ZNF85 zinc finger protein 85
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 92 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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92 |
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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 |
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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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 | HPF4 |
SYNONYM | HTF1 |
MIM | 603899 OMIM |
HGNC | HGNC:13160 HGNC |
Ensembl | ENSG00000105750 Ensembl |
AllianceGenome | HGNC:13160 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000300540.7 | hg38 | chr19 | 20,923,276 | 20,943,977 | 20,702 |
ENST00000328178.13 | hg38 | chr19 | 20,923,251 | 20,950,697 | 27,447 |
ENST00000596476.1 | hg38 | chr19 | 20,923,310 | 20,943,726 | 20,417 |
ENST00000597314.5 | hg38 | chr19 | 20,923,222 | 20,948,915 | 25,694 |
ENST00000345030.6 | hg38 | chr19 | 20,923,401 | 20,950,302 | 26,902 |
ENST00000597314.5 | hg19 | chr19 | 21,106,028 | 21,131,721 | 25,694 |
ENST00000328178.13 | hg19 | chr19 | 21,106,057 | 21,133,503 | 27,447 |
ENST00000300540.7 | hg19 | chr19 | 21,106,082 | 21,126,783 | 20,702 |
ENST00000596476.1 | hg19 | chr19 | 21,106,116 | 21,126,532 | 20,417 |
ENST00000345030.6 | hg19 | chr19 | 21,106,207 | 21,133,108 | 26,902 |
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