PLEKHG7 pleckstrin homology and RhoGEF domain containing G7
Information
- Symbol
- PLEKHG7
- Type
- protein-coding
- Description
- pleckstrin homology and RhoGEF domain containing G7
- Entrez Gene ID
- 440107
- Genome
- hg19
- Position
- chr12:93,096,765-93,166,231
- Genome
- hg38
- Position
- chr12:92,702,989-92,772,455
- HGNC
- HGNC:33829 HGNC
- Ensembl
- ENSG00000187510 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 30 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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38 |
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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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | C12orf74 |
| HGNC | HGNC:33829 HGNC |
| Ensembl | ENSG00000187510 Ensembl |
| AllianceGenome | HGNC:33829 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000544406.2 | hg38 | chr12 | 92,703,028 | 92,708,549 | 5,522 |
| ENST00000344636.6 | hg38 | chr12 | 92,702,989 | 92,772,455 | 69,467 |
| ENST00000397833.3 | hg38 | chr12 | 92,702,843 | 92,708,547 | 5,705 |
| ENST00000397833.3 | hg19 | chr12 | 93,096,619 | 93,102,323 | 5,705 |
| ENST00000344636.6 | hg19 | chr12 | 93,096,765 | 93,166,231 | 69,467 |
| ENST00000544406.2 | hg19 | chr12 | 93,096,804 | 93,102,325 | 5,522 |
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