SLC15A3 solute carrier family 15 member 3
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 68 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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72 |
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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 | |||||
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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 |
---|---|
SYNONYM | OCTP |
SYNONYM | PHT2 |
SYNONYM | PTR3 |
SYNONYM | hPHT2 |
MIM | 610408 OMIM |
HGNC | HGNC:18068 HGNC |
Ensembl | ENSG00000110446 Ensembl |
AllianceGenome | HGNC:18068 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000227880.8 | hg38 | chr11 | 60,937,084 | 60,952,176 | 15,093 |
ENST00000681275.1 | hg38 | chr11 | 60,937,084 | 60,952,080 | 14,997 |
ENST00000681882.1 | hg38 | chr11 | 60,937,084 | 60,952,176 | 15,093 |
ENST00000681951.1 | hg38 | chr11 | 60,937,084 | 60,952,176 | 15,093 |
ENST00000681275.1 | hg19 | chr11 | 60,704,556 | 60,719,552 | 14,997 |
ENST00000681882.1 | hg19 | chr11 | 60,704,556 | 60,719,648 | 15,093 |
ENST00000681951.1 | hg19 | chr11 | 60,704,556 | 60,719,648 | 15,093 |
ENST00000227880.8 | hg19 | chr11 | 60,704,556 | 60,719,648 | 15,093 |
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