SPATA31E1 SPATA31 subfamily E member 1
Information
- Symbol
- SPATA31E1
- Type
- protein-coding
- Description
- SPATA31 subfamily E member 1
- Entrez Gene ID
- 286234
- Genome
- hg19
- Position
- chr9:90,497,792-90,503,818
- Genome
- hg38
- Position
- chr9:87,882,877-87,888,903
- HGNC
- HGNC:26672 HGNC
- Ensembl
- ENSG00000177992 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 16 |
| Uncertain significance | 0 | 232 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
248 |
 |
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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| 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 | C9orf79 |
| SYNONYM | FAM75E1 |
| HGNC | HGNC:26672 HGNC |
| Ensembl | ENSG00000177992 Ensembl |
| AllianceGenome | HGNC:26672 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000325643.6 | hg38 | chr9 | 87,882,877 | 87,888,903 | 6,027 |
| ENST00000325643.6 | hg19 | chr9 | 90,497,792 | 90,503,818 | 6,027 |
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