LILRA6 leukocyte immunoglobulin like receptor A6
Information
- Symbol
- LILRA6
- Type
- protein-coding
- Description
- leukocyte immunoglobulin like receptor A6
- Entrez Gene ID
- 79168
- Genome
- hg19
- Position
- chr19:54,742,425-54,746,640
- Genome
- hg38
- Position
- chr19:54,236,590-54,242,790
- HGNC
- HGNC:15495 HGNC
- Ensembl
- ENSG00000244482 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 14 |
| Uncertain significance | 0 | 63 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
79 |
 |
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 | CD85b |
| SYNONYM | ILT-8 |
| SYNONYM | ILT5 |
| SYNONYM | ILT8 |
| SYNONYM | LILRB3 |
| SYNONYM | LILRB6 |
| HGNC | HGNC:15495 HGNC |
| Ensembl | ENSG00000244482 Ensembl |
| AllianceGenome | HGNC:15495 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000245621.6 | hg38 | chr19 | 54,238,953 | 54,242,751 | 3,799 |
| ENST00000396365.7 | hg38 | chr19 | 54,236,590 | 54,242,790 | 6,201 |
| ENST00000440558.2 | hg19 | chr19 | 54,720,737 | 54,746,649 | 25,913 |
| ENST00000270464.5 | hg19 | chr19 | 54,720,797 | 54,746,602 | 25,806 |
| ENST00000419410.2 | hg19 | chr19 | 54,720,797 | 54,746,602 | 25,806 |
| ENST00000391735.3 | hg19 | chr19 | 54,720,797 | 54,746,602 | 25,806 |
| ENST00000396365.2 | hg19 | chr19 | 54,742,425 | 54,746,640 | 4,216 |
| ENST00000245621.5 | hg19 | chr19 | 54,742,829 | 54,746,600 | 3,772 |
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