RGSL1 regulator of G protein signaling like 1
Information
- Symbol
- RGSL1
- Type
- protein-coding
- Description
- regulator of G protein signaling like 1
- Entrez Gene ID
- 353299
- Genome
- hg19
- Position
- chr1:182,419,281-182,529,732
- Genome
- hg38
- Position
- chr1:182,450,146-182,560,597
- MIM
- 611012 OMIM
- HGNC
- HGNC:18636 HGNC
- Ensembl
- ENSG00000121446 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
Uncertain significance | 0 | 112 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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120 |
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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 |
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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 |
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | RGSL |
SYNONYM | RGSL2 |
MIM | 611012 OMIM |
HGNC | HGNC:18636 HGNC |
Ensembl | ENSG00000121446 Ensembl |
AllianceGenome | HGNC:18636 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000294854.13 | hg38 | chr1 | 182,450,146 | 182,560,597 | 110,452 |
ENST00000294854.13 | hg19 | chr1 | 182,419,281 | 182,529,732 | 110,452 |
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