Busch Lab

ZMP

ENSDARG00000034467

Ensembl ID:
ENSDARG00000034467
Human Orthologues:
AHNAK2, PRX
Human Descriptions:
AHNAK nucleoprotein 2 [Source:HGNC Symbol;Acc:20125]
periaxin [Source:HGNC Symbol;Acc:13797]
Mouse Orthologues:
Ahnak2, Prx
Mouse Descriptions:
AHNAK nucleoprotein 2 Gene [Source:MGI Symbol;Acc:MGI:2144831]
periaxin Gene [Source:MGI Symbol;Acc:MGI:108176]

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa28063 Nonsense Mutation detected in F1 DNA Not yet available
sa13531 Essential Splice Site, Missense Available for shipment Available now
sa42135 Nonsense Mutation detected in F1 DNA Not yet available
sa35416 Essential Splice Site, Missense Mutation detected in F1 DNA Not yet available
sa10978 Nonsense Available for shipment Available now
sa22215 Essential Splice Site Available for shipment Available now
sa22214 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa28063
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
ENSDART00000064001 Nonsense 132 1062 4 17
ENSDART00000064005 Nonsense 217 1272 2 18
Genomic Location (Zv9):
Chromosome 13 (position 6924486)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 6976827
GRCz11 13 7309133
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGGAAATCATCCAAAGTGAAAGACATGCCAGATGTAGACATAGATGTT[A/T]AAGGACTTGATGTGAGCCTTCCAGAAACAGAAGTAAATGTGAAGCTAAAA
Long Flanking Sequence:
GTGCTGATATTCATATTCCTGATGTCAGCACAGAGGAAACTACAGTGAATGTTGAGTTGCCAGAAGCTAAATTGTCTGTAGAATCGACAACACTATCTGAAAATAAAGGCATGGACATGCCTCTCAGTGTATGCAAACCTAAAGTTGACTTGTCTCTGCCTGAGGGAAAAGTAGGCATTAAAGATATAAGTATTCCAAAAGTAGATGATTTTCAGAAAAAAACAGAGGCTGATGCTAGTATCACTGGCCATGATGTAGAAATTTCAAAAAAAGACATCAAAGATGATATCAGTCCCCCACAGGTTGATGCGCCCATTCCAGAAGCTTCTGTTGAAATAAAAGTGCCAGAAGTGGATTTCACAACTTCAAAGGAAGATGCTGAAGATAAAAACATAACAGGTGGTGCACCAATAAAGATTAAACTACCCTCTATCCACTTACCAACATTTGGTGGGAAATCATCCAAAGTGAAAGACATGCCAGATGTAGACATAGATGTT[A/T]AAGGACTTGATGTGAGCCTTCCAGAAACAGAAGTAAATGTGAAGCTAAAAGATGATGCACCTTCATTTGAAGTCAAGGATTCTTTTGTGACTATGAGAGGTGTAGACATGAAGGTTGAAGAAGCAAAGCTCAAAGACCAAGATGTTATGGTTACACTGCCTAAATTTGGCATTAGCCTTCCAAAGGTTCAAGCCCACAAACAAGAGGATATTACTGACAAAGAATCAAGTACAGACACCAAAGAATCAAAACCAGAGTCTGACCAGGCTGAGAAAGGTTCAAGGTCTCCAACAAAAGTTAAACTTCCTACTTTTAAATTTCCAAAGATTGGTGTCTCATATCCAAAATCACCAGATGTAGACTTAGACAATCAAGTCACTATGGTCAACACAGATGAACCTACTATAGAATTTAAAGAACCTTCTGGAGAAATACCAGCATTGCCTAAACTGAAAACCCAGCACATTACTCTCAGCGTTTCCAAACCTGAAGTTGATGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13531
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
Order Allele From EZRC
Mutation:
G > A
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000064001 Essential Splice Site 179 1062 5 17
ENSDART00000064005 Missense 388 1272 4 18
Genomic Location (Zv9):
Chromosome 13 (position 6923651)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 6977662
GRCz11 13 7309968
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
MTTTTCCAAATCGGACACTAAGGTCCCTGATGTTGATACAAATCTTCAAG[G/A]TACATCAGTGCAAGAAATTGAGACTGAGRTGACTGTTCCTGCTCCAGAGC
Long Flanking Sequence:
CTCATATCCAAAATCACCAGATGTAGACTTAGACAATCAAGTCACTATGGTCAACACAGATGAACCTACTATAGAATTTAAAGAACCTTCTGGAGAAATACCAGCATTGCCTAAACTGAAAACCCAGCACATTACTCTCAGCGTTTCCAAACCTGAAGTTGATGTTTCTATGCCAAAGGGAGATAAGACTGCTGATGCCCACTGTGAAAAGAAAAAAGAAAAGATTTTGTCTTCAGACAACAAAATTTCCAAATCAGAGGTAAAGACGATCCATGTAGATCATGATCTTGATCAAAAGACAGATTTAGAAGATTTGGAAATGCAAGGCAAGCAACTTGACATGAAAATCAAACTTCCTTCAGGTACAGTGGATGTAGTTATCCCAGAGGCTAAAGAAAAAGAGAGTGAAACTAAACTCAAAAAACGTAAAATATCATTTCCTAAATTTGGCTTTTCCAAATCGGACACTAAGGTCCCTGATGTTGATACAAATCTTCAAG[G/A]TACATCAGTGCAAGAAATTGAGACTGAGGTGACTGTTCCTGCTCCAGAGCTTGAGGTTCAGATGAAAAACAAAACTTCAGGTTCTCCATCTAAATTCAAGCTTCCTACAATTTCTCTCCCTAAGTTTGACATTTCCATTTCAAAAATGGAGGAAGAATCTACTGCAAAAGCTGATGAAGCTGCACATGAAGTAAAGGTACCATCAGGAGATACATTGCAAGATCAAGATACAGGGAAAGAAGGTACAGAAGCATCAAAGCTAATTTTGGAAACCCTTCCAGAAAATGTTGAAATAAAGACAAAAGACTCTGATCCTGAAAGCCAAGGCAGCAAATTTACTATGCCCAAATTTGAATTTTCATTTCCAAAGCTAAAGGGACCAGAATTCAAAAAGGGTGCATCAAAAATAGATACAGACAAAACAGAGGCTACACTGAAATCTTATATGGAGAGAGCAGAGGGGGAAACTGAAATACCGGAGGCTTCTGTGGAATTTGAGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42135
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
ENSDART00000064001 Nonsense 210 1062 6 17
ENSDART00000064005 Nonsense 558 1272 7 18
Genomic Location (Zv9):
Chromosome 13 (position 6922752)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 6978561
GRCz11 13 7310867
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAAGGAGAACTCTGGGAACCATCAGCTGAAGTGGAAGTACCAAAAGTT[A/T]AACTAGAATGCAAAATAGACCAAGAAGCTGATTTAAAAGACACAGGAATT
Long Flanking Sequence:
CATCAAAAATAGATACAGACAAAACAGAGGCTACACTGAAATCTTATATGGAGAGAGCAGAGGGGGAAACTGAAATACCGGAGGCTTCTGTGGAATTTGAGGTAACATCTGCATCCGTCCAAGCAGGTGAACTGGATGTGAATGTTGAATCTGACTTGAAAATTCACACAACAGACATGTTAAAAGATGATACAACCACGGGAGGGTCACCAATTAAATTTAAACTACCTTCTTTTAAACTACCCAAATTTGGAAGTTCATATTCCAAAGAAAAACCTGAAATAACTGATTTGAAGGGTGGGGAAATTACTTTGAAGGCTGAAGAAATAGAAGCATCGGATTTAAAAATGGACTTCGGTCTAGAGCTAAAGAAACCATCAATCAGTGTTCAACAGCCAAAGGTTCTTACAGAGGCCCAAACATCAAAAGCAGAAGGTGATATTTCCTTACCAGAAGGAGAACTCTGGGAACCATCAGCTGAAGTGGAAGTACCAAAAGTT[A/T]AACTAGAATGCAAAATAGACCAAGAAGCTGATTTAAAAGACACAGGAATTAACATAAAAAGACCAGGCTTTTCACTTCCTAAATTTGGATTTTCTAAACCAGATAAGGTGCCTGAGATCGATGTCAATCTGATGCAAGTTGATTTCTCTAAAACAACAGGTGATGTGAAAATAAACGATCAAAGTATGAATATCACTGCACCAAGTGTTGAGCAAAAAGATCTAACTCTTGATGCCACAACAAAAGATACACTTTCCTCAATTAACTTACCAAAGTTTGGAGGACCTTCTATTAAGGTTGAGAAAACTATGCAAGTTGTGGATATATCGGTAAAAGAACCTGAGGTGAGTACTCCAGATGCACAAGTAAGTGTGGACTTAAAGGTTAAAGATGCCGAACTTGGAGGACAGGAGAAAAAGCTTAAGATGCCAAAGCTTGCTATAGGTCTTCCCAAAGTTAAAGGGTTTGAATTAAGTACAAAGACTGAGGATGTAGCTGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35416
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, Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000064001 Missense 465 1062 7 17
ENSDART00000064005 Essential Splice Site 766 1272 None 18
Genomic Location (Zv9):
Chromosome 13 (position 6921837)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 6979476
GRCz11 13 7311782
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTAGAGGGAGCAAATATAAAACATGACATTTCAAAACCTGATGTCAAA[T/A]TAGAAATAAAACCATCTAGTATTGAAGCTAAAGTTGAAAGCAGCACAGAC
Long Flanking Sequence:
AAAAGCTTAAGATGCCAAAGCTTGCTATAGGTCTTCCCAAAGTTAAAGGGTTTGAATTAAGTACAAAGACTGAGGATGTAGCTGAAGTACAACCAATTGATGTCAAACAACCCGATATGACAACTGAAGGGAAAGTTCCCCCACCAGAATACGATTCTAAGACACTAGATGTGCAGATGAAGACATTACCTGGACTTGGGTTCTCAAAACCAGAAGTAAAATCCCCTGAGGTTGATGTAAGTACCCAAAAAACAGATATTCTCATACCAGAAGGCAGTCTAGACCTGGGAGAAGCAAATGTGGATGTTAATGTTTCAAAGGTGGAATGTGAACAGAAGGGTTCAACATTTTTTGGATCTCCTACAAAATTTAAACTCCCTTCAATTAGCTTCCCAAAATTTGGTGTTAAATCACAAAAAGTAGCGTTAGACACTAATGTAACAGAATCAGAACTAGAGGGAGCAAATATAAAACATGACATTTCAAAACCTGATGTCAAA[T/A]TAGAAATAAAACCATCTAGTATTGAAGCTAAAGTTGAAAGCAGCACAGACACACCTGATGTTGATTCGAAAGAACCACAAGTAAAAGTGAAGAGACCAAGCTTTTCATTCCCTAAGTTTGGATTTTCTAAATCAGACACTGCAACTCCAGAAGTAGATGTTAGTGTTCATAAGGTTGAACCATCCATACCAGAGACCACTGTAACAATTAAAGAACAAACAGCAGAAATTGCTCTTCCAGGAGGGGAGGCTGAACAGAAAGATCTAACTAGTGTTATTTCCCCAATCAAAATTAAGCTGCCAGAAGTCAACCTGCCAAAATTTGGAGTCAAAACCTCAAAAGGTACAGTAAGTTTACCATCACCAGATAAAGACATTATAGAAATTACAAATCAACAACCAGACATCAAGGTGGCAGGTGAAATTGTAAAAATGGGAAAAGAGGCTGATGTAAACATCACATTAGGAGAAGCTGATGTTCTTCCAAAAGAAGAAAAAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10978
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
Order Allele From EZRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000064001 Nonsense 627 1062 9 17
ENSDART00000064005 Nonsense 924 1272 12 18
Genomic Location (Zv9):
Chromosome 13 (position 6920787)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 6980526
GRCz11 13 7312832
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGGAAKTAAACCCAAGCTACCAAAAATGGGAATTAGTATGCCAAAAGTA[A/T]AGGAGATGGAACAAGAAAGTAAAGACATAAAAATAGAGACTGACCTGCTA
Long Flanking Sequence:
AAGCAGACATACCTGAAGTTGATCTGAGAGGACTTGATGTGAAACTGAAGAAACCAAGCTTTTCATTTCCAAAATTTGGTTTTTCAAAGCCAGATAAGGGGCAAAGCGTTGATGCAAGTCTTCCAAAGACAGAAATGTCTATAAAAGAGGGTGACATACCTGTTAAAGAAAAAGATGTAGAACTTGCCTTCACACGTGAAGAAAATAAGCAGGAAGATCCAAACACTCAAACAAAATTTAGACTGCCCTCTATTAACCTTCCAAAGTTTGGTCTCAAATATCCAAAAGCCACACCTGAAATTTCATCAACTGAAGTAGACATCAGAAAACCTGAAATATCTTTCTCTGAAACAGGAGAAGTGCAAACTACTGACACAAAAATAAATATTGACATTAAAGGGCCCACCACTGATGTGGAAAGTAAAGATATGGAGGTGGACATTGATGTGACAGGAAGTAAACCCAAGCTACCAAAAATGGGAATTAGTATGCCAAAAGTA[A/T]AGGAGATGGAACAAGAAAGTAAAGACATAAAAATAGAGACTGACCTGCTATGCAAAGAAAAGGTAAATGTACAACAGCCTATTGAGGGGAAATTAGATAAAGCAGAAGTTGATTCCAAAGGACTAAAAGTAAAACTTCCAAAGCTGGGATTTTCAAAATCAGATCTTAAGACTCCTGAAATTGATTCGAGACTGCCCAAAGCTGACATGAGCATATCGGTGGGAAATGTTGATTTTGCAGAGCTATCGGCTGATAATAAATTACAAGAACAAGAACAAGATTTGAAGGTTGACACTTCTGGCTCACCAACAAGATTTAAACTACCAACAGTAAATTTGCCAAAATTTGGAATTAAAGCATCAAAAGACACAGTGGACATTAGTACAGCCCACATTGACACCAAAAGCCCTGAAGTTAGCCTTCCGGATAAGAAATTACTGTCTGGAGAAGTGTCAACCATTGACACGAAGGAACTAACAGAAGTAGATCCATCTATTGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22215
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000064001 None None 1062 None 17
ENSDART00000064005 Essential Splice Site 1011 1272 14 18
Genomic Location (Zv9):
Chromosome 13 (position 6920360)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 6980953
GRCz11 13 7313259
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTAGTACAGCCCACATTGACACCAAAAGCCCTGAAGTTAGCCTTCCGG[A/T]TAAGAAATTACTGTCTGGAGAAGTGTCAACCATTGACACGAAGGAACTAA
Long Flanking Sequence:
TATGGAGGTGGACATTGATGTGACAGGAAGTAAACCCAAGCTACCAAAAATGGGAATTAGTATGCCAAAAGTAAAGGAGATGGAACAAGAAAGTAAAGACATAAAAATAGAGACTGACCTGCTATGCAAAGAAAAGGTAAATGTACAACAGCCTATTGAGGGGAAATTAGATAAAGCAGAAGTTGATTCCAAAGGACTAAAAGTAAAACTTCCAAAGCTGGGATTTTCAAAATCAGATCTTAAGACTCCTGAAATTGATTCGAGACTGCCCAAAGCTGACATGAGCATATCGGTGGGAAATGTTGATTTTGCAGAGCTATCGGCTGATAATAAATTACAAGAACAAGAACAAGATTTGAAGGTTGACACTTCTGGCTCACCAACAAGATTTAAACTACCAACAGTAAATTTGCCAAAATTTGGAATTAAAGCATCAAAAGACACAGTGGACATTAGTACAGCCCACATTGACACCAAAAGCCCTGAAGTTAGCCTTCCGG[A/T]TAAGAAATTACTGTCTGGAGAAGTGTCAACCATTGACACGAAGGAACTAACAGAAGTAGATCCATCTATTGAGATTGAAATTAAAGGAGATAAAAAAGAGCTACAAGATGGCAAATTCAAGATTCCAAAATTTGGAATTGGTCTACCAACCATAAAAGGTCCAGATAGCGGAGTGCTGGCCAAACGTGAAGAAGGAACAGTTTCAGGGGATGTATTATCTACAGACAAGAAGGAGCTAAAGTTACCCAAAGGATCAGTAGAAGTGGATATGAAGGCTAAAGGTGTTAAACTTGAAGTAGAAAAAAGTAAATTCAAACTACCAGAGCTTGGAATTTCACATGAATTGAAAGGTCCAGAAATTGACATAAGCATTTCCAAAGCCGAAGTTCCTCAAACTGAAGTTAAAGAAGTCAAACCTGCTGAAGCAGAAATGGATGTCAGTTCTAAGGGACTTAAAACGAAGAAGCCAGGCTTTGGATTGCCCAAAATTGGATTTTCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22214
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000064001 Nonsense 954 1062 16 17
ENSDART00000064005 Nonsense 1264 1272 18 18
Genomic Location (Zv9):
Chromosome 13 (position 6919167)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 6982146
GRCz11 13 7314452
KASP Assay ID:
2260-6012.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTTAAAATGCCAAAATTTGGAATTTCAGGTCCAAAAATATCCGATGCA[A/T]AAGCAAAACTGGGAGCAGACGTACCAGATAATGCTGACCTAAATATTGAG
Long Flanking Sequence:
AGGTGACTAAGGATGCACTAAAGTCTGATTCTGACATCAAGGACATTAAAGTTAGTTCAGTGGATAACAAGATAGAAACAACAAAGGTGGAAATATCTGGTGACATCAAAGGCAAAACTGCAGAGATTGAAGCCCCATCTGTTAGCATCAATATAAAGGGAAAGGAGATTAATCAGGAGGTTCAGGAATCTAAATTTCAAATTCCAAAATTTGGGATTTCATTACCCAAAGTAAAAGGTCCTGAGGTAACAGTGACTGCGAAAGAGGTCAAGACAGGAACACCTGACACTGGGATTACTGAACCAGAAATTAAGATTCCAGGTGATGTAAGTGTCCCAAAAGTAGATATTGCTTTAGAGGGAAGTTCCAGCCTTGAAAAAAAAGAGGTAGAGACAGAGGTGAAAAATGATGAACCTGTTTCAGGTTCACCAAGTAAATTCAAATTGCCTGCCTTTAAAATGCCAAAATTTGGAATTTCAGGTCCAAAAATATCCGATGCA[A/T]AAGCAAAACTGGGAGCAGACGTACCAGATAATGCTGACCTAAATATTGAGAACAAGCCTAAACAAGTGTCTACAGATATACACAGAGAAGGTGAAATTAAAGAAACCTCTGAACCTCCTCCAGAGGCTGCTGTCAAAAAACTAGATGGAGAAAAGGGTTCCCCAAGTAAATTCAAACTTCCAACTATAAAAATGCCAAAGATTAGCCTTTCAAGAACAAAATCTCAGGATGAAGATGACACAACCATTAAAGCCAAAGCTCCAGAAGCTAAAACAGAACACAAAGATGATGCACAAGCACCTGGAAAATCACCCAGATTTGCAATGCCTGCACTCGAGGATGTTCTCAGGGGCTTTGAGGTTGAATTTAACGTCCCAACAATAGAACAAACAGACGGTCAATTGGACAAACCTTCTGTCAAGCAAGATCAAGAAGCAGGAGAAAAAACTCAGGAAGCAGCAGAGCAGAAGGAAAAAGGAGCTCAGGAAAAATCCAAATTT
Associated Phenotype:
Not determined