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SIN3A

SIN3 transcription regulator family member A

HCNC Approved Symbol
SIN3A (HGNC:19353)
Genomic Coordinates
15:75,369,379 - 75,455,815 (15q24.2)
Synonyms
KIAA0700, DKFZP434K2235
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

4Patients

In total, 4 patients were diagnosed with a variant in the SIN3A gene.

Frequently observed phenotypes

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

Global development delay
 2 (50.0%)
Anosmia
 1 (25.0%)
Bicuspid aortic valve
 1 (25.0%)
Broad forehead
 1 (25.0%)
Curved middle phalanx of the 5th finger
 1 (25.0%)
SIN3A - Gene browser | 3billion