SLC15A4 solute carrier family 15 member 4
Information
- Symbol
- SLC15A4
- Type
- protein-coding
- Description
- solute carrier family 15 member 4
- Entrez Gene ID
- 121260
- Genome
- hg19
- Position
- chr12:129,277,739-129,308,503
- Genome
- hg38
- Position
- chr12:128,793,194-128,823,958
- MIM
- 615806 OMIM
- HGNC
- HGNC:23090 HGNC
- Ensembl
- ENSG00000139370 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
not provided | 2 | 0 |
Uncertain significance | 0 | 52 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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54 |
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2 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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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Category | : |
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Filtering | : |
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 | FP12591 |
SYNONYM | PHT1 |
SYNONYM | PTR4 |
MIM | 615806 OMIM |
HGNC | HGNC:23090 HGNC |
Ensembl | ENSG00000139370 Ensembl |
AllianceGenome | HGNC:23090 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000266771.10 | hg38 | chr12 | 128,793,194 | 128,823,958 | 30,765 |
ENST00000266771.10 | hg19 | chr12 | 129,277,739 | 129,308,503 | 30,765 |
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