Name

SPOP Gene

speckle-type POZ protein

This gene encodes a protein that may modulate the transcriptional repression activities of death-associated protein 6 (DAXX), which interacts with histone deacetylase, core histones, and other histone-associated proteins. In mouse, the encoded protein binds to the putative leucine zipper domain of macroH2A1.2, a variant H2A histone that is enriched on inactivated X chromosomes. The BTB/POZ domain of this protein has been shown in other proteins to mediate transcriptional repression and to interact with components of histone deacetylase co-repressor complexes. Alternative splicing of this gene results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]

spop Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term spop in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

SPOP Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for SPOP from the Pathway Commons Protein-Protein Interactions dataset.

SPOP Gene Set

From CM4AI KOLF21J CRISPRi Gene Perturbation Atlas

genes differentially expressed following the SPOP gene perturbation from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas.

Ubiquitin E3 ligase (H2AFY, SPOP, CUL3) Gene Set

From CORUM Protein Complexes

proteins in the Ubiquitin E3 ligase (H2AFY, SPOP, CUL3) protein complex from the CORUM Protein Complexes dataset.

Ubiquitin E3 ligase (BMI1, SPOP, CUL3) Gene Set

From CORUM Protein Complexes

proteins in the Ubiquitin E3 ligase (BMI1, SPOP, CUL3) protein complex from the CORUM Protein Complexes dataset.

Ubiquitin E3 ligase (SPOP, DAXX, CUL3) Gene Set

From CORUM Protein Complexes

proteins in the Ubiquitin E3 ligase (SPOP, DAXX, CUL3) protein complex from the CORUM Protein Complexes dataset.

SPOP-related neurodevelopmental condition Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the SPOP-related neurodevelopmental condition phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.