NPIPA2 nuclear pore complex interacting protein family member A2
Information
- Symbol
- NPIPA2
- Type
- protein-coding
- Description
- nuclear pore complex interacting protein family member A2
- Entrez Gene ID
- 642799
- Genome
- hg19
- Position
- chr16:14,836,390-14,859,319
- Genome
- hg38
- Position
- chr16:14,742,533-14,765,462
- HGNC
- HGNC:41979 HGNC
- Ensembl
- ENSG00000254852 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| not provided | 1 | 0 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
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0 |
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0 |
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0 |
 |
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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| 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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| 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
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | NPIP |
| SYNONYM | NPIPA1 |
| HGNC | HGNC:41979 HGNC |
| Ensembl | ENSG00000254852 Ensembl |
| AllianceGenome | HGNC:41979 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000530328.5 | hg38 | chr16 | 14,748,066 | 14,763,898 | 15,833 |
| ENST00000553201.1 | hg38 | chr16 | 14,750,813 | 14,765,413 | 14,601 |
| ENST00000529166.6 | hg38 | chr16 | 14,742,533 | 14,765,462 | 22,930 |
| ENST00000529166.6 | hg19 | chr16 | 14,836,390 | 14,859,319 | 22,930 |
| ENST00000530328.5 | hg19 | chr16 | 14,841,923 | 14,857,755 | 15,833 |
| ENST00000553201.1 | hg19 | chr16 | 14,844,670 | 14,859,270 | 14,601 |
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