GO_REF:0000002
Gene Ontology annotation through association of InterPro records with GO terms
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
PMID:15372022
The DNA sequence and comparative analysis of human chromosome 5.
PMID:24619944
A frameshift mutation in GRXCR2 causes recessively inherited hearing loss.
PMID:30380417
GRXCR2 Regulates Taperin Localization Critical for Stereocilia Morphology and Hearing.
UniProt:A6NFK2
UniProt entry A6NFK2
file:human/GRXCR2/GRXCR2-source-evidence.json
GRXCR2 original contexts, independent PAINT replay and ontology evidence