NTNG2 - Gene browser | 3billion

NTNG2

NTNG2

netrin G2

HCNC Approved Symbol: NTNG2 (HGNC:14288)
Genomic Coordinates: 9:132,161,689 - 132,244,526 (9q34.13)
Synonyms: KIAA1857, Lmnt2, NetrinG2, NTNG1
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 NTNG2 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

Global development delay: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Hypotonia: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Macrocephaly: 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

NTNG2 - Gene browser | 3billion