TCEAL1 transcription elongation factor A like 1

Information
Symbol
TCEAL1
Type
protein-coding
Description
transcription elongation factor A like 1
Entrez Gene ID
9338
Genome
hg19
Position
chrX:102,883,903-102,885,881
Genome
hg38
Position
chrX:103,628,975-103,630,953
MIM
300237 OMIM
HGNC
HGNC:11616 HGNC
Ensembl
ENSG00000172465 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Likely pathogenic 0 14
Likely benign 0 6
not provided 6 0
Uncertain significance 0 16
Ranking
ClinVar
0
0
0
38
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 HIJRS
SYNONYM NEDGFAX
SYNONYM SIIR
SYNONYM WEX9
SYNONYM p21
SYNONYM pp21
MIM 300237 OMIM
HGNC HGNC:11616 HGNC
Ensembl ENSG00000172465 Ensembl
AllianceGenome HGNC:11616
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000372625.8 hg38 chrX 103,628,975 103,630,953 1,979
ENST00000372624.3 hg38 chrX 103,628,999 103,630,953 1,955
ENST00000372626.7 hg38 chrX 103,628,704 103,630,447 1,744
ENST00000372626.7 hg19 chrX 102,883,632 102,885,375 1,744
ENST00000372625.8 hg19 chrX 102,883,903 102,885,881 1,979
ENST00000372624.3 hg19 chrX 102,883,927 102,885,881 1,955
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