CYTH2 cytohesin 2
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 18 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
18 |
 |
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
|
| 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 | ARNO |
| SYNONYM | CTS18 |
| SYNONYM | CTS18.1 |
| SYNONYM | PSCD2 |
| SYNONYM | PSCD2L |
| SYNONYM | SEC7L |
| SYNONYM | Sec7p-L |
| SYNONYM | Sec7p-like |
| SYNONYM | cytohesin-2 |
| MIM | 602488 OMIM |
| HGNC | HGNC:9502 HGNC |
| Ensembl | ENSG00000105443 Ensembl |
| AllianceGenome | HGNC:9502 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000704950.1 | hg38 | chr19 | 48,469,369 | 48,482,314 | 12,946 |
| ENST00000452733.7 | hg38 | chr19 | 48,469,369 | 48,482,314 | 12,946 |
| ENST00000641098.1 | hg38 | chr19 | 48,469,433 | 48,480,653 | 11,221 |
| ENST00000427476.4 | hg38 | chr19 | 48,469,208 | 48,482,313 | 13,106 |
| ENST00000427476.4 | hg19 | chr19 | 48,972,465 | 48,985,570 | 13,106 |
| ENST00000452733.7 | hg19 | chr19 | 48,972,626 | 48,985,571 | 12,946 |
| ENST00000704950.1 | hg19 | chr19 | 48,972,626 | 48,985,571 | 12,946 |
| ENST00000641098.1 | hg19 | chr19 | 48,972,690 | 48,983,910 | 11,221 |
Genome browser