TCF21 transcription factor 21

Information
Symbol
TCF21
Type
protein-coding
Description
transcription factor 21
Entrez Gene ID
6943
Genome
hg19
Position
chr6:134,210,473-134,216,691
Genome
hg38
Position
chr6:133,889,335-133,895,553
MIM
603306 OMIM
HGNC
HGNC:11632 HGNC
Ensembl
ENSG00000118526 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 4
Uncertain significance 0 18
Ranking
ClinVar
0
0
0
26
2
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
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Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM POD1
SYNONYM bHLHa23
MIM 603306 OMIM
HGNC HGNC:11632 HGNC
Ensembl ENSG00000118526 Ensembl
AllianceGenome HGNC:11632
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000237316.3 hg38 chr6 133,889,335 133,895,553 6,219
ENST00000367882.5 hg38 chr6 133,889,113 133,892,257 3,145
ENST00000367882.5 hg19 chr6 134,210,251 134,213,395 3,145
ENST00000237316.3 hg19 chr6 134,210,473 134,216,691 6,219
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