CUL7
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Lua error in Module:Infobox_gene at line 53: attempt to index field 'wikibase' (a nil value). Cullin-7 is a RING-E3 ligase protein that in humans is encoded by the CUL7 gene.[1][2][3]
Clinical significance
[edit | edit source]It is associated with 3-M syndrome.
Interactions
[edit | edit source]CUL7 has been shown to interact with RBX1.[1]
References
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Further reading
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External links
[edit | edit source]- GeneReviews/NIH/NCBI/UW entry on 3-M syndrome
- OMIM entries entry on 3-M syndrome
- Human CUL7 genome location and CUL7 gene details page in the UCSC Genome Browser.
- Overview of all the structural information available in the PDB for UniProt: Q14999 (Human Cullin-7) at the PDBe-KB.
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