TSEN34 tRNA splicing endonuclease subunit 34
Information
- Symbol
- TSEN34
- Type
- protein-coding
- Description
- tRNA splicing endonuclease subunit 34
- Entrez Gene ID
- 79042
- Genome
- hg19
- Position
- chr19:54,694,138-54,697,585
- Genome
- hg38
- Position
- chr19:54,190,287-54,193,730
- MIM
- 608754 OMIM
- HGNC
- HGNC:15506 HGNC
- Ensembl
- ENSG00000170892 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 2 |
Likely pathogenic | 0 | 2 |
Benign | 0 | 60 |
Likely benign | 0 | 91 |
Conflicting classifications of pathogenicity | 0 | 16 |
Uncertain significance | 0 | 156 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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55 |
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242 |
![]() |
4 |
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
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Category | : |
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 |
Type | ID |
---|---|
SYNONYM | LENG5 |
SYNONYM | PCH2C |
SYNONYM | SEN34 |
SYNONYM | SEN34L |
MIM | 608754 OMIM |
HGNC | HGNC:15506 HGNC |
Ensembl | ENSG00000170892 Ensembl |
AllianceGenome | HGNC:15506 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000429671.7 | hg38 | chr19 | 54,190,268 | 54,194,532 | 4,265 |
ENST00000653273.2 | hg38 | chr19 | 54,191,306 | 54,194,532 | 3,227 |
ENST00000665674.2 | hg38 | chr19 | 54,190,738 | 54,194,532 | 3,795 |
ENST00000667261.1 | hg38 | chr19 | 54,190,287 | 54,193,730 | 3,444 |
ENST00000302937.8 | hg38 | chr19 | 54,190,268 | 54,194,536 | 4,269 |
ENST00000396388.3 | hg38 | chr19 | 54,191,308 | 54,194,532 | 3,225 |
ENST00000396383.5 | hg38 | chr19 | 54,190,731 | 54,193,666 | 2,936 |
ENST00000455798.6 | hg38 | chr19 | 54,189,938 | 54,194,532 | 4,595 |
ENST00000455798.6 | hg19 | chr19 | 54,693,789 | 54,698,390 | 4,602 |
ENST00000429671.7 | hg19 | chr19 | 54,694,119 | 54,698,390 | 4,272 |
ENST00000302937.8 | hg19 | chr19 | 54,694,119 | 54,698,394 | 4,276 |
ENST00000667261.1 | hg19 | chr19 | 54,694,138 | 54,697,585 | 3,448 |
ENST00000396383.5 | hg19 | chr19 | 54,694,582 | 54,697,521 | 2,940 |
ENST00000665674.2 | hg19 | chr19 | 54,694,589 | 54,698,390 | 3,802 |
ENST00000653273.2 | hg19 | chr19 | 54,695,157 | 54,698,390 | 3,234 |
ENST00000396388.3 | hg19 | chr19 | 54,695,159 | 54,698,390 | 3,232 |
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