ORC5 origin recognition complex subunit 5
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 38 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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38 |
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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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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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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 | ORC5L |
SYNONYM | ORC5P |
SYNONYM | ORC5T |
SYNONYM | PPP1R117 |
MIM | 602331 OMIM |
HGNC | HGNC:8491 HGNC |
Ensembl | ENSG00000164815 Ensembl |
AllianceGenome | HGNC:8491 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000447452.6 | hg38 | chr7 | 104,167,994 | 104,207,957 | 39,964 |
ENST00000297431.9 | hg38 | chr7 | 104,126,341 | 104,208,013 | 81,673 |
ENST00000626700.1 | hg38 | chr7 | 104,202,509 | 104,208,047 | 5,539 |
ENST00000297431.9 | hg19 | chr7 | 103,766,788 | 103,848,461 | 81,674 |
ENST00000447452.6 | hg19 | chr7 | 103,808,442 | 103,848,405 | 39,964 |
ENST00000626700.1 | hg19 | chr7 | 103,842,957 | 103,848,495 | 5,539 |
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