LILRB2 leukocyte immunoglobulin like receptor B2
Information
- Symbol
- LILRB2
- Type
- protein-coding
- Description
- leukocyte immunoglobulin like receptor B2
- Entrez Gene ID
- 10288
- Genome
- hg19
- Position
- chr19:54,778,320-54,785,039
- Genome
- hg38
- Position
- chr19:54,274,466-54,281,184
- MIM
- 604815 OMIM
- HGNC
- HGNC:6606 HGNC
- Ensembl
- ENSG00000131042 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 26 |
| Uncertain significance | 0 | 82 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
108 |
 |
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
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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 | CD85D |
| SYNONYM | ILT-4 |
| SYNONYM | ILT4 |
| SYNONYM | LIR-2 |
| SYNONYM | LIR2 |
| SYNONYM | MIR-10 |
| SYNONYM | MIR10 |
| MIM | 604815 OMIM |
| HGNC | HGNC:6606 HGNC |
| Ensembl | ENSG00000131042 Ensembl |
| AllianceGenome | HGNC:6606 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000434421.5 | hg38 | chr19 | 54,273,822 | 54,281,178 | 7,357 |
| ENST00000391749.4 | hg38 | chr19 | 54,274,466 | 54,281,184 | 6,719 |
| ENST00000391748.5 | hg38 | chr19 | 54,273,821 | 54,280,883 | 7,063 |
| ENST00000314446.10 | hg38 | chr19 | 54,273,812 | 54,281,110 | 7,299 |
| ENST00000391746.5 | hg38 | chr19 | 54,274,466 | 54,280,498 | 6,033 |
| ENST00000314446.10 | hg19 | chr19 | 54,777,666 | 54,784,965 | 7,300 |
| ENST00000391748.5 | hg19 | chr19 | 54,777,675 | 54,784,738 | 7,064 |
| ENST00000434421.5 | hg19 | chr19 | 54,777,676 | 54,785,033 | 7,358 |
| ENST00000391746.5 | hg19 | chr19 | 54,778,320 | 54,784,353 | 6,034 |
| ENST00000391749.4 | hg19 | chr19 | 54,778,320 | 54,785,039 | 6,720 |
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