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SERPINB7

serpin family B member 7

HCNC Approved Symbol
SERPINB7 (HGNC:13902)
Genomic Coordinates
18:63,753,057 - 63,805,370 (18q21.33)
Synonyms
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

10Patients

In total, 10 patients were diagnosed with a variant in the SERPINB7 gene.

Frequently observed phenotypes

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

Palmoplantar hyperkeratosis
 7 (70.0%)
Hyperkeratosis
 
1 (10.0%)
Ichthyosis
 
1 (10.0%)
Thickened skin
 
1 (10.0%)
Palmoplantar keratoderma
 
1 (10.0%)
SERPINB7 - Gene browser | 3billion