MYT1L - Gene browser

MYT1L

myelin transcription factor 1 like

HCNC Approved Symbol: MYT1L (HGNC:7623)
Genomic Coordinates: 2:1,789,113 - 2,331,275 (2p25.3)
Synonyms: KIAA1106, NZF1, ZC2HC4B, ZC2H2C2
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

7Patients

In total, 7 patients were diagnosed with a variant in the MYT1L gene.

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

07
Patient count

Global developmental delay: 5 (71.4%)
Patient Count: 5 (71.4%)
% of total patients presenting each phenotype is shown in parentheses.
5 (71.4%)
Hypertelorism: 2 (28.6%)
Patient Count: 2 (28.6%)
% of total patients presenting each phenotype is shown in parentheses.
2 (28.6%)
Obesity: 2 (28.6%)
Patient Count: 2 (28.6%)
% of total patients presenting each phenotype is shown in parentheses.
2 (28.6%)
Autistic behavior: 2 (28.6%)
Patient Count: 2 (28.6%)
% of total patients presenting each phenotype is shown in parentheses.
2 (28.6%)
Ventriculomegaly: 2 (28.6%)
Patient Count: 2 (28.6%)
% of total patients presenting each phenotype is shown in parentheses.
2 (28.6%)