OPN1MW3 opsin 1, medium wave sensitive 3
Information
- Symbol
- OPN1MW3
- Type
- protein-coding
- Description
- opsin 1, medium wave sensitive 3
- Entrez Gene ID
- 101060233
- Genome
- hg19
- Position
- chrX:153,485,247-153,498,755
- Genome
- hg38
- Position
- chrX:154,257,582-154,271,090
- HGNC
- HGNC:51831 HGNC
- Ensembl
- ENSG00000269433 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| not provided | 8 | 0 |
| Uncertain significance | 0 | 9 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
13 |
 |
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
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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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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| Category | : |
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| 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 | GCP |
| SYNONYM | GOP |
| SYNONYM | OPN1MW |
| SYNONYM | OPN1MW2 |
| HGNC | HGNC:51831 HGNC |
| Ensembl | ENSG00000269433 Ensembl |
| AllianceGenome | HGNC:51831 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000599405.4 | hg38 | chrX | 154,257,582 | 154,271,090 | 13,509 |
| ENST00000599405.4 | hg19 | chrX | 153,485,247 | 153,498,755 | 13,509 |
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