TAGLN transgelin

Information
Symbol
TAGLN
Type
protein-coding
Description
transgelin
Entrez Gene ID
6876
Genome
hg19
Position
chr11:117,070,086-117,078,180
Genome
hg38
Position
chr11:117,199,370-117,207,464
MIM
600818 OMIM
HGNC
HGNC:11553 HGNC
Ensembl
ENSG00000149591 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 10
Likely benign 0 2
Uncertain significance 0 40
Ranking
ClinVar
0
0
0
52
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
[No Data.]
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 SM22
SYNONYM SM22-alpha
SYNONYM SMCC
SYNONYM TAGLN1
SYNONYM TGLN
SYNONYM WS3-10
MIM 600818 OMIM
HGNC HGNC:11553 HGNC
Ensembl ENSG00000149591 Ensembl
AllianceGenome HGNC:11553
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000392951.9 hg38 chr11 117,199,370 117,207,464 8,095
ENST00000532870.5 hg38 chr11 117,201,873 117,204,778 2,906
ENST00000530649.5 hg38 chr11 117,201,750 117,204,776 3,027
ENST00000392951.9 hg19 chr11 117,070,086 117,078,180 8,095
ENST00000530649.5 hg19 chr11 117,072,466 117,075,492 3,027
ENST00000532870.5 hg19 chr11 117,072,589 117,075,494 2,906
Genome browser