CAND1 cullin associated and neddylation dissociated 1
Information
- Symbol
- CAND1
- Type
- protein-coding
- Description
- cullin associated and neddylation dissociated 1
- Entrez Gene ID
- 55832
- Genome
- hg19
- Position
- chr12:67,663,138-67,713,733
- Genome
- hg38
- Position
- chr12:67,269,358-67,319,953
- MIM
- 607727 OMIM
- HGNC
- HGNC:30688 HGNC
- Ensembl
- ENSG00000111530 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 50 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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48 |
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2 |
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 |
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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 | TIP120 |
SYNONYM | TIP120A |
MIM | 607727 OMIM |
HGNC | HGNC:30688 HGNC |
Ensembl | ENSG00000111530 Ensembl |
AllianceGenome | HGNC:30688 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000545606.6 | hg38 | chr12 | 67,269,358 | 67,319,953 | 50,596 |
ENST00000545606.6 | hg19 | chr12 | 67,663,138 | 67,713,733 | 50,596 |
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