Busch Lab

ZMP

PARP14

Ensembl ID:
ENSDARG00000074139
Description:
poly (ADP-ribose) polymerase family, member 14 [Source:HGNC Symbol;Acc:29232]
Human Orthologues:
PARP14, PARP15
Human Descriptions:
poly (ADP-ribose) polymerase family, member 14 [Source:HGNC Symbol;Acc:29232]
poly (ADP-ribose) polymerase family, member 15 [Source:HGNC Symbol;Acc:26876]
Mouse Orthologues:
Parp14, Zc3hav1
Mouse Descriptions:
poly (ADP-ribose) polymerase family, member 14 Gene [Source:MGI Symbol;Acc:MGI:1919489]
zinc finger CCCH type, antiviral 1 Gene [Source:MGI Symbol;Acc:MGI:1926031]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa34897 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa41647 Nonsense Mutation detected in F1 DNA Not yet available
sa44723 Nonsense Mutation detected in F1 DNA Not yet available
sa6170 Nonsense Mutation detected in F1 DNA Not yet available
sa34896 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa34897
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112054 Essential Splice Site 263 1807 5 18
Genomic Location (Zv9):
Chromosome 10 (position 22150918)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 21981346
GRCz11 10 21950860
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAATTCCATCAGAGCATGCAGCCATTATTACATTTAAGGATGAAGAAGG[T/A]AAGTACATGCGCAATTGCTTGTAGTATTTTCTTGTTTGGCTCCATTTCCT
Long Flanking Sequence:
GATCTAGATTAGGAATAAGACATGTGTTTATACCATTATACCTTGGAATGCATCATTTGTAAGCTTTATTTTCCAAGCTTTTGACAGAGCCTTTAAACTGTCACCATTCACATCATTATTGTCTGAGCTCATTGCTGTTTCTCCAGTCCTACAACATTTGTTTAATGTGAGGAGGCAGCTTTTGTCTTGTTTGTCATGTGGATTGTTCAGCAAAGTTTATTGTGTGTATCATGTATTTCTGACTAAGTAATTTGAACAAATTTTCTTACAGCTGCAGGAAAGTTCCTCGAGGACAGCAAAATGCATGAAAAAATCAAGAAGAATAATCTAAAGGTGCGTTCACTGGAGAGAAGCACATGTGTGCGGGTGGAGGATCTTCCAGCTGAAGCTAATGAGATGCTGCTGGAACTGTTGTTTGAGAAATGGGGTGGTCCAATACAACAAATTGATACAATTCCATCAGAGCATGCAGCCATTATTACATTTAAGGATGAAGAAGG[T/A]AAGTACATGCGCAATTGCTTGTAGTATTTTCTTGTTTGGCTCCATTTCCTTCATTTTGACAGCATCAGTACATTTCATTGTACCTGCAACTTTCATATTTTTTCAGCCAAAGAGAGAGTTTTGAAGCAGCAGAATATGATCAGTAATGTTCCAGTCAAGATGTATCCCTACTTTAAATCACTGGATATGGTCTTCTATGGTGACAACAAGCCACATTTAAAGCTGCCTGAACCTATCACAGTCAGTGTACATCCTGCCATCAGGGCATTCCTCCTCAAGAAAGGGCTTATTTTTTCTATTGAAGATAAAATGAGTTCACACTTCTGCCTGATAAACATGGATAAACCTGATGTTTTGCTCAGTCCTGATCCAGCATTACTGAAACAGAAAGGAGTCAGCAGAAGACACATTGATGGCTGGAGTAAGAATGCTTTAGATGCCTTCAAGAAAATTATCTCAGACTACACAACATCTGAGTGGCCGGTGTCACATGCCTTGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41647
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112054 Nonsense 987 1807 6 18
Genomic Location (Zv9):
Chromosome 10 (position 22147812)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 21978240
GRCz11 10 21948580
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTATAACCCCAAAATGGCTTTCCCACATCAAAGCAAACCTCATGAGTA[T/G]AGTAACTATGAGCATGGACATCGTGGAGGTGGTCGTGGTCGTGGTCATGG
Long Flanking Sequence:
GCTTTTGCACTTCTCCAAGCTGCAGGACGATGTCTGCAGGAATACTGTGATCTACACATAAAGGTAAATGGGCGTTTGAGTCCTGGAGATGCCATCATCACTGAAGCTGGTCGTCTTCCATGTAAATATGTTGTGCATGCTGTTGGGCCTCGATTCAGAGGTTCAGACAAACGTACAGCTGTGCAACAATGCCTGAGACGTGCTGTGAGGGAGAGTTTGAACCAGGCATCAAGCAAAAAATGCTCCTCCATTGCAATTCCAGTGATCAGCTCAGGAATATTTGGTTGTCCTCTTGATCTTTGCACTGAATCAATCGCCAAAGAGGTGCGTCAATACATTGAAAATCACAACTACAGTGGCTCCAATTCCACACTGACTGAGATTCAATTAGTTGACAACAACGACAAGAATGTGAATGCCATGGCTCAAGCTGTCAGAAATGAGTTTGCTGCTTATAACCCCAAAATGGCTTTCCCACATCAAAGCAAACCTCATGAGTA[T/G]AGTAACTATGAGCATGGACATCGTGGAGGTGGTCGTGGTCGTGGTCATGGTCATGGTCATGGTCATGAAAACTATAACCAAAGAAACCATCGTGGTCATAGCAATAGAGAATTTGAAGAACAAGCACACTCACAGTCTGGTGACAGAACAGATAATTCTGAGGGGTTGAGGGTTCTTGAGACCAAAACTACACAAGACGGACTAAAAATTTGTCTGTATGAAGGGAACATCCAGGATGCAAGCGTAAGTGTATCAAGAGGTTGGGGTGGGTCAGGGAATGGGATCAAGCTATTTTGTTTTTAAGAAAAATTAACTTTGCTCAAGGTTTTAATTTATATTATTTTATTATATTATTTATTATCTTTATTATATGGAATATATCAAATCTAAATTAATTAAAACAAAGGACCATTTTTTAAATGGAATATTTGTTAAGATATATATTTTGGTTCAAACACTTTGCTAATATTACATAAATTTTCTGTGCCAGCACACATCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44723
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112054 Nonsense 1133 1807 9 18
Genomic Location (Zv9):
Chromosome 10 (position 22146730)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 21977158
GRCz11 10 21947498
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAATTCAATAGTTTTCCCTGCTATCGGCACTGGAAACCTTGGCTTTCCT[A/T]AAGATCTGGTGGCCAAAATCATTCTGACAGAAGTCCAGCAATTTAACACT
Long Flanking Sequence:
ATTTCTCCTGCAGGCTGATGTCATTGTCAACACTATATCAGAGGATATGGATCTGAGAAAAGGTGCCGTCTCTAAAGCACTCCTTCAGGCTGCTGGTCATCAGCTCCAGTCTGAAGTGAACAGAGCTGCTAAGTCATTCAGGCTGAATACTGGTGAAATTGTCATCACAGATGGTTATAATCTGAAATGTTCCCGAGTCTTTCATGTAGTTTGTCCATTTTGGAGTCAAGGCTCAGAGGACAAGGTGAGTAAATTAGATACAAAACTGTCATTGACTGTTACAGTTTATTGATTTTGAGATTAAGCGTTGTGCCTCATATGTAGGCTCCGTTTATGTATTTAGATGGTACTTTTTATAAAAAAAATTATAATGTAAATATTTCTTTACATTTTAAAAGGTTCTCTGTCAGATCATTAGAAACTGCCTAAAAAATGCAGAAACCCAGAGAATGAATTCAATAGTTTTCCCTGCTATCGGCACTGGAAACCTTGGCTTTCCT[A/T]AAGATCTGGTGGCCAAAATCATTCTGACAGAAGTCCAGCAATTTAACACTACAAACCTTCGAAAGGTCACTGTGATTGTGCACCCTTCTGACAAGGAGAGTGTTCAGGTGAGTGAAGGAAAAATACAGAACAATAAAAACATTTTATTTAAAATAGTTTACCGTAGTTTCTCATGTTAAGTTTTCTTTTACTGTATATTTCTGTGTTTTATCTATTAGTGCTTTATTAGCATCTTCAGACATGGGTATCAGGGTCCCATCACAAAAGAAGCACATCAACATTTCAAGCCTAAAAAATCAGCTCAGACCTCTGGTAATGTTTTTATTATTTGATGTCCATGAGACTTTTTGAGTACATTTTGTAAAATGATTTACAGTAATATATCTAAATCACAATACATTTTTAGGGTATTGAAAAAAATTGTAAAGATTTTTTATTTTTGTTCAGGAACTCATGGCAAAGTCTCCTCTCCTTCTCTTGGGGTTTACATTATGCAGCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6170
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112054 Nonsense 1315 1807 13 18
Genomic Location (Zv9):
Chromosome 10 (position 22144738)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 21975166
GRCz11 10 21945506
KASP Assay ID:
554-5379.1 (used for ordering genotyping assays)
KASP Sequence:
ATGCAATGGTCTATCTACARTWAAAGAGGTTGTTTTGTCTGTTCTGAAGT[T/A]GTGTGAATCACAKCAGTTTACCTCCATTGCCTTCCCTGCTCTTGGCACAG
Long Flanking Sequence:
ACTTTTTACATGAAATAATTAGTAATGTAATTAGATTACAATTTTCCAGTAGTAATCAGTAATTTGTAATCGATAACTTTTTAAAAGTAACTTACCCACCACTGCTCATTTGAATCTTCATTCATTATTAATTTCTCATTCACAGAGAATCATAATGTTATTGTTTTTATTTTTGTAATTCAGGAGTATCCAAGGCCATCTTAGATGCTGCTGGAGGAAAAGTAGAACATGAATGTTCACAAATTGGTTCGTTTACATATATAAAATATTTTATATTTTAATTGATATTTTGTTATGTTGATGAATATTACTTAATGAGATATAATGAACTTTATATTTTGCTGGTAAACCCACTTTTTTTTCAATAGTGGCATCACAAAACAAGCAGCTTAGAGAAATTGTGACCTCATCCGGACGACTCCCGTGTGGAAAGATCATCCATATTTCTGGATGCAATGGTCTATCTACAATTAAAGAGGTTGTTTTGTCTGTTCTGAAGT[T/A]GTGTGAATCACAGCAGTTTACCTCCATTGCCTTCCCTGCTCTTGGCACAGGTAACACGTGGTCCATAGTTAAAGTAAGTTTTGATTATTTACTTAACTAACAATTTGTCAAAATTCTTCACTATTCTTTTCTTTTTGGGAAATGTTGTGAAACATTTAGGTCAGGGTGGTGCGGAACCTGGTGATGTTGCAGATGCAATGGTTGATGCAGTTGTTGACTTTGTGAAGAAGAAGAAACCGGTGCATGTAAAGTTCGTGAAGTTCCTTATATTCCAGCCAAAAATGCTGGCAGATTTTCACCAAAGCATGGTGAGAAGATCTGGTGAGAAGGTTGAAGAGGAAAAAGGTCTGTTCACCAAAATTAAAGGTCAGTAAAAATTCTAAGGTTTGCTAATCCTATATATTGTAATTTTTGAACAGTTATTGATCTCTCCTTTTTTCATCAAACATGGGCCTTGGAAAAAAAAGATTATTTTTTAGGGGAAAGTTCAGAATCTTCCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34896
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112054 Nonsense 1487 1807 15 18
Genomic Location (Zv9):
Chromosome 10 (position 22144010)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 21974438
GRCz11 10 21944778
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGAAATGCTGAACGCCATGCAGAAGGAGCTCACAGTCAGTATCAAACTA[G/T]AGAGGAAAGGCCAAGACTCTGTCGTTACTATGGAGGGTCTGACAAGAGAT
Long Flanking Sequence:
AAGAAGAAACCGGTGCATGTAAAGTTCGTGAAGTTCCTTATATTCCAGCCAAAAATGCTGGCAGATTTTCACCAAAGCATGGTGAGAAGATCTGGTGAGAAGGTTGAAGAGGAAAAAGGTCTGTTCACCAAAATTAAAGGTCAGTAAAAATTCTAAGGTTTGCTAATCCTATATATTGTAATTTTTGAACAGTTATTGATCTCTCCTTTTTTCATCAAACATGGGCCTTGGAAAAAAAAGATTATTTTTTAGGGGAAAGTTCAGAATCTTCCGCAAATGAAGAGTTTGTGATGGTGGGTGAAGAAATTGAGCCGGCTGTGTTTCAGCTGTGTGGAGAGACACCACAGGACCTGAGTGAAGCCAAGGAAATGATCAACAATTTTATAATACGGGAGCATTTGACCATCCCAATCCATGATCCAGCCATTGCTTATTTCACCAGAGAGGATGTAGAAATGCTGAACGCCATGCAGAAGGAGCTCACAGTCAGTATCAAACTA[G/T]AGAGGAAAGGCCAAGACTCTGTCGTTACTATGGAGGGTCTGACAAGAGATGTTCACACTGCAGAGAGTCGGGTTCGGGACATGATCCGCAAGGTGGAAAGAAATGAAAGCAAAAAACGTGAAGCATTAATGATCAGAACTATAATTAAATGGCAGTATCAGGAGAATGGGCAGAGATTCGAAAACTTTGACATGCTGACCAATTTTGACTTGGAACAAGCCTTTCAGAATCAGCAGCCCTCAGTAAAAATCAAGATTAACAATGATGAATATGAGGCTGATTTAGTTAGCAAAGAGGCCAAAAGAAGAGGAATAAGGATTAAATTGAATAGAGTAGATCTGGAAGGTGGGATTATTATTTAAATATTAATTAAAATGTCATCCTGTACAAATATCAGGTATTAATGTTTTTCTTTTTCCCTTTGTAGATACAGCTGAGGCTGCATCCCAAAGCTCTTTGCCTTCACACTGGGAGAACATGAAAGGAAATTCAGTCATTCT
Associated Phenotype:
Not determined