ARFGAP2 ADP ribosylation factor GTPase activating protein 2
Information
- Symbol
- ARFGAP2
- Type
- protein-coding
- Description
- ADP ribosylation factor GTPase activating protein 2
- Entrez Gene ID
- 84364
- Genome
- hg19
- Position
- chr11:47,185,923-47,198,433
- Genome
- hg38
- Position
- chr11:47,164,372-47,176,882
- MIM
- 606908 OMIM
- HGNC
- HGNC:13504 HGNC
- Ensembl
- ENSG00000149182 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 14 |
| Likely benign | 0 | 16 |
| Uncertain significance | 0 | 56 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
86 |
 |
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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| 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 |
|---|---|
| SYNONYM | IRZ |
| SYNONYM | NBLA10535 |
| SYNONYM | ZFP289 |
| SYNONYM | ZNF289 |
| MIM | 606908 OMIM |
| HGNC | HGNC:13504 HGNC |
| Ensembl | ENSG00000149182 Ensembl |
| AllianceGenome | HGNC:13504 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000524782.6 | hg38 | chr11 | 47,164,301 | 47,176,879 | 12,579 |
| ENST00000629231.2 | hg38 | chr11 | 47,171,779 | 47,176,853 | 5,075 |
| ENST00000525314.6 | hg38 | chr11 | 47,164,372 | 47,176,882 | 12,511 |
| ENST00000627920.2 | hg38 | chr11 | 47,164,299 | 47,177,125 | 12,827 |
| ENST00000426335.6 | hg38 | chr11 | 47,164,299 | 47,177,125 | 12,827 |
| ENST00000426335.6 | hg19 | chr11 | 47,185,850 | 47,198,676 | 12,827 |
| ENST00000524782.6 | hg19 | chr11 | 47,185,852 | 47,198,430 | 12,579 |
| ENST00000525314.6 | hg19 | chr11 | 47,185,923 | 47,198,433 | 12,511 |
| ENST00000627920.2 | hg19 | chr11 | 47,185,850 | 47,198,676 | 12,827 |
| ENST00000629231.2 | hg19 | chr11 | 47,193,330 | 47,198,404 | 5,075 |
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