| Type | Description |
|---|---|
| Definition | interferon lambda receptor 1 |
| Date | Results | Publications |
|---|---|---|
| 2019-09-28 12:40:00 | This study was designed to explore the genetic etiology of deafness in a large Chinese family with autosomal dominant, nonsyndromic, progressive sensorineural hearing loss (ADNSHL). Inner ear expression of Ifnlr1 was investigated by immunostaining in mice. ifnlr1 Morpholino knockdown Zebrafish were constructed to explore the deafness mechanism.. IFNLR1 mutations are associated with ADNSHL | 29453195 |
| Type | IDs |
|---|---|
| Synonymous | crfb14 |
| Gene |
UniProtKB-ID:
D9IL84_DANRE
UniprotKB:
D9IL84
UniParc:
UPI0001DE0B4C
EMBL:
HM149255
KO:
dre:100332149
|
| Nucleutide sequences |
EMBL-CDS:
ADK22853.1
|
| Protein sequencees |
RefSeq:
XP_021322267.1,
NP_001184131.1
|
| Others |
UniRef100:
UniRef100_D9IL84
UniRef90:
UniRef90_D9IL84
UniRef50:
UniRef50_D9IL84
UniGene:
Dr.118705
|
| {{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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||||
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