PCGEM1 PCGEM1 prostate-specific transcript
Information
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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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
[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 | LINC00071 |
SYNONYM | NCRNA00071 |
SYNONYM | PCAT9 |
MIM | 605443 OMIM |
HGNC | HGNC:30145 HGNC |
Ensembl | ENSG00000227418 Ensembl |
AllianceGenome | HGNC:30145 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000454040.5 | hg38 | chr2 | 192,749,845 | 192,776,899 | 27,055 |
ENST00000606314.1 | hg38 | chr2 | 192,749,967 | 192,776,068 | 26,102 |
ENST00000454040.5 | hg19 | chr2 | 193,614,571 | 193,641,625 | 27,055 |
ENST00000606314.1 | hg19 | chr2 | 193,614,693 | 193,640,794 | 26,102 |
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