PNRC1 proline rich nuclear receptor coactivator 1
Information
- Symbol
- PNRC1
- Type
- protein-coding
- Description
- proline rich nuclear receptor coactivator 1
- Entrez Gene ID
- 10957
- Genome
- hg19
- Position
- chr6:89,790,470-89,794,879
- Genome
- hg38
- Position
- chr6:89,080,751-89,085,160
- MIM
- 606714 OMIM
- HGNC
- HGNC:17278 HGNC
- Ensembl
- ENSG00000146278 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 2 | 0 |
Uncertain significance | 0 | 60 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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60 |
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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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | B4-2 |
SYNONYM | PNAS-145 |
SYNONYM | PROL2 |
SYNONYM | PRR2 |
MIM | 606714 OMIM |
HGNC | HGNC:17278 HGNC |
Ensembl | ENSG00000146278 Ensembl |
AllianceGenome | HGNC:17278 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000369472.1 | hg38 | chr6 | 89,080,751 | 89,084,345 | 3,595 |
ENST00000336032.4 | hg38 | chr6 | 89,080,751 | 89,085,160 | 4,410 |
ENST00000354922.3 | hg38 | chr6 | 89,081,836 | 89,084,197 | 2,362 |
ENST00000369472.1 | hg19 | chr6 | 89,790,470 | 89,794,064 | 3,595 |
ENST00000336032.4 | hg19 | chr6 | 89,790,470 | 89,794,879 | 4,410 |
ENST00000354922.3 | hg19 | chr6 | 89,791,555 | 89,793,916 | 2,362 |
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