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

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

Combined Automated Annotation using Multiple IEA Methods

A reference map of the human binary protein interactome.

Role for Spi-C in the development of red pulp macrophages and splenic iron homeostasis.

Heme-mediated SPI-C induction promotes monocyte differentiation into iron-recycling macrophages.

Spi-C, a novel Ets protein that is temporally regulated during B lymphocyte development.

SPI-C, a PU-box binding ETS protein expressed temporarily during B-cell development and in macrophages, contains an acidic transactivation domain located to the N-terminus.

Genomic structure of mouse SPI-C and genomic structure and expression pattern of human SPI-C.

Spi-C has opposing effects to PU.1 on gene expression in progenitor B cells.

SPI-C and STAT6 can cooperate to stimulate IgE germline transcription.

Identification of a negative regulatory role for spi-C in the murine B cell lineage.

Regulation of follicular B cell differentiation by the related E26 transformation-specific transcription factors PU.1, Spi-B, and Spi-C.

Opposing Roles for the Related ETS-Family Transcription Factors Spi-B and Spi-C in Regulating B Cell Differentiation and Function.

RAG-Mediated DNA Breaks Attenuate PU.1 Activity in Early B Cells through Activation of a SPIC-BCLAF1 Complex.

Spi-C and PU.1 Counterregulate Rag1 and Igκ Transcription to Effect Vκ-Jκ Recombination in Small Pre-B Cells.

Counter Regulation of Spic by NF-κB and STAT Signaling Controls Inflammation and Iron Metabolism in Macrophages.

Inflammation induces stress erythropoiesis through heme-dependent activation of SPI-C.

Spi-C positively regulates RANKL-mediated osteoclast differentiation and function.

Extracellular Vesicles From Stored Red Blood Cells Convey Heme and Induce Spic Expression on Human Monocytes.

UniProt record for human SPIC (Q8N5J4)

Role for Spi-C in the development of red pulp macrophages and splenic iron homeostasis.

Heme-mediated SPI-C induction promotes monocyte differentiation into iron-recycling macrophages.

Spi-C, a novel Ets protein that is temporally regulated during B lymphocyte development.

SPI-C, a PU-box binding ETS protein expressed temporarily during B-cell development and in macrophages, contains an acidic transactivation domain located to the N-terminus.

Genomic structure of mouse SPI-C and genomic structure and expression pattern of human SPI-C.

Spi-C has opposing effects to PU.1 on gene expression in progenitor B cells.

SPI-C and STAT6 can cooperate to stimulate IgE germline transcription.

Identification of a negative regulatory role for spi-C in the murine B cell lineage.

Regulation of follicular B cell differentiation by the related E26 transformation-specific transcription factors PU.1, Spi-B, and Spi-C.

Opposing Roles for the Related ETS-Family Transcription Factors Spi-B and Spi-C in Regulating B Cell Differentiation and Function.

RAG-Mediated DNA Breaks Attenuate PU.1 Activity in Early B Cells through Activation of a SPIC-BCLAF1 Complex.

Spi-C and PU.1 Counterregulate Rag1 and Igκ Transcription to Effect Vκ-Jκ Recombination in Small Pre-B Cells.

Counter Regulation of Spic by NF-κB and STAT Signaling Controls Inflammation and Iron Metabolism in Macrophages.

Inflammation induces stress erythropoiesis through heme-dependent activation of SPI-C.

Spi-C positively regulates RANKL-mediated osteoclast differentiation and function.

Extracellular Vesicles From Stored Red Blood Cells Convey Heme and Induce Spic Expression on Human Monocytes.

UniProt record for human SPIC (Q8N5J4)