ARHGAP36 Rho GTPase activating protein 36
Information
- Symbol
- ARHGAP36
- Type
- protein-coding
- Description
- Rho GTPase activating protein 36
- Entrez Gene ID
- 158763
- Genome
- hg19
- Position
- chrX:130,192,320-130,223,859
- Genome
- hg38
- Position
- chrX:131,058,346-131,089,885
- MIM
- 300937 OMIM
- HGNC
- HGNC:26388 HGNC
- Ensembl
- ENSG00000147256 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| not provided | 6 | 0 |
| Uncertain significance | 0 | 44 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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48 |
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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
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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| Search word | : | |
| 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 |
|---|---|
| MIM | 300937 OMIM |
| HGNC | HGNC:26388 HGNC |
| Ensembl | ENSG00000147256 Ensembl |
| AllianceGenome | HGNC:26388 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000639280.1 | hg38 | chrX | 131,078,717 | 131,089,882 | 11,166 |
| ENST00000276211.10 | hg38 | chrX | 131,058,346 | 131,089,885 | 31,540 |
| ENST00000370921.1 | hg38 | chrX | 131,083,710 | 131,089,883 | 6,174 |
| ENST00000370922.5 | hg38 | chrX | 131,058,357 | 131,089,883 | 31,527 |
| ENST00000276211.10 | hg19 | chrX | 130,192,320 | 130,223,859 | 31,540 |
| ENST00000370922.5 | hg19 | chrX | 130,192,331 | 130,223,857 | 31,527 |
| ENST00000639280.1 | hg19 | chrX | 130,212,691 | 130,223,856 | 11,166 |
| ENST00000370921.1 | hg19 | chrX | 130,217,684 | 130,223,857 | 6,174 |
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