TEDC2 tubulin epsilon and delta complex 2
Information
- Symbol
- TEDC2
- Type
- protein-coding
- Description
- tubulin epsilon and delta complex 2
- Entrez Gene ID
- 80178
- Genome
- hg19
- Position
- chr16:2,510,110-2,514,964
- Genome
- hg38
- Position
- chr16:2,460,109-2,464,963
- HGNC
- HGNC:25849 HGNC
- Ensembl
- ENSG00000162062 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 14 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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16 |
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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 | C16orf59 |
HGNC | HGNC:25849 HGNC |
Ensembl | ENSG00000162062 Ensembl |
AllianceGenome | HGNC:25849 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000361837.9 | hg38 | chr16 | 2,460,109 | 2,464,963 | 4,855 |
ENST00000483320.5 | hg38 | chr16 | 2,460,145 | 2,464,963 | 4,819 |
ENST00000563531.5 | hg38 | chr16 | 2,460,134 | 2,464,927 | 4,794 |
ENST00000569496.5 | hg38 | chr16 | 2,460,086 | 2,464,926 | 4,841 |
ENST00000569496.5 | hg19 | chr16 | 2,510,087 | 2,514,927 | 4,841 |
ENST00000361837.9 | hg19 | chr16 | 2,510,110 | 2,514,964 | 4,855 |
ENST00000563531.5 | hg19 | chr16 | 2,510,135 | 2,514,928 | 4,794 |
ENST00000483320.5 | hg19 | chr16 | 2,510,146 | 2,514,964 | 4,819 |
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