TCTN2 - Gene browser

TCTN2

tectonic family member 2

HCNC Approved Symbol: TCTN2 (HGNC:25774)
Genomic Coordinates: 12:123,671,113 - 123,708,399 (12q24.31)
Synonyms: FLJ12975, TECT2, MKS8, JBTS24, C12orf38
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

1Patient

In total, 1 patient was diagnosed with a variant in the TCTN2 gene.

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

01
Patient count

Abnormality of fibula morphology: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Clenched hands: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Hyperechogenic kidneys: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Occipital encephalocele: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)