GO_REF:0000024
Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
GO_REF:0000033
Annotation inferences using phylogenetic trees
GO_REF:0000044
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
GO_REF:0000107
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
GO_REF:0000120
Combined Automated Annotation using Multiple IEA Methods
PMID:19606496
EYA4, deleted in a case with middle interhemispheric variant of holoprosencephaly, interacts with SIX3 both physically and functionally.
PMID:9887327
EYA4, a novel vertebrate gene related to Drosophila eyes absent.
PMID:38360978
The Eyes Absent family members EYA4 and EYA1 promote PLK1 activation and successful mitosis through tyrosine dephosphorylation.
PMID:19234442
Tyrosine dephosphorylation of H2AX modulates apoptosis and survival decisions.
PMID:18219393
Eya4-deficient mice are a model for heritable otitis media.
PMID:18799547
Eya4 regulation of Na+/K+-ATPase is required for sensory system development in zebrafish.
PMID:11159937
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus.
HPA:ENSG00000112319
Human Protein Atlas EYA4 subcellular localization
file:human/EYA4/EYA4-uniprot.txt
UniProtKB O95677 (EYA4_HUMAN) curated record