NOG - Gene browser

NOG

noggin

HCNC Approved Symbol: NOG (HGNC:7866)
Genomic Coordinates: 17:56,593,699 - 56,595,611 (17q22)
Synonyms: SYNS1, SYM1
Disease Associations: This gene is associated with the following 5 diseases in OMIM.

2Patients

In total, 2 patients were diagnosed with a variant in the NOG gene.

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

02
Patient count

Brachydactyly: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Craniosynostosis: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Symphalangism affecting the proximal phalanx of the 4th finger: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Symphalangism affecting the proximal phalanx of the 5th finger: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Symphalangism of middle phalanx of finger: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)