TFG gene homepage

General information
Gene symbol TFG
Gene name TRK-fused gene
Chromosome 3
Chromosomal band q12.2
Imprinted Unknown
Genomic reference NG_027821.1
Transcript reference NM_001007565.2
Exon/intron information NM_001007565.2 exon/intron table
Associated with diseases SPG-57, Epithelial-myoepithelial carcinoma, neuropathy, motor and sensory, hereditary, Okinawa type
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 17
Unique public DNA variants reported 12
Individuals with public variants 9
Hidden variants 0
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created May 03, 2013
Date last updated July 07, 2016
Version TFG:160707

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_001007565.2.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL http://www.LOVD.nl/TFG
HGNC 11758
Entrez Gene 10342
PubMed articles TFG
OMIM - Gene 602498
OMIM - Diseases SPG-57 (paraplegia, spastic, type 57, autosomal recessive (SPG-57))
Epithelial-myoepithelial carcinoma
neuropathy, motor and sensory, hereditary, Okinawa type
HGMD TFG
GeneCards TFG
GeneTests TFG


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00024112 3 transcript variant 2 NM_001007565.2 NP_001007566.1 17


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