ZMP
si:ch211-14c7.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate periaxin (PRX) [Source:UniProtKB/TrEMBL;Acc:Q1L8A1]
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 13 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32221 | Nonsense | Available for shipment | Available now |
sa23379 | Nonsense | Available for shipment | Available now |
sa23378 | Nonsense | Available for shipment | Available now |
sa18071 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32221
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 |
---|---|---|---|---|---|
ENSDART00000059039 | Nonsense | 1190 | 4197 | 4 | 4 |
ENSDART00000134244 | None | None | 84 | None | 5 |
ENSDART00000145999 | None | None | 149 | None | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 44628689)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 46222218 |
GRCz11 | 18 | 46220236 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTAGATATCTCTCTACCAGGAGGTAAAGCTGGAGGTAATGTAGATGTC[A/T]AAGCTCATGGAGGACAAGGAGAAAAATTTGAAATGCCAAAATTGGATGTC
Long Flanking Sequence:
CCAAATTTGATGTTTCATTGCCCAAATTAAAACCATCTGAGGCTGAAGTTAACATTGAAGGTCCCGATATCAAAAGTGGAAAGTTTCACATGCCCTCTCTAGATATCTCTCCACAAAGAGAGGGAGCAGAAGGTGATGTAGATGTTAAAGCTCATGGAAGAAAAGGAGGAAAATTGGAAATGCCAAAATTGGACGTTTCCCTGCCTAAATTTAAAGCTTTTGGAGCAGAAATCAACACTGAAGATCCCAATATCAAAGGTGAAAAGCTTCACATGCCCTCTTTAGATATCTCTCTACCAGGAGGTGATGTAGATGTTGAAGAGTATGGAGGAAAAGGAGGAAATTTTGAAATGCCAAAGTTGGATGTTTCCTTGCCTAAGTTTAAACCATCTGGGGCTAAAATTAATGTTGAAGGTCCCGATATCAAAGGTGGAAAGTTTAACATGCCCTCTGTAGATATCTCTCTACCAGGAGGTAAAGCTGGAGGTAATGTAGATGTC[A/T]AAGCTCATGGAGGACAAGGAGAAAAATTTGAAATGCCAAAATTGGATGTCTCCTTGCCCAAATTAAAAACATCAGGAGGTGAAATCAACATTGAAGGTCCCGATATCAAAGGTGAAAAGTTTCACATGCCCTCTGTAGATATCTCTCTACCAGGGGGTAGAGCAGAAGGTGATGTAGTTGTCGAAACTCATGGAGGACAAGGAGGAAAATTTGAAATGCCAAAATTGGATATTTCCTTGCCCAAATTTAAACCATCTGGAGCTAAAGTCAATGTTGAAGGTCCCGATTTCAAAGGTGGCAAGTTTCACATGCCCTCTCTAGATATCTCTTTACCAAGAGGTGGAGCAGAAAGTGATGTAGATGTTGCTGGACATGGAGGAAAAGGAGGAAAATTTGAAATTCCAAAATTGGATGTCTCCTTGCCCAAATTAAAACCATCAGGAGGTGAAATCAACATTGAAGGTCCCGATATCAAAGGTGGAAAGTTTCACATGCCCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23379
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 |
---|---|---|---|---|---|
ENSDART00000059039 | Nonsense | 2359 | 4197 | 4 | 4 |
ENSDART00000134244 | None | None | 84 | None | 5 |
ENSDART00000145999 | None | None | 149 | None | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 44625182)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 46218711 |
GRCz11 | 18 | 46216729 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGGAGGAAAATTTGAAATGCCAAAATTGGATGTCTCCTTGCCTAAATTA[A/T]AACCATCAGGAGGTGAAATCAACATGAAAGGTCCAGACATCGAAAGTGGA
Long Flanking Sequence:
GAAAGTTTCACATGCCCTCTCTAGATATCTCTTTACCAAGAGGTGGAGCAGAAGGTGATGTAGATGTTGAAGGACATGGAGGAAAAGGAGGAAAATTTGAAATGCCCAAATTTGATGTTTCCATGCCTAAATTTAAACCGTCTGGGGCTGATGTCAATGTTGAAGGTCCCGATATCAAAGGTGGAAAGTTTCACATGCCCTCTTTAGATATCTCTCTACCTGGAGGTAAAGCTGAAGGAGGTGTAGATGTCAAAGCTCATGGAGGAAAAGGAGGAAAATTTGAAATGCCCAAATTGGACGTTTCCTTGCCCAAATTAAAAACATCTGGAGGTGAAATCAACATTGAAGGTCCCGATATCAAAGGTGAAAAGTTTCACATGCCCTCTGTAGATATCTCTCTACCAGGGGGTAGAGCAGAAGGAGATGTAGTTGTCGAAACTCATGGAGGACAAGGAGGAAAATTTGAAATGCCAAAATTGGATGTCTCCTTGCCTAAATTA[A/T]AACCATCAGGAGGTGAAATCAACATGAAAGGTCCAGACATCGAAAGTGGAAAGTTTCACATGCCCTCTGTAGATATCTCTTTACCAAAAGGAGGCGCAGAAGGTGATGTAGGTGTCAAAGCTCATGGAGGAAAAGGAGGAAAATTTGAAATGCCAAAATTGGATATTTCCTTGCCCAAATTTAAACCATCTGGAGCTAAAGTCAATGTTGAAGGTCCCGATTTCAAAGGTGGCAAGTTTCACATGCCCTCTCTAGATATCTCTCTACCAGGAGGTGGAGCAGAAAGTGATGTAGATGTTGCTGGACATGGAGGAAAAGGAGGAAAATTTGAAATTCCAAAATTGGATGTCTCCTTGCCCAAATTAAAACCATCAGGAGGTGAAATCAACATTGAAGGTCCCGATATCAAAGGTGGAAAGTTTCACATGCCCTCTGTAGATATCTCTCTACCAAGAGGTGGAGCAGAAGGTGATGTAGATGTTGAAGGACATGGTGGAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23378
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 |
---|---|---|---|---|---|
ENSDART00000059039 | Nonsense | 2961 | 4197 | 4 | 4 |
ENSDART00000134244 | None | None | 84 | None | 5 |
ENSDART00000145999 | None | None | 149 | None | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 44623376)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 46216905 |
GRCz11 | 18 | 46214923 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTAAAAGGAGGACAATTTGAAATGCCAAAATTGGATGTTTCCTTGCCC[A/T]AATTAAAACCATCAGGAGGTGAAATCAACATTGAAGGTCCCGATATCGAA
Long Flanking Sequence:
AAGGTGGAAAGTTTCACATGCCCTCTGTAGATATCTCTCTACCAGGAGGTAAAGCTGAAGGAGGTGTAGATGTCAAAGGACATAAAGTAAAAGGAGGAAAATTTGAAATGCCCAAATTAGATGTTTCCTTGCCCAAATTAAAAACATCTGGAGGTGAAATAAACATTGAAGGTCCTGATATCGAAGGTGGAAAGTTTCACATGCCCTCTGTAGATATCTCTTTACCAAAAGGTGGAGCAGGAGGTGATGTAGGTGTCAAAGCTCGTGGAGAAAAAGGAGGAAAATTTGAAATGCCCAAATTTGATGTTTCCTTGCCCAAATTTAAACGATCTGGAGCTGACGTCAATGTTGAAGGTCCAGATATCGAAGGTGGAAAGTTTCACATGCCCTCTGTAGATATCTCTCAACCAGGAGGTGGAGCTAAAGGAAATGTAGATGTCAAAGGGCATGGAGTAAAAGGAGGACAATTTGAAATGCCAAAATTGGATGTTTCCTTGCCC[A/T]AATTAAAACCATCAGGAGGTGAAATCAACATTGAAGGTCCCGATATCGAAAGTGGAAAGTTTAACATTCCCTCTGTAGACATATCTTTACCAAAAGGAGGAGCAGAAGGTGATGTAGATGTCAAAGCTCATGGAGGAAAAGGAGGAAAATTTGAAATGCCCAAATTGGACGTTTCCTTGCCCAAATTTAAACCATCTGGAGCTAAAGTCAATGTTGAAGGTCCCAACATCGAAGGTGGAAAGTTTCACATGCCCTCTATAGATATCTCTCTACCAGGAGGTAGAGCTGAAGGAGGTGTAGATGTCAAAGGGCTAGGAGGAAAAGGGGGAAAATTGCCAAAATTGGATGTTTCCTTGCCTAAATTTAAACAATCACGGGCTGAAGTCAATGTTGAAGGTGCTAATATTGAAGGTGGATGTTTTCAAATGCCTTTAATAGATATTTCTCTTCCAAGAGAAGGAGCAGAAGGTGATGTAGATGCCAAAGGACATCCAGGAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18071
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059039 | Nonsense | 4044 | 4197 | 4 | 4 |
ENSDART00000134244 | None | None | 84 | None | 5 |
ENSDART00000145999 | None | None | 149 | None | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 44620126)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 46213655 |
GRCz11 | 18 | 46211673 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAAGAGACCTCATGGGAACTCAAAGAGACCAAGGAGACAAAGACGAYAT[C/A]AAGCACAATGTCTTTCCCAGGTCTTAAGAAGAAACCAGGGAAGGAYGAGG
Long Flanking Sequence:
CTCTGAAGTAGAATACGAGGGCCCACGTTTGCCAAAGGTAACGAAAGCAGTCTTTGTCATGGTGAATCCACAAACGGAGAGCTCTGCAAGTGCAGCTGGTGAAACAAGTGCCGAAATCGAAAAAGAAAAGCTCAAGCAGACAAAGATCACAATGAAGCAGAGTTTTGGCAAGTCAACAGAAAAGGGGAAAGCAATACATTACGGAGAGGAGGTTGAATTTGAAGGAAAGTCAAAAACTGGAAAGCTTAAGTTGCCCAAAGTCACATTTTCATCAGGCCAAAAAGGATCGTTTGATGTAACACCAAGTGGGTCTGATGATGGAGCAAGTCCAAGTCTAAATGGCGGCGACAAAGATGAAAGAGCAAAGTTTGGGAAGCTTAAATTGCCCAAGTTGGAGTTTTTCTCACCATATTCAAAAGACACAGAAGAGGAACTGGAAATAAGCATGAGGAAAGAGACCTCATGGGAACTCAAAGAGACCAAGGAGACAAAGACGACAT[C/A]AAGCACAATGTCTTTCCCAGGTCTTAAGAAGAAACCAGGGAAGGATGAGGAGGTACAGGAGATTGGCACTTTAGTGTCCTCAAAAGCACGGACTGAAATGTTGGCAGAACGGGAGGGATCAGAGTCGCCAGCACACATTGAATCAGCTGGATTTGTCTCTTTAAAGAAAAGTGAAGAAAGAGAGGAGACGACATGGTTCAAAGTACCCAAAGTAACCCTCAGTCCCCATTCTACCGGCATCCTTCACATCACTCCAGAAAGCTCTCCGAAAGCAAGCAAGTCCTCTATTCCTGGCTCTAGTGAGCAAGCCTCTGGAGGTTTCTATGTGAAGATGCCAAGCGTTGAATATTTGACCCAGGAAATGTCCTCGGAGCATACGACAAGCAAAACAGAGGGAACTCGTACTGTAGTGACTAAGATGACAAAGTATACAGAAACAAAAACTAGCAGCTCCAAACAATAAGCATCTCAGTTACTGAATAGGTAGGGAAATATATTGG
Associated Phenotype:
Not determined