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MBTPS2

membrane bound transcription factor peptidase, site 2

HCNC Approved Symbol
MBTPS2 (HGNC:15455)
Genomic Coordinates
23:21,839,617 - 21,885,423 (Xp22.12)
Synonyms
S2P, KFSD
Disease Associations
This gene is associated with the following 4 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Olmsted syndrome, X-linked
300918X-linked recessive
IFAP syndrome with or without BRESHECK syndrome
308205X-linked recessive
Keratosis follicularis spinulosa decalvans, X-linked
308800X-linked recessive
Osteogenesis imperfecta, type XIX
301014X-linked recessive

Diagnosed Cases

3Patients

In total, 3 patients were diagnosed with a variant in the MBTPS2 gene.

Frequently observed phenotypes

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

Alopecia
 2 (66.7%)
Seizure
 2 (66.7%)
Congenital ichthyosis
 1 (33.3%)
Keratosis pilaris
 1 (33.3%)
Papillomatous papule
 1 (33.3%)