CUL7 Chromosome 6

Cullin 7
155 variants 155 Health Risk

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What This Gene Does
The protein encoded by this gene is a component of an E3 ubiquitin-protein ligase complex. The encoded protein interacts with TP53, CUL9, and FBXW8 proteins. Defects in this gene are a cause of 3M syndrome type 1 (3M1). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]
Gene Info
Gene Group
"Cullins|3M complex subunits"
Locus Type
gene with protein product
Location
6p21.1
Ensembl
ENSG00000044090
Associated Conditions (7)
3M syndrome 1
Inborn genetic diseases
CUL7-related disorder
Hepatocellular carcinoma
Cervical cancer
3-M syndrome
Yakut short stature syndrome
Key Variants
All Variants (155)
RSID Category Clinical Significance Conditions
RS61752334 Health Risk Pathogenic/Likely pathogenic Inborn genetic diseases, 3M syndrome 1, 3-M syndrome
RS746333044 Health Risk Pathogenic/Likely pathogenic 3M syndrome 1, 3M syndrome 1
RS748555538 Health Risk Pathogenic/Likely pathogenic 3-M syndrome, 3M syndrome 1, 3-M syndrome
RS759300846 Health Risk Pathogenic/Likely pathogenic 3M syndrome 1, 3-M syndrome, 3M syndrome 1
RS786205651 Health Risk Pathogenic/Likely pathogenic 3M syndrome 1, 3M syndrome 1
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