AGTRAP angiotensin II receptor associated protein
Information
- Symbol
- AGTRAP
- Type
- protein-coding
- Description
- angiotensin II receptor associated protein
- Entrez Gene ID
- 57085
- Genome
- hg19
- Position
- chr1:11,796,193-11,810,826
- Genome
- hg38
- Position
- chr1:11,736,136-11,750,769
- MIM
- 608729 OMIM
- HGNC
- HGNC:13539 HGNC
- Ensembl
- ENSG00000177674 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 28 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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34 |
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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
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 | |||||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | ATRAP |
MIM | 608729 OMIM |
HGNC | HGNC:13539 HGNC |
Ensembl | ENSG00000177674 Ensembl |
AllianceGenome | HGNC:13539 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000510878.1 | hg38 | chr1 | 11,736,175 | 11,750,633 | 14,459 |
ENST00000314340.10 | hg38 | chr1 | 11,736,136 | 11,750,769 | 14,634 |
ENST00000400895.6 | hg38 | chr1 | 11,736,124 | 11,750,316 | 14,193 |
ENST00000376629.8 | hg38 | chr1 | 11,736,147 | 11,750,771 | 14,625 |
ENST00000376627.6 | hg38 | chr1 | 11,736,153 | 11,750,578 | 14,426 |
ENST00000452018.6 | hg38 | chr1 | 11,736,173 | 11,750,409 | 14,237 |
ENST00000376637.7 | hg38 | chr1 | 11,736,084 | 11,750,710 | 14,627 |
ENST00000376637.7 | hg19 | chr1 | 11,796,141 | 11,810,767 | 14,627 |
ENST00000400895.6 | hg19 | chr1 | 11,796,181 | 11,810,373 | 14,193 |
ENST00000314340.10 | hg19 | chr1 | 11,796,193 | 11,810,826 | 14,634 |
ENST00000376629.8 | hg19 | chr1 | 11,796,204 | 11,810,828 | 14,625 |
ENST00000376627.6 | hg19 | chr1 | 11,796,210 | 11,810,635 | 14,426 |
ENST00000452018.6 | hg19 | chr1 | 11,796,230 | 11,810,466 | 14,237 |
ENST00000510878.1 | hg19 | chr1 | 11,796,232 | 11,810,690 | 14,459 |
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