STARD10 StAR related lipid transfer domain containing 10
Information
- Symbol
- STARD10
- Type
- protein-coding
- Description
- StAR related lipid transfer domain containing 10
- Entrez Gene ID
- 10809
- Genome
- hg19
- Position
- chr11:72,465,774-72,505,092
- Genome
- hg38
- Position
- chr11:72,754,729-72,794,047
- MIM
- 617382 OMIM
- HGNC
- HGNC:10666 HGNC
- Ensembl
- ENSG00000214530 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Uncertain significance | 0 | 40 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
42 |
 |
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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| 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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| 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 | CGI-52 |
| SYNONYM | NY-CO-28 |
| SYNONYM | PCTP2 |
| SYNONYM | SDCCAG28 |
| MIM | 617382 OMIM |
| HGNC | HGNC:10666 HGNC |
| Ensembl | ENSG00000214530 Ensembl |
| AllianceGenome | HGNC:10666 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000545082.5 | hg38 | chr11 | 72,754,893 | 72,781,842 | 26,950 |
| ENST00000334805.11 | hg38 | chr11 | 72,754,729 | 72,794,047 | 39,319 |
| ENST00000543304.5 | hg38 | chr11 | 72,754,729 | 72,793,657 | 38,929 |
| ENST00000538536.5 | hg38 | chr11 | 72,754,839 | 72,793,643 | 38,805 |
| ENST00000334805.11 | hg19 | chr11 | 72,465,774 | 72,505,092 | 39,319 |
| ENST00000538536.5 | hg19 | chr11 | 72,465,884 | 72,504,688 | 38,805 |
| ENST00000543304.5 | hg19 | chr11 | 72,465,774 | 72,504,702 | 38,929 |
| ENST00000545082.5 | hg19 | chr11 | 72,465,938 | 72,492,887 | 26,950 |
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