PAF1 PAF1 homolog, Paf1/RNA polymerase II complex component
Information
- Symbol
- PAF1
- Type
- protein-coding
- Description
- PAF1 homolog, Paf1/RNA polymerase II complex component
- Entrez Gene ID
- 54623
- Genome
- hg19
- Position
- chr19:39,876,269-39,881,746
- Genome
- hg38
- Position
- chr19:39,385,629-39,391,106
- MIM
- 610506 OMIM
- HGNC
- HGNC:25459 HGNC
- Ensembl
- ENSG00000006712 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 14 |
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 38 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
52 |
 |
2 |
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
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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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| 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 | F23149_1 |
| SYNONYM | PD2 |
| MIM | 610506 OMIM |
| HGNC | HGNC:25459 HGNC |
| Ensembl | ENSG00000006712 Ensembl |
| AllianceGenome | HGNC:25459 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000221265.8 | hg38 | chr19 | 39,385,629 | 39,391,106 | 5,478 |
| ENST00000595564.5 | hg38 | chr19 | 39,385,853 | 39,391,154 | 5,302 |
| ENST00000221265.8 | hg19 | chr19 | 39,876,269 | 39,881,746 | 5,478 |
| ENST00000595564.5 | hg19 | chr19 | 39,876,493 | 39,881,794 | 5,302 |
| Key | Value |
|---|---|
| strand | - |
| UniProt | TSG |
| start | 39,876,269 |
| Gene Symbol | PAF1 |
| Entrez GeneId | 54,623 |
| Chr Band | 19q13.1 |
| end | 39,881,834 |
| chr | chr19 |
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