Gene entry
TFG
trafficking from ER to golgi regulator
- Chromosome
- 3
- Cytoband
- 3q12.2
- Variants (rsID)
- 11
TFG is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q12.2). Its official name is “trafficking from ER to golgi regulator”. The reference table lists 11 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs6772054Benignsingle nucleotide variantHereditary motor and sensory neuropathy, Okinawa type|Hereditary spastic paraplegia 57
- rs111356679Conflicting interpretationssingle nucleotide variantHereditary motor and sensory neuropathy, Okinawa type|Hereditary spastic paraplegia 57
- rs207482230Pathogenicsingle nucleotide variantHereditary motor and sensory neuropathy, Okinawa type|Hereditary motor and sensory neuropathy, Okinawa type|Hereditary spastic paraplegia 57|Amyotrophic Lateral Sclerosis with Sensory Neuropathy|See cases
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.