Risk Conflicting classifications of pathogenicity Drash syndrome, Frasier syndrome, Wilms tumor 1
RS147241955 Health Risk Conflicting classifications of pathogenicity Wilms tumor 1, 11p partial monosomy syndrome, Drash syndrome
RS1473590912 Health Risk Conflicting classifications of pathogenicity Wilms tumor 1, 11p partial monosomy syndrome, Drash syndrome
RS1475923286 Health Risk Conflicting classifications of pathogenicity Drash syndrome, Frasier syndrome, 11p partial monosomy syndrome
RS147939483 Health Risk Conflicting classifications of pathogenicity Wilms tumor 1, 11p partial monosomy syndrome, Drash syndrome
RS148856160 Health Risk Conflicting classifications of pathogenicity Wilms tumor 1, 11p partial monosomy syndrome, Drash syndrome
RS151034312 Health Risk Conflicting classifications of pathogenicity Wilms tumor 1, 11p partial monosomy syndrome, Drash syndrome
RS1554943492 Health Risk Conflicting classifications of pathogenicity Drash syndrome, Frasier syndrome, 11p partial monosomy syndrome
RS1564975924 Health Risk Conflicting classifications of pathogenicity Wilms tumor 1, 11p partial monosomy syndrome, Drash syndrome
RS1565001804 Health Risk Conflicting classifications of pathogenicity Wilms tumor 1, 11p partial monosomy syndrome, Drash syndrome
RS1590338659 Health Risk Conflicting classifications of pathogenicity Male infertility with azoospermia or oligozoospermia due to single gene mutation, Inborn genetic diseases, Frasier syndrome
RS1590410967 Health Risk Conflicting classifications of pathogenicity Wilms tumor 1, 11p partial monosomy syndrome, Drash syndrome
RS1590411426 Health Risk Conflicting classifications of pathogenicity Frasier syndrome, Wilms tumor 1, 11p partial monosomy syndrome
RS1712081462 Health Risk Conflicting classifications of pathogenicity Nephrotic syndrome, type 4, Wilms tumor 1
RS1851829640 Health Risk Conflicting classifications of pathogenicity Ambiguous genitalia, Disorder of sexual differentiation, Ambiguous genitalia
RS1851834162 Health Risk Conflicting classifications of pathogenicity Wilms tumor 1, 11p partial monosomy syndrome, Frasier syndrome
RS1851851609 Health Risk Conflicting classifications of pathogenicity
RS1852677213 Health Risk Conflicting classifications of pathogenicity Drash syndrome, Wilms tumor 1, 11p partial monosomy syndrome
RS1853454967 Health Risk Conflicting classifications of pathogenicity Drash syndrome, Inborn genetic diseases, Drash syndrome
RS1853462729 Health Risk Conflicting classifications of pathogenicity Wilms tumor 1, 11p partial monosomy syndrome, Frasier syndrome
RS1853481697 Health Risk Conflicting classifications of pathogenicity Drash syndrome, Frasier syndrome, Wilms tumor 1
RS200222400 Health Risk Conflicting classifications of pathogenicity Wilms tumor 1, 11p partial monosomy syndrome, Drash syndrome
RS2132898640 Health Risk Conflicting classifications of pathogenicity Drash syndrome, Frasier syndrome, Wilms tumor 1
RS2132913596 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, WT1-related disorder, Inborn genetic diseases
RS2132919246 Health Risk Conflicting classifications of pathogenicity
RS2133032654 Health Risk Conflicting classifications of pathogenicity 11p partial monosomy syndrome, Frasier syndrome, Drash syndrome
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