TMUB2 transmembrane and ubiquitin like domain containing 2
Information
- Symbol
- TMUB2
- Type
- protein-coding
- Description
- transmembrane and ubiquitin like domain containing 2
- Entrez Gene ID
- 79089
- Genome
- hg19
- Position
- chr17:42,264,340-42,269,297
- Genome
- hg38
- Position
- chr17:44,186,972-44,191,929
- HGNC
- HGNC:28459 HGNC
- Ensembl
- ENSG00000168591 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 38 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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42 |
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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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Category | : |
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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 | FP2653 |
HGNC | HGNC:28459 HGNC |
Ensembl | ENSG00000168591 Ensembl |
AllianceGenome | HGNC:28459 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000446571.7 | hg38 | chr17 | 44,186,970 | 44,191,226 | 4,257 |
ENST00000319511.6 | hg38 | chr17 | 44,187,206 | 44,191,726 | 4,521 |
ENST00000587989.1 | hg38 | chr17 | 44,187,049 | 44,191,714 | 4,666 |
ENST00000592825.1 | hg38 | chr17 | 44,187,272 | 44,191,711 | 4,440 |
ENST00000589785.1 | hg38 | chr17 | 44,187,262 | 44,191,712 | 4,451 |
ENST00000589184.5 | hg38 | chr17 | 44,187,275 | 44,191,711 | 4,437 |
ENST00000589856.1 | hg38 | chr17 | 44,187,654 | 44,190,349 | 2,696 |
ENST00000538716.7 | hg38 | chr17 | 44,186,972 | 44,191,929 | 4,958 |
ENST00000590235.5 | hg38 | chr17 | 44,187,050 | 44,191,731 | 4,682 |
ENST00000357984.7 | hg38 | chr17 | 44,186,986 | 44,191,730 | 4,745 |
ENST00000587172.1 | hg38 | chr17 | 44,188,933 | 44,191,731 | 2,799 |
ENST00000446571.7 | hg19 | chr17 | 42,264,338 | 42,268,594 | 4,257 |
ENST00000538716.7 | hg19 | chr17 | 42,264,340 | 42,269,297 | 4,958 |
ENST00000357984.7 | hg19 | chr17 | 42,264,354 | 42,269,098 | 4,745 |
ENST00000587989.1 | hg19 | chr17 | 42,264,417 | 42,269,082 | 4,666 |
ENST00000590235.5 | hg19 | chr17 | 42,264,418 | 42,269,099 | 4,682 |
ENST00000319511.6 | hg19 | chr17 | 42,264,574 | 42,269,094 | 4,521 |
ENST00000589785.1 | hg19 | chr17 | 42,264,630 | 42,269,080 | 4,451 |
ENST00000592825.1 | hg19 | chr17 | 42,264,640 | 42,269,079 | 4,440 |
ENST00000589184.5 | hg19 | chr17 | 42,264,643 | 42,269,079 | 4,437 |
ENST00000589856.1 | hg19 | chr17 | 42,265,022 | 42,267,717 | 2,696 |
ENST00000587172.1 | hg19 | chr17 | 42,266,301 | 42,269,099 | 2,799 |
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