PPP1R14B protein phosphatase 1 regulatory inhibitor subunit 14B
Information
- Symbol
- PPP1R14B
- Type
- protein-coding
- Description
- protein phosphatase 1 regulatory inhibitor subunit 14B
- Entrez Gene ID
- 26472
- Genome
- hg19
- Position
- chr11:64,011,951-64,014,415
- Genome
- hg38
- Position
- chr11:64,244,479-64,246,943
- MIM
- 601140 OMIM
- HGNC
- HGNC:9057 HGNC
- Ensembl
- ENSG00000173457 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 20 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
20 |
 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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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| 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 | PHI-1 |
| SYNONYM | PLCB3N |
| SYNONYM | PNG |
| SYNONYM | SOM172 |
| MIM | 601140 OMIM |
| HGNC | HGNC:9057 HGNC |
| Ensembl | ENSG00000173457 Ensembl |
| AllianceGenome | HGNC:9057 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000309318.8 | hg38 | chr11 | 64,244,479 | 64,246,943 | 2,465 |
| ENST00000392210.6 | hg38 | chr11 | 64,244,480 | 64,246,193 | 1,714 |
| ENST00000542235.1 | hg38 | chr11 | 64,244,549 | 64,245,816 | 1,268 |
| ENST00000309318.8 | hg19 | chr11 | 64,011,951 | 64,014,415 | 2,465 |
| ENST00000392210.6 | hg19 | chr11 | 64,011,952 | 64,013,665 | 1,714 |
| ENST00000542235.1 | hg19 | chr11 | 64,012,021 | 64,013,288 | 1,268 |
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