PCIF1 phosphorylated CTD interacting factor 1
Information
- Symbol
- PCIF1
- Type
- protein-coding
- Description
- phosphorylated CTD interacting factor 1
- Entrez Gene ID
- 63935
- Genome
- hg19
- Position
- chr20:44,563,322-44,576,659
- Genome
- hg38
- Position
- chr20:45,934,683-45,948,020
- MIM
- 618626 OMIM
- HGNC
- HGNC:16200 HGNC
- Ensembl
- ENSG00000100982 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| not provided | 1 | 0 |
| Uncertain significance | 0 | 72 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
72 |
 |
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
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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| 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 | C20orf67 |
| SYNONYM | CAPAM |
| SYNONYM | MT-A70 |
| SYNONYM | PPP1R121 |
| SYNONYM | hCAPAM |
| SYNONYM | hPCIF1 |
| MIM | 618626 OMIM |
| HGNC | HGNC:16200 HGNC |
| Ensembl | ENSG00000100982 Ensembl |
| AllianceGenome | HGNC:16200 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000372409.8 | hg38 | chr20 | 45,934,683 | 45,948,020 | 13,338 |
| ENST00000372409.8 | hg19 | chr20 | 44,563,322 | 44,576,659 | 13,338 |
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