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ProteomicsProteomic analysis of ANO10 SH-SY5Y mutant cell lines
To investigate the effects of ANO10 pathogenic variants in cell proteome, four SH-SY5Y mutant cell lines (a knockout cell line,and three lines bearing the following variants: ANO10 c.289delA, ANO10 c.1009T>G, and ANO10 c.1529T>G) were engineered via CRISPR-Cas9 editing. After establishment and chara...
ORGANISM(S): Homo sapiens (Human) 
2026-09-07 | PXD067059 | Pride
Lc-ms/ms Ano10 Sh-sy5y 
UnknownANO10 Function in Health and Disease.
Not available
S-EPMC10126014 | biostudies-literature
UnknownANO10 is a potential prognostic biomarker and correlates with immune infiltration in breast cancer.
Not available
S-EPMC10244099 | biostudies-literature
UnknownExpanding the Allelic Heterogeneity of ANO10-Associated Autosomal Recessive Cerebellar Ataxia.
Not available
S-EPMC9872716 | biostudies-literature
UnknownA Coding Variant of ANO10, Affecting Volume Regulation of Macrophages, Is Associated with Borrelia Seropositivity.
Not available
S-EPMC4461583 | biostudies-literature
UnknownTargeted next-generation sequencing of a 12.5 Mb homozygous region reveals ANO10 mutations in patients with autosomal-recessive cerebellar ataxia.
Not available
S-EPMC2997370 | biostudies-literature
UnknownThe ion channel Anoctamin 10/TMEM16K coordinates organ morphogenesis across scales in the urochordate notochord.
Not available
S-EPMC11341064 | biostudies-literature
ProteomicsTMEM16K is an interorganelle regulator of endosomal sorting.
Using proximity biotinylation proteomics based on TMEM16K/Ano10 (an endoplasmic reticulum lipid scramblase causative for spinocerebellar ataxia) BioID chimeras, we identify endosomal transport as a major functional cluster of interacting proteins.
ORGANISM(S): Homo sapiens (Human) Mus musculus (Mouse) 
2020-05-30 | PXD018990 | Pride
Bioid Endosomal sorting Tmem16k 
UnknownAnoctamin 10-Related Autosomal Recessive Cerebellar Ataxia: Comprehensive Clinical Phenotyping of an Irish Sibship.
Not available
S-EPMC6353423 | biostudies-literature
UnknownAutosomal Recessive Spinocerebellar Ataxia Caused by a Novel Homozygous ANO10 Mutation in a Consanguineous Chinese Family.
Not available
S-EPMC7174130 | biostudies-literature
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