LSR lipolysis stimulated lipoprotein receptor
Information
- Symbol
- LSR
- Type
- protein-coding
- Description
- lipolysis stimulated lipoprotein receptor
- Entrez Gene ID
- 51599
- Genome
- hg19
- Position
- chr19:35,739,623-35,758,863
- Genome
- hg38
- Position
- chr19:35,248,720-35,267,960
- MIM
- 616582 OMIM
- HGNC
- HGNC:29572 HGNC
- Ensembl
- ENSG00000105699 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 34 |
Likely benign | 0 | 52 |
Conflicting classifications of pathogenicity | 0 | 2 |
Uncertain significance | 0 | 152 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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20 |
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212 |
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4 |
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 |
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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 | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | ILDR3 |
SYNONYM | LISCH7 |
MIM | 616582 OMIM |
HGNC | HGNC:29572 HGNC |
Ensembl | ENSG00000105699 Ensembl |
AllianceGenome | HGNC:29572 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000602122.5 | hg38 | chr19 | 35,248,392 | 35,267,962 | 19,571 |
ENST00000360798.7 | hg38 | chr19 | 35,248,765 | 35,267,962 | 19,198 |
ENST00000605618.6 | hg38 | chr19 | 35,249,002 | 35,267,964 | 18,963 |
ENST00000361790.7 | hg38 | chr19 | 35,248,720 | 35,267,960 | 19,241 |
ENST00000427250.5 | hg38 | chr19 | 35,249,002 | 35,267,962 | 18,961 |
ENST00000354900.7 | hg38 | chr19 | 35,248,772 | 35,267,964 | 19,193 |
ENST00000621372.4 | hg38 | chr19 | 35,248,656 | 35,267,960 | 19,305 |
ENST00000347609.8 | hg38 | chr19 | 35,248,879 | 35,267,963 | 19,085 |
ENST00000602122.5 | hg19 | chr19 | 35,739,295 | 35,758,865 | 19,571 |
ENST00000621372.4 | hg19 | chr19 | 35,739,559 | 35,758,863 | 19,305 |
ENST00000361790.7 | hg19 | chr19 | 35,739,623 | 35,758,863 | 19,241 |
ENST00000360798.7 | hg19 | chr19 | 35,739,668 | 35,758,865 | 19,198 |
ENST00000354900.7 | hg19 | chr19 | 35,739,675 | 35,758,867 | 19,193 |
ENST00000347609.8 | hg19 | chr19 | 35,739,782 | 35,758,866 | 19,085 |
ENST00000427250.5 | hg19 | chr19 | 35,739,905 | 35,758,865 | 18,961 |
ENST00000605618.6 | hg19 | chr19 | 35,739,905 | 35,758,867 | 18,963 |
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