GPAT2 glycerol-3-phosphate acyltransferase 2, mitochondrial
Information
- Symbol
- GPAT2
- Type
- protein-coding
- Description
- glycerol-3-phosphate acyltransferase 2, mitochondrial
- Entrez Gene ID
- 150763
- Genome
- hg19
- Position
- chr2:96,687,694-96,700,664
- Genome
- hg38
- Position
- chr2:96,021,946-96,034,916
- MIM
- 616431 OMIM
- HGNC
- HGNC:27168 HGNC
- Ensembl
- ENSG00000186281 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 10 |
| Uncertain significance | 0 | 76 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
88 |
 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | CT123 |
| MIM | 616431 OMIM |
| HGNC | HGNC:27168 HGNC |
| Ensembl | ENSG00000186281 Ensembl |
| AllianceGenome | HGNC:27168 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000434632.6 | hg38 | chr2 | 96,021,946 | 96,034,916 | 12,971 |
| ENST00000691940.1 | hg38 | chr2 | 96,021,958 | 96,034,921 | 12,964 |
| ENST00000453542.5 | hg38 | chr2 | 96,021,947 | 96,034,925 | 12,979 |
| ENST00000687910.1 | hg38 | chr2 | 96,022,029 | 96,035,974 | 13,946 |
| ENST00000359548.8 | hg38 | chr2 | 96,021,946 | 96,034,916 | 12,971 |
| ENST00000359548.8 | hg19 | chr2 | 96,687,694 | 96,700,664 | 12,971 |
| ENST00000434632.6 | hg19 | chr2 | 96,687,694 | 96,700,664 | 12,971 |
| ENST00000453542.5 | hg19 | chr2 | 96,687,695 | 96,700,673 | 12,979 |
| ENST00000691940.1 | hg19 | chr2 | 96,687,706 | 96,700,669 | 12,964 |
| ENST00000687910.1 | hg19 | chr2 | 96,687,777 | 96,701,722 | 13,946 |
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