LPCAT3 lysophosphatidylcholine acyltransferase 3
Information
- Symbol
- LPCAT3
- Type
- protein-coding
- Description
- lysophosphatidylcholine acyltransferase 3
- Entrez Gene ID
- 10162
- Genome
- hg19
- Position
- chr12:7,085,347-7,125,780
- Genome
- hg38
- Position
- chr12:6,976,185-7,018,476
- MIM
- 611950 OMIM
- HGNC
- HGNC:30244 HGNC
- Ensembl
- ENSG00000111684 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Uncertain significance | 0 | 44 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
48 |
 |
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
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | C3F |
| SYNONYM | LPCAT |
| SYNONYM | LPLAT 5 |
| SYNONYM | LPLAT12 |
| SYNONYM | LPSAT |
| SYNONYM | MBOAT5 |
| SYNONYM | OACT5 |
| SYNONYM | nessy |
| MIM | 611950 OMIM |
| HGNC | HGNC:30244 HGNC |
| Ensembl | ENSG00000111684 Ensembl |
| AllianceGenome | HGNC:30244 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000261407.9 | hg38 | chr12 | 6,976,185 | 7,018,476 | 42,292 |
| ENST00000261407.9 | hg19 | chr12 | 7,085,347 | 7,125,780 | 40,434 |
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