| Type | Description |
|---|---|
| Definition | myosin XVA |
| Date | Results | Publications |
|---|---|---|
| 2013-02-05 18:07:00 | Myo15 and Kcnj12 can be regarded as candidate genes for the deafblind phenotype of the LEW-ci2 rat. | 14629112 |
| 2011-07-30 11:05:00 | Mutations in binding domains of myosin XV do not only cause non-syndromic hearing loss but can also lead to syndromic disorders including retinal dysfunction. | 21479269 |
| Type | IDs |
|---|---|
| Synonymous | Myo15, RGD1561873 |
| Gene | |
| Nucleutide sequences | |
| Protein sequencees |
RefSeq:
XP_017453130.1,
XP_017459557.1,
XP_001077498.1,
XP_008766109.1
|
| Others |
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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| Location | {{protein.contigId}} ( {{protein.positionStart}}..{{protein.positionEnd}} , {{protein.orientation}} ) | |||||||
| Conserved domain | Region: {{conservedDomain.region == '' || conservedDomain.region == null ? "-": conservedDomain.region}} GFID: {{conservedDomain.gfid == '' || conservedDomain.gfid == null ? "-": conservedDomain.gfid}} Family: {{conservedDomain.family == '' || conservedDomain.family == null ? "-": conservedDomain.family}} CDD: {{conservedDomain.cdd}} - |
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