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Items: 3

1.

OTX2 loss causes rod differentiation defect in CRX-associated congenital blindness

(Submitter supplied) Leber congenital amaurosis (LCA) includes congenital or early-onset blinding diseases, characterized by vision loss together with nystagmus and nonrecordable electroretinogram (ERG). At least 19 genes are associated with LCA. While most LCA is recessive, mutations in the homeodomain transcription factor gene CRX lead to autosomal dominant LCA. The mechanism of CRX-LCA is not understood. Here, we report a new spontaneous mouse mutant carrying a frameshift mutation in Crx (CrxRip). more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11002
20 Samples
Download data: TXT
Series
Accession:
GSE52006
ID:
200052006

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2.

Illumina Genome Analyzer IIx (Mus musculus)

Organism:
Mus musculus
896 Series
7716 Samples
Download data
Platform
Accession:
GPL11002
ID:
100011002

3.

P21_WT_rep2

Organism:
Mus musculus
Source name:
wild type mouse retina at age postnatal day 21
Platform:
GPL11002
Series:
GSE52006
Download data
Sample
Accession:
GSM1257275
ID:
301257275

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db=gds|term=GSM1257275[Accession]|query=1|qty=2|blobid=MCID_67594472df415c74f8af6447|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
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