TFCP2 transcription factor CP2

Information
Symbol
TFCP2
Type
protein-coding
Description
transcription factor CP2
Entrez Gene ID
7024
Genome
hg19
Position
chr12:51,487,439-51,566,918
Genome
hg38
Position
chr12:51,093,656-51,173,135
MIM
189889 OMIM
HGNC
HGNC:11748 HGNC
Ensembl
ENSG00000135457 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 2
not provided 15 0
Uncertain significance 0 22
Ranking
ClinVar
0
0
2
26
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
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 LBP1C
SYNONYM LSF
SYNONYM LSF1D
SYNONYM SEF
SYNONYM TFCP2C
MIM 189889 OMIM
HGNC HGNC:11748 HGNC
Ensembl ENSG00000135457 Ensembl
AllianceGenome HGNC:11748
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000548115.5 hg38 chr12 51,095,222 51,172,912 77,691
ENST00000257915.10 hg38 chr12 51,093,656 51,173,135 79,480
ENST00000549867.5 hg38 chr12 51,094,883 51,173,134 78,252
ENST00000257915.10 hg19 chr12 51,487,439 51,566,918 79,480
ENST00000549867.5 hg19 chr12 51,488,666 51,566,917 78,252
ENST00000548115.5 hg19 chr12 51,489,005 51,566,695 77,691
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