FB2026_03 , released September 17, 2026
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Ma, M., Ganapathi, M., Zheng, Y., Tan, K.L., Kanca, O., Bove, K.E., Quintanilla, N., Sag, S.O., Temel, S.G., LeDuc, C.A., McPartland, A.J., Pereira, E.M., Shen, Y., Hagen, J., Thomas, C.P., Nguyen Galván, N.T., Pan, X., Lu, S., Rosenfeld, J.A., Calame, D.G., Wangler, M.F., Lupski, J.R., Pehlivan, D., Hertel, P.M., Chung, W.K., Bellen, H.J. (2024). Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellular carcinoma.  Genet Med 26(7): 101125.
FlyBase ID
FBrf0259938
Publication Type
Research paper
Abstract
YKT6 plays important roles in multiple intracellular vesicle trafficking events but has not been associated with Mendelian diseases. We report 3 unrelated individuals with rare homozygous missense variants in YKT6 who exhibited neurological disease with or without a progressive infantile liver disease. We modeled the variants in Drosophila. We generated wild-type and variant genomic rescue constructs of the fly ortholog dYkt6 and compared their ability in rescuing the loss-of-function phenotypes in mutant flies. We also generated a dYkt6[KozakGAL4] allele to assess the expression pattern of dYkt6. Two individuals are homozygous for YKT6 [NM_006555.3:c.554A>G p.(Tyr185Cys)] and exhibited normal prenatal course followed by failure to thrive, developmental delay, and progressive liver disease. Haplotype analysis identified a shared homozygous region flanking the variant, suggesting a common ancestry. The third individual is homozygous for YKT6 [NM_006555.3:c.191A>G p.(Tyr64Cys)] and exhibited neurodevelopmental disorders and optic atrophy. Fly dYkt6 is essential and is expressed in the fat body (analogous to liver) and central nervous system. Wild-type genomic rescue constructs can rescue the lethality and autophagic flux defects, whereas the variants are less efficient in rescuing the phenotypes. The YKT6 variants are partial loss-of-function alleles, and the p.(Tyr185Cys) is more severe than p.(Tyr64Cys).
PubMed ID
PubMed Central ID
PMC11335040 (PMC) (EuropePMC)
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    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Genet Med
    Title
    Genetics in medicine
    ISBN/ISSN
    1098-3600 1530-0366
    Data From Reference
    Aberrations (1)
    Alleles (7)
    Genes (4)
    Human Disease Models (1)
    Natural transposons (1)
    Insertions (6)
    Transgenic Constructs (4)