CLDN19 - Gene browser

CLDN19

claudin 19

HCNC Approved Symbol: CLDN19 (HGNC:2040)
Genomic Coordinates: 1:42,733,093 - 42,740,236 (1p34.2)
Synonyms
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

14Patients

In total, 14 patients were diagnosed with a variant in the CLDN19 gene.

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

014
Patient count

Hypomagnesemia: 9 (64.3%)
Patient Count: 9 (64.3%)
% of total patients presenting each phenotype is shown in parentheses.
9 (64.3%)
Medullary nephrocalcinosis: 9 (64.3%)
Patient Count: 9 (64.3%)
% of total patients presenting each phenotype is shown in parentheses.
9 (64.3%)
Nephrocalcinosis: 5 (35.7%)
Patient Count: 5 (35.7%)
% of total patients presenting each phenotype is shown in parentheses.
5 (35.7%)
Hypercalciuria: 5 (35.7%)
Patient Count: 5 (35.7%)
% of total patients presenting each phenotype is shown in parentheses.
5 (35.7%)
Chronic renal disease: 3 (21.4%)
Patient Count: 3 (21.4%)
% of total patients presenting each phenotype is shown in parentheses.
3 (21.4%)