SIGLEC9 sialic acid binding Ig like lectin 9
Information
- Symbol
- SIGLEC9
- Type
- protein-coding
- Description
- sialic acid binding Ig like lectin 9
- Entrez Gene ID
- 27180
- Genome
- hg19
- Position
- chr19:51,628,165-51,639,908
- Genome
- hg38
- Position
- chr19:51,124,908-51,136,651
- MIM
- 605640 OMIM
- HGNC
- HGNC:10878 HGNC
- Ensembl
- ENSG00000129450 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 6 |
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 50 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
58 |
 |
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
|
| 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 | CD329 |
| SYNONYM | CDw329 |
| SYNONYM | FOAP-9 |
| SYNONYM | OBBP-LIKE |
| SYNONYM | siglec-9 |
| MIM | 605640 OMIM |
| HGNC | HGNC:10878 HGNC |
| Ensembl | ENSG00000129450 Ensembl |
| AllianceGenome | HGNC:10878 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000250360.8 | hg38 | chr19 | 51,124,906 | 51,130,310 | 5,405 |
| ENST00000440804.7 | hg38 | chr19 | 51,124,908 | 51,136,651 | 11,744 |
| ENST00000250360.8 | hg19 | chr19 | 51,628,163 | 51,633,567 | 5,405 |
| ENST00000440804.7 | hg19 | chr19 | 51,628,165 | 51,639,908 | 11,744 |
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