LILRB4 leukocyte immunoglobulin like receptor B4
Information
- Symbol
- LILRB4
- Type
- protein-coding
- Description
- leukocyte immunoglobulin like receptor B4
- Entrez Gene ID
- 11006
- Genome
- hg19
- Position
- chr19:55,174,472-55,179,848
- Genome
- hg38
- Position
- chr19:54,663,020-54,668,397
- MIM
- 604821 OMIM
- HGNC
- HGNC:6608 HGNC
- Ensembl
- ENSG00000186818 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 8 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
8 |
 |
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 | B4 |
| SYNONYM | CD85K |
| SYNONYM | ILT-3 |
| SYNONYM | ILT3 |
| SYNONYM | LIR-5 |
| SYNONYM | LIR5 |
| MIM | 604821 OMIM |
| HGNC | HGNC:6608 HGNC |
| Ensembl | ENSG00000186818 Ensembl |
| AllianceGenome | HGNC:6608 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000391736.5 | hg38 | chr19 | 54,662,128 | 54,670,359 | 8,232 |
| ENST00000391734.7 | hg38 | chr19 | 54,662,998 | 54,668,397 | 5,400 |
| ENST00000391733.7 | hg38 | chr19 | 54,663,020 | 54,668,397 | 5,378 |
| ENST00000695418.1 | hg38 | chr19 | 54,662,985 | 54,668,718 | 5,734 |
| ENST00000430952.6 | hg38 | chr19 | 54,662,995 | 54,668,397 | 5,403 |
| ENST00000391736.5 | hg19 | chr19 | 55,173,579 | 55,181,810 | 8,232 |
| ENST00000695418.1 | hg19 | chr19 | 55,174,437 | 55,180,169 | 5,733 |
| ENST00000430952.6 | hg19 | chr19 | 55,174,447 | 55,179,848 | 5,402 |
| ENST00000391734.7 | hg19 | chr19 | 55,174,450 | 55,179,848 | 5,399 |
| ENST00000391733.7 | hg19 | chr19 | 55,174,472 | 55,179,848 | 5,377 |
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