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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

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Protein   

Orthologues

    View homologues in other Mines:

    FlyMine
      MouseMine
        YeastMine
          RatMine
            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)

              Gene --> Alleles and Disease (clinVar data)

              Mouse Gene --> Allele [Phenotype]

              Homology

              Gene --> Orthologues

              Interactions

              Gene --> Physical and Genetic Interactions

              Expression

              Gene(s) --> Significant SNPs (GTex data)

              Gene Ontology

              Gene --> GO terms.