1. Gene
  2. TFG - trafficking from ER to golgi regulator Gene

TFG - trafficking from ER to golgi regulator Gene

Homo sapiens

Also known as TF6; HMSNP; SPG57; TRKT3

Gene ID: 10342 | Gene type: protein coding

About TFG

Cytogenetic location: 3q12.2 Genomic coordinates (GRCh38): 3:100,709,290-100,748,967 (from NCBI)

This gene has 36 transcripts (splice variants), 217 orthologues and is associated with 67 phenotypes. Ubiquitous expression in duodenum (RPKM 35.2), placenta (RPKM 33.3) and 25 other tissues.

Summary

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]

TFG Products(4)

mRNA Protein Name
NM_001007565.2 NP_001007566.1 protein TFG isoform 1
NM_001195478.2 NP_001182407.1 protein TFG isoform 1
NM_001195479.2 NP_001182408.1 protein TFG isoform 2
NM_006070.6 NP_006061.2 protein TFG isoform 1
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
16169070 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
Biological Process GO Annotation Evidence Reference Source
involved in endoplasmic reticulum to Golgi vesicle-mediated transport IMP
IMP: Inferred from mutant phenotype
21478858 GOA
Cellular Component GO Annotation Evidence Reference Source
located in endoplasmic reticulum exit site IDA
IDA: Inferred from direct assay
21478858 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

TFG Protein Structure

PB1

PB1: PB1 domain (12 - 90)

  • 0
  • 100
  • 200
  • 300
  • 400 a.a.
Protein Preferred Names Protein Names

protein TFG

TRK-fused

TFG Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
TFG Q92734 UBE2I Homo sapiens Q7KZS0 32296183
Intra
TFG Q92734 UBE2I Homo sapiens Q7KZS0 32296183
Intra
TFG Q92734 ANXA11 Homo sapiens Q5T0G8 25416956
Intra
TFG Q92734 ANXA11 Homo sapiens Q5T0G8 25416956
Intra
TFG Q92734 ANXA11 Homo sapiens Q5T0G8 25416956
Intra
TFG Q92734 NID2 Homo sapiens Q8IV28 32296183
Intra
TFG Q92734 NID2 Homo sapiens Q8IV28 32296183
Intra
TFG Q92734 ARHGEF16 Homo sapiens Q5VV41 25416956
Intra
TFG Q92734 MSS51 Homo sapiens Q4VC12 32296183
Intra
TFG Q92734 ACTMAP Homo sapiens Q5BKX5-3 32296183
Intra
TFG Q92734 ACTMAP Homo sapiens Q5BKX5-3 32296183
Intra
TFG Q92734 FAM168A Homo sapiens Q92567-2 32296183
Intra
TFG Q92734 FAM168A Homo sapiens Q92567-2 32296183
Intra
TFG Q92734 BOLL Homo sapiens Q8N9W6-4 32296183
Intra
TFG Q92734 BOLL Homo sapiens Q8N9W6-4 32296183
Intra
TFG Q92734 SAXO4 Homo sapiens Q7Z5V6-2 32296183
Intra
TFG Q92734 SAXO4 Homo sapiens Q7Z5V6-2 32296183
Intra
TFG Q92734 WWOX Homo sapiens Q9NZC7-5 32296183
Intra
TFG Q92734 WWOX Homo sapiens Q9NZC7-5 32296183
Intra
TFG Q92734 WWOX Homo sapiens Q9NZC7-5 32296183
Intra
TFG Q92734 TBX19 Homo sapiens O60806 32296183
Intra
TFG Q92734 TBX19 Homo sapiens O60806 32296183
Intra
TFG Q92734 SMUG1 Homo sapiens Q53HV7-2 32296183
Intra
TFG Q92734 SMUG1 Homo sapiens Q53HV7-2 32296183
Intra
TFG Q92734 PRR20D Homo sapiens P86480 32296183
Intra
TFG Q92734 PRR20D Homo sapiens P86480 32296183
Intra
TFG Q92734 EYA2 Homo sapiens O00167-2 32296183
Intra
TFG Q92734 EYA2 Homo sapiens O00167-2 32296183
Intra
TFG Q92734 OXER1 Homo sapiens Q8TDS5 32296183
Intra
TFG Q92734 OXER1 Homo sapiens Q8TDS5 32296183
Intra
TFG Q92734 STH Homo sapiens Q8IWL8 32296183
Intra
TFG Q92734 STH Homo sapiens Q8IWL8 32296183
Intra
TFG Q92734 FOXH1 Homo sapiens O75593 32296183
Intra
TFG Q92734 FOXH1 Homo sapiens O75593 32296183
Intra
TFG Q92734 ZMYM5 Homo sapiens Q9UJ78-2 32296183
Intra
TFG Q92734 ZMYM5 Homo sapiens Q9UJ78-2 32296183
Intra
TFG Q92734 ZMYM5 Homo sapiens Q9UJ78-2 32296183
Intra
TFG Q92734 RNF4 Homo sapiens P78317 32296183
Intra
TFG Q92734 RNF4 Homo sapiens P78317 32296183
Intra
TFG Q92734 SF3A2 Homo sapiens Q15428 32296183
Intra
TFG Q92734 SF3A2 Homo sapiens Q15428 32296183
Intra
TFG Q92734 UBAP2 Homo sapiens Q5T6F2 32296183
Intra
TFG Q92734 UBAP2 Homo sapiens Q5T6F2 32296183
Intra
TFG Q92734 VPS37C Homo sapiens A5D8V6 25416956
Intra
TFG Q92734 VPS37C Homo sapiens A5D8V6 32296183
Intra
TFG Q92734 VPS37C Homo sapiens A5D8V6 25416956
Intra
TFG Q92734 VPS37C Homo sapiens A5D8V6 25416956
Intra
TFG Q92734 VPS37C Homo sapiens A5D8V6 32296183
Intra
TFG Q92734 SF3B4 Homo sapiens Q15427 32296183
Intra
TFG Q92734 SF3B4 Homo sapiens Q15427 32296183
Intra
TFG Q92734 HNRNPF Homo sapiens P52597 25416956
Intra
TFG Q92734 TFG Homo sapiens Q92734 32296183
Intra
TFG Q92734 TFG Homo sapiens Q92734 32296183
Intra
TFG Q92734 TFG Homo sapiens Q92734 25416956
Intra
TFG Q92734 TFG Homo sapiens Q92734 16169070
Intra
TFG Q92734 TFG Homo sapiens Q92734 27107012
Intra
TFG Q92734 TFG Homo sapiens Q92734 32296183
Intra
TFG Q92734 TFG Homo sapiens Q92734 27107012
Intra
TFG Q92734 PFDN5 Homo sapiens Q99471 32296183
Intra
TFG Q92734 PFDN5 Homo sapiens Q99471 32296183
Intra
TFG Q92734 PFDN5 Homo sapiens Q99471 32296183
Intra
TFG Q92734 KRTAP26-1 Homo sapiens Q6PEX3 32296183
Intra
TFG Q92734 KRTAP26-1 Homo sapiens Q6PEX3 32296183
Intra
TFG Q92734 INCA1 Homo sapiens Q0VD86 32296183
Intra
TFG Q92734 INCA1 Homo sapiens Q0VD86 32296183
Intra
TFG Q92734 CSTF2 Homo sapiens P33240 25416956
Intra
TFG Q92734 CSTF2 Homo sapiens P33240 25416956
Intra
TFG Q92734 ANXA11 Homo sapiens P50995 31515488
Intra
TFG Q92734 MAGED1 Homo sapiens Q9Y5V3 32296183
Intra
TFG Q92734 MAGED1 Homo sapiens Q9Y5V3 25416956
Intra
TFG Q92734 MAGED1 Homo sapiens Q9Y5V3 32296183
Intra
TFG Q92734 MAGED1 Homo sapiens Q9Y5V3 25416956
Intra
TFG Q92734 MAGED1 Homo sapiens Q9Y5V3 32296183
Intra
TFG Q92734 MAGED1 Homo sapiens Q9Y5V3 25416956
Intra
TFG Q92734 DAZAP2 Homo sapiens Q15038 32296183
Intra
TFG Q92734 DAZAP2 Homo sapiens Q15038 32296183
Intra
TFG Q92734 PEF1 Homo sapiens Q9UBV8 32296183
Intra
TFG Q92734 PEF1 Homo sapiens Q9UBV8 32296183
Intra
TFG Q92734 PEF1 Homo sapiens Q9UBV8 32296183
Intra
TFG Q92734 PLA2G10 Homo sapiens O15496 32296183
Intra
TFG Q92734 PLA2G10 Homo sapiens O15496 32296183
Intra
TFG Q92734 LENG8 Homo sapiens Q96PV6 32296183
Intra
TFG Q92734 EWSR1 Homo sapiens Q01844 25416956
Intra
TFG Q92734 DVL3 Homo sapiens Q92997 32296183
Intra
TFG Q92734 DVL3 Homo sapiens Q92997 32296183
Intra
TFG Q92734 DVL3 Homo sapiens Q92997 32296183
Intra
TFG Q92734 PLSCR1 Homo sapiens O15162 16189514
Intra
TFG Q92734 RBPMS Homo sapiens Q93062 25416956
Intra
TFG Q92734 RBPMS Homo sapiens Q93062 25416956
Intra
TFG Q92734 MAPK1IP1L Homo sapiens Q8NDC0 25416956
Intra
TFG Q92734 MAPK1IP1L Homo sapiens Q8NDC0 25416956
Intra
TFG Q92734 MAPK1IP1L Homo sapiens Q8NDC0 32296183
Intra
TFG Q92734 MAPK1IP1L Homo sapiens Q8NDC0 25416956
Intra
TFG Q92734 MAPK1IP1L Homo sapiens Q8NDC0 32296183
Intra
TFG Q92734 SPG21 Homo sapiens Q9NZD8 25416956
Intra
TFG Q92734 SPG21 Homo sapiens Q9NZD8 25416956
Intra
TFG Q92734 SPMIP9 Homo sapiens Q96LM6 32296183
Intra
TFG Q92734 SPMIP9 Homo sapiens Q96LM6 32296183
Intra
TFG Q92734 SPMIP9 Homo sapiens Q96LM6 32296183
Intra
TFG Q92734 CEP55 Homo sapiens Q53EZ4 32296183
Intra
TFG Q92734 CEP55 Homo sapiens Q53EZ4 32296183
Intra
TFG Q92734 CRX Homo sapiens O43186 32296183
Intra
TFG Q92734 CRX Homo sapiens O43186 32296183
Intra
TFG Q92734 INTS11 Homo sapiens Q5TA45 32296183
Intra
TFG Q92734 INTS11 Homo sapiens Q5TA45 32296183
Intra
TFG Q92734 NADSYN1 Homo sapiens Q6IA69 32296183
Intra
TFG Q92734 NADSYN1 Homo sapiens Q6IA69 32296183
Intra
TFG Q92734 SEC24A Homo sapiens O95486 25416956
Intra
TFG Q92734 SEC24A Homo sapiens O95486 25416956
Intra
TFG Q92734 METTL27 Homo sapiens Q8N6F8 32296183
Intra
TFG Q92734 METTL27 Homo sapiens Q8N6F8 32296183
Intra
TFG Q92734 LASP1 Homo sapiens Q14847-2 32296183
Intra
TFG Q92734 LASP1 Homo sapiens Q14847-2 32296183
Intra
TFG Q92734 POU2AF1 Homo sapiens Q16633 32296183
Intra
TFG Q92734 POU2AF1 Homo sapiens Q16633 32296183
Intra
TFG Q92734 PLEKHG4 Homo sapiens Q58EX7 32296183
Intra
TFG Q92734 PLEKHG4 Homo sapiens Q58EX7 32296183
Intra
TFG Q92734 BPIFA1 Homo sapiens Q9NP55 32296183
Intra
TFG Q92734 BPIFA1 Homo sapiens Q9NP55 32296183
Intra
TFG Q92734 BPIFA1 Homo sapiens Q9NP55 32296183
Intra
TFG Q92734 BOLL Homo sapiens Q8N9W6 25416956
Intra
TFG Q92734 BOLL Homo sapiens Q8N9W6 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

TFG Antibodies

Cat. No. Product Name Application Reactivity
HY-P82536 TFG Antibody (YA2281) WB, IHC-F, IHC-P, ICC/IF Human, Mouse, Rat

Related Diseases

Diseases Alias
Spastic Paraplegia 57, Autosomal Recessive

SPG57

Hereditary Spastic Paraplegia 57

Autosomal Recessive Spastic Paraplegia Type 57

Autosomal Recessive Spastic Paraplegia 57

Spastic Paraplegia Due To Partial Tfg Deficiency

Paraplegia, Spastic, Type 57, Autosomal Recessive

Neuropathy, Hereditary Motor And Sensory, Okinawa Type

Hereditary Motor And Sensory Neuropathy, Okinawa Type

HMSNO

Hereditary Motor And Sensory Neuropathy, Proximal Type

Hmsnp

Hereditary Motor And Sensory Neuropathy, Proximal Type, Formerly

Hmsnp, Formerly

Hereditary Motor And Sensory Neuropathy Okinawa

Neuropathy, Motor And Sensory, Hereditary, Okinawa Type

Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due To Tfg Mutation

Cmt2 Due To Tfg Mutation

Chondrosarcoma, Extraskeletal Myxoid

Extraskeletal Myxoid Chondrosarcoma

Emc

Myxoid Extraosseous Chondrosarcoma

Differentiated Thyroid Carcinoma

Papillary Or Follicular Thyroid Carcinoma

Well-Differentiated Thyroid Carcinoma

Differentiated Thyroid Gland Carcinoma

Charcot-Marie-Tooth Disease

Cmt

Hmsn

Hereditary Motor And Sensory Neuropathy

Pma

Cmt - Charcot-Marie-Tooth Disease

Charcot Marie Tooth Disease

Charcot-Marie-Tooth Hereditary Neuropathy

Charcot-Marie-Tooth Syndrome

Peroneal Muscular Atrophy

Hereditary Motor And Sensory Neuropathies

Anaplastic Large Cell Lymphoma

Alcl

Cd30 Positive Anaplastic Large Cell Lymphoma

Ki-1 Positive Anaplastic Large Cell Lymphoma

Primary Systemic Alcl

Sacl

Ki-1+ Anaplastic Large Cell Lymphoma

Chondrosarcoma

Cartilaginous Cancer

Chondrosarcoma Of Bone

Primary Chondrosarcoma Of The Bone

CHDSA

Occipital Lobe Neoplasm

Neoplasm Of Occipital Lobe

Malignant Neoplasm Of Occipital Lobe

Tumor Of Occipital Lobe

Paraplegia

Paraplegia, Lower

Severe Or Complete Loss Of Motor Function In The Lower Extremities And Lower Portions Of The Trunk

Lymphoma

Lymphoid Cancer

Lymphomas

Lymphoid Cancers

Lymphoid Neoplasm

Lymphoma Nos

Nhl - [Non-Hodgkin Lymphoma]

Non-Hodgkin Lymphoma

Non-Hodgkin Lymphoma, Nos

Non-Hodgkin Malignant Lymphoma Nos

Dental Fluorosis

Mottled Teeth

Intrinsic Enamel Discolouration Of Fluorosis

Mottling Of Enamel

Fluorosis, Dental

Dental Fluorosis, Acquired

Bone Chondrosarcoma
Spondylometaphyseal Dysplasia, Corner Fracture Type

SMDCF

Spondylometaphyseal Dysplasia, Sutcliffe Type

Spondylometaphyseal Dysplasia Corner Fracture Type

Spondylometaphyseal Dysplasia, 'Corner Fracture' Type

Spondylometaphyseal Dysplasia Sutcliffe Type

Sutcliffe Type Of Spondylometaphyseal Dysplasia

Spondylometaphyseal Dysplasia - Sutcliffe Type

Smd, Corner Fractures Type

Smd, Sutcliffe Type

Sutcliffe Smd

Dysplasia, Spondylometaphyseal, Corner Fracture Type

Inflammatory Myofibroblastic Tumor

Inflammatory Fibrosarcoma

Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive

Charcot-Marie-Tooth Disease Type 4

Charcot-Marie-Tooth Disease Type 4e

Hereditary Motor And Sensory Neuropathy

Cmt4e

CHN1

Hypomyelinating Neuropathy, Congenital, 1

Charcot-Marie-Tooth Neuropathy Type 4e

Neuropathy, Congenital Hypomyelinating, 1

Ar-Cmt1

Autosomal Recessive Demyelinating Charcot-Marie-Tooth

Cmt4

Neuropathy, Congenital Hypomyelinating Or Amyelinating, Autosomal Recessive

Hypomyelination, Severe Congenital

Charcot-Marie-Tooth Disease, Type 4e

Charcot-Marie-Tooth Neuropathy, Type 4e

Autosomal Recessive Congenital Hypomyelinating Or Amyelinating Neuropathy

Autosomal Recessive Congenital Hypomyelinating Neuropathy

Congenital Amyelinating Neuropathy

Congenital Hypomyelinating Neuropathy Autosomal Recessive

Neuropathy, Congenital Hypomyelinating Or Amyelinating

Severe Congenital Hypomyelination

Hereditary Sensory Motor Neuropathy

Charcot-Marie-Tooth Disease, Demyelinating, Autosomal Recessive

Neuropathy, Hypomyelinating, Congenital, Type 1

Neuropathy, Motor And Sensory, Hereditary

Congenital Hypomyelinating Neuropathy

Hereditary Motor And Sensory Neuropathies

Hereditary Sensorimotor Neuropathy

Hmsn - [Hereditary Motor And Sensory Neuropathy]

Hsmn - [Hereditary Sensory And Motor Neuropathy]

Hereditary Motor And Sensory Neuropathy, Types I-Iv

Hereditary Spastic Paraplegia

Familial Spastic Paraplegia

Hereditary Spastic Paraparesis

Strumpell-Lorrain Disease

Familial Spastic Paraparesis

Hsp

Spg

Strümpell-Lorrain Disease

Spastic Paraplegia, Hereditary

French Settlement Disease

Strumpell-Lorrain Syndrome

Fsp

Spastic Paraplegia, Familial

Spastic Paraplegia Hereditary

Spastic Paraplegia 3, Autosomal Dominant

Spastic Paraparesis

Hereditary Spastic Paralysis

Familial Spastic Paralysis

Hereditary Spastic Ataxia

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus TFG RGD RGD:1309751
Macaca mulatta TFG VGNC VGNC:82715
Canis familiaris TFG VGNC VGNC:47299
Mus musculus TFG MGD MGI:1338041
Felis catus TFG VGNC VGNC:66122
Others TFG NCBI