CDON cell adhesion associated, oncogene regulated
Information
- Symbol
- CDON
- Type
- protein-coding
- Description
- cell adhesion associated, oncogene regulated
- Entrez Gene ID
- 50937
- Genome
- hg19
- Position
- chr11:125,825,691-125,933,187
- Genome
- hg38
- Position
- chr11:125,955,796-126,063,292
- MIM
- 608707 OMIM
- HGNC
- HGNC:17104 HGNC
- Ensembl
- ENSG00000064309 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 6 |
Likely pathogenic | 0 | 4 |
Benign | 0 | 348 |
Likely benign | 0 | 258 |
Conflicting classifications of pathogenicity | 0 | 50 |
Uncertain significance | 0 | 624 |
Ranking
ClinVar | |
---|---|
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0 |
![]() |
0 |
![]() |
180 |
![]() |
1,018 |
![]() |
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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
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 | |||
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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 | CDO |
SYNONYM | CDON1 |
SYNONYM | HPE11 |
SYNONYM | Ihog |
SYNONYM | ORCAM |
MIM | 608707 OMIM |
HGNC | HGNC:17104 HGNC |
Ensembl | ENSG00000064309 Ensembl |
AllianceGenome | HGNC:17104 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000263577.11 | hg38 | chr11 | 125,960,679 | 126,063,292 | 102,614 |
ENST00000531738.6 | hg38 | chr11 | 125,956,821 | 126,062,866 | 106,046 |
ENST00000392693.7 | hg38 | chr11 | 125,955,796 | 126,063,292 | 107,497 |
ENST00000684078.1 | hg38 | chr11 | 125,955,796 | 126,063,335 | 107,540 |
ENST00000392693.7 | hg19 | chr11 | 125,825,691 | 125,933,187 | 107,497 |
ENST00000684078.1 | hg19 | chr11 | 125,825,691 | 125,933,230 | 107,540 |
ENST00000263577.11 | hg19 | chr11 | 125,830,574 | 125,933,187 | 102,614 |
ENST00000531738.6 | hg19 | chr11 | 125,826,716 | 125,932,761 | 106,046 |
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