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TFG

trafficking from ER to golgi regulator

HCNC Approved Symbol
TFG (HGNC:11758)
Genomic Coordinates
3:100,709,290 - 100,748,967 (3q12.2)
Synonyms
TF6, FLJ36137, SPG57
Disease Associations
This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

3Patients

In total, 3 patients were diagnosed with a variant in the TFG gene.

Frequently observed phenotypes

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

Delayed walking
 1 (33.3%)
Optic atrophy
 1 (33.3%)
Hypohidrosis
 1 (33.3%)
Intellectual disability
 1 (33.3%)
Pain insensitivity
 1 (33.3%)
TFG - Gene browser | 3billion