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SCUBE3

signal peptide, CUB domain and EGF like domain containing 3

HCNC Approved Symbol
SCUBE3 (HGNC:13655)
Genomic Coordinates
6:35,213,956 - 35,253,079 (6p21.3)
Synonyms
FLJ34743, CEGF3
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the SCUBE3 gene.

Frequently observed phenotypes

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

Growth failure
 1 (100.0%)
Intrauterine growth retardation
 1 (100.0%)
Postnatal growth retardation
 1 (100.0%)
Short stature
 1 (100.0%)
Skeletal dysplasia
 1 (100.0%)
SCUBE3 - Gene browser | 3billion