TCEAL2 transcription elongation factor A like 2

Information
Symbol
TCEAL2
Type
protein-coding
Description
transcription elongation factor A like 2
Entrez Gene ID
140597
Genome
hg19
Position
chrX:101,380,651-101,382,684
Genome
hg38
Position
chrX:102,125,679-102,127,712
HGNC
HGNC:29818 HGNC
Ensembl
ENSG00000184905 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
not provided 6 0
Uncertain significance 0 24
Ranking
ClinVar
0
0
0
30
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 MY0876G05
SYNONYM WEX1
SYNONYM my048
HGNC HGNC:29818 HGNC
Ensembl ENSG00000184905 Ensembl
AllianceGenome HGNC:29818
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000329035.2 hg38 chrX 102,125,703 102,127,711 2,009
ENST00000372780.6 hg38 chrX 102,125,679 102,127,712 2,034
ENST00000372780.6 hg19 chrX 101,380,651 101,382,684 2,034
ENST00000329035.2 hg19 chrX 101,380,675 101,382,683 2,009
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