SLC25A52 solute carrier family 25 member 52
Information
- Symbol
- SLC25A52
- Type
- protein-coding
- Description
- solute carrier family 25 member 52
- Entrez Gene ID
- 147407
- Genome
- hg19
- Position
- chr18:29,339,547-29,340,843
- Genome
- hg38
- Position
- chr18:31,759,584-31,760,880
- MIM
- 616153 OMIM
- HGNC
- HGNC:23324 HGNC
- Ensembl
- ENSG00000141437 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 4 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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4 |
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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 |
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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 | |||
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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 | MCART2 |
MIM | 616153 OMIM |
HGNC | HGNC:23324 HGNC |
Ensembl | ENSG00000141437 Ensembl |
AllianceGenome | HGNC:23324 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000672005.1 | hg38 | chr18 | 31,759,696 | 31,760,880 | 1,185 |
ENST00000269205.7 | hg38 | chr18 | 31,759,584 | 31,760,880 | 1,297 |
ENST00000269205.7 | hg19 | chr18 | 29,339,547 | 29,340,843 | 1,297 |
ENST00000672005.1 | hg19 | chr18 | 29,339,659 | 29,340,843 | 1,185 |
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