Transcriptome of Human Primary Corneal Endothelial... (ID 597782) - BioProject

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Accession: PRJNA597782 ID: 597782

Transcriptome of Human Primary Corneal Endothelial Cells with SLC4A11 deficiency (human)

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88717 additional projects are related by organism.

Mutations in the solute-linked carrier family 4 member 11 (SLC4A11) gene are associated with several corneal endothelial dystrophies, in all of which visually significant cornea edema may require corneal transplantation. More...

Accession	PRJNA597782; GEO: GSE142636
Data Type	Transcriptome or Gene expression
Scope	Multiisolate
Organism	Homo sapiens[Taxonomy ID: 9606] Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
Publications	Zhang W et al., "Energy Shortage in Human and Mouse Models of SLC4A11-Associated Corneal Endothelial Dystrophies.", Invest Ophthalmol Vis Sci, 2020 Jul 1;61(8):39
Submission	Registration date: 26-Dec-2019 UCLA, Jules Stein Eye Institute
Relevance	Medical

Project Data:

Resource Name	Number of Links
Sequence data
SRA Experiments	6
Publications
PubMed	1
PMC	1
Other datasets
BioSample	6
GEO DataSets	1

GEO Data Details

Parameter	Value
Data volume, Supplementary Mbytes	1

SRA Data Details

Parameter	Value
Data volume, Gbases	107
Data volume, Mbytes	40884

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Transcriptome of Human Primary Corneal Endothelial Cells with SLC4A11 deficiency (human)

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