CDX2 caudal type homeobox 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 0 | 4 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 40 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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46 |
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0 |
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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | CDX-3 |
SYNONYM | CDX2/AS |
SYNONYM | CDX3 |
MIM | 600297 OMIM |
HGNC | HGNC:1806 HGNC |
Ensembl | ENSG00000165556 Ensembl |
AllianceGenome | HGNC:1806 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000381020.8 | hg38 | chr13 | 27,960,918 | 27,969,315 | 8,398 |
ENST00000381020.8 | hg19 | chr13 | 28,535,055 | 28,543,452 | 8,398 |
Key | Value |
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strand | - |
start | 28,536,204 |
Gene Symbol | CDX2 |
Entrez GeneId | 1,045 |
Chr Band | 13q12.3 |
end | 28,543,504 |
chr | chr13 |
Name | caudal type homeo box transcription factor 2 |
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