UBALD1 UBA like domain containing 1
Information
- Symbol
- UBALD1
- Type
- protein-coding
- Description
- UBA like domain containing 1
- Entrez Gene ID
- 124402
- Genome
- hg19
- Position
- chr16:4,658,885-4,664,889
- Genome
- hg38
- Position
- chr16:4,608,884-4,614,888
- HGNC
- HGNC:29576 HGNC
- Ensembl
- ENSG00000153443 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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26 |
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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 | FAM100A |
SYNONYM | PP11303 |
HGNC | HGNC:29576 HGNC |
Ensembl | ENSG00000153443 Ensembl |
AllianceGenome | HGNC:29576 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000283474.12 | hg38 | chr16 | 4,608,884 | 4,614,888 | 6,005 |
ENST00000587649.1 | hg38 | chr16 | 4,609,721 | 4,614,873 | 5,153 |
ENST00000587615.1 | hg38 | chr16 | 4,609,368 | 4,614,872 | 5,505 |
ENST00000591897.5 | hg38 | chr16 | 4,608,883 | 4,615,027 | 6,145 |
ENST00000590965.1 | hg38 | chr16 | 4,608,883 | 4,614,874 | 5,992 |
ENST00000590891.1 | hg38 | chr16 | 4,608,883 | 4,611,523 | 2,641 |
ENST00000591401.5 | hg38 | chr16 | 4,608,883 | 4,614,881 | 5,999 |
ENST00000590891.1 | hg19 | chr16 | 4,658,884 | 4,661,524 | 2,641 |
ENST00000590965.1 | hg19 | chr16 | 4,658,884 | 4,664,875 | 5,992 |
ENST00000591401.5 | hg19 | chr16 | 4,658,884 | 4,664,882 | 5,999 |
ENST00000591897.5 | hg19 | chr16 | 4,658,884 | 4,665,028 | 6,145 |
ENST00000283474.12 | hg19 | chr16 | 4,658,885 | 4,664,889 | 6,005 |
ENST00000587615.1 | hg19 | chr16 | 4,659,369 | 4,664,873 | 5,505 |
ENST00000587649.1 | hg19 | chr16 | 4,659,722 | 4,664,874 | 5,153 |
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