Cullin 7 | |||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
PDB rendering based on 2jng. |
|||||||||||||
|
|||||||||||||
Identifiers | |||||||||||||
Symbols | CUL7; KIAA0076; dJ20C7.5 | ||||||||||||
External IDs | OMIM: 609577 MGI: 1913765 HomoloGene: 56683 GeneCards: CUL7 Gene | ||||||||||||
|
|||||||||||||
RNA expression pattern | |||||||||||||
More reference expression data | |||||||||||||
Orthologs | |||||||||||||
Species | Human | Mouse | |||||||||||
Entrez | 9820 | 66515 | |||||||||||
Ensembl | ENSG00000044090 | ENSMUSG00000038545 | |||||||||||
UniProt | Q14999 | Q3U270 | |||||||||||
RefSeq (mRNA) | NM_001168370.1 | NM_025611.5 | |||||||||||
RefSeq (protein) | NP_001161842.1 | NP_079887.3 | |||||||||||
Location (UCSC) | Chr 6: 43.01 – 43.02 Mb |
Chr 17: 46.79 – 46.8 Mb |
|||||||||||
PubMed search | [1] | [2] |
Cullin-7 is a protein that in humans is encoded by the CUL7 gene.[1][2][3]
Contents |
It is associated with 3-M syndrome.
CUL7 has been shown to interact with RBX1.[1]
|
|