NFRKB nuclear factor related to kappaB binding protein
Information
- Symbol
- NFRKB
- Type
- protein-coding
- Description
- nuclear factor related to kappaB binding protein
- Entrez Gene ID
- 4798
- Genome
- hg19
- Position
- chr11:129,734,365-129,762,904
- Genome
- hg38
- Position
- chr11:129,864,470-129,893,009
- MIM
- 164013 OMIM
- HGNC
- HGNC:7802 HGNC
- Ensembl
- ENSG00000170322 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 12 |
| Conflicting classifications of pathogenicity | 0 | 2 |
| Uncertain significance | 0 | 124 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
136 |
 |
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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| 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
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | INO80G |
| MIM | 164013 OMIM |
| HGNC | HGNC:7802 HGNC |
| Ensembl | ENSG00000170322 Ensembl |
| AllianceGenome | HGNC:7802 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000526940.1 | hg38 | chr11 | 129,888,313 | 129,892,876 | 4,564 |
| ENST00000524794.5 | hg38 | chr11 | 129,864,470 | 129,893,009 | 28,540 |
| ENST00000682444.1 | hg38 | chr11 | 129,863,636 | 129,895,578 | 31,943 |
| ENST00000524746.5 | hg38 | chr11 | 129,864,704 | 129,894,441 | 29,738 |
| ENST00000446488.7 | hg38 | chr11 | 129,863,636 | 129,894,441 | 30,806 |
| ENST00000446488.7 | hg19 | chr11 | 129,733,531 | 129,764,336 | 30,806 |
| ENST00000682444.1 | hg19 | chr11 | 129,733,531 | 129,765,473 | 31,943 |
| ENST00000524794.5 | hg19 | chr11 | 129,734,365 | 129,762,904 | 28,540 |
| ENST00000524746.5 | hg19 | chr11 | 129,734,599 | 129,764,336 | 29,738 |
| ENST00000526940.1 | hg19 | chr11 | 129,758,208 | 129,762,771 | 4,564 |
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