TCEAL7 transcription elongation factor A like 7

Information
Symbol
TCEAL7
Type
protein-coding
Description
transcription elongation factor A like 7
Entrez Gene ID
56849
Genome
hg19
Position
chrX:102,585,167-102,587,254
Genome
hg38
Position
chrX:103,330,239-103,332,326
MIM
300771 OMIM
HGNC
HGNC:28336 HGNC
Ensembl
ENSG00000182916 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 6 0
Uncertain significance 0 8
Ranking
ClinVar
0
0
0
8
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 WEX5
MIM 300771 OMIM
HGNC HGNC:28336 HGNC
Ensembl ENSG00000182916 Ensembl
AllianceGenome HGNC:28336
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000372666.1 hg38 chrX 103,330,229 103,332,088 1,860
ENST00000332431.5 hg38 chrX 103,330,239 103,332,326 2,088
ENST00000372666.1 hg19 chrX 102,585,157 102,587,016 1,860
ENST00000332431.5 hg19 chrX 102,585,167 102,587,254 2,088
Genome browser