Gene Ontology annotation through association of InterPro records with GO terms

Gene Ontology annotation based on Enzyme Commission mapping

Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity

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

Electronic Gene Ontology annotations created by ARBA machine learning models

Combined Automated Annotation using Multiple IEA Methods

MTABC3, a novel mitochondrial ATP-binding cassette protein involved in iron homeostasis.

Isolation of a genomic clone containing the promoter region of the human ATP binding cassette (ABC) transporter, ABCB6.

ABCB6 (MTABC3) excluded as the causative gene for the growth retardation syndrome with aminoaciduria, cholestasis, iron overload, and lactacidosis.

Identification of a mammalian mitochondrial porphyrin transporter.

Human ABCB6 localizes to both the outer mitochondrial membrane and the plasma membrane.

Human ABC transporter isoform B6 (ABCB6) localizes primarily in the Golgi apparatus.

Large-scale proteomics and phosphoproteomics of urinary exosomes.

Conserved intramolecular disulfide bond is critical to trafficking and fate of ATP-binding cassette (ABC) transporters ABCB6 and sulfonylurea receptor 1 (SUR1)/ABCC8.

Recessive mutations in ELOVL4 cause ichthyosis, intellectual disability, and spastic quadriplegia.

ABCB6 mutations cause ocular coloboma.

ABCB6 is dispensable for erythropoiesis and specifies the new blood group system Langereis.

Shifting the paradigm: the putative mitochondrial protein ABCB6 resides in the lysosomes of cells and in the plasma membrane of erythrocytes.

Missense mutations in the ABCB6 transporter cause dominant familial pseudohyperkalemia.

Efficient purification and reconstitution of ATP binding cassette transporter B6 (ABCB6) for functional and structural studies.

Role of the N-terminal transmembrane domain in the endo-lysosomal targeting and function of the human ABCB6 protein.

The severity of hereditary porphyria is modulated by the porphyrin exporter and Lan antigen ABCB6.

ABCB6 Resides in Melanosomes and Regulates Early Steps of Melanogenesis Required for PMEL Amyloid Matrix Formation.

The human ABCB6 protein is the functional homologue of HMT-1 proteins mediating cadmium detoxification.

Cryo-electron microscopy structure of human ABCB6 transporter.

Quantitative high-confidence human mitochondrial proteome and its dynamics in cellular context.

ABCB6 transports porphyrin from cytosol to mitchondrial matrix

Defective ABCB6 does not transport porphyrin from cytosol into mitochondria matrix

UniProtKB entry Q9NP58 (ABCB6_HUMAN)

Structural Insights into Porphyrin Recognition by the Human ATP-Binding Cassette Transporter ABCB6.

Drosophila ABC transporter, DmHMT-1, confers tolerance to cadmium. DmHMT-1 and its yeast homolog, SpHMT-1, are not essential for vacuolar phytochelatin sequestration.