| Type | Description |
|---|---|
| Definition | solute carrier family 16 member 2 |
| Date | Results | Publications |
|---|---|---|
| 2015-04-18 10:52:00 | the cellular and molecular consequences of MCT8 knockdown during embryonic development in zebrafish provides new insight into the potential role of thyroid hormones in X-linked mental retardation in humans. | 24877564 |
| 2013-03-02 10:52:00 | MCT8 is a crucial regulator during embryonic development; zebrafish is a model for MCT8 deficiency that exhibits a neurological phenotype | 23161551 |
| Type | IDs |
|---|---|
| Synonymous | mct8 |
| Gene |
UniProtKB-ID:
G8XYX6_DANRE
UniprotKB:
G8XYX6
UniParc:
UPI000238D870
EMBL:
FN687448
KO:
dre:100884148
|
| Nucleutide sequences |
EMBL-CDS:
CBK52149.2
|
| Protein sequencees |
RefSeq:
NP_001245159.1
|
| Others |
UniRef100:
UniRef100_G8XYX6
UniRef90:
UniRef90_L7T0T8
UniRef50:
UniRef50_L7T0T8
UniGene:
Dr.162105
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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| 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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