ISCU iron-sulfur cluster assembly enzyme
Information
- Symbol
- ISCU
- Type
- protein-coding
- Description
- iron-sulfur cluster assembly enzyme
- Entrez Gene ID
- 23479
- Genome
- hg19
- Position
- chr12:108,956,372-108,963,144
- Genome
- hg38
- Position
- chr12:108,562,596-108,569,368
- MIM
- 611911 OMIM
- HGNC
- HGNC:29882 HGNC
- Ensembl
- ENSG00000136003 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 2 |
Likely pathogenic | 0 | 2 |
Benign | 0 | 66 |
Likely benign | 0 | 132 |
Conflicting classifications of pathogenicity | 0 | 2 |
Uncertain significance | 0 | 100 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
![]() |
64 |
![]() |
232 |
![]() |
2 |
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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Category | : |
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Filtering | : |
Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
|
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 | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | 2310020H20Rik |
SYNONYM | HML |
SYNONYM | ISU2 |
SYNONYM | NIFU |
SYNONYM | NIFUN |
SYNONYM | hnifU |
MIM | 611911 OMIM |
HGNC | HGNC:29882 HGNC |
Ensembl | ENSG00000136003 Ensembl |
AllianceGenome | HGNC:29882 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000535729.5 | hg38 | chr12 | 108,562,601 | 108,568,547 | 5,947 |
ENST00000431221.6 | hg38 | chr12 | 108,562,601 | 108,569,092 | 6,492 |
ENST00000547005.5 | hg38 | chr12 | 108,562,601 | 108,569,099 | 6,499 |
ENST00000392807.8 | hg38 | chr12 | 108,562,606 | 108,569,368 | 6,763 |
ENST00000311893.14 | hg38 | chr12 | 108,562,596 | 108,569,368 | 6,773 |
ENST00000539593.1 | hg38 | chr12 | 108,562,610 | 108,567,908 | 5,299 |
ENST00000311893.14 | hg19 | chr12 | 108,956,372 | 108,963,144 | 6,773 |
ENST00000535729.5 | hg19 | chr12 | 108,956,377 | 108,962,323 | 5,947 |
ENST00000431221.6 | hg19 | chr12 | 108,956,377 | 108,962,868 | 6,492 |
ENST00000547005.5 | hg19 | chr12 | 108,956,377 | 108,962,875 | 6,499 |
ENST00000392807.8 | hg19 | chr12 | 108,956,382 | 108,963,144 | 6,763 |
ENST00000539593.1 | hg19 | chr12 | 108,956,386 | 108,961,684 | 5,299 |
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