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CNOT2

CCR4-NOT transcription complex subunit 2

HCNC Approved Symbol
CNOT2 (HGNC:7878)
Genomic Coordinates
12:70,243,018 - 70,354,993 (12q15)
Synonyms
CDC36, NOT2H, NOT2
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies
618608AD

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the CNOT2 gene.

Frequently observed phenotypes

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

No Results