GO_REF:0000033
Annotation inferences using phylogenetic trees
GO_REF:0000044
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping
GO_REF:0000107
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
PMID:23793029
ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3.
PMID:24998259
Characterization of the SAM domain of the PKD-related protein ANKS6 and its interaction with ANKS3.
PMID:25599650
ANKS6 is the critical activator of NEK8 kinase in embryonic situs determination and organ patterning.
PMID:26967905
Novel NEK8 Mutations Cause Severe Syndromic Renal Cystic Dysplasia through YAP Dysregulation.
PMID:26638075
A Dynamic Protein Interaction Landscape of the Human Centrosome-Cilium Interface.
PMID:27173435
An organelle-specific protein landscape identifies novel diseases and molecular mechanisms.
PMID:32296183
A reference map of the human binary protein interactome.
PMID:32707033
Kinase Interaction Network Expands Functional and Disease Roles of Human Kinases.
PMID:33961781
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
PMID:29290488
Crystal Structure of Bicc1 SAM Polymer and Mapping of Interactions between the Ciliopathy-Associated Proteins Bicc1, ANKS3, and ANKS6.
PMID:37733651
Bicc1 ribonucleoprotein complexes specifying organ laterality are licensed by ANKS6-induced structural remodeling of associated ANKS3.
PMID:32886109
Loss of Anks6 leads to YAP deficiency and liver abnormalities.
PMID:37525964
Biallelic ANKS6 null variants cause notable extrarenal phenotypes in a nephronophthisis patient and lead to hepatobiliary abnormalities by YAP1 deficiency.
PMID:32994509
Nephronophthisis gene products display RNA-binding properties and are recruited to stress granules.
PMID:24610927
Mutations in ANKS6 cause a nephronophthisis-like phenotype with ESRD.
file:human/ANKS6/ANKS6-notes.md
ANKS6 research notes and published-figure provenance