RBMXL3 RBMX like 3
Information
- Symbol
- RBMXL3
- Type
- protein-coding
- Description
- RBMX like 3
- Entrez Gene ID
- 139804
- Genome
- hg19
- Position
- chrX:114,423,973-114,427,431
- Genome
- hg38
- Position
- chrX:115,189,410-115,192,868
- HGNC
- HGNC:26859 HGNC
- Ensembl
- ENSG00000175718 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 42 |
Conflicting classifications of pathogenicity | 0 | 6 |
not provided | 7 | 0 |
Uncertain significance | 0 | 244 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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286 |
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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
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 | |||||
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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 | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | CXorf55 |
HGNC | HGNC:26859 HGNC |
Ensembl | ENSG00000175718 Ensembl |
AllianceGenome | HGNC:26859 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000424776.5 | hg38 | chrX | 115,189,410 | 115,192,868 | 3,459 |
ENST00000424776.5 | hg19 | chrX | 114,423,973 | 114,427,431 | 3,459 |
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