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Items: 3

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    Name/Gene IDDescriptionLocationAliasesMIM
    ID: 7249
    tuberous sclerosis 2 [Homo sapiens (human)]Chromosome 16, NC_000016.10 (2047804..2088720)LAM, PPP1R160, TSC4191092
    ID: 2915
    glutamate metabotropic receptor 5 [Homo sapiens (human)]Chromosome 11, NC_000011.10 (88504576..89065971, complement)GPRC1E, MGLUR5, PPP1R86, mGlu5604102
    ID: 2332
    fragile X mental retardation 1 [Homo sapiens (human)]Chromosome X, NC_000023.11 (147911951..147951127)FMRP, FRAXA, POF, POF1309550
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