CALY calcyon neuron specific vesicular protein
Information
- Symbol
- CALY
- Type
- protein-coding
- Description
- calcyon neuron specific vesicular protein
- Entrez Gene ID
- 50632
- Genome
- hg19
- Position
- chr10:135,137,576-135,150,400
- Genome
- hg38
- Position
- chr10:133,324,072-133,336,896
- MIM
- 604647 OMIM
- HGNC
- HGNC:17938 HGNC
- Ensembl
- ENSG00000130643 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 26 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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28 |
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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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | DRD1IP |
| SYNONYM | NSG3 |
| MIM | 604647 OMIM |
| HGNC | HGNC:17938 HGNC |
| Ensembl | ENSG00000130643 Ensembl |
| AllianceGenome | HGNC:17938 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000368558.1 | hg38 | chr10 | 133,325,932 | 133,336,935 | 11,004 |
| ENST00000368555.3 | hg38 | chr10 | 133,327,427 | 133,336,872 | 9,446 |
| ENST00000252939.9 | hg38 | chr10 | 133,324,072 | 133,336,896 | 12,825 |
| ENST00000252939.9 | hg19 | chr10 | 135,137,576 | 135,150,400 | 12,825 |
| ENST00000368558.1 | hg19 | chr10 | 135,139,436 | 135,150,439 | 11,004 |
| ENST00000368555.3 | hg19 | chr10 | 135,140,931 | 135,150,376 | 9,446 |
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