Gene Ontology annotation through association of InterPro records with GO terms

Annotation inferences using phylogenetic trees

Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt

Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara

Automatic assignment of GO terms using logical inference, based on on inter-ontology links

Gene Ontology annotation of human sequence-specific DNA binding transcription factors (DbTFs) based on the TFClass database

Combined Automated Annotation using Multiple IEA Methods

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

Generation and annotation of the DNA sequences of human chromosomes 2 and 4.

Impact of cytosine methylation on DNA binding specificities of human transcription factors.

Septal contributions to olfactory bulb interneuron diversity in the embryonic mouse telencephalon: role of the homeobox gene Gsx2.

Agenesis of the putamen and globus pallidus caused by recessive mutations in the homeobox gene GSX2.

Many Faces of Diencephalic-Mesencephalic Junction Dysplasia Syndrome with GSX2 and PCDH12 Variants.

Modelling a pathological GSX2 variant that selectively alters DNA binding reveals hypomorphic mouse brain defects.

An inducible system to study the regulatory functions of GSX2 in human lateral ganglionic eminence-like progenitors.

GSX2 (Q9BZM3), Homo sapiens

GSX2 independent phylogeny, target motif and typed ontology evidence