Functional expression of the new gap junction gene connexin47 transcribed in mouse brain and spinal cord neurons.
Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease.
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
The DNA sequence and biological annotation of human chromosome 1.
Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus-Merzbacher-like disease.
Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations.
GJC2 missense mutations cause human lymphedema.
Dynamic expression of Cx47 in mouse brain development and in the cuprizone model of myelin plasticity.
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
Gene Ontology annotation based on curation of immunofluorescence data
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
Combined Automated Annotation using Multiple IEA Methods
Gap junction gamma-2 protein
Gap junction gamma-2 protein
GJC2 manual evidence and source boundaries