Detailed information for OPN1MW
Basic information
| Official symbol | OPN1MW |
|---|---|
| Official full name | opsin 1 (cone pigments), medium-wave-sensitive |
| Location | Xq28 |
| Gene type | protein-coding |
| Synonyms | CBBM|CBD|COD5|GCP|GOP|OPN1MW1 |
| Quick links | Entrez ID:2652; HGNC:4206; MIM:300821; Ensembl:02365; HPRD:; Vega: |
GO related
| GO term accession | GO term name | Number of reference genes | Number of genes | Expected number | Ratio of enrichment | P-value | Adjusted P-Value |
|---|
Pathway related
| Term | Surce | Number of reference genes | Number of genes | Expected number | Ratio of enrichment | P-value | Adjusted P-value |
|---|
PPI related
| ID | Number of reference genes | Number of genes | Expected number | Ratio of enrichment | P-value | Adjusted P-value |
|---|---|---|---|---|---|---|
| Hsapiens_Module_56 | 6 | 3 | 0.06 | 48.69 | 2.08e-05 | 0.0004 |
| Hsapiens_Module_9 | 127 | 5 | 1.30 | 3.83 | 0.0100 | 0.0350 |
OMIM related
| chromosome | begin | end | disorder MIM number | disorder | phene mapping key | gene/locus MIM number | cytogenetic loaction |
|---|---|---|---|---|---|---|---|
| chrX | 153484202 | 153500470 | 303700 | Blue cone monochromacy | 3 | 300821 | Xq28 |
| chrX | 153484202 | 153500470 | 303800 | "Colorblindness, deutan" | 3 | 300821 | Xq28 |
MGI related
| chromosome | begin | end | gene ID | gene symbol of mouse | MGI | MP | phenotype description |
|---|---|---|---|---|---|---|---|
| chrX | 153484202 | 153500470 | 2652 | Opn1mw | MGI:1097692 | MP:0005391 | vision/eye phenotype |
Mutation spectrum
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Gene-disease network
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