| Type | Description |
|---|---|
| Definition | rp1 like 1a |
| Date | Results | Publications |
|---|---|---|
| 2017-11-18 13:42:00 | We propose that the combination of heterozygous loss-of-function mutations in these genes drives syndromic retinal dystrophy, likely through the genetic interaction of at least two loci. | 27029556 |
| Type | IDs |
|---|---|
| Synonymous | rp1l1 |
| Gene |
UniProtKB-ID:
E7F630_DANRE
UniprotKB:
E7F630
UniParc:
UPI0001E9007F
EMBL:
CR388223,
CU929322
Ensembl:
ENSDARG00000089458
KO:
dre:101882236
|
| Nucleutide sequences |
Ensembl_TRS:
ENSDART00000153743
|
| Protein sequencees |
Ensembl_PRO:
ENSDARP00000127535
RefSeq:
XP_005169866.1,
XP_005169865.1,
XP_021328722.1,
XP_021328720.1,
XP_021328721.1,
XP_009291061.1
|
| Others |
UniRef100:
UniRef100_E7F630
UniRef90:
UniRef90_E7F630
UniRef50:
UniRef50_E7F630
|
| {{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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