ZNF177 zinc finger protein 177
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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20 |
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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
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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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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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Target data | : |
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 | PIGX |
MIM | 601276 OMIM |
HGNC | HGNC:12966 HGNC |
Ensembl | ENSG00000188629 Ensembl |
AllianceGenome | HGNC:12966 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000683217.1 | hg38 | chr19 | 9,363,013 | 9,382,617 | 19,605 |
ENST00000589262.5 | hg38 | chr19 | 9,376,411 | 9,382,185 | 5,775 |
ENST00000343499.8 | hg38 | chr19 | 9,363,020 | 9,382,190 | 19,171 |
ENST00000590616.2 | hg38 | chr19 | 9,378,269 | 9,382,617 | 4,349 |
ENST00000683217.1 | hg19 | chr19 | 9,473,689 | 9,493,293 | 19,605 |
ENST00000343499.8 | hg19 | chr19 | 9,473,696 | 9,492,866 | 19,171 |
ENST00000589262.5 | hg19 | chr19 | 9,487,087 | 9,492,861 | 5,775 |
ENST00000590616.2 | hg19 | chr19 | 9,488,945 | 9,493,293 | 4,349 |
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