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FAR1

fatty acyl-CoA reductase 1

HCNC Approved Symbol
FAR1 (HGNC:26222)
Genomic Coordinates
11:13,668,668 - 13,732,346 (11p15.3)
Synonyms
FLJ22728, SDR10E1, MLSTD2
Disease Associations
This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

4Patients

In total, 4 patients were diagnosed with a variant in the FAR1 gene.

Frequently observed phenotypes

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

Intellectual disability
 2 (50.0%)
Neurodevelopmental delay
 2 (50.0%)
Toe walking
 1 (25.0%)
Seizures
 1 (25.0%)
Cerebral palsy
 1 (25.0%)
FAR1 - Gene browser | 3billion