YPEL2 yippee like 2
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 2 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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2 |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
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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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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 | FKSG4 |
MIM | 609723 OMIM |
HGNC | HGNC:18326 HGNC |
Ensembl | ENSG00000175155 Ensembl |
AllianceGenome | HGNC:18326 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000585166.1 | hg38 | chr17 | 59,345,156 | 59,397,376 | 52,221 |
ENST00000312655.9 | hg38 | chr17 | 59,331,655 | 59,401,729 | 70,075 |
ENST00000672916.2 | hg38 | chr17 | 59,353,311 | 59,397,190 | 43,880 |
ENST00000312655.9 | hg19 | chr17 | 57,409,016 | 57,479,090 | 70,075 |
ENST00000585166.1 | hg19 | chr17 | 57,422,517 | 57,474,737 | 52,221 |
ENST00000672916.2 | hg19 | chr17 | 57,430,672 | 57,474,551 | 43,880 |
Key | Value |
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strand | + |
start | 57,409,052 |
Gene Symbol | YPEL2 |
Entrez GeneId | 388,403 |
Chr Band | 17q22 |
end | 57,479,094 |
chr | chr17 |
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