ZMP
ENSDARG00000034467
Ensembl ID:
Human Orthologues:
AHNAK2, PRX
Human Descriptions:
AHNAK nucleoprotein 2 [Source:HGNC Symbol;Acc:20125]
periaxin [Source:HGNC Symbol;Acc:13797]
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]
periaxin Gene [Source:MGI Symbol;Acc:MGI:108176]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13531 | Essential Splice Site, Missense | Available for shipment | Available now |
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:
sa13531
Status:
Available for shipment
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:
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:
sa10978
Status:
Available for shipment
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:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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