Busch Lab

ZMP

papolg

Ensembl ID:
ENSDARG00000012141
ZFIN ID:
ZDB-GENE-040426-1256
Description:
poly(A) polymerase gamma [Source:RefSeq peptide;Acc:NP_956915]
Human Orthologue:
PAPOLG
Human Description:
poly(A) polymerase gamma [Source:HGNC Symbol;Acc:14982]
Mouse Orthologue:
Papolg
Mouse Description:
poly(A) polymerase gamma Gene [Source:MGI Symbol;Acc:MGI:2442119]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa1701 Essential Splice Site F2 line generated Not yet available
sa22310 Nonsense Available for shipment Available now
sa30972 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa1701
Status:
F2 line generated
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
ENSDART00000015154 Essential Splice Site 84 744 3 23
ENSDART00000124089 Essential Splice Site 84 744 3 24

The following transcripts of ENSDARG00000012141 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 26060957)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 25706617
GRCz11 13 25837067
KASP Assay ID:
554-1647.1 (used for ordering genotyping assays)
KASP Sequence:
AGCTAAATTCGTTTGTGAAGGAGTGGATTTCTGAAATCAGTGAATCAAAG[G/T]TAGGTAAACCTGCAGGTTTCTTAGTTTGATCATCAGGTTGGATGAGATGC
Long Flanking Sequence:
TGGATGTCACTGTGACCTCGCTGTGGCCAATTGATAATCATGACACAAGCACTGACCCTGAAAATCTTCCAGACATAATATTTTTGTAAATTTGTCCATCGGTGGTGCAATGAGAAAAATGTGAGTTCTTCACTAAAATCAGTTGTTCTTCAACTGTTATTTATACACAAAAACATAATTATATTCAGATATTCACGTTCTATACACCTATATCAGTTGTGCTGAAACCTTTATGTACAGCTTTTTGCATTGAGATAATAAAAAGAATCTCATCTTGTGTTTTTTTTTTTCCCACATAACTTTTTTTACTTATAAAATAACTTTTCCTTTGTTACAATTTTGTGTAGTTGGAAACTTGGTATCCTACAAATGAGCTTTTTGCATGTTCTGAGTGACTGTGAATACTAAGAGAAGCATGTGTGTGTTTTTGAAGGCTTGCGGTTCTTGGGAAGCTAAATTCGTTTGTGAAGGAGTGGATTTCTGAAATCAGTGAATCAAAG[G/T]TAGGTAAACCTGCAGGTTTCTTAGTTTGATCATCAGGTTGGATGAGATGCTTTTCTAAATCATTCCTTTTAATCTACAGAATCTTCCACCGTCAGCAGTAGCGAATGTTGGTGGCAAAATCTTTACGTTTGGGTCCTATAGGTTGGGAGTGCACACAAAAGGTACATTTGATAAGCTGCTGAATAAGATCTTGGGAGAGAGCCATTGCACAAAACGGTACATGAGCCATTGCTAATCAAAATATTGTTTCTTTAGGTGCTGATATAGATGCTTTGTGTGTTGCCCCACGTCATGTTGAAAGAACAGACTTTTTTTCATCCTTCTTTGAAAAACTAAAACGGCATGATGAGATTAAGGACCTACGCGTGAGTACTTTTAATGTGCTTCATAGTTTATTCCTCTGGCTTTTTTATAAGAAGTGAATTTTTAATATTGTGTGAAATTCTTTTTCAGGCTGTGGAAGATGCATTTGTACCAGTGATCAAGTTCAAGTTTGATGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22310
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000015154 Nonsense 301 744 10 23
ENSDART00000124089 Nonsense 301 744 10 24

The following transcripts of ENSDARG00000012141 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 26056431)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 25702091
GRCz11 13 25832541
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGTGCTTTTAAAACAACCCGAAGACAGCAATTTGAATCTGCCGGTCTG[G/A]GATCCACGGGTCAGCACTCATGTTCATTGTGATTAATATACTGTTCTTGG
Long Flanking Sequence:
TAACGTGTTAACCACACTTCTCATATCTGCTTTGAAATGGAGACTTTTGATATCTTTTGTTCTCGGTTTTAACTTGAATAAACATGTTAAGAATGCATTTCACTGATATTGTCTTTTTTTTCCCCCCTTCCTTTTTTTTTTTAAGGCCGTGGAATCTATTCCAACATGCTAGGCTTTCTCGGCGGAGTTTCCTGGGCTATGCTGGTGGCCAGAACATGTCAGCTTTACCCAAATGCTGTTGCCGCCACGCTTGTGCATAAGTTCTTTCTGGTCTTCTCTAAATGGTGAGGTCACATCACACCAGGTTCATATAGTGGAACTGAAACTTCACGTATCGTGTGCTGAAATTGTCTAGTCCCTATCATGTAGCAATGGAATGTCCTGTTTCCTTCCTAATTCTATTTGTATGCATTTGTCCTCTGATTTGACTTCTTCAGGGAATGGCCAAACCCTGTGCTTTTAAAACAACCCGAAGACAGCAATTTGAATCTGCCGGTCTG[G/A]GATCCACGGGTCAGCACTCATGTTCATTGTGATTAATATACTGTTCTTGGTTTTACATGCTTTCTGATTTGACTATACCATTGTTTGTTCTTCTGCTTTCAGGTGAATCCATCAGACCGGTATCACTTAATGCCAATCATCACTCCTGCATATCCACAACAGAACTCCACCTACAACGTGTCCACTTCCACACGCACTATCATGAATGAGGAGTTCAAGAATGGTGCGTAACTGAAGTCGAAGAAGGAACAATTTGTGTTTTTACTGATCATTACAATTGACAGATACATTTCTGGTTTTAGGTCTCACTGTTACAGATGAAATTCTTCAGGGTAAAGCCGACTGGTCCAAGTTGTTTGAACCTCCCAACTTTTTCCAACAGTATAGGTACGTGGATCTCTACAATGTCATATTCAAGATTTAATTTTAAGCAATCCACTTTTTCATAGTTATGATGGTTAGCCCTGGCTCATTCTAAACCCCAGGTAAAAAAACTCCCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30972
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
ENSDART00000015154 Essential Splice Site 468 744 15 23
ENSDART00000124089 Essential Splice Site 468 744 15 24

The following transcripts of ENSDARG00000012141 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 26053751)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 25699411
GRCz11 13 25829861
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTGAATATTGACTTGACCTACGACATTCAGTCTTTCACAGATACTGG[T/A]AAGCTGCTCCTGAATTTTATTAAATTACATTGCTACCTTTTAATATCCAA
Long Flanking Sequence:
ATAATGCAAATCCCTTCTGCAGATTTATAGCCATCATTCAGACTATTTAAATGTCATATTTCTGCCATTTTGTACTACATCTGTTGTAGTAACTCCTTTACAATAAGGTTGTGTTTAATGCATTTACTAACATTTATAAAGAATAAACAAATTTATTAAAGTATTGTTTATGTTCGTTAATAAAAATACAGTTTATTGTTAGTTCATGTTAACTCGCGTTGCTTTAATGTTAACAAGCATGAATGGGGATTTTAATAAGGCATTAGTAAATTTTGAGCCATGATTAATAAATGTTGTACATCAGGCTAACGATTTGGTGTGGTTTTTCTTTTTCATAAACCAATATGCTCATCAGCTTTTAAATGTAGAAATCGGTTTTTGTTTTGCAGGAATGATTTTGTTTCCATGTGGTTTATTGGAATCAGCTTTAAAAAACTGGACAATTCTGACTGTGTGAATATTGACTTGACCTACGACATTCAGTCTTTCACAGATACTGG[T/A]AAGCTGCTCCTGAATTTTATTAAATTACATTGCTACCTTTTAATATCCAAATATTGTGTTTTGCTGTAGTTTATAGACAGGCCAGCAACATCAACATGCTGAAGGATGGCATGACGATTGAGGCTACACATGTGAAGAAGAAACAGCTGCATCATTACCTGCCTCCTGAGCTGGTGCAGAGGAAAAAGAAGGTAAAATCAGTGTCTGAGTGTTTACAGTAAAAGTCAAAACATTTATAGTCTCTATAGATGTTATACATGTATTCCCTCTCTTTTTTTTTTTTTCTAACAGAGTTTGGGAGATATAAACCGGAGCTCAAATGGTGGCGGGTCAAAGCGCTGCTCTCTGGATAGCAGTCAGCTGGACAGCTCCAGGGACACAGACATTGGCACGCCATTCAGCTCTCCTACACCCATCAGCAAACCATGCCAGCCAGCCTCCACACCTGAAGACAAGTAAAGTTTAGCTATATTTTCATCCACATTTTGACATTCATAGAA
Associated Phenotype:
Not determined