SAT1 spermidine/spermine N1-acetyltransferase 1
Information
- Symbol
- SAT1
- Type
- protein-coding
- Description
- spermidine/spermine N1-acetyltransferase 1
- Entrez Gene ID
- 6303
- Genome
- hg19
- Position
- chrX:23,801,290-23,804,327
- Genome
- hg38
- Position
- chrX:23,783,173-23,786,210
- MIM
- 313020 OMIM
- HGNC
- HGNC:10540 HGNC
- Ensembl
- ENSG00000130066 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
not provided | 6 | 0 |
Uncertain significance | 0 | 4 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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8 |
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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
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
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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Category | : |
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Search word | : | |
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
|
Category | : |
|
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 | DC21 |
SYNONYM | KFSD |
SYNONYM | KFSDX |
SYNONYM | SAT |
SYNONYM | SSAT |
SYNONYM | SSAT-1 |
MIM | 313020 OMIM |
HGNC | HGNC:10540 HGNC |
Ensembl | ENSG00000130066 Ensembl |
AllianceGenome | HGNC:10540 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000379254.5 | hg38 | chrX | 23,783,173 | 23,786,113 | 2,941 |
ENST00000379270.5 | hg38 | chrX | 23,783,173 | 23,786,210 | 3,038 |
ENST00000379254.5 | hg19 | chrX | 23,801,290 | 23,804,230 | 2,941 |
ENST00000379270.5 | hg19 | chrX | 23,801,290 | 23,804,327 | 3,038 |
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