TIPARP TCDD inducible poly(ADP-ribose) polymerase
Information
- Symbol
- TIPARP
- Type
- protein-coding
- Description
- TCDD inducible poly(ADP-ribose) polymerase
- Entrez Gene ID
- 25976
- Genome
- hg19
- Position
- chr3:156,392,634-156,424,539
- Genome
- hg38
- Position
- chr3:156,674,845-156,706,750
- MIM
- 612480 OMIM
- HGNC
- HGNC:23696 HGNC
- Ensembl
- ENSG00000163659 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Uncertain significance | 0 | 58 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
62 |
 |
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 | ARTD14 |
| SYNONYM | PARP7 |
| SYNONYM | pART14 |
| MIM | 612480 OMIM |
| HGNC | HGNC:23696 HGNC |
| Ensembl | ENSG00000163659 Ensembl |
| AllianceGenome | HGNC:23696 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000461166.5 | hg38 | chr3 | 156,674,845 | 156,706,750 | 31,906 |
| ENST00000295924.12 | hg38 | chr3 | 156,674,590 | 156,706,770 | 32,181 |
| ENST00000542783.5 | hg38 | chr3 | 156,676,664 | 156,706,766 | 30,103 |
| ENST00000486483.5 | hg38 | chr3 | 156,673,235 | 156,705,139 | 31,905 |
| ENST00000486483.5 | hg19 | chr3 | 156,391,024 | 156,422,928 | 31,905 |
| ENST00000295924.12 | hg19 | chr3 | 156,392,379 | 156,424,559 | 32,181 |
| ENST00000461166.5 | hg19 | chr3 | 156,392,634 | 156,424,539 | 31,906 |
| ENST00000542783.5 | hg19 | chr3 | 156,394,453 | 156,424,555 | 30,103 |
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