RBM4B RNA binding motif protein 4B
Information
- Symbol
- RBM4B
- Type
- protein-coding
- Description
- RNA binding motif protein 4B
- Entrez Gene ID
- 83759
- Genome
- hg19
- Position
- chr11:66,432,469-66,445,219
- Genome
- hg38
- Position
- chr11:66,664,998-66,677,748
- HGNC
- HGNC:28842 HGNC
- Ensembl
- ENSG00000173914 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 56 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
58 |
 |
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 | RBM30 |
| SYNONYM | RBM4L |
| SYNONYM | ZCCHC15 |
| SYNONYM | ZCCHC21B |
| SYNONYM | ZCRB3B |
| HGNC | HGNC:28842 HGNC |
| Ensembl | ENSG00000173914 Ensembl |
| AllianceGenome | HGNC:28842 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000531969.5 | hg38 | chr11 | 66,665,295 | 66,677,824 | 12,530 |
| ENST00000531036.2 | hg38 | chr11 | 66,675,560 | 66,677,877 | 2,318 |
| ENST00000525754.5 | hg38 | chr11 | 66,664,998 | 66,677,748 | 12,751 |
| ENST00000310046.9 | hg38 | chr11 | 66,664,998 | 66,677,887 | 12,890 |
| ENST00000524637.1 | hg38 | chr11 | 66,668,971 | 66,677,837 | 8,867 |
| ENST00000525754.5 | hg19 | chr11 | 66,432,469 | 66,445,219 | 12,751 |
| ENST00000310046.9 | hg19 | chr11 | 66,432,469 | 66,445,358 | 12,890 |
| ENST00000531969.5 | hg19 | chr11 | 66,432,766 | 66,445,295 | 12,530 |
| ENST00000524637.1 | hg19 | chr11 | 66,436,442 | 66,445,308 | 8,867 |
| ENST00000531036.2 | hg19 | chr11 | 66,443,031 | 66,445,348 | 2,318 |
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