ZMP
LOC564886
Ensembl ID:
Human Orthologue:
PARP10
Human Description:
poly (ADP-ribose) polymerase family, member 10 [Source:HGNC Symbol;Acc:25895]
Mouse Orthologues:
Parp10, Zc3hav1
Mouse Descriptions:
poly (ADP-ribose) polymerase family, member 10 Gene [Source:MGI Symbol;Acc:MGI:3712326]
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23477 | Nonsense | Available for shipment | Available now |
sa9947 | Nonsense | Available for shipment | Available now |
sa43246 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39238 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23477
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 |
---|---|---|---|---|---|
ENSDART00000123409 | Nonsense | 25 | 581 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 19 (position 12589097)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 12047443 |
GRCz11 | 19 | 11965785 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCAGTGATCCTTTAGAGTTAATTGCACTTGTGTTTTCCACAGGATATTT[T/A]GGAGCTGGCATGGAAAATGACACCCTGTCAGAACTTCCAGAAGAGTTCCT
Long Flanking Sequence:
CTTACATATACAGTAGGAGCAGTATAGCAGAAAATTATGCCGTTTTTTTAAAACCTTGACTTTTCCTAACTGCGGTATACTTTGTAAACGTTTTTGTCCCGTGCCTAGTATTATGATTGTCTTTAAATGTTTTCTGTAACTGCTTACACTTTTTTTATATATTTGTTTGTTTGTAATTTCTTAATTTCATTGGTAGATTCAAGGAGATGCAAATGTTTGCCAGTCAGCGGCAGAACTGCTAAGTGCTATCATCGGCTCAGTATTTACAAGGAGCATTGTAGTCAAACACCCTGGCATTTCCCGCTTCTTGCTAGACGATGAAGGTACCAGCATACTGGCAGAGATGACAGCCAAGTTTGAGGTCTATATAGACATGACCAAAGTGCACTGGGAGCCTCTAGAAGATAAAGTAATGTATCCAGCCTTGTTCTTCATCATGTAACTCAGATAATCAGTGATCCTTTAGAGTTAATTGCACTTGTGTTTTCCACAGGATATTT[T/A]GGAGCTGGCATGGAAAATGACACCCTGTCAGAACTTCCAGAAGAGTTCCTCTGCAAATTCCATTCAGGAATTCACTGCTGGTGTACCGAATGGCGCTACTGATGCACATGCATCAGGTCATTACAGAAGATATCCCTGATTCATTCTACACATTTTAATATAACTGTAAATAAAGAATTCAATAAATACAGAATCATGAATACATCAAAGCCCCAAACAAGAACCATTTTAAAATATAGATAGAGATATAGCATTGAGTGGCTCCACCCCATTTATTAAACAGCCAATTGCATTTGTTTTATTACAGCTCTGCTAGTAAGAGTGGTTGAGCTCAAGAGAATTAAATGAAAAGCAAACTAAAAGTGTCTTAACTGGGGTGTGACATGTCAAATACTAGAGAGCATTTGATTAGTCAAGACTTGATGAGAAACTGAAGTATGAAGTCAAATGAAAAAAAAAACTGTTGATCCATTTACTTTGAAGTGACAAACCGGAAGGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9947
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123409 | Nonsense | 177 | 581 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 19 (position 12587393)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 12045739 |
GRCz11 | 19 | 11964081 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAWCCAGAAAGCTCTAGAACTTTCCAAGAGGGACTCCGTACCAAGGGAG[G/T]AGAACAAACAGCTGGAGATGGCRTTTGAAATGTCAATGGAGGAAGCCATT
Long Flanking Sequence:
TTCAAGTAAAGTGAGTGTTCCTTTAGTTTTTTACCTTGGAAGATTAAAGTTTCTTCGCCAAATAAAAAATAAAAAATTTAGCTTTTTGTTTTTTTGTTGTTTGTTTTTAAACTACTGGCAACTAATATGTTGATTCTAATGTTTGCTGGTATGTTTTCTCAGCTCGTATTGAAGAAGCTAAGAAGATTCTGGCAGTGATTGGGAGTGATTTCAACCCCGCTCCTTCAAGTTCAGGATCCACAAACACTGATACTCAAGATATCTATTCTGACCCAAGTGAAGAAATTATAGAAGTGAACTCCGACTCGGACGATCAACCCCAACCCCTGCAGACGCTTGACCTCCCGAGCTTCTCAGCACCTACGAATGTCTGCAACCTTGACGAAGATGCGAGCCTCTTGTTGGCGATTCAGTTATCAATGGAGATCAACCAAAGAAAGGACAATGATGACATCCAGAAAGCTCTAGAACTTTCCAAGAGGGACTCCGTACCAAGGGAG[G/T]AGAACAAACAGCTGGAGATGGCGTTTGAAATGTCAATGGAGGAAGCCATTAGATTATCCAACACTGCTGAGATATTTGTATACGCAAACTACAACCATGATCTTGTAAGGGTTGATATTGCATTGGGCAAGAAGGTGGGACTAAGACAGTGTGAGGAAAAAATTGAGAACAAAATCCTCCGGAAACTTTCCTCGTTTCAGAAGAGATGCATAGATCTCATTAAAAGGAAGCATGCTGTGGAAATCAACATCCAGGGCACCACCGCCATCCTCTCTGGCTTTAAAGAGTACGTCTCTGTGGCCGTTCCTGACCTGAAGGACGTCCTGAGAAGAACAGAGCACATGATGAGTGATGCTGGCATTGCTAAGTCTGTTCAGTGGGTGTGGTATGAGCAGGGCTCGTCTAAGGGCACACCGTACTCGCCCGAGGCCACAGTATTCATAGAGAATGCTTGGAAGCTGAAGCAGAAGAAGATTGATATTTTATTCAACAATCAGCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43246
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 |
---|---|---|---|---|---|
ENSDART00000123409 | Nonsense | 367 | 581 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 19 (position 12586823)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 12045169 |
GRCz11 | 19 | 11963511 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATGGAAGAGCACAGTTTGGCATCTGGGAAATCTGTGCCTATTAAACGA[A/T]AAATGATGAGCACAGAGGACTTGTACACAGACGGTGCAGGTAGGAATTCA
Long Flanking Sequence:
AGATATTTGTATACGCAAACTACAACCATGATCTTGTAAGGGTTGATATTGCATTGGGCAAGAAGGTGGGACTAAGACAGTGTGAGGAAAAAATTGAGAACAAAATCCTCCGGAAACTTTCCTCGTTTCAGAAGAGATGCATAGATCTCATTAAAAGGAAGCATGCTGTGGAAATCAACATCCAGGGCACCACCGCCATCCTCTCTGGCTTTAAAGAGTACGTCTCTGTGGCCGTTCCTGACCTGAAGGACGTCCTGAGAAGAACAGAGCACATGATGAGTGATGCTGGCATTGCTAAGTCTGTTCAGTGGGTGTGGTATGAGCAGGGCTCGTCTAAGGGCACACCGTACTCGCCCGAGGCCACAGTATTCATAGAGAATGCTTGGAAGCTGAAGCAGAAGAAGATTGATATTTTATTCAACAATCAGCCATACAGCATTGACTTAGAGAAGATGGAAGAGCACAGTTTGGCATCTGGGAAATCTGTGCCTATTAAACGA[A/T]AAATGATGAGCACAGAGGACTTGTACACAGACGGTGCAGGTAGGAATTCAGCTTGATTATTTAAAAATCCATTAAAAAAGGAATTTTTTTATCTGTTAAAGTCCAATTTAGTGAATGAATAGTTTAATCTGTTCATTATAACAATGATAATAATAATAACTAAATTGTTCATTTCCTAAAGAAAGTGTGTGTGAGGTTTGCCGTGGCAAATTGATGGGGTAAAATGCATTACCGTTCTGCCCAAAAGCAATGGAGTGCTAAGAAATGGACAAATATGTGTTGATGTAGCTGCTAGGGTATTGTAAATGGTTGCTCGGCTGTGCCAATGCAGTTTAATAGGTAAAAGCACAAGAGGATTTTAACAGCCTGAATCAATTCAATTCAGCTTTATTTGTATAGTGCTTTTACAATGTAGATTGTGTCAAAGCAGCTTCACATAAATGGTCATAGTAACTGGAACAGTGTAGTTCAGTTTTTTGTGTTTAAGTTCAGTTCAGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39238
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123409 | Nonsense | 491 | 581 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 19 (position 12579073)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 12037419 |
GRCz11 | 19 | 11955761 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCGATTTTTTTTCTTCTCTTCCAGCCACTGTATACGGTCAGGGTGTGTA[T/A]TTTGCGGTCAACGCCTCTCTGTCTGTGTCAGACACCTACTCTCCACCTAA
Long Flanking Sequence:
GCATATTGGTGGTTCATTCCACTGTGGTGACCCCTGATTAATAAAGGGATTGAGCTGAAAACAAAATGAATGAATGAATAAATCCATATTATGAGGCAATGAGAGTGTTTTTTGACCTTGTATGCAAATCAGTCTGTTATTAGAGACCCTAAAACTAAAATATGACATGTAATAGGGGCTCTTTAAATCTTTAACTAACATTGAAGCGAAAACAGATTTTAAAAAATATGTTTTCCATCACTGTCCACTATTTTTCTCTAAACTGTGCTTTTGTAGTTCACACAGAGGCAATAAAATTTTCATATCTCTATTAACAACTAACACTTTAAAACACATATTTAACAAACTGTTTTCTGTTTTTGTTGTTGTTGAAAGTGTGTAAATGCCCCAAACATGTTTTTTAAACAAAATGTAATAAAATGAATTAATTCAACTAATTATTTTTTAATATTCGATTTTTTTTCTTCTCTTCCAGCCACTGTATACGGTCAGGGTGTGTA[T/A]TTTGCGGTCAACGCCTCTCTGTCTGTGTCAGACACCTACTCTCCACCTAATGCAGATGGGCACAAGTTTATTTTTGTAGCCAAAGTGCTCACCGGTGAGTTCACTGTAGGAAAACACGAGATGAAGGCAGCTCCGCTCAAGGAGAATTCAGCCGTACCGTTCAGATACCACAGCGTGACGGATCAGATCAACTCCCCGACTTTATTCGTCATCTTTAATGACACACAGGCTTATCCGAAATACCTTATTACATGCAAGAAGATCTACGGTTAATCACATGCTTTCAGATCCTAATGCTGGCATGCATTTACAGCAACTGCCAATCATGTACAGTTATTAAACTGATTAGAGCTACTTTAATTTACAGCTTTACTGTATTATTATTTGAAACAAAGGTTTGTCTGTTTGTGTTTTATTTAATTTTATTATTTGATTGTTATGTTTGGAAATGACATTTTCATATTTAGCCGTTCTTCTTTAATCATACTATTTTTGTTACA
Associated Phenotype:
Not determined