TCF12 - Gene browser

TCF12

transcription factor 12

HCNC Approved Symbol: TCF12 (HGNC:11623)
Genomic Coordinates: 15:56,918,090 - 57,291,310 (15q21.3)
Synonyms: HEB, HTF4, HsT17266, bHLHb20, p64
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

13Patients

In total, 13 patients were diagnosed with a variant in the TCF12 gene.

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

013
Patient count

Autism spectrum disorder: 3 (23.1%)
Patient Count: 3 (23.1%)
% of total patients presenting each phenotype is shown in parentheses.
3 (23.1%)
Seizures: 3 (23.1%)
Patient Count: 3 (23.1%)
% of total patients presenting each phenotype is shown in parentheses.
3 (23.1%)
Autism: 2 (15.4%)
Patient Count: 2 (15.4%)
% of total patients presenting each phenotype is shown in parentheses.
2 (15.4%)
Craniosynostosis: 2 (15.4%)
Patient Count: 2 (15.4%)
% of total patients presenting each phenotype is shown in parentheses.
2 (15.4%)
Microcephaly: 2 (15.4%)
Patient Count: 2 (15.4%)
% of total patients presenting each phenotype is shown in parentheses.
2 (15.4%)