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Accession: PRJNA153265 ID: 153265

Homo sapiens (human)

Rare and common variants in CARD14, an epidermal regulator of NF-kappaB, in psoriasis

See Genome Information for Homo sapiens
Psoriasis is a common inflammatory disorder of the skin and other organs. We have determined that mutations in CARD14, encoding an NF-kB activator within skin epidermis, account for PSORS2. More...
AccessionPRJNA153265; GEO: GSE36381
Data TypeTranscriptome or Gene expression
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
PublicationsJordan CT et al., "Rare and common variants in CARD14, encoding an epidermal regulator of NF-kappaB, in psoriasis.", Am J Hum Genet, 2012 Apr 19;90(5):796-808
SubmissionRegistration date: 9-May-2012
Roberson Lab, Internal Medicine & Genetics, Washington University in St. Louis
Project Data:
Resource NameNumber
of Links
Other datasets
GEO DataSets1
GEO Data Details
Data volume, Spots804406
Data volume, Processed Mbytes26
Data volume, Supplementary Mbytes6

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