TPGS2 tubulin polyglutamylase complex subunit 2
Information
- Symbol
- TPGS2
- Type
- protein-coding
- Description
- tubulin polyglutamylase complex subunit 2
- Entrez Gene ID
- 25941
- Genome
- hg19
- Position
- chr18:34,366,536-34,408,805
- Genome
- hg38
- Position
- chr18:36,786,573-36,828,842
- MIM
- 620710 OMIM
- HGNC
- HGNC:24561 HGNC
- Ensembl
- ENSG00000134779 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 24 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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30 |
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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
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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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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | C18orf10 |
SYNONYM | HMFN0601 |
SYNONYM | L17 |
SYNONYM | PGs2 |
MIM | 620710 OMIM |
HGNC | HGNC:24561 HGNC |
Ensembl | ENSG00000134779 Ensembl |
AllianceGenome | HGNC:24561 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000590842.5 | hg38 | chr18 | 36,786,573 | 36,828,842 | 42,270 |
ENST00000589049.5 | hg38 | chr18 | 36,798,018 | 36,828,781 | 30,764 |
ENST00000610723.4 | hg38 | chr18 | 36,786,485 | 36,829,216 | 42,732 |
ENST00000587129.5 | hg38 | chr18 | 36,782,985 | 36,828,804 | 45,820 |
ENST00000614939.4 | hg38 | chr18 | 36,780,027 | 36,829,216 | 49,190 |
ENST00000383056.7 | hg38 | chr18 | 36,796,072 | 36,828,986 | 32,915 |
ENST00000334295.9 | hg38 | chr18 | 36,794,108 | 36,829,002 | 34,895 |
ENST00000593035.5 | hg38 | chr18 | 36,796,072 | 36,828,963 | 32,892 |
ENST00000587129.5 | hg19 | chr18 | 34,362,948 | 34,408,767 | 45,820 |
ENST00000334295.9 | hg19 | chr18 | 34,374,071 | 34,408,965 | 34,895 |
ENST00000383056.7 | hg19 | chr18 | 34,376,035 | 34,408,949 | 32,915 |
ENST00000589049.5 | hg19 | chr18 | 34,377,981 | 34,408,744 | 30,764 |
ENST00000590842.5 | hg19 | chr18 | 34,366,536 | 34,408,805 | 42,270 |
ENST00000593035.5 | hg19 | chr18 | 34,376,035 | 34,408,926 | 32,892 |
ENST00000610723.4 | hg19 | chr18 | 34,366,448 | 34,409,179 | 42,732 |
ENST00000614939.4 | hg19 | chr18 | 34,359,990 | 34,409,179 | 49,190 |
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