ZNF664 zinc finger protein 664
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 8 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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10 |
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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
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 |
Search Word
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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Search word | : | |
Filtering | : |
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 | ZFOC1 |
SYNONYM | ZNF176 |
MIM | 617890 OMIM |
HGNC | HGNC:25406 HGNC |
Ensembl | ENSG00000179195 Ensembl |
AllianceGenome | HGNC:25406 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000392404.7 | hg38 | chr12 | 123,973,212 | 124,015,426 | 42,215 |
ENST00000337815.9 | hg38 | chr12 | 123,973,215 | 124,015,427 | 42,213 |
ENST00000539644.5 | hg38 | chr12 | 123,973,123 | 124,015,422 | 42,300 |
ENST00000538932.6 | hg38 | chr12 | 123,973,215 | 124,015,439 | 42,225 |
ENST00000539644.5 | hg19 | chr12 | 124,457,670 | 124,499,969 | 42,300 |
ENST00000392404.7 | hg19 | chr12 | 124,457,759 | 124,499,973 | 42,215 |
ENST00000337815.9 | hg19 | chr12 | 124,457,762 | 124,499,974 | 42,213 |
ENST00000538932.6 | hg19 | chr12 | 124,457,762 | 124,499,986 | 42,225 |
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