APEX2 apurinic/apyrimidinic endodeoxyribonuclease 2
Information
- Symbol
- APEX2
- Type
- protein-coding
- Description
- apurinic/apyrimidinic endodeoxyribonuclease 2
- Entrez Gene ID
- 27301
- Genome
- hg19
- Position
- chrX:55,026,796-55,035,490
- Genome
- hg38
- Position
- chrX:55,000,363-55,009,057
- MIM
- 300773 OMIM
- HGNC
- HGNC:17889 HGNC
- Ensembl
- ENSG00000169188 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 8 |
Likely benign | 0 | 18 |
not provided | 6 | 0 |
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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52 |
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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
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | APE2 |
SYNONYM | APEXL2 |
SYNONYM | XTH2 |
SYNONYM | ZGRF2 |
MIM | 300773 OMIM |
HGNC | HGNC:17889 HGNC |
Ensembl | ENSG00000169188 Ensembl |
AllianceGenome | HGNC:17889 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000374987.4 | hg38 | chrX | 55,000,363 | 55,009,057 | 8,695 |
ENST00000374987.4 | hg19 | chrX | 55,026,796 | 55,035,490 | 8,695 |
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