ANP32A acidic nuclear phosphoprotein 32 family member A
Information
- Symbol
- ANP32A
- Type
- protein-coding
- Description
- acidic nuclear phosphoprotein 32 family member A
- Entrez Gene ID
- 8125
- Genome
- hg19
- Position
- chr15:69,070,874-69,113,234
- Genome
- hg38
- Position
- chr15:68,778,535-68,820,895
- MIM
- 600832 OMIM
- HGNC
- HGNC:13233 HGNC
- Ensembl
- ENSG00000140350 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Uncertain significance | 0 | 10 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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14 |
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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 |
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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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | C15orf1 |
SYNONYM | HPPCn |
SYNONYM | I1PP2A |
SYNONYM | LANP |
SYNONYM | MAPM |
SYNONYM | PHAP1 |
SYNONYM | PHAPI |
SYNONYM | PP32 |
MIM | 600832 OMIM |
HGNC | HGNC:13233 HGNC |
Ensembl | ENSG00000140350 Ensembl |
AllianceGenome | HGNC:13233 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000560303.1 | hg38 | chr15 | 68,780,420 | 68,820,886 | 40,467 |
ENST00000465139.6 | hg38 | chr15 | 68,778,535 | 68,820,895 | 42,361 |
ENST00000465139.6 | hg19 | chr15 | 69,070,874 | 69,113,234 | 42,361 |
ENST00000560303.1 | hg19 | chr15 | 69,072,759 | 69,113,225 | 40,467 |
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