PAN2 poly(A) specific ribonuclease subunit PAN2
Information
- Symbol
- PAN2
- Type
- protein-coding
- Description
- poly(A) specific ribonuclease subunit PAN2
- Entrez Gene ID
- 9924
- Genome
- hg19
- Position
- chr12:56,710,731-56,727,527
- Genome
- hg38
- Position
- chr12:56,316,947-56,333,743
- MIM
- 617447 OMIM
- HGNC
- HGNC:20074 HGNC
- Ensembl
- ENSG00000135473 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely pathogenic | 0 | 6 |
| Benign | 0 | 4 |
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 124 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
130 |
 |
6 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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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
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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 | USP52 |
| MIM | 617447 OMIM |
| HGNC | HGNC:20074 HGNC |
| Ensembl | ENSG00000135473 Ensembl |
| AllianceGenome | HGNC:20074 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000425394.7 | hg38 | chr12 | 56,316,947 | 56,333,693 | 16,747 |
| ENST00000610546.4 | hg38 | chr12 | 56,316,223 | 56,334,053 | 17,831 |
| ENST00000440411.8 | hg38 | chr12 | 56,316,936 | 56,334,000 | 17,065 |
| ENST00000548043.5 | hg38 | chr12 | 56,316,947 | 56,333,743 | 16,797 |
| ENST00000257931.9 | hg38 | chr12 | 56,316,937 | 56,334,006 | 17,070 |
| ENST00000440411.8 | hg19 | chr12 | 56,710,720 | 56,727,784 | 17,065 |
| ENST00000257931.9 | hg19 | chr12 | 56,710,721 | 56,727,790 | 17,070 |
| ENST00000425394.7 | hg19 | chr12 | 56,710,731 | 56,727,477 | 16,747 |
| ENST00000548043.5 | hg19 | chr12 | 56,710,731 | 56,727,527 | 16,797 |
| ENST00000610546.4 | hg19 | chr12 | 56,710,007 | 56,727,837 | 17,831 |
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