STAP2 signal transducing adaptor family member 2
Information
- Symbol
- STAP2
- Type
- protein-coding
- Description
- signal transducing adaptor family member 2
- Entrez Gene ID
- 55620
- Genome
- hg19
- Position
- chr19:4,324,040-4,338,818
- Genome
- hg38
- Position
- chr19:4,324,043-4,338,821
- MIM
- 607881 OMIM
- HGNC
- HGNC:30430 HGNC
- Ensembl
- ENSG00000178078 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 12 |
| Uncertain significance | 0 | 48 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
60 |
 |
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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| 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 | BKS |
| MIM | 607881 OMIM |
| HGNC | HGNC:30430 HGNC |
| Ensembl | ENSG00000178078 Ensembl |
| AllianceGenome | HGNC:30430 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000600324.5 | hg38 | chr19 | 4,324,043 | 4,338,821 | 14,779 |
| ENST00000594605.6 | hg38 | chr19 | 4,324,043 | 4,338,827 | 14,785 |
| ENST00000600324.5 | hg19 | chr19 | 4,324,040 | 4,338,818 | 14,779 |
| ENST00000594605.6 | hg19 | chr19 | 4,324,040 | 4,338,824 | 14,785 |
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