MRPL11 mitochondrial ribosomal protein L11
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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26 |
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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
[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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 |
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | CGI-113 |
SYNONYM | L11MT |
SYNONYM | MRP-L11 |
SYNONYM | uL11m |
MIM | 611826 OMIM |
HGNC | HGNC:14042 HGNC |
Ensembl | ENSG00000174547 Ensembl |
AllianceGenome | HGNC:14042 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000310999.11 | hg38 | chr11 | 66,435,075 | 66,438,848 | 3,774 |
ENST00000329819.4 | hg38 | chr11 | 66,435,838 | 66,438,834 | 2,997 |
ENST00000430466.6 | hg38 | chr11 | 66,435,075 | 66,438,848 | 3,774 |
ENST00000310999.11 | hg19 | chr11 | 66,202,546 | 66,206,319 | 3,774 |
ENST00000430466.6 | hg19 | chr11 | 66,202,546 | 66,206,319 | 3,774 |
ENST00000329819.4 | hg19 | chr11 | 66,203,309 | 66,206,305 | 2,997 |
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