NUBP1 NUBP iron-sulfur cluster assembly factor 1, cytosolic
Information
- Symbol
- NUBP1
- Type
- protein-coding
- Description
- NUBP iron-sulfur cluster assembly factor 1, cytosolic
- Entrez Gene ID
- 4682
- Genome
- hg19
- Position
- chr16:10,837,699-10,863,208
- Genome
- hg38
- Position
- chr16:10,743,842-10,769,351
- MIM
- 600280 OMIM
- HGNC
- HGNC:8041 HGNC
- Ensembl
- ENSG00000103274 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 58 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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64 |
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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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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 | CIAO5 |
SYNONYM | NBP |
SYNONYM | NBP1 |
SYNONYM | NBP35 |
MIM | 600280 OMIM |
HGNC | HGNC:8041 HGNC |
Ensembl | ENSG00000103274 Ensembl |
AllianceGenome | HGNC:8041 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000433392.6 | hg38 | chr16 | 10,743,855 | 10,769,351 | 25,497 |
ENST00000283027.10 | hg38 | chr16 | 10,743,842 | 10,769,351 | 25,510 |
ENST00000283027.10 | hg19 | chr16 | 10,837,699 | 10,863,208 | 25,510 |
ENST00000433392.6 | hg19 | chr16 | 10,837,712 | 10,863,208 | 25,497 |
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