UBALD2 UBA like domain containing 2
Information
- Symbol
- UBALD2
- Type
- protein-coding
- Description
- UBA like domain containing 2
- Entrez Gene ID
- 283991
- Genome
- hg19
- Position
- chr17:74,261,429-74,267,379
- Genome
- hg38
- Position
- chr17:76,265,348-76,271,298
- HGNC
- HGNC:28438 HGNC
- Ensembl
- ENSG00000185262 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 10 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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14 |
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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 |
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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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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 | FAM100B |
HGNC | HGNC:28438 HGNC |
Ensembl | ENSG00000185262 Ensembl |
AllianceGenome | HGNC:28438 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000589240.1 | hg38 | chr17 | 76,265,703 | 76,270,586 | 4,884 |
ENST00000327490.8 | hg38 | chr17 | 76,265,348 | 76,271,298 | 5,951 |
ENST00000327490.8 | hg19 | chr17 | 74,261,429 | 74,267,379 | 5,951 |
ENST00000589240.1 | hg19 | chr17 | 74,261,784 | 74,266,667 | 4,884 |
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