TFG gene

trafficking from ER to golgi regulator

The information on this page was automatically extracted from online scientific databases.

From NCBI Gene:

There are several documented fusion oncoproteins encoded partially by this gene. This gene also participates in several oncogenic rearrangements resulting in anaplastic lymphoma and mixoid chondrosarcoma, and may play a role in the NF-kappaB pathway. Multiple transcript variants have been found for this gene. [provided by RefSeq, Sep 2010]

From UniProt:

Plays a role in the normal dynamic function of the endoplasmic reticulum (ER) and its associated microtubules (PubMed:23479643, PubMed:27813252). Required for secretory cargo traffic from the endoplasmic reticulum to the Golgi apparatus (PubMed:21478858).

From NCBI Gene:

  • Spastic paraplegia 57, autosomal recessive
  • Hereditary motor and sensory neuropathy, Okinawa type

From UniProt:

A chromosomal aberration involving TFG is found in papillary thyroid carcinomas (PTCs). Translocation t(1;3)(q21;q11) with NTRK1. The TFG sequence is fused to the 3'-end of NTRK1 generating the TRKT3 (TRK-T3) fusion transcript.

Neuropathy, hereditary motor and sensory, Okinawa type (HMSNO): A neurodegenerative disorder characterized by young adult onset of proximal muscle weakness and atrophy, muscle cramps, and fasciculations, with later onset of distal sensory impairment. The disorder is slowly progressive and clinically resembles amyotrophic lateral sclerosis. [MIM:604484]

Spastic paraplegia 57, autosomal recessive (SPG57): A complicated form of spastic paraplegia, a neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. Rate of progression and the severity of symptoms are quite variable. Initial symptoms may include difficulty with balance, weakness and stiffness in the legs, muscle spasms, and dragging the toes when walking. Complicated forms are recognized by additional variable features including spastic quadriparesis, seizures, dementia, amyotrophy, extrapyramidal disturbance, cerebral or cerebellar atrophy, optic atrophy, and peripheral neuropathy, as well as by extra neurological manifestations. [MIM:615658]

Cytogenetic Location: 3q12.2, which is the long (q) arm of chromosome 3 at position 12.2

Molecular Location: base pairs 100,709,290 to 100,748,967 on chromosome 3 (Homo sapiens Updated Annotation Release 109.20200522, GRCh38.p13) (NCBI)

Cytogenetic Location: 3q12.2, which is the long (q) arm of chromosome 3 at position 12.2
  • SPG57
  • TF6
  • TRKT3