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SCYL2

SCY1 like pseudokinase 2

HCNC Approved Symbol
SCYL2 (HGNC:19286)
Genomic Coordinates
12:100,267,177 - 100,341,715 (12q23.1)
Synonyms
KIAA1360, CVAK104
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum
618766AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the SCYL2 gene.

Frequently observed phenotypes

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

No Results