WNT3 Wnt family member 3
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 2 |
| Likely pathogenic | 0 | 2 |
| Benign | 0 | 22 |
| Likely benign | 0 | 114 |
| Conflicting classifications of pathogenicity | 0 | 2 |
| Uncertain significance | 0 | 66 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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20 |
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174 |
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6 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
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| 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 | |||||||||||
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| Target data | : |
MGeND data only
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| 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
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| 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 | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | INT4 |
| SYNONYM | TETAMS |
| MIM | 165330 OMIM |
| HGNC | HGNC:12782 HGNC |
| Ensembl | ENSG00000108379 Ensembl |
| AllianceGenome | HGNC:12782 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000706485.1 | hg38 | chr17 | 46,763,878 | 46,771,447 | 7,570 |
| ENST00000706483.1 | hg38 | chr17 | 46,762,618 | 46,772,287 | 9,670 |
| ENST00000225512.6 | hg38 | chr17 | 46,762,506 | 46,818,692 | 56,187 |
| ENST00000706495.1 | hg38 | chr17 | 46,762,643 | 46,833,084 | 70,442 |
| ENST00000225512.6 | hg19 | chr17 | 44,839,872 | 44,896,058 | 56,187 |
| ENST00000706483.1 | hg19 | chr17 | 44,839,984 | 44,849,653 | 9,670 |
| ENST00000706495.1 | hg19 | chr17 | 44,840,009 | 44,910,450 | 70,442 |
| ENST00000706485.1 | hg19 | chr17 | 44,841,244 | 44,848,813 | 7,570 |
| Key | Value |
|---|---|
| strand | - |
| UniProt | OG |
| start | 44,839,871 |
| Gene Symbol | WNT3 |
| Entrez GeneId | 7,473 |
| Chr Band | 17q21 |
| end | 44,896,125 |
| chr | chr17 |
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