SLC25A6 solute carrier family 25 member 6
Information
- Symbol
- SLC25A6
- Type
- protein-coding
- Description
- solute carrier family 25 member 6
- Entrez Gene ID
- 293
- Genome
- hg19
- Position
- chrX:1,505,045-1,511,006
- Genome
- hg19
- Position
- chrY:1,455,045-1,461,006
- Genome
- hg38
- Position
- chrX:1,386,152-1,392,113
- Genome
- hg38
- Position
- chrY:1,386,152-1,392,113
- MIM
- 300151 OMIM
- HGNC
- HGNC:10992 HGNC
- Ensembl
- ENSG00000169100 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 16 |
Likely benign | 0 | 32 |
not provided | 7 | 0 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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48 |
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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
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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Filtering | : |
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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Search word | : | |
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
|
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 | AAC3 |
SYNONYM | ANT |
SYNONYM | ANT 2 |
SYNONYM | ANT 3 |
SYNONYM | ANT3 |
SYNONYM | ANT3Y |
MIM | 300151 OMIM |
MIM | 403000 OMIM |
HGNC | HGNC:10992 HGNC |
Ensembl | ENSG00000169100 Ensembl |
Ensembl | ENSG00000292334 Ensembl |
AllianceGenome | HGNC:10992 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000381401.11 | hg38 | chrX | 1,386,152 | 1,392,113 | 5,962 |
ENST00000711214.1 | hg38 | chrY | 1,386,152 | 1,392,113 | 5,962 |
ENST00000381401.11 | hg19 | chrX | 1,505,045 | 1,511,006 | 5,962 |
ENST00000711214.1 | hg19 | chrY | 1,455,045 | 1,461,006 | 5,962 |
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