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Links from OMIM

Items: 3

    • Showing Current items.

    Name/Gene IDDescriptionLocationAliasesMIM
    ID: 100217370
    Chromosome 1q21.1 deletion syndrome [Homo sapiens (human)]C1DELq21612474
    ID: 2703
    gap junction protein alpha 8 [Homo sapiens (human)]Chromosome 1, NC_000001.11 (147902795..147914486)CAE, CAE1, CTRCT1, CX50, CZP1, MP70600897
    ID: 2702
    gap junction protein alpha 5 [Homo sapiens (human)]Chromosome 1, NC_000001.11 (147756199..147773351, complement)ATFB11, CX40121013
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