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List Analysis for PL_PraderWilliRegion_Genes (120 Genes)

 
Description: Genes located in the Prader-Willi region of chromosome 15. Prader–Willi syndrome (abbreviated PWS) is a rare genetic disorder in which seven genes (or some subset thereof) on chromosome 15 (q 11-13: 20,700,000-33,600,000) are deleted or unexpressed (chromosome 15q partial deletion) on the paternal chromosome. PWS is characterized by severe hypotonia and feeding difficulties in early infancy, followed in later infancy or early childhood by excessive eating and gradual development of morbid obesity (unless eating is externally controlled). 31Jan2011
Date Created: 1433250041482

esyN Network Diagram

Physical (Orange) and Genetic (Green) interactions between the genes in the list. Visit esyN for more details or click the Edit in esyN button if you wish to extend or modify the network.


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Protein   

Orthologues

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      MouseMine
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            ZebrafishMine

              The template queries below have been executed for this list.

              Function

              Gene --> GO terms.

              Mouse Gene --> Allele [Phenotype]

              Genomics

              Gene --> Chromosomal location.

              Gene --> GO terms.

              Gene --> Overlapping genes.

              Proteins

              Gene --> Proteins.

              SNPs

              Gene Report --> GWAS hit

              Disease

              Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

              Mouse Gene --> Allele [Phenotype]

              Homology

              Gene --> Orthologues

              Interactions

              Gene --> Physical and Genetic Interactions

              Gene Ontology

              Gene --> GO terms.