PAQR6 progestin and adipoQ receptor family member 6
Information
- Symbol
- PAQR6
- Type
- protein-coding
- Description
- progestin and adipoQ receptor family member 6
- Entrez Gene ID
- 79957
- Genome
- hg19
- Position
- chr1:156,213,112-156,217,908
- Genome
- hg38
- Position
- chr1:156,243,321-156,248,117
- MIM
- 614579 OMIM
- HGNC
- HGNC:30132 HGNC
- Ensembl
- ENSG00000160781 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
association | 0 | 2 |
Uncertain significance | 0 | 44 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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52 |
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2 |
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 | |||||
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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 | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | PRdelta |
MIM | 614579 OMIM |
HGNC | HGNC:30132 HGNC |
Ensembl | ENSG00000160781 Ensembl |
AllianceGenome | HGNC:30132 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000292291.10 | hg38 | chr1 | 156,243,320 | 156,248,056 | 4,737 |
ENST00000652405.1 | hg38 | chr1 | 156,243,496 | 156,248,090 | 4,595 |
ENST00000540423.5 | hg38 | chr1 | 156,243,321 | 156,248,117 | 4,797 |
ENST00000612424.4 | hg38 | chr1 | 156,243,321 | 156,248,117 | 4,797 |
ENST00000623241.3 | hg38 | chr1 | 156,243,321 | 156,248,117 | 4,797 |
ENST00000335852.6 | hg38 | chr1 | 156,243,321 | 156,248,117 | 4,797 |
ENST00000356983.7 | hg38 | chr1 | 156,243,912 | 156,248,056 | 4,145 |
ENST00000368270.2 | hg38 | chr1 | 156,243,423 | 156,248,031 | 4,609 |
ENST00000613336.4 | hg38 | chr1 | 156,243,321 | 156,248,117 | 4,797 |
ENST00000292291.10 | hg19 | chr1 | 156,213,111 | 156,217,847 | 4,737 |
ENST00000335852.6 | hg19 | chr1 | 156,213,112 | 156,217,908 | 4,797 |
ENST00000356983.7 | hg19 | chr1 | 156,213,703 | 156,217,847 | 4,145 |
ENST00000368270.2 | hg19 | chr1 | 156,213,214 | 156,217,822 | 4,609 |
ENST00000623241.3 | hg19 | chr1 | 156,213,112 | 156,217,908 | 4,797 |
ENST00000613336.4 | hg19 | chr1 | 156,213,112 | 156,217,908 | 4,797 |
ENST00000612424.4 | hg19 | chr1 | 156,213,112 | 156,217,908 | 4,797 |
ENST00000540423.5 | hg19 | chr1 | 156,213,112 | 156,217,908 | 4,797 |
ENST00000652405.1 | hg19 | chr1 | 156,213,287 | 156,217,881 | 4,595 |
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