Busch Lab

ZMP

parp12a

Ensembl ID:
ENSDARG00000042496
ZFIN ID:
ZDB-GENE-050419-6
Description:
Novel protein similar to vertebrate zinc finger CCCH type domain containing 1 (ZC3HDC1) [Source:UniP
Human Orthologue:
PARP12
Human Description:
poly (ADP-ribose) polymerase family, member 12 [Source:HGNC Symbol;Acc:21919]
Mouse Orthologues:
Parp12, Zc3hav1
Mouse Descriptions:
poly (ADP-ribose) polymerase family, member 12 Gene [Source:MGI Symbol;Acc:MGI:2143990]
zinc finger CCCH type, antiviral 1 Gene [Source:MGI Symbol;Acc:MGI:1926031]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa28994 Nonsense Mutation detected in F1 DNA Not yet available
sa43063 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa23246 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa28994
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000130343 Nonsense 431 663 8 12
Genomic Location (Zv9):
Chromosome 18 (position 12292752)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 12875481
GRCz11 18 12844199
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTAAAGTTTGACATTCATTTTCAGAGATGTGCCAACAAAATCTGAAGTA[C/A]AAAACTGAGAGAGATGTTCGAAGGAGACCTCGTTTTGTATCTGCTCAAGA
Long Flanking Sequence:
CAGATGCTGTTTCTGTGTGGAGTTTGCATGTTCTCACATGAGCATGTGTTCACATGGGTTTCCTCCAGGTGCTCCAGTTTTCCTCACAGTTGAAGGGCATCTACTGCGTAAAACATACTGTATACTGGATAAGTCAGCGGTTCTTTCCGCTGTGGCGACCCCGGTTTAATAAATGGACTAAGCCGAAAAAGAAAATGAATGAATGAATGATTCCCAGTAATTAAATTAATTGTCATATATTATGTTAAGGGGTGGGACTATTTATTTATTTATTTATTTATTTATCTAGCATTTTAGAGTGAAAAATTAAATTAGCCATAAAATTGTCAATGTAAAAAAAAAAAAAAAAATTGTGATTTCCTATAAGATTGGGTTAGTATACAATATAAATAAGACTAAACTAATCATGCAAGCGAAATGATCCAACAGTGAAATGATCTTTTTATAGAGAGTAAAGTTTGACATTCATTTTCAGAGATGTGCCAACAAAATCTGAAGTA[C/A]AAAACTGAGAGAGATGTTCGAAGGAGACCTCGTTTTGTATCTGCTCAAGACGTCAAGAGTAAAATCAAGGGGTAAGATATCCTGTGCCATTTGTCCATTACATGCACACACATTTGACCTGCTGTTCACTTTAATGTGTGGTGTTTTAATTAGAGGTGATTCTACAGAAAGCTCAGCATCTTCTTCTGCAGATGTTCCTTCTTACTGGGACAAAGGAGCTCCTGATACCGGCACCTACAAGGTACATAGTCATGCGGGCTGGTCAAGTAGCTGTGGAATCATTGTACTTTGGGTTATAGATTAGTACTTCTAATTAAAGCAGCTAAATTCACCTTCTTTTTCGCGTACGAGCAGGCATAGCCGTTTGAATCTTTTTGGCTCGAGACTTGCGCTCTAATTTACTTTCATTCAATTTTACATGTAAAATACAGCTCATTCTGCTGCTTGATGTTGCAAACTTATATTTTCTTTTTTATATTATTCTGCTTTGTCTGTATAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43063
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000130343 Essential Splice Site 485 663 10 12
Genomic Location (Zv9):
Chromosome 18 (position 12291567)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 12874296
GRCz11 18 12843014
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCTTTAAAATACTGATGACATTTCACTAATCAAATTTAATATCTCCTC[A/T]GATTGTTTCACTGCAAAAAACTTGCAAGGAGTATGAGAGAGTGAGCTCAA
Long Flanking Sequence:
TAGATATTTTTCTGAGCTAAATAAAAAAAAAGACTTTGAAACAGCACAAATGATTGAAATGACTTTGTCTCCTTGCATCAGTGCTTATTTTTTTTTAGCTCTAGGTCCACCTAACAGAACCTACTGAAGATATGGGGATGAAGATAGTAAAGGCCCCATCTGATTGGTCAGATGTTGATAAACAACCTATGCATGCAGCACACAACTGCTTGGCACATAAGATTAGCTTAATTTAGTGCACTGAATTTATAGATATTGAATATACTATTATTGCGATAACAATAATTTTTGATATACTCTGCAGCCCTACATCTAATGCTACTACTTGTATATTATTTTATCTAACCCAGCTTACGAACTGCTGTGTTTTACAATTGCTGAAAAGCACCAGTTTTTCTATATTTATTATTATTGAAAGTTATCTGTTTGAGTAAATTACAACTACCTTTTATTCTTTAAAATACTGATGACATTTCACTAATCAAATTTAATATCTCCTC[A/T]GATTGTTTCACTGCAAAAAACTTGCAAGGAGTATGAGAGAGTGAGCTCAATGTTTAATAGAACTCTGCCTGGAAGCATCATTCACCGCATTGACAGAGTGCAGAATCCTTCACTCTGGAAAGTCTTTGAGTGGTACGTTTCTTTCTATATTTCACTAGAAAAACAACAACAATAGTGTCTATGTGTGTGTAGTATTATTTATTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACAGTAGGTAGTGCTGTCGACTTACAGCAAGAAGGTCACTGGTTCGAGCCTCGGCTGGGTCAGTTGGCGTTTCTGTGTGGAGATTTTATGTTCTCCCTGCGTTCGTGTGGGTTTCCTCCGGGTGCTCCGGTTTCCCCCACAGTCCAAAGACATGCGGTATAGGTGAATTGGGTAGGCTAAATTGTCCATAGTGTATAAGTGTGTATGGATGTTTCCCAGAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23246
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000130343 Nonsense 655 663 12 12
Genomic Location (Zv9):
Chromosome 18 (position 12288036)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 12870765
GRCz11 18 12839483
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACGAGGCAAACCCGGCCATTTTTGTCGTGTTTGAGAAATTTCAGATCTA[T/A]CCGGAGTACATCATTGAATACTCCTGATATGTGCCGTGTCAAATTATGTT
Long Flanking Sequence:
TTTGTTGTCCTAGGCAAAAAGAGCAAATGAACTTAAAGAGTGGAGGAAAGGTAGTGGACCAGCGCTACCTGTTTCATGGTACAGATGAATCTCACATGGATGCCATTTGTGATCAAAACTTTGACTGGAGGATTTGCGGAAGTAACGGGACACTTTATGGGAAAGGTATTTACACATTTGCTTCTACTACAGCAGCTTTTTACCATGACAATTACAATAACGAGACATTACTGAACGTTTAACCAAATATTCAAATCATCACGTTCAACAGGAAGCTATTTTGCCAGAGATGCTTCATACTCGGACAGATACGCCAGATCTAGGAACGGAAAGACCAAGAAGATGTTCATGGCGCTTGTGCTGGTTGGAGACTTCATTAGGGGTAACAATAGTTTAGTTCGTCCACCACAAAAACCACACAGCCAAAGATTTTACGACAGCTGTGTCGACAACGAGGCAAACCCGGCCATTTTTGTCGTGTTTGAGAAATTTCAGATCTA[T/A]CCGGAGTACATCATTGAATACTCCTGATATGTGCCGTGTCAAATTATGTTTGGATATATTTGACGCACTCAAACATTCTAAGCAGATCTACTTGTTTCTCGAAATCCTTCTGAAACGGTTAATATCGCTGAACAACCAAAATCTTCAACTTTAGGGCATTTAAGCTTCTTCTTTAGTGAATACTAATGGGATGTTACATAGTAGATAGTTAGATGAGTAAATTTAATTAGTTTCAGTCTCTATTCAATCATCTATGTGTGATGGAAATGGCAAACTGGTAAAAAAACGAAATATCTGAATTTTATTGTGATTTATTATGTTATTTTCCTTATTGACTTTTGTGCTGAGAGAAAAAAAAAAGAGTTTAACCAGTAGCTTTCAACTAACAGTTTTTGATTGCTCAAGATTATAAAAACGTGAAAACTAAATGGTTTAGTCCATTGTTTCTCATCCATGTTGCTGCAAGACCACCAGCTCTGCACATTTTCCATGTATTCTTA
Associated Phenotype:
Not determined