PAPPA-AS1 PAPPA antisense RNA 1
Clinical Significance
MGeND | ClinVar | |
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Likely pathogenic | 1 | 0 |
Ranking
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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
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 | DIPAS |
SYNONYM | NCRNA00156 |
SYNONYM | PAPPA-AS |
SYNONYM | PAPPAAS |
SYNONYM | PAPPAS |
SYNONYM | TAF2C2 |
SYNONYM | TAF4B |
SYNONYM | TAFII105 |
MIM | 610689 OMIM |
HGNC | HGNC:35152 HGNC |
Ensembl | ENSG00000256040 Ensembl |
AllianceGenome | HGNC:35152 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000445861.3 | hg38 | chr9 | 116,398,157 | 116,400,606 | 2,450 |
ENST00000445861.3 | hg19 | chr9 | 119,160,436 | 119,162,885 | 2,450 |
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