CUL7

Protein-coding gene in humans From Wikipedia, the free encyclopedia

Cullin-7 is a RING-E3 ligase protein that in humans is encoded by the CUL7 gene.[5][6][7]

PDBOrtholog search: PDBe RCSB
AliasesCUL7, 3M1, KIAA0076, dJ20C7.5, cullin 7, CUL-7
Quick facts Available structures, PDB ...
CUL7
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesCUL7, 3M1, KIAA0076, dJ20C7.5, cullin 7, CUL-7
External IDsOMIM: 609577; MGI: 1913765; HomoloGene: 56683; GeneCards: CUL7; OMA:CUL7 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001168370
NM_014780
NM_001374872
NM_001374873
NM_001374874

NM_025611

RefSeq (protein)

NP_001161842
NP_055595
NP_001361801
NP_001361802
NP_001361803

NP_079887

Location (UCSC)Chr 6: 43.04 – 43.05 MbChr 17: 46.96 – 46.98 Mb
PubMed search[3][4]
Wikidata
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Clinical significance

It is associated with 3-M syndrome.

Interactions

CUL7 has been shown to interact with RBX1.[5]

References

Further reading

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