ARHGAP20 Rho GTPase activating protein 20
Information
- Symbol
- ARHGAP20
- Type
- protein-coding
- Description
- Rho GTPase activating protein 20
- Entrez Gene ID
- 57569
- Genome
- hg19
- Position
- chr11:110,447,766-110,583,451
- Genome
- hg38
- Position
- chr11:110,577,042-110,712,728
- MIM
- 609568 OMIM
- HGNC
- HGNC:18357 HGNC
- Ensembl
- ENSG00000137727 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 112 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
114 |
 |
2 |
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 | RARHOGAP |
| MIM | 609568 OMIM |
| HGNC | HGNC:18357 HGNC |
| Ensembl | ENSG00000137727 Ensembl |
| AllianceGenome | HGNC:18357 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000529591.5 | hg38 | chr11 | 110,577,043 | 110,589,685 | 12,643 |
| ENST00000683387.1 | hg38 | chr11 | 110,577,043 | 110,712,437 | 135,395 |
| ENST00000524756.5 | hg38 | chr11 | 110,577,054 | 110,712,050 | 134,997 |
| ENST00000260283.8 | hg38 | chr11 | 110,577,042 | 110,712,728 | 135,687 |
| ENST00000528829.5 | hg38 | chr11 | 110,577,054 | 110,712,728 | 135,675 |
| ENST00000533353.5 | hg38 | chr11 | 110,577,054 | 110,713,189 | 136,136 |
| ENST00000527598.1 | hg38 | chr11 | 110,577,054 | 110,713,189 | 136,136 |
| ENST00000260283.8 | hg19 | chr11 | 110,447,766 | 110,583,451 | 135,686 |
| ENST00000529591.5 | hg19 | chr11 | 110,447,767 | 110,460,409 | 12,643 |
| ENST00000683387.1 | hg19 | chr11 | 110,447,767 | 110,583,160 | 135,394 |
| ENST00000524756.5 | hg19 | chr11 | 110,447,778 | 110,582,773 | 134,996 |
| ENST00000528829.5 | hg19 | chr11 | 110,447,778 | 110,583,451 | 135,674 |
| ENST00000533353.5 | hg19 | chr11 | 110,447,778 | 110,583,912 | 136,135 |
| ENST00000527598.1 | hg19 | chr11 | 110,447,778 | 110,583,912 | 136,135 |
| Key | Value |
|---|---|
| strand | - |
| UniProt | TSG |
| start | 110,447,758 |
| Gene Symbol | ARHGAP20 |
| Entrez GeneId | 57,569 |
| Chr Band | 11q23.1 |
| end | 110,583,911 |
| chr | chr11 |
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