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Human Disease and Mouse Model Detail
Human Disease Renpenning Syndrome 1; RENS1
OMIM ID: 309500
Human Phenotype Ontology associations
Synonyms Golabi-Ito-Hall Syndrome; Mental Retardation, X-Linked 55; MRX55; Mental Retardation, X-Linked, Renpenning Type; Mental Retardation, X-Linked, Syndromic; Mental Retardation, X-Linked, Syndromic 3; MRXS3; Mental Retardation, X-Linked, Syndromic 8; MRXS8; Mental Retardation, X-Linked, with Spastic Diplegia; Sutherland-Haan X-Linked Mental Retardation Syndrome; SHS
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     PQBP1* Pqbp1   HomoloGene and HGNC

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory