LAIR1 leukocyte associated immunoglobulin like receptor 1
Information
- Symbol
- LAIR1
- Type
- protein-coding
- Description
- leukocyte associated immunoglobulin like receptor 1
- Entrez Gene ID
- 3903
- Genome
- hg19
- Position
- chr19:54,862,991-54,876,538
- Genome
- hg38
- Position
- chr19:54,351,384-54,364,931
- MIM
- 602992 OMIM
- HGNC
- HGNC:6477 HGNC
- Ensembl
- ENSG00000167613 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
26 |
![]() |
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
|
Category | : |
|
Search word | : | |
Filtering | : |
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
|
Category | : |
|
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 | CD305 |
SYNONYM | LAIR-1 |
MIM | 602992 OMIM |
HGNC | HGNC:6477 HGNC |
Ensembl | ENSG00000167613 Ensembl |
AllianceGenome | HGNC:6477 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000391742.7 | hg38 | chr19 | 54,351,384 | 54,364,931 | 13,548 |
ENST00000391743.7 | hg38 | chr19 | 54,353,624 | 54,370,558 | 16,935 |
ENST00000348231.8 | hg38 | chr19 | 54,354,675 | 54,364,865 | 10,191 |
ENST00000434277.6 | hg38 | chr19 | 54,354,675 | 54,364,995 | 10,321 |
ENST00000474878.5 | hg38 | chr19 | 54,355,267 | 54,364,807 | 9,541 |
ENST00000391742.7 | hg19 | chr19 | 54,862,991 | 54,876,538 | 13,548 |
ENST00000391743.7 | hg19 | chr19 | 54,865,233 | 54,882,165 | 16,933 |
ENST00000348231.8 | hg19 | chr19 | 54,866,284 | 54,876,472 | 10,189 |
ENST00000434277.6 | hg19 | chr19 | 54,866,284 | 54,876,602 | 10,319 |
ENST00000474878.5 | hg19 | chr19 | 54,866,876 | 54,876,414 | 9,539 |
Genome browser