NALCN - Gene browser

NALCN

sodium leak channel, non-selective

HCNC Approved Symbol: NALCN (HGNC:19082)
Genomic Coordinates: 13:101,053,776 - 101,417,179 (13q32.3-q33.1)
Synonyms: bA430M15.1, CanIon, VGCNL1
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

23Patients

In total, 23 patients were diagnosed with a variant in the NALCN gene.

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

023
Patient count

Global developmental delay: 5 (21.7%)
Patient Count: 5 (21.7%)
% of total patients presenting each phenotype is shown in parentheses.
5 (21.7%)
Intellectual disability: 4 (17.4%)
Patient Count: 4 (17.4%)
% of total patients presenting each phenotype is shown in parentheses.
4 (17.4%)
Hypotonia: 4 (17.4%)
Patient Count: 4 (17.4%)
% of total patients presenting each phenotype is shown in parentheses.
4 (17.4%)
Global development delay: 4 (17.4%)
Patient Count: 4 (17.4%)
% of total patients presenting each phenotype is shown in parentheses.
4 (17.4%)
Prematurity: 4 (17.4%)
Patient Count: 4 (17.4%)
% of total patients presenting each phenotype is shown in parentheses.
4 (17.4%)