SMPD4 - Gene browser | 3billion

SMPD4

SMPD4

sphingomyelin phosphodiesterase 4

HCNC Approved Symbol: SMPD4 (HGNC:32949)
Genomic Coordinates: 2:130,151,392 - 130,181,757 (2q21.1)
Synonyms: FLJ20297, FLJ20756, nSMase-3, KIAA1418, NSMASE3, NET13
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the SMPD4 gene.

Frequently observed phenotypes(Top 5 only)

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

01
Patient count

Brisk reflexes: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Delayed psychomotor development: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Hypertonia: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Seizures: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)

Last updated: 2024-06-30

SMPD4 - Gene browser | 3billion