例如:"NBL1", "4681", "drought"
收藏
568982 ush2a

568982

ush2a

Usher syndrome 2A (autosomal recessive, mild)

protein-coding

Danio rerio

基因描述

Type Description
Definition Usher syndrome 2A (autosomal recessive, mild)

研究结论

Date Results Publications
2019-01-12 10:43:00 This study shows that mutant ush2a zebrafish models present with early-onset retinal dysfunction that is exacerbated by light exposure. These models provide a better understanding of the pathophysiology underlying USH2A-associated RP and a unique opportunity to evaluate future therapeutic strategies. 29777677
2018-11-03 11:44:00 The expression of Ush1b and Ush1c was up-regulated when Ush2a was null. We also found that disruption of fibronectin assembly at the retinal basement membrane weakened cell adhesion in ush2a(-/-) mutants. 30242501

名称对应

Type IDs
Synonymous si:ch211-279e11.1
Gene
Nucleutide sequences
Protein sequencees
RefSeq: XP_009291422.1
Others
UniGene: Dr.118940, Dr.158626

全选

{{proteinIndex+1}}
mRNA Protein UniprotKB Description
Refseq {{protein.nucleotideVersion}}

Ensembl: {{protein.nucleotideEnsembl}}

{{protein.proteinVersion}}

Ensembl: {{protein.proteinEnsembl}}

{{uniprot}}
Definition: {{{protein.definition}}}

Transcript Veriant:{{protein.transcriptVeriant}}

Status: {{protein.status}}

Location ( {{protein.positionStart}}..{{protein.positionEnd}} )

暂无数据

研究热度

热点单位
排名 科研单位 文献
{{affIndex+1}}

{{aff.value}}

{{aff.size}}

目前还没有研究热点单位

热点人员
排名 研究人员 文献
{{authorIndex+1}}

{{author.value}}

{{author.size}}

目前还没有研究热点人员