1 | ALG5, PKD7
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| Monoallelic pathogenic ALG5 variants cause atypical polycystic kidney disease and interstitial fibrosis
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| Lemoine H, Raud L, Foulquier F, Sayer JA, Lambert B, Olinger E, Lefèvre S, Knebelmann B, Harris PC, Trouvé P, Desprès A, Duneau G, Matignon M, Poyet A, Jourde-Chiche N, Guerrot D, Lemoine S, Seret G, Barroso-Gil M, Bingham C, Gilbert R; Genomics England Research Consortium; Genkyst Study Group, Le Meur Y, Audrézet MP, Cornec-Le Gall E.
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| Am J Hum Genet. Aug 4;109(8):1484-1499. doi: 10.1016/j.ajhg.2022.06.013. Epub 2022 Jul 26. 2022
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2 | ALG5
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| Wollknauel is required for embryo patterning and encodes the Drosophila ALG5 UDP-glucose:dolichyl-phosphate glucosyltransferase
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| Haecker A, Bergman M, Neupert C, Moussian B, Luschnig S, Aebi M, Mannervik M.
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| Development. May;135(10):1745-9. doi: 10.1242/dev.020891. Epub 2008 Apr 9. 2008
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3 | ADGRG1, ALG5, APLP2, B3GNT3, BGN, C14orf1, CD151, CD99, CDH1, CDH32, CLPTM1, CNPY3, DAG1, DHX8, FXYD5, GDF15, HSP90B1, HSPA5, KRTCAP2, LAMA3, LMAN2, LYPD3, SPINT2, TEX261, TNFRSF12A
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| Identification of novel genes for secreted and membrane-anchored proteins in human keratinocytes.
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| Bonkobara M, Das A, Takao J, Cruz PD, Ariizumi K.
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| Br J Dermatol 148(4):654-64. 2003
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4 | ALG5, ALG6, CDG1C
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| A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-deficient glycoprotein syndrome type-Ic.
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| Imbach T, Burda P, Kuhnert P, Wevers RA, Aebi M, Berger EG, Hennet T.
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| Proc Natl Acad Sci U S A 96(12):6982-7. 1999
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