NUB1 negative regulator of ubiquitin like proteins 1
Information
- Symbol
- NUB1
- Type
- protein-coding
- Description
- negative regulator of ubiquitin like proteins 1
- Entrez Gene ID
- 51667
- Genome
- hg19
- Position
- chr7:151,038,898-151,075,517
- Genome
- hg38
- Position
- chr7:151,341,812-151,378,431
- MIM
- 607981 OMIM
- HGNC
- HGNC:17623 HGNC
- Ensembl
- ENSG00000013374 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 4 |
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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20 |
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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
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 |
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Target data | : |
MGeND data only
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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 | BS4 |
SYNONYM | NUB1L |
SYNONYM | NYREN18 |
MIM | 607981 OMIM |
HGNC | HGNC:17623 HGNC |
Ensembl | ENSG00000013374 Ensembl |
AllianceGenome | HGNC:17623 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000470229.6 | hg38 | chr7 | 151,341,812 | 151,378,431 | 36,620 |
ENST00000568733.6 | hg38 | chr7 | 151,341,812 | 151,378,449 | 36,638 |
ENST00000413040.7 | hg38 | chr7 | 151,341,772 | 151,378,449 | 36,678 |
ENST00000413040.7 | hg19 | chr7 | 151,038,858 | 151,075,535 | 36,678 |
ENST00000470229.6 | hg19 | chr7 | 151,038,898 | 151,075,517 | 36,620 |
ENST00000568733.6 | hg19 | chr7 | 151,038,898 | 151,075,535 | 36,638 |
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