TCEAL9 transcription elongation factor A like 9

Information
Symbol
TCEAL9
Type
protein-coding
Description
transcription elongation factor A like 9
Entrez Gene ID
51186
Genome
hg19
Position
chrX:102,611,446-102,613,383
Genome
hg38
Position
chrX:103,356,518-103,358,455
HGNC
HGNC:30084 HGNC
Ensembl
ENSG00000185222 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 6 0
Uncertain significance 0 2
Ranking
ClinVar
0
0
0
2
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 WBP5
SYNONYM WEX6
HGNC HGNC:30084 HGNC
Ensembl ENSG00000185222 Ensembl
AllianceGenome HGNC:30084
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000372661.6 hg38 chrX 103,356,506 103,358,462 1,957
ENST00000646896.1 hg38 chrX 103,356,518 103,358,455 1,938
ENST00000372656.5 hg38 chrX 103,356,489 103,358,195 1,707
ENST00000372656.5 hg19 chrX 102,611,417 102,613,123 1,707
ENST00000372661.6 hg19 chrX 102,611,434 102,613,390 1,957
ENST00000646896.1 hg19 chrX 102,611,446 102,613,383 1,938
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