CPSF6 cleavage and polyadenylation specific factor 6
Information
- Symbol
- CPSF6
- Type
- protein-coding
- Description
- cleavage and polyadenylation specific factor 6
- Entrez Gene ID
- 11052
- Genome
- hg19
- Position
- chr12:69,633,396-69,663,719
- Genome
- hg38
- Position
- chr12:69,239,616-69,269,939
- MIM
- 604979 OMIM
- HGNC
- HGNC:13871 HGNC
- Ensembl
- ENSG00000111605 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 40 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
40 |
 |
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
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| 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
|
| Category | : |
|
| 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
|
| Category | : |
|
| 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 | CFIM |
| SYNONYM | CFIM68 |
| SYNONYM | CFIM72 |
| SYNONYM | HPBRII-4 |
| SYNONYM | HPBRII-7 |
| MIM | 604979 OMIM |
| HGNC | HGNC:13871 HGNC |
| Ensembl | ENSG00000111605 Ensembl |
| AllianceGenome | HGNC:13871 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000266679.8 | hg38 | chr12 | 69,239,616 | 69,269,939 | 30,324 |
| ENST00000551516.1 | hg38 | chr12 | 69,239,642 | 69,269,573 | 29,932 |
| ENST00000435070.7 | hg38 | chr12 | 69,239,569 | 69,274,358 | 34,790 |
| ENST00000456847.7 | hg38 | chr12 | 69,239,600 | 69,269,939 | 30,340 |
| ENST00000435070.7 | hg19 | chr12 | 69,633,349 | 69,668,138 | 34,790 |
| ENST00000456847.7 | hg19 | chr12 | 69,633,380 | 69,663,719 | 30,340 |
| ENST00000266679.8 | hg19 | chr12 | 69,633,396 | 69,663,719 | 30,324 |
| ENST00000551516.1 | hg19 | chr12 | 69,633,422 | 69,663,353 | 29,932 |
Genome browser