SLC39A1 solute carrier family 39 member 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 34 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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36 |
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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.]
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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 |
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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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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 | ZIP1 |
SYNONYM | ZIRTL |
MIM | 604740 OMIM |
HGNC | HGNC:12876 HGNC |
Ensembl | ENSG00000143570 Ensembl |
AllianceGenome | HGNC:12876 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000356205.9 | hg38 | chr1 | 153,959,110 | 153,963,537 | 4,428 |
ENST00000617697.4 | hg38 | chr1 | 153,959,099 | 153,968,184 | 9,086 |
ENST00000368623.7 | hg38 | chr1 | 153,959,110 | 153,963,475 | 4,366 |
ENST00000368621.5 | hg38 | chr1 | 153,959,111 | 153,963,462 | 4,352 |
ENST00000621013.4 | hg38 | chr1 | 153,959,099 | 153,963,492 | 4,394 |
ENST00000537590.5 | hg38 | chr1 | 153,959,099 | 153,963,641 | 4,543 |
ENST00000310483.10 | hg38 | chr1 | 153,959,112 | 153,967,712 | 8,601 |
ENST00000621013.4 | hg19 | chr1 | 153,931,575 | 153,935,968 | 4,394 |
ENST00000537590.5 | hg19 | chr1 | 153,931,575 | 153,936,117 | 4,543 |
ENST00000617697.4 | hg19 | chr1 | 153,931,575 | 153,940,660 | 9,086 |
ENST00000368623.7 | hg19 | chr1 | 153,931,586 | 153,935,951 | 4,366 |
ENST00000356205.9 | hg19 | chr1 | 153,931,586 | 153,936,013 | 4,428 |
ENST00000368621.5 | hg19 | chr1 | 153,931,587 | 153,935,938 | 4,352 |
ENST00000310483.10 | hg19 | chr1 | 153,931,588 | 153,940,188 | 8,601 |
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