ZMP
tiparp
Ensembl ID:
ZFIN IDs:
Description:
TCDD-inducible poly [Source:RefSeq peptide;Acc:NP_001038484]
Human Orthologue:
TIPARP
Human Description:
TCDD-inducible poly(ADP-ribose) polymerase [Source:HGNC Symbol;Acc:23696]
Mouse Orthologues:
Tiparp, Zc3hav1
Mouse Descriptions:
TCDD-inducible poly(ADP-ribose) polymerase Gene [Source:MGI Symbol;Acc:MGI:2159210]
zinc finger CCCH type, antiviral 1 Gene [Source:MGI Symbol;Acc:MGI:1926031]
zinc finger CCCH type, antiviral 1 Gene [Source:MGI Symbol;Acc:MGI:1926031]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43140 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15738 | Nonsense | Available for shipment | Available now |
sa43141 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36690 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa10114 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43140
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088673 | Nonsense | 161 | 646 | 1 | 5 |
ENSDART00000088675 | Nonsense | 161 | 279 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 18 (position 32943868)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 34625413 |
GRCz11 | 18 | 34601437 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGGAGCGCGACGAGGCGGCGCCCCCCTCCGATGTTTCGGGCTCCAAGT[T/G]AAATGACATCTACACTGCTGAGACTTTGCAGGGAGCAAATTGCCTCGCCA
Long Flanking Sequence:
GTGGAGACAGTTTTGCACCATGCAGGAGGCAGTTGACACCGCCGAGCCCGCTTTAGCTCTGCCCATGGGGACCGGAGAGTTCACAGAGCAGCAGATGGGACTCGCAGACAAGATCCCGTTAGTGAAGCCCTGCTTCAAAAAGAAGCACGCACAGAGGAAGCTGGACACAAAATGCTTACGCGCTTTAGAGGACCCTATTTTGAGCACGTTATTAAGCTCAGATGCTCTCGTCTCAGGGGACGGAGTGTTTGTTCCACGTAACCCGCCTCGACCTCAGCGGAATATATGCACCGCCGCCGTGGAAAAGCAGTCGAGGATTAGTCAGGTGTGCCTGAAGGAGGAGGACGAGAGCACGGATGCCGACGTGGCCGCGAGCGAGCTTGCGGTGGAGCAGAAGGTGACGGATATTCAGCGAGTGTCAATAGACGCTAATGAGCGTCGCTTCCCGCCCCAGGAGCGCGACGAGGCGGCGCCCCCCTCCGATGTTTCGGGCTCCAAGT[T/G]AAATGACATCTACACTGCTGAGACTTTGCAGGGAGCAAATTGCCTCGCCATCAAAGAGGGCGAGATCTTTCAGGATAAAAGCGAGGAGGCCTCTTTGGATCTAGTGTTTGAACTGCTGACCCAGCTCCAGTATCACACGCATCAAGGGGATGCTGTATCGATTTGTGTGGATTTCCTCCAGGGCGTTTGCGTCTATGGCAGTGACTGTGCCCAGCATCACACCGTTTTACCTTACCACTGGCAAATCCGCAGAGTAGATACGCAAATCTGGCAGAGCATATCGGACGACTCTCAAGAACAACTGGAAAGGCTTTATTGCAACCCGGATAACGAACATGTCAGACTTAAGTTCCTGTAAGTGCTTTTGGTTTATGCCACTTTTCACTAAAATTTTTTTTGTTTTGCCTAACCCAATAGCAAAAAGGAAGTATAGGTATGCAAAGCTTTTAGTTCAGTGAGAAAACAAACATAATTGGTAAAAGGGAGGGACTGGTGTGACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15738
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088673 | Nonsense | 237 | 646 | 1 | 5 |
ENSDART00000088675 | Nonsense | 237 | 279 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 18 (position 32944096)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 34625641 |
GRCz11 | 18 | 34601665 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAGGGCGTTTGCGTCTATGGCAGTGACTGTGCCCAGCATCACACCGTTT[T/A]ACCTTACCACTGGCAAATCCGCAGAGTAGAWACGCAAATCTGGCAGAGCA
Long Flanking Sequence:
CGTCTCAGGGGACGGAGTGTTTGTTCCACGTAACCCGCCTCGACCTCAGCGGAATATATGCACCGCCGCCGTGGAAAAGCAGTCGAGGATTAGTCAGGTGTGCCTGAAGGAGGAGGACGAGAGCACGGATGCCGACGTGGCCGCGAGCGAGCTTGCGGTGGAGCAGAAGGTGACGGATATTCAGCGAGTGTCAATAGACGCTAATGAGCGTCGCTTCCCGCCCCAGGAGCGCGACGAGGCGGCGCCCCCCTCCGATGTTTCGGGCTCCAAGTTAAATGACATCTACACTGCTGAGACTTTGCAGGGAGCAAATTGCCTCGCCATCAAAGAGGGCGAGATCTTTCAGGATAAAAGCGAGGAGGCCTCTTTGGATCTAGTGTTTGAACTGCTGACCCAGCTCCAGTATCACACGCATCAAGGGGATGCTGTATCGATTTGTGTGGATTTCCTCCAGGGCGTTTGCGTCTATGGCAGTGACTGTGCCCAGCATCACACCGTTT[T/A]ACCTTACCACTGGCAAATCCGCAGAGTAGATACGCAAATCTGGCAGAGCATATCGGACGACTCTCAAGAACAACTGGAAAGGCTTTATTGCAACCCGGATAACGAACATGTCAGACTTAAGTTCCTGTAAGTGCTTTTGGTTTATGCCACTTTTCACTAAAATTTTTTTTGTTTTGCCTAACCCAATAGCAAAAAGGAAGTATAGGTATGCAAAGCTTTTAGTTCAGTGAGAAAACAAACATAATTGGTAAAAGGGAGGGACTGGTGTGACTTTCACCTAAAAATACAAAAAAAAAAAACAAAAGCTACCTAAACCAGTCTGGTTCACAGATCTTATTTCATTCAGCTGGTCAGCCAGCCAGACCTGATAAAAAAAGTGGACAAAAAACATTCTAAACCCAACAACTAGGCTGCAGTATATTGAGTGACTACTGAGGGAGGCAGAGAGTTTGAGTGAAAGAGTGCAGTACGTGACAGGAAGTTGCCCTGTGTGCAGGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43141
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088673 | Nonsense | 277 | 646 | 1 | 5 |
ENSDART00000088675 | Nonsense | 277 | 279 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 18 (position 32944215)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 34625760 |
GRCz11 | 18 | 34601784 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAACTGGAAAGGCTTTATTGCAACCCGGATAACGAACATGTCAGACTT[A/T]AGTTCCTGTAAGTGCTTTTGGTTTATGCCACTTTTCACTAAAATTTTTTT
Long Flanking Sequence:
AGAGCACGGATGCCGACGTGGCCGCGAGCGAGCTTGCGGTGGAGCAGAAGGTGACGGATATTCAGCGAGTGTCAATAGACGCTAATGAGCGTCGCTTCCCGCCCCAGGAGCGCGACGAGGCGGCGCCCCCCTCCGATGTTTCGGGCTCCAAGTTAAATGACATCTACACTGCTGAGACTTTGCAGGGAGCAAATTGCCTCGCCATCAAAGAGGGCGAGATCTTTCAGGATAAAAGCGAGGAGGCCTCTTTGGATCTAGTGTTTGAACTGCTGACCCAGCTCCAGTATCACACGCATCAAGGGGATGCTGTATCGATTTGTGTGGATTTCCTCCAGGGCGTTTGCGTCTATGGCAGTGACTGTGCCCAGCATCACACCGTTTTACCTTACCACTGGCAAATCCGCAGAGTAGATACGCAAATCTGGCAGAGCATATCGGACGACTCTCAAGAACAACTGGAAAGGCTTTATTGCAACCCGGATAACGAACATGTCAGACTT[A/T]AGTTCCTGTAAGTGCTTTTGGTTTATGCCACTTTTCACTAAAATTTTTTTTGTTTTGCCTAACCCAATAGCAAAAAGGAAGTATAGGTATGCAAAGCTTTTAGTTCAGTGAGAAAACAAACATAATTGGTAAAAGGGAGGGACTGGTGTGACTTTCACCTAAAAATACAAAAAAAAAAAACAAAAGCTACCTAAACCAGTCTGGTTCACAGATCTTATTTCATTCAGCTGGTCAGCCAGCCAGACCTGATAAAAAAAGTGGACAAAAAACATTCTAAACCCAACAACTAGGCTGCAGTATATTGAGTGACTACTGAGGGAGGCAGAGAGTTTGAGTGAAAGAGTGCAGTACGTGACAGGAAGTTGCCCTGTGTGCAGGAGCGTGTGTGTTGTGAGTGAGGTATATATGTGACTAAGAGATTGTGTTTTTCCCATAAGCCTTCCGCTGGCTGGCTTGACATGTGGAAGCGTACTGACAGCTGTAAGCCGTGAACTTGCTCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36690
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088673 | Essential Splice Site | 344 | 646 | 3 | 5 |
ENSDART00000088675 | None | None | 279 | None | 2 |
Genomic Location (Zv9):
Chromosome 18 (position 32965856)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 34647401 |
GRCz11 | 18 | 34623425 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTCTCTTTCTTTGCGTAACTCATTTCCTCTCTGCTTCTTCATCCCACA[G/T]CCGGTGGTTCGGCTGATTGAGGAGGCCAGTGGTCGAGGTTTGAAGGAGGT
Long Flanking Sequence:
TATATCTTAAAGTAATTTCTCACATTAAATCTGAACATTAAATCTAACCTTGTGAATTGTAGTTTCAAATAGTTTTTGATTTTGGTTTGAAATTAAAAAATAAACCTGATGTTACAGATTTTATGAGCTCCCCATATTTTGAAATAGCACATATTGTGCACAAAAGCAACAGATTTGTTCAGTTCTCAAGAGTTAGAATGTGTGTGCGGCTGGCTCAGTGTATAAACGTGTGATCGCATTGTGTGTTCGGTCTCAAGTCGAGCTGGCTTGCACAAACCAGAGACGTCCTGTTCTACTCAGAAGTGCCTGACATCAGAACATTGGATAAGCATTCCTTTGAAAACAAAGCTTTTTATTTCCTGTGAAAATCTCTTATGATGGATACATTCTGACCAGTGCTCCGGATGAATTGAATGGGAGTTGGAGCACATTTAAATGTCCTGTTGTTCCCTCTCTCTTTCTTTGCGTAACTCATTTCCTCTCTGCTTCTTCATCCCACA[G/T]CCGGTGGTTCGGCTGATTGAGGAGGCCAGTGGTCGAGGTTTGAAGGAGGTCCGTTTCATCACGCTGCAGAATCAGTACATCCTGAACATTCGTGAGGGCTTCCAGCAGAATGCTGTATTTGGGTTCCGCAGACAGATTAAAAAACGGCCGCTGTTTAGGTCCTCCATCATGCTCACGCCTTACCTCCAGTAAGTAACTTCATATTTACCTTCAGTTGCAAACAGTGTCCTAAATCTCTTGTTCGACAATCCTTATTTCTTATTGAACATCCCATAATTACCAACTTGGTACCATTTTGTTTTCCTCATAATATGAAAATCATATGAGGCAATGGCTCCCATTCACTAATAAATGTTACAAGTATGACTGTTTAGAGCACATGCTGCAATGTCTTTAATAAAGATGTAACAATATGAAAAGTGTCATATCATTAGTGACAGATATGATTACGGTTTTCAGTATTATCATGGTTTTGCTAAAATGACCTGAACATTTTCTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10114
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088673 | Nonsense | 560 | 646 | 5 | 5 |
ENSDART00000088675 | None | None | 279 | None | 2 |
Genomic Location (Zv9):
Chromosome 18 (position 32983678)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 34665223 |
GRCz11 | 18 | 34641247 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACGCCACCATGTTCGGCCAAGGCAGCTACTTTGCACGCAAGGCTGTGYA[T/G]TCCCRCAACTTCTCCAAGCGCTCGCCTAATGGTGTGCACTACATGTTCCT
Long Flanking Sequence:
GCATGATAATTTGCATGAAGTGTAGTGAAGTAGAAGCTTATGATGCTACGTTTTAATCTTTGTATGGTTTTGACAGTTGTTTACTTTAGTTTATTTGCTTTGTATGTTTTTAATTTGAATCCTTCATCTACTAGCATCAAATGATTGTTTTTAGAATTGAATGAAAATGATGATTTATGCTTCAGTTCTTAAAGTTACTGGCCAACTGGTTTGAATCCTGGTTGTTTACACAAACTTGGTTCTCACTGCTTTAATTTGTTTGCCTTTTGATAAGGATGTGTAATTGAAACGTCTGTTTCTCCTTCTCTTTATAGGAAGAAGGAGTACATGTCACGGCGCATGACAGATATGGACCGCATGCTGAACGAGCGTCACCTGTTCCACGGCACGTCACAGGATGTAGTGGAGGGCATCTGCAAGCACAACTTCGACCCCCGTGTGTGCGGCAAGCACGCCACCATGTTCGGCCAAGGCAGCTACTTTGCACGCAAGGCTGTGTA[T/G]TCCCACAACTTCTCCAAGCGCTCGCCTAATGGTGTGCACTACATGTTCCTGGCCAAAGTCTTGACAGGCAAGTTCACAGTGGGCAACCCTTCCATGCGTCGACCACCTCCCCTGAATCCAAGAGACGCCTCAAGCGACCTGTTTGACTCCTGCGTGGACAACTGGATGGACCCGCAGATCTTTGTCATCTTTAATGATGATCAGAGTTATCCGTACTTCATCGTTCAGTATGAAGAGGTAGGCAGTACAGTGGCTATCTGAATAGTGCTGCACCTCTGGAGACTTGCACCAAGGCCTGTGCGCATATTCGGCCAGTACGAAAAGAGACGGGAGTGGCTGTGCGCCGGCACTCTGAATGGAACTCATGGACCATACGGGATACGTTTTGAAACGGTTCCCACCCTCAGTCGTGCGCGAGGGTTTCTGTGTGACCTTTCAGTGCCCGTCTTCTCATACCCTCATTTATAAAAATGGGGATTGTGTGTATGTGTTCGCATGTA
Associated Phenotype:
Not determined