CALCOCO1 calcium binding and coiled-coil domain 1
Information
- Symbol
- CALCOCO1
- Type
- protein-coding
- Description
- calcium binding and coiled-coil domain 1
- Entrez Gene ID
- 57658
- Genome
- hg19
- Position
- chr12:54,102,301-54,121,236
- Genome
- hg38
- Position
- chr12:53,708,517-53,727,452
- HGNC
- HGNC:29306 HGNC
- Ensembl
- ENSG00000012822 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 10 |
Uncertain significance | 0 | 76 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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86 |
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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 |
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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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Category | : |
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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 |
---|---|
SYNONYM | Cocoa |
SYNONYM | PP13275 |
SYNONYM | calphoglin |
HGNC | HGNC:29306 HGNC |
Ensembl | ENSG00000012822 Ensembl |
AllianceGenome | HGNC:29306 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000548263.5 | hg38 | chr12 | 53,711,159 | 53,727,428 | 16,270 |
ENST00000262059.8 | hg38 | chr12 | 53,708,517 | 53,727,745 | 19,229 |
ENST00000430117.6 | hg38 | chr12 | 53,711,119 | 53,727,439 | 16,321 |
ENST00000550804.6 | hg38 | chr12 | 53,708,517 | 53,727,452 | 18,936 |
ENST00000262059.8 | hg19 | chr12 | 54,102,301 | 54,121,529 | 19,229 |
ENST00000430117.6 | hg19 | chr12 | 54,104,903 | 54,121,223 | 16,321 |
ENST00000550804.6 | hg19 | chr12 | 54,102,301 | 54,121,236 | 18,936 |
ENST00000548263.5 | hg19 | chr12 | 54,104,943 | 54,121,212 | 16,270 |
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