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UFSP2

UFM1 specific peptidase 2

HCNC Approved Symbol
UFSP2 (HGNC:25640)
Genomic Coordinates
4:185,399,537 - 185,425,964 (4q35.1)
Synonyms
FLJ11200, C4orf20
Disease Associations
This gene is associated with the following 3 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Hip dysplasia, Beukes type
142669AD
Developmental and epileptic encephalopathy 106
620028AR
Spondyloepimetaphyseal dysplasia, Di Rocco type
617974AD

Diagnosed Cases

4Patients

In total, 4 patients were diagnosed with a variant in the UFSP2 gene.

Frequently observed phenotypes

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

Atonic seizures
 1 (25.0%)
Eeg with generalized spikes
 1 (25.0%)
Epileptic encephalopathy
 1 (25.0%)
Febrile seizures
 1 (25.0%)
Generalized myoclonic seizures
 1 (25.0%)