| Type | Description |
|---|---|
| Definition | chaperonin containing TCP1, subunit 2 (beta) |
| Date | Results | Publications |
|---|---|---|
| 2018-08-11 10:40:00 | The retinal pathology observed in the homozygous cct2-L394H-7del mutants resembles the retinal pathology of human leber congenital amaurosis (LCA) patients. | 29450543 |
| Type | IDs |
|---|---|
| Synonymous | CHUNP6883, fa26a01, fc58a11, wu:fa26a01, wu:fc58a11 |
| Gene |
UniProtKB-ID:
Q6PBW6_DANRE
UniprotKB:
Q6PBW6
UniParc:
UPI00001D94CF
EMBL:
BC059558
KO:
dre:192326
|
| Nucleutide sequences |
EMBL-CDS:
AAH59558.1
|
| Protein sequencees |
RefSeq:
NP_958863.1
|
| Others |
UniRef100:
UniRef100_Q6PBW6
UniRef90:
UniRef90_Q6PBW6
UniRef50:
UniRef50_Q6PBW6
UniGene:
Dr.117647
|
| {{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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