CUL7 (cullin 7)

2007-12-01  

Identity

HGNC
LOCATION
6p21.1
LOCUSID
ALIAS
3M1,CUL-7,KIAA0076,dJ20C7.5
FUSION GENES

Other Information

Locus ID:

NCBI: 9820
MIM: 609577
HGNC: 21024
Ensembl: ENSG00000044090

Variants:

dbSNP: 9820
ClinVar: 9820
TCGA: ENSG00000044090
COSMIC: CUL7

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000044090ENST00000265348Q14999
ENSG00000044090ENST00000535468Q14999

Expression (GTEx)

0
10
20
30
40
50
60
70
80

Pathways

PathwaySourceExternal ID
Ubiquitin mediated proteolysisKEGGko04120
Ubiquitin mediated proteolysisKEGGhsa04120
Metabolism of proteinsREACTOMER-HSA-392499
Unfolded Protein Response (UPR)REACTOMER-HSA-381119
IRE1alpha activates chaperonesREACTOMER-HSA-381070
XBP1(S) activates chaperone genesREACTOMER-HSA-381038
Immune SystemREACTOMER-HSA-168256
Adaptive Immune SystemREACTOMER-HSA-1280218
Class I MHC mediated antigen processing & presentationREACTOMER-HSA-983169
Antigen processing: Ubiquitination & Proteasome degradationREACTOMER-HSA-983168

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
363044722022Identification and verification of the prognostic value of CUL7 in colon adenocarcinoma.0
363044722022Identification and verification of the prognostic value of CUL7 in colon adenocarcinoma.0
332582892021A rare cause of syndromic short stature: 3M syndrome in three families.4
345978592021Natural history of facial and skeletal features from neonatal period to adulthood in a 3M syndrome cohort with biallelic CUL7 or OBSL1 variants.2
332582892021A rare cause of syndromic short stature: 3M syndrome in three families.4
345978592021Natural history of facial and skeletal features from neonatal period to adulthood in a 3M syndrome cohort with biallelic CUL7 or OBSL1 variants.2
318982342020Cullin-RING E3 Ubiquitin Ligase 7 in Growth Control and Cancer.11
321416542020Identification of two CUL7 variants in two Chinese families with 3-M syndrome by whole-exome sequencing.2
322528022020Cullin-7 (CUL7) is overexpressed in glioma cells and promotes tumorigenesis via NF-κB activation.30
322786982020A novel mutation within intron 17 of the CUL7 gene results in appearance of premature termination codon.2
318982342020Cullin-RING E3 Ubiquitin Ligase 7 in Growth Control and Cancer.11
321416542020Identification of two CUL7 variants in two Chinese families with 3-M syndrome by whole-exome sequencing.2
322528022020Cullin-7 (CUL7) is overexpressed in glioma cells and promotes tumorigenesis via NF-κB activation.30
322786982020A novel mutation within intron 17 of the CUL7 gene results in appearance of premature termination codon.2
308076462019CUL7 promotes cancer cell survival through promoting Caspase-8 ubiquitination.13

Citation

Dessen P

CUL7 (cullin 7)

Atlas Genet Cytogenet Oncol Haematol. 2007-12-01

Online version: http://atlasgeneticsoncology.org/gene/49921/cul7-(cullin-7)