SLC30A8 solute carrier family 30 member 8
Information
- Symbol
- SLC30A8
- Type
- protein-coding
- Description
- solute carrier family 30 member 8
- Entrez Gene ID
- 169026
- Genome
- hg19
- Position
- chr8:118,147,234-118,188,953
- Genome
- hg38
- Position
- chr8:117,134,995-117,176,714
- MIM
- 611145 OMIM
- HGNC
- HGNC:20303 HGNC
- Ensembl
- ENSG00000164756 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 8 |
Likely benign | 0 | 12 |
Conflicting classifications of pathogenicity | 0 | 2 |
protective | 0 | 4 |
Uncertain significance | 0 | 36 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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56 |
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4 |
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 | ZNT8 |
SYNONYM | ZnT-8 |
MIM | 611145 OMIM |
HGNC | HGNC:20303 HGNC |
Ensembl | ENSG00000164756 Ensembl |
AllianceGenome | HGNC:20303 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000519688.5 | hg38 | chr8 | 117,135,259 | 117,176,714 | 41,456 |
ENST00000521243.5 | hg38 | chr8 | 116,950,273 | 117,172,791 | 222,519 |
ENST00000456015.7 | hg38 | chr8 | 117,134,995 | 117,176,714 | 41,720 |
ENST00000427715.2 | hg38 | chr8 | 116,950,951 | 117,176,714 | 225,764 |
ENST00000521243.5 | hg19 | chr8 | 117,962,512 | 118,185,030 | 222,519 |
ENST00000427715.2 | hg19 | chr8 | 117,963,190 | 118,188,953 | 225,764 |
ENST00000456015.7 | hg19 | chr8 | 118,147,234 | 118,188,953 | 41,720 |
ENST00000519688.5 | hg19 | chr8 | 118,147,498 | 118,188,953 | 41,456 |
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