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Items: 3

1.

Hippocampus RNA-seq in CD x Gtf2i*

(Submitter supplied) Williams syndrome is a neurodevelopmental disorder caused by a 1.5-1.8Mbp deletion on chromosome 7q11.23, affecting the copy number of 26-28 genes. Phenotypes of Williams syndrome include cardiovascular problems, craniofacial dysmorphology, deficits in visual spatial cognition, and a characteristic hypersocial personality. There are still no genes in the region that have been consistently linked to the cognitive and behavioral phenotypes, although human studies and mouse models have led to the current hypothesis that the general transcription factor 2 I family of genes, GTF2I and GTF2IRD1, are responsible. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21493
18 Samples
Download data: CSV
Series
Accession:
GSE127723
ID:
200127723
2.

Illumina HiSeq 3000 (Mus musculus)

Platform
Accession:
GPL21493
ID:
100021493
3.

hippocampus_Gtf2i*_17.3

Organism:
Mus musculus
Source name:
hippocampus
Platform:
GPL21493
Series:
GSE127723
Download data
Sample
Accession:
GSM3637734
ID:
303637734
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db=gds|term=GSM3637734[Accession]|query=1|qty=2|blobid=MCID_666fa9c5ce9c6e4cac165e59|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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