ZMP
PARP14
Ensembl ID:
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]
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]
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.
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.
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.
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.
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.
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