MKRN1 makorin ring finger protein 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 2 | 0 |
Uncertain significance | 0 | 40 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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42 |
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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 |
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SYNONYM | RNF61 |
MIM | 607754 OMIM |
HGNC | HGNC:7112 HGNC |
Ensembl | ENSG00000133606 Ensembl |
AllianceGenome | HGNC:7112 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000255977.7 | hg38 | chr7 | 140,453,033 | 140,479,505 | 26,473 |
ENST00000474576.5 | hg38 | chr7 | 140,454,268 | 140,478,984 | 24,717 |
ENST00000480552.5 | hg38 | chr7 | 140,456,180 | 140,478,926 | 22,747 |
ENST00000443720.6 | hg38 | chr7 | 140,456,192 | 140,479,499 | 23,308 |
ENST00000255977.7 | hg19 | chr7 | 140,152,833 | 140,179,305 | 26,473 |
ENST00000474576.5 | hg19 | chr7 | 140,154,068 | 140,178,784 | 24,717 |
ENST00000480552.5 | hg19 | chr7 | 140,155,980 | 140,178,726 | 22,747 |
ENST00000443720.6 | hg19 | chr7 | 140,155,992 | 140,179,299 | 23,308 |
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