LLGL2 LLGL scribble cell polarity complex component 2
Information
- Symbol
- LLGL2
- Type
- protein-coding
- Description
- LLGL scribble cell polarity complex component 2
- Entrez Gene ID
- 3993
- Genome
- hg19
- Position
- chr17:73,521,778-73,571,290
- Genome
- hg38
- Position
- chr17:75,525,697-75,575,209
- MIM
- 618483 OMIM
- HGNC
- HGNC:6629 HGNC
- Ensembl
- ENSG00000073350 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 18 |
| Likely benign | 0 | 16 |
| Uncertain significance | 0 | 194 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
2 |
 |
224 |
 |
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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| 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 | HGL |
| SYNONYM | Hugl-2 |
| SYNONYM | LGL2 |
| MIM | 618483 OMIM |
| HGNC | HGNC:6629 HGNC |
| Ensembl | ENSG00000073350 Ensembl |
| AllianceGenome | HGNC:6629 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000375227.8 | hg38 | chr17 | 75,525,732 | 75,564,721 | 38,990 |
| ENST00000578363.5 | hg38 | chr17 | 75,525,779 | 75,564,723 | 38,945 |
| ENST00000392550.8 | hg38 | chr17 | 75,525,697 | 75,575,209 | 49,513 |
| ENST00000167462.9 | hg38 | chr17 | 75,525,726 | 75,575,208 | 49,483 |
| ENST00000577200.5 | hg38 | chr17 | 75,532,493 | 75,574,906 | 42,414 |
| ENST00000392550.8 | hg19 | chr17 | 73,521,778 | 73,571,290 | 49,513 |
| ENST00000167462.9 | hg19 | chr17 | 73,521,807 | 73,571,289 | 49,483 |
| ENST00000375227.8 | hg19 | chr17 | 73,521,813 | 73,560,802 | 38,990 |
| ENST00000577200.5 | hg19 | chr17 | 73,528,574 | 73,570,987 | 42,414 |
| ENST00000578363.5 | hg19 | chr17 | 73,521,860 | 73,560,804 | 38,945 |
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