NME8 - Gene browser | 3billion

NME8

NME8

NME/NM23 family member 8

HCNC Approved Symbol: NME8 (HGNC:16473)
Genomic Coordinates: 7:37,848,597 - 37,900,397 (7p14.1)
Synonyms: CILD6, SPTRX2, NM23-H8, DNAI8, TXNDC3
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 NME8 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

Elevated serum cpk: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Muscle weakness: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Respiratory insufficiency due to muscle weakness: 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

NME8 - Gene browser | 3billion