The TCF20 gene homepage

General information
Gene symbol TCF20
Gene name transcription factor 20 (AR1)
Chromosome 22
Chromosomal band q13.3
Imprinted Unknown
Genomic reference NG_028982.3
Transcript reference NM_005650.2
Exon/intron information NM_005650.2 exon/intron table
Associated with diseases DDVIBA
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 99
Unique public DNA variants reported 87
Individuals with public variants 45
Hidden variants 19
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 April 19, 2024
Version TCF20:240419

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_005650.2.
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 https://www.LOVD.nl/TCF20
HGNC 11631
Entrez Gene 6942
PubMed articles TCF20
OMIM - Gene 603107
OMIM - Diseases DDVIBA (Developmental delay with variable intellectual impairment and behavioral abnormalities)
HGMD TCF20
GeneCards TCF20
GeneTests TCF20
Orphanet TCF20


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00025260 22 transcript variant 1 NM_005650.2 NP_005641.1 99


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