RBMX RNA binding motif protein X-linked
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 2 |
| Likely pathogenic | 0 | 2 |
| Benign | 0 | 4 |
| Likely benign | 0 | 8 |
| not provided | 6 | 6 |
| Uncertain significance | 0 | 34 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
48 |
 |
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
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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| 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 | HNRNPG |
| SYNONYM | HNRPG |
| SYNONYM | MRXS11 |
| SYNONYM | MRXSG |
| SYNONYM | MRXSH |
| SYNONYM | RBMXP1 |
| SYNONYM | RBMXRT |
| SYNONYM | RNMX |
| SYNONYM | hnRNP-G |
| MIM | 300199 OMIM |
| HGNC | HGNC:9910 HGNC |
| Ensembl | ENSG00000147274 Ensembl |
| AllianceGenome | HGNC:9910 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000320676.11 | hg38 | chrX | 136,873,461 | 136,880,725 | 7,265 |
| ENST00000565438.1 | hg38 | chrX | 136,873,978 | 136,880,764 | 6,787 |
| ENST00000431446.7 | hg38 | chrX | 136,869,187 | 136,880,725 | 11,539 |
| ENST00000562646.5 | hg38 | chrX | 136,873,958 | 136,880,725 | 6,768 |
| ENST00000431446.7 | hg19 | chrX | 135,951,346 | 135,962,884 | 11,539 |
| ENST00000320676.11 | hg19 | chrX | 135,955,620 | 135,962,884 | 7,265 |
| ENST00000562646.5 | hg19 | chrX | 135,956,117 | 135,962,884 | 6,768 |
| ENST00000565438.1 | hg19 | chrX | 135,956,137 | 135,962,923 | 6,787 |
| Key | Value |
|---|---|
| strand | - |
| UniProt | TSG |
| start | 135,951,352 |
| Gene Symbol | RBMX |
| Entrez GeneId | 27,316 |
| Chr Band | Xq26.3 |
| end | 135,962,938 |
| chr | chrX |
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