CUL7 - Gene browser

CUL7

cullin 7

HCNC Approved Symbol: CUL7 (HGNC:21024)
Genomic Coordinates: 6:43,037,617 - 43,053,851 (6p21.1)
Synonyms: dJ20C7.5, KIAA0076
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

11Patients

In total, 11 patients were diagnosed with a variant in the CUL7 gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

011
Patient count

Short stature: 6 (54.5%)
Patient Count: 6 (54.5%)
% of total patients presenting each phenotype is shown in parentheses.
6 (54.5%)
Midface hypoplasia: 3 (27.3%)
Patient Count: 3 (27.3%)
% of total patients presenting each phenotype is shown in parentheses.
3 (27.3%)
Skeletal dysplasia: 3 (27.3%)
Patient Count: 3 (27.3%)
% of total patients presenting each phenotype is shown in parentheses.
3 (27.3%)
Large head: 3 (27.3%)
Patient Count: 3 (27.3%)
% of total patients presenting each phenotype is shown in parentheses.
3 (27.3%)
Blue sclerae: 2 (18.2%)
Patient Count: 2 (18.2%)
% of total patients presenting each phenotype is shown in parentheses.
2 (18.2%)