Human Disease and Mouse Model Detail
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Human Disease
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Renpenning Syndrome 1; RENS1
OMIM ID: 309500
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Synonyms
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Golabi-Ito-Hall Syndrome;
Mental Retardation, X-Linked 55; MRX55;
Mental Retardation, X-Linked, Renpenning Type;
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
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Pqbp1
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PQBP1*
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1:1 Homology
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Analysis Tools