SAAL1 serum amyloid A like 1
Information
- Symbol
- SAAL1
- Type
- protein-coding
- Description
- serum amyloid A like 1
- Entrez Gene ID
- 113174
- Genome
- hg19
- Position
- chr11:18,101,839-18,127,629
- Genome
- hg38
- Position
- chr11:18,080,292-18,106,082
- HGNC
- HGNC:25158 HGNC
- Ensembl
- ENSG00000166788 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 32 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
36 |
 |
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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| 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 | SPACIA1 |
| HGNC | HGNC:25158 HGNC |
| Ensembl | ENSG00000166788 Ensembl |
| AllianceGenome | HGNC:25158 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000300013.8 | hg38 | chr11 | 18,080,344 | 18,106,082 | 25,739 |
| ENST00000529318.5 | hg38 | chr11 | 18,080,373 | 18,106,087 | 25,715 |
| ENST00000524803.6 | hg38 | chr11 | 18,080,292 | 18,106,082 | 25,791 |
| ENST00000524803.6 | hg19 | chr11 | 18,101,839 | 18,127,629 | 25,791 |
| ENST00000300013.8 | hg19 | chr11 | 18,101,891 | 18,127,629 | 25,739 |
| ENST00000529318.5 | hg19 | chr11 | 18,101,920 | 18,127,634 | 25,715 |
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