CIAO2B cytosolic iron-sulfur assembly component 2B
Information
- Symbol
- CIAO2B
- Type
- protein-coding
- Description
- cytosolic iron-sulfur assembly component 2B
- Entrez Gene ID
- 51647
- Genome
- hg19
- Position
- chr16:66,965,968-66,968,305
- Genome
- hg38
- Position
- chr16:66,932,065-66,934,402
- MIM
- 614778 OMIM
- HGNC
- HGNC:24261 HGNC
- Ensembl
- ENSG00000166595 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 14 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
16 |
 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | CGI-128 |
| SYNONYM | CIA2B |
| SYNONYM | FAM96B |
| SYNONYM | MIP18 |
| MIM | 614778 OMIM |
| HGNC | HGNC:24261 HGNC |
| Ensembl | ENSG00000166595 Ensembl |
| AllianceGenome | HGNC:24261 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000422424.7 | hg38 | chr16 | 66,932,065 | 66,934,402 | 2,338 |
| ENST00000422424.7 | hg19 | chr16 | 66,965,968 | 66,968,305 | 2,338 |
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