DYNLT2 dynein light chain Tctex-type 2

Information
Symbol
DYNLT2
Type
protein-coding
Description
dynein light chain Tctex-type 2
Entrez Gene ID
6991
Genome
hg19
Position
chr6:170,140,205-170,151,668
Genome
hg38
Position
chr6:169,740,109-169,751,572
MIM
186977 OMIM
HGNC
HGNC:11695 HGNC
Ensembl
ENSG00000184786 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 8
Uncertain significance 0 18
Ranking
ClinVar
0
0
0
26
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 TCTE3
SYNONYM TCTEX1D3
SYNONYM TCTEX2
SYNONYM Tctex4
SYNONYM oda12
MIM 186977 OMIM
HGNC HGNC:11695 HGNC
Ensembl ENSG00000184786 Ensembl
AllianceGenome HGNC:11695
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000366774.4 hg38 chr6 169,740,109 169,751,572 11,464
ENST00000366774.4 hg19 chr6 170,140,205 170,151,668 11,464
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