PABPN1L PABPN1 like, cytoplasmic
Information
- Symbol
- PABPN1L
- Type
- protein-coding
- Description
- PABPN1 like, cytoplasmic
- Entrez Gene ID
- 390748
- Genome
- hg19
- Position
- chr16:88,929,741-88,933,068
- Genome
- hg38
- Position
- chr16:88,863,333-88,866,660
- HGNC
- HGNC:37237 HGNC
- Ensembl
- ENSG00000205022 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 68 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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70 |
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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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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 |
Type | ID |
---|---|
SYNONYM | PABPNL1 |
SYNONYM | ePABP2 |
HGNC | HGNC:37237 HGNC |
Ensembl | ENSG00000205022 Ensembl |
AllianceGenome | HGNC:37237 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000411789.6 | hg38 | chr16 | 88,863,686 | 88,866,660 | 2,975 |
ENST00000419291.7 | hg38 | chr16 | 88,863,333 | 88,866,660 | 3,328 |
ENST00000419291.7 | hg19 | chr16 | 88,929,741 | 88,933,068 | 3,328 |
ENST00000411789.6 | hg19 | chr16 | 88,930,094 | 88,933,068 | 2,975 |
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