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Items: 3

1.

Non-coding cause of congenital heart defects: Abnormal RNA splicing with multiple isoforms as a mechanism for heterotaxy

(Submitter supplied) Heterotaxy is a disorder characterized by severe congenital heart defects (CHDs) and abnormal left-right patterning in other thoracic or abdominal organs. Clinical and research-based genetic testing has previously focused on evaluation of coding variants to identify causes of CHDs, leaving non-coding causes of CHDs largely unknown. Variants in the transcription factor Zinc finger of the cerebellum 3 (ZIC3) cause X-linked heterotaxy. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL26167 GPL24676
17 Samples
Download data: TXT
Series
Accession:
GSE263414
ID:
200263414

PubMed

2.

Illumina NovaSeq 6000 (Homo sapiens)

Organism:
Homo sapiens
17287 Series
937751 Samples
Download data
Platform
Accession:
GPL24676
ID:
100024676

3.

ZIC3 AtoG_C2, short-read, biol rep 1 of 1

Organism:
Homo sapiens
Source name:
H1-OCT4-eGFP
Platform:
GPL24676
Series:
GSE263414
Download data
Sample
Accession:
GSM8191371
ID:
308191371

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db=gds|term=GSM8191371[Accession]|query=1|qty=2|blobid=MCID_6748b9d3462e1a751e0e4d0a|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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