PNISR PNN interacting serine and arginine rich protein
Information
- Symbol
- PNISR
- Type
- protein-coding
- Description
- PNN interacting serine and arginine rich protein
- Entrez Gene ID
- 25957
- Genome
- hg19
- Position
- chr6:99,845,505-99,873,205
- Genome
- hg38
- Position
- chr6:99,397,629-99,425,329
- MIM
- 616653 OMIM
- HGNC
- HGNC:21222 HGNC
- Ensembl
- ENSG00000132424 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 78 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
82 |
 |
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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| 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 | C6orf111 |
| SYNONYM | HSPC306 |
| SYNONYM | SFRS18 |
| SYNONYM | SRrp130 |
| SYNONYM | bA98I9.2 |
| MIM | 616653 OMIM |
| HGNC | HGNC:21222 HGNC |
| Ensembl | ENSG00000132424 Ensembl |
| AllianceGenome | HGNC:21222 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000481229.2 | hg38 | chr6 | 99,398,069 | 99,425,292 | 27,224 |
| ENST00000438806.5 | hg38 | chr6 | 99,399,964 | 99,425,331 | 25,368 |
| ENST00000647811.1 | hg38 | chr6 | 99,398,051 | 99,425,277 | 27,227 |
| ENST00000369239.10 | hg38 | chr6 | 99,398,050 | 99,425,308 | 27,259 |
| ENST00000681611.1 | hg38 | chr6 | 99,398,989 | 99,425,315 | 26,327 |
| ENST00000681615.1 | hg38 | chr6 | 99,397,629 | 99,425,329 | 27,701 |
| ENST00000681615.1 | hg19 | chr6 | 99,845,505 | 99,873,205 | 27,701 |
| ENST00000369239.10 | hg19 | chr6 | 99,845,926 | 99,873,184 | 27,259 |
| ENST00000647811.1 | hg19 | chr6 | 99,845,927 | 99,873,153 | 27,227 |
| ENST00000481229.2 | hg19 | chr6 | 99,845,945 | 99,873,168 | 27,224 |
| ENST00000681611.1 | hg19 | chr6 | 99,846,865 | 99,873,191 | 26,327 |
| ENST00000438806.5 | hg19 | chr6 | 99,847,840 | 99,873,207 | 25,368 |
| Key | Value |
|---|---|
| strand | - |
| start | 99,845,926 |
| Gene Symbol | PNISR |
| Entrez GeneId | 25,957 |
| Chr Band | 6q16.3 |
| end | 99,873,220 |
| chr | chr6 |
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