GIRGL glutamine insufficiency regulator of glutaminase lncRNA
Information
- Symbol
- GIRGL
- Type
- ncRNA
- Description
- glutamine insufficiency regulator of glutaminase lncRNA
- Entrez Gene ID
- 100506098
- Genome
- hg19
- Position
- chr7:20,257,162-20,261,325
- Genome
- hg38
- Position
- chr7:20,217,539-20,221,702
- HGNC
- HGNC:55702 HGNC
- Ensembl
- ENSG00000233834 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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0 |
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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
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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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| 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 | MACC1-DT |
| HGNC | HGNC:55702 HGNC |
| Ensembl | ENSG00000233834 Ensembl |
| AllianceGenome | HGNC:55702 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000688687.1 | hg38 | chr7 | 20,217,539 | 20,221,702 | 4,164 |
| ENST00000688687.1 | hg19 | chr7 | 20,257,162 | 20,261,325 | 4,164 |
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