STARD7 StAR related lipid transfer domain containing 7
Information
- Symbol
- STARD7
- Type
- protein-coding
- Description
- StAR related lipid transfer domain containing 7
- Entrez Gene ID
- 56910
- Genome
- hg19
- Position
- chr2:96,850,597-96,874,565
- Genome
- hg38
- Position
- chr2:96,184,859-96,208,827
- MIM
- 616712 OMIM
- HGNC
- HGNC:18063 HGNC
- Ensembl
- ENSG00000084090 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| not provided | 2 | 0 |
| Uncertain significance | 0 | 54 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
2 |
 |
54 |
 |
2 |
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 | ADCME |
| SYNONYM | BAFME2 |
| SYNONYM | FAME |
| SYNONYM | FAME2 |
| SYNONYM | FCMTE2 |
| SYNONYM | GTT1 |
| MIM | 616712 OMIM |
| HGNC | HGNC:18063 HGNC |
| Ensembl | ENSG00000084090 Ensembl |
| AllianceGenome | HGNC:18063 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000337288.10 | hg38 | chr2 | 96,184,859 | 96,208,827 | 23,969 |
| ENST00000337288.10 | hg19 | chr2 | 96,850,597 | 96,874,565 | 23,969 |
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