LILRA2 leukocyte immunoglobulin like receptor A2
Information
- Symbol
- LILRA2
- Type
- protein-coding
- Description
- leukocyte immunoglobulin like receptor A2
- Entrez Gene ID
- 11027
- Genome
- hg19
- Position
- chr19:55,085,257-55,101,752
- Genome
- hg38
- Position
- chr19:54,573,790-54,590,287
- MIM
- 604812 OMIM
- HGNC
- HGNC:6603 HGNC
- Ensembl
- ENSG00000239998 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 6 |
| Uncertain significance | 2 | 110 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
116 |
 |
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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| 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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| 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 | CD85H |
| SYNONYM | ILT1 |
| SYNONYM | LIR-7 |
| SYNONYM | LIR7 |
| MIM | 604812 OMIM |
| HGNC | HGNC:6603 HGNC |
| Ensembl | ENSG00000239998 Ensembl |
| AllianceGenome | HGNC:6603 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000391737.3 | hg38 | chr19 | 54,573,841 | 54,587,395 | 13,555 |
| ENST00000391738.8 | hg38 | chr19 | 54,573,790 | 54,590,287 | 16,498 |
| ENST00000251376.7 | hg38 | chr19 | 54,573,792 | 54,590,287 | 16,496 |
| ENST00000251377.7 | hg38 | chr19 | 54,573,351 | 54,587,560 | 14,210 |
| ENST00000251377.7 | hg19 | chr19 | 55,084,818 | 55,099,027 | 14,210 |
| ENST00000391738.8 | hg19 | chr19 | 55,085,257 | 55,101,752 | 16,496 |
| ENST00000251376.7 | hg19 | chr19 | 55,085,259 | 55,101,752 | 16,494 |
| ENST00000391737.3 | hg19 | chr19 | 55,085,308 | 55,098,862 | 13,555 |
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