SLC25A14 solute carrier family 25 member 14
Information
- Symbol
- SLC25A14
- Type
- protein-coding
- Description
- solute carrier family 25 member 14
- Entrez Gene ID
- 9016
- Genome
- hg19
- Position
- chrX:129,474,253-129,506,924
- Genome
- hg38
- Position
- chrX:130,340,279-130,372,950
- MIM
- 300242 OMIM
- HGNC
- HGNC:10984 HGNC
- Ensembl
- ENSG00000102078 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| not provided | 6 | 0 |
| Uncertain significance | 0 | 2 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
2 |
 |
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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| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | BMCP1 |
| SYNONYM | UCP5 |
| MIM | 300242 OMIM |
| HGNC | HGNC:10984 HGNC |
| Ensembl | ENSG00000102078 Ensembl |
| AllianceGenome | HGNC:10984 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000361980.9 | hg38 | chrX | 130,340,279 | 130,372,950 | 32,672 |
| ENST00000545805.6 | hg38 | chrX | 130,339,919 | 130,373,357 | 33,439 |
| ENST00000218197.9 | hg38 | chrX | 130,340,052 | 130,373,361 | 33,310 |
| ENST00000612248.4 | hg38 | chrX | 130,339,888 | 130,373,361 | 33,474 |
| ENST00000543953.5 | hg38 | chrX | 130,339,888 | 130,373,361 | 33,474 |
| ENST00000339231.3 | hg38 | chrX | 130,340,279 | 130,372,950 | 32,672 |
| ENST00000543953.5 | hg19 | chrX | 129,473,862 | 129,507,335 | 33,474 |
| ENST00000612248.4 | hg19 | chrX | 129,473,862 | 129,507,335 | 33,474 |
| ENST00000545805.6 | hg19 | chrX | 129,473,893 | 129,507,331 | 33,439 |
| ENST00000218197.9 | hg19 | chrX | 129,474,026 | 129,507,335 | 33,310 |
| ENST00000339231.3 | hg19 | chrX | 129,474,253 | 129,506,924 | 32,672 |
| ENST00000361980.9 | hg19 | chrX | 129,474,253 | 129,506,924 | 32,672 |
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