SATL1 spermidine/spermine N1-acetyl transferase like 1
Information
- Symbol
- SATL1
- Type
- protein-coding
- Description
- spermidine/spermine N1-acetyl transferase like 1
- Entrez Gene ID
- 340562
- Genome
- hg19
- Position
- chrX:84,347,317-84,498,785
- Genome
- hg38
- Position
- chrX:85,092,311-85,243,779
- HGNC
- HGNC:27992 HGNC
- Ensembl
- ENSG00000184788 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 14 |
Likely benign | 0 | 16 |
not provided | 6 | 0 |
Uncertain significance | 0 | 60 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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90 |
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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 | |||
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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000395409.7 | hg38 | chrX | 85,092,287 | 85,108,968 | 16,682 |
ENST00000644105.2 | hg38 | chrX | 85,092,284 | 85,243,779 | 151,496 |
ENST00000646235.1 | hg38 | chrX | 85,092,300 | 85,243,911 | 151,612 |
ENST00000509231.1 | hg38 | chrX | 85,092,294 | 85,109,048 | 16,755 |
ENST00000646118.1 | hg38 | chrX | 85,092,311 | 85,243,779 | 151,469 |
ENST00000644105.2 | hg19 | chrX | 84,347,290 | 84,498,785 | 151,496 |
ENST00000395409.7 | hg19 | chrX | 84,347,293 | 84,363,974 | 16,682 |
ENST00000509231.1 | hg19 | chrX | 84,347,300 | 84,364,054 | 16,755 |
ENST00000646235.1 | hg19 | chrX | 84,347,306 | 84,498,917 | 151,612 |
ENST00000646118.1 | hg19 | chrX | 84,347,317 | 84,498,785 | 151,469 |
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