SAT2 spermidine/spermine N1-acetyltransferase family member 2
Information
- Symbol
- SAT2
- Type
- protein-coding
- Description
- spermidine/spermine N1-acetyltransferase family member 2
- Entrez Gene ID
- 112483
- Genome
- hg19
- Position
- chr17:7,529,552-7,531,139
- Genome
- hg38
- Position
- chr17:7,626,234-7,627,821
- MIM
- 611463 OMIM
- HGNC
- HGNC:23160 HGNC
- Ensembl
- ENSG00000141504 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 20 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
22 |
 |
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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| 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 | SSAT-2 |
| SYNONYM | SSAT2 |
| MIM | 611463 OMIM |
| HGNC | HGNC:23160 HGNC |
| Ensembl | ENSG00000141504 Ensembl |
| AllianceGenome | HGNC:23160 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000573566.1 | hg38 | chr17 | 7,626,388 | 7,627,805 | 1,418 |
| ENST00000269298.10 | hg38 | chr17 | 7,626,234 | 7,627,821 | 1,588 |
| ENST00000269298.10 | hg19 | chr17 | 7,529,552 | 7,531,139 | 1,588 |
| ENST00000573566.1 | hg19 | chr17 | 7,529,706 | 7,531,123 | 1,418 |
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