ERICH2 glutamate rich 2
Information
- Symbol
- ERICH2
- Type
- protein-coding
- Description
- glutamate rich 2
- Entrez Gene ID
- 285141
- Genome
- hg19
- Position
- chr2:171,626,888-171,655,487
- Genome
- hg38
- Position
- chr2:170,770,378-170,798,977
- HGNC
- HGNC:44395 HGNC
- Ensembl
- ENSG00000204334 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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2 |
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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000689478.1 | hg38 | chr2 | 170,770,978 | 170,778,109 | 7,132 |
ENST00000697325.1 | hg38 | chr2 | 170,770,378 | 170,798,977 | 28,600 |
ENST00000688829.1 | hg38 | chr2 | 170,770,937 | 170,778,113 | 7,177 |
ENST00000697344.1 | hg38 | chr2 | 170,771,008 | 170,798,977 | 27,970 |
ENST00000409885.1 | hg38 | chr2 | 170,783,786 | 170,798,971 | 15,186 |
ENST00000653024.2 | hg38 | chr2 | 170,770,977 | 170,778,584 | 7,608 |
ENST00000664870.2 | hg38 | chr2 | 170,770,935 | 170,778,729 | 7,795 |
ENST00000653024.2 | hg19 | chr2 | 171,627,487 | 171,635,094 | 7,608 |
ENST00000409885.1 | hg19 | chr2 | 171,640,296 | 171,655,481 | 15,186 |
ENST00000664870.2 | hg19 | chr2 | 171,627,445 | 171,635,239 | 7,795 |
ENST00000688829.1 | hg19 | chr2 | 171,627,447 | 171,634,623 | 7,177 |
ENST00000689478.1 | hg19 | chr2 | 171,627,488 | 171,634,619 | 7,132 |
ENST00000697344.1 | hg19 | chr2 | 171,627,518 | 171,655,487 | 27,970 |
ENST00000697325.1 | hg19 | chr2 | 171,626,888 | 171,655,487 | 28,600 |
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