DKK3 dickkopf WNT signaling pathway inhibitor 3
Information
- Symbol
- DKK3
- Type
- protein-coding
- Description
- dickkopf WNT signaling pathway inhibitor 3
- Entrez Gene ID
- 27122
- Genome
- hg19
- Position
- chr11:11,985,938-12,031,316
- Genome
- hg38
- Position
- chr11:11,964,391-12,009,769
- MIM
- 605416 OMIM
- HGNC
- HGNC:2893 HGNC
- Ensembl
- ENSG00000050165 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely pathogenic | 0 | 4 |
| Benign | 0 | 4 |
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 42 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
46 |
 |
8 |
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 | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| 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
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| Category | : |
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| 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 | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | CRRL |
| SYNONYM | REIC |
| SYNONYM | RIG |
| MIM | 605416 OMIM |
| HGNC | HGNC:2893 HGNC |
| Ensembl | ENSG00000050165 Ensembl |
| AllianceGenome | HGNC:2893 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000326932.8 | hg38 | chr11 | 11,963,106 | 12,009,370 | 46,265 |
| ENST00000683431.1 | hg38 | chr11 | 11,963,036 | 12,008,626 | 45,591 |
| ENST00000525493.5 | hg38 | chr11 | 11,964,391 | 12,009,769 | 45,379 |
| ENST00000396505.7 | hg38 | chr11 | 11,956,207 | 12,009,082 | 52,876 |
| ENST00000396505.7 | hg19 | chr11 | 11,977,754 | 12,030,629 | 52,876 |
| ENST00000326932.8 | hg19 | chr11 | 11,984,653 | 12,030,917 | 46,265 |
| ENST00000525493.5 | hg19 | chr11 | 11,985,938 | 12,031,316 | 45,379 |
| ENST00000683431.1 | hg19 | chr11 | 11,984,583 | 12,030,173 | 45,591 |
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