PATL1 PAT1 homolog 1, processing body mRNA decay factor
Information
- Symbol
- PATL1
- Type
- protein-coding
- Description
- PAT1 homolog 1, processing body mRNA decay factor
- Entrez Gene ID
- 219988
- Genome
- hg19
- Position
- chr11:59,404,189-59,436,510
- Genome
- hg38
- Position
- chr11:59,636,716-59,669,037
- MIM
- 614660 OMIM
- HGNC
- HGNC:26721 HGNC
- Ensembl
- ENSG00000166889 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 8 |
Likely benign | 0 | 10 |
Uncertain significance | 0 | 56 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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74 |
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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 | Pat1b |
SYNONYM | hPat1b |
MIM | 614660 OMIM |
HGNC | HGNC:26721 HGNC |
Ensembl | ENSG00000166889 Ensembl |
AllianceGenome | HGNC:26721 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000300146.10 | hg38 | chr11 | 59,636,716 | 59,669,037 | 32,322 |
ENST00000300146.10 | hg19 | chr11 | 59,404,189 | 59,436,510 | 32,322 |
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