LILRB1 leukocyte immunoglobulin like receptor B1
Information
- Symbol
- LILRB1
- Type
- protein-coding
- Description
- leukocyte immunoglobulin like receptor B1
- Entrez Gene ID
- 10859
- Genome
- hg19
- Position
- chr19:55,141,935-55,149,473
- Genome
- hg38
- Position
- chr19:54,630,484-54,638,022
- MIM
- 604811 OMIM
- HGNC
- HGNC:6605 HGNC
- Ensembl
- ENSG00000104972 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 3 |
Likely benign | 0 | 12 |
Uncertain significance | 0 | 116 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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131 |
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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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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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 | CD85J |
SYNONYM | ILT-2 |
SYNONYM | ILT2 |
SYNONYM | LIR-1 |
SYNONYM | LIR1 |
SYNONYM | MIR-7 |
SYNONYM | MIR7 |
SYNONYM | PIR-B |
SYNONYM | PIRB |
MIM | 604811 OMIM |
HGNC | HGNC:6605 HGNC |
Ensembl | ENSG00000104972 Ensembl |
AllianceGenome | HGNC:6605 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000396331.5 | hg38 | chr19 | 54,617,158 | 54,637,528 | 20,371 |
ENST00000396332.8 | hg38 | chr19 | 54,630,512 | 54,637,528 | 7,017 |
ENST00000396327.7 | hg38 | chr19 | 54,630,410 | 54,637,528 | 7,119 |
ENST00000427581.6 | hg38 | chr19 | 54,630,633 | 54,637,190 | 6,558 |
ENST00000324602.12 | hg38 | chr19 | 54,630,484 | 54,638,022 | 7,539 |
ENST00000396317.5 | hg38 | chr19 | 54,631,074 | 54,637,076 | 6,003 |
ENST00000396315.5 | hg38 | chr19 | 54,631,074 | 54,637,076 | 6,003 |
ENST00000396331.5 | hg19 | chr19 | 55,128,612 | 55,148,979 | 20,368 |
ENST00000396327.7 | hg19 | chr19 | 55,141,861 | 55,148,979 | 7,119 |
ENST00000324602.12 | hg19 | chr19 | 55,141,935 | 55,149,473 | 7,539 |
ENST00000396332.8 | hg19 | chr19 | 55,141,963 | 55,148,979 | 7,017 |
ENST00000427581.6 | hg19 | chr19 | 55,142,084 | 55,148,641 | 6,558 |
ENST00000396315.5 | hg19 | chr19 | 55,142,525 | 55,148,527 | 6,003 |
ENST00000396317.5 | hg19 | chr19 | 55,142,525 | 55,148,527 | 6,003 |
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