GPATCH11 G-patch domain containing 11
Information
- Symbol
- GPATCH11
- Type
- protein-coding
- Description
- G-patch domain containing 11
- Entrez Gene ID
- 253635
- Genome
- hg19
- Position
- chr2:37,311,661-37,326,387
- Genome
- hg38
- Position
- chr2:37,084,518-37,099,244
- HGNC
- HGNC:26768 HGNC
- Ensembl
- ENSG00000152133 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 8 |
| Uncertain significance | 0 | 34 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
34 |
 |
8 |
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
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| 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
|
| Category | : |
|
| Search word | : | |
| 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
|
| Category | : |
|
| 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 | CCDC75 |
| SYNONYM | CENP-Y |
| SYNONYM | CENPY |
| HGNC | HGNC:26768 HGNC |
| Ensembl | ENSG00000152133 Ensembl |
| AllianceGenome | HGNC:26768 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000281932.6 | hg38 | chr2 | 37,084,518 | 37,099,244 | 14,727 |
| ENST00000674370.2 | hg38 | chr2 | 37,084,518 | 37,099,244 | 14,727 |
| ENST00000281932.6 | hg19 | chr2 | 37,311,661 | 37,326,387 | 14,727 |
| ENST00000674370.2 | hg19 | chr2 | 37,311,661 | 37,326,387 | 14,727 |
| Key | Value |
|---|---|
| strand | + |
| start | 37,311,593 |
| Gene Symbol | GPATCH11 |
| Entrez GeneId | 253,635 |
| Chr Band | 2p22.2 |
| end | 37,326,386 |
| chr | chr2 |
Genome browser