ZIM2 zinc finger imprinted 2
Information
- Symbol
- ZIM2
- Type
- protein-coding
- Description
- zinc finger imprinted 2
- Entrez Gene ID
- 23619
- Genome
- hg19
- Position
- chr19:57,285,915-57,352,094
- Genome
- hg38
- Position
- chr19:56,774,547-56,840,726
- HGNC
- HGNC:12875 HGNC
- Ensembl
- ENSG00000269699 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 42 |
Likely benign | 0 | 64 |
Uncertain significance | 0 | 190 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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10 |
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280 |
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2 |
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 |
---|---|
SYNONYM | ZNF656 |
HGNC | HGNC:12875 HGNC |
Ensembl | ENSG00000269699 Ensembl |
AllianceGenome | HGNC:12875 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000593931.1 | hg38 | chr19 | 56,822,497 | 56,824,314 | 1,818 |
ENST00000715564.1 | hg38 | chr19 | 56,774,594 | 56,795,511 | 20,918 |
ENST00000629319.3 | hg38 | chr19 | 56,774,547 | 56,840,726 | 66,180 |
ENST00000599935.5 | hg38 | chr19 | 56,774,594 | 56,840,729 | 66,136 |
ENST00000601070.5 | hg38 | chr19 | 56,774,594 | 56,836,078 | 61,485 |
ENST00000689654.1 | hg38 | chr19 | 56,774,547 | 56,840,726 | 66,180 |
ENST00000593711.6 | hg38 | chr19 | 56,774,547 | 56,840,726 | 66,180 |
ENST00000593711.6 | hg19 | chr19 | 57,285,915 | 57,352,094 | 66,180 |
ENST00000629319.3 | hg19 | chr19 | 57,285,915 | 57,352,094 | 66,180 |
ENST00000689654.1 | hg19 | chr19 | 57,285,915 | 57,352,094 | 66,180 |
ENST00000715564.1 | hg19 | chr19 | 57,285,962 | 57,306,879 | 20,918 |
ENST00000601070.5 | hg19 | chr19 | 57,285,962 | 57,347,446 | 61,485 |
ENST00000599935.5 | hg19 | chr19 | 57,285,962 | 57,352,097 | 66,136 |
ENST00000593931.1 | hg19 | chr19 | 57,333,865 | 57,335,682 | 1,818 |
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