ZMP
si:ch211-120p12.4
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate pecanex-like 3 (Drosophila) (PCNXL3) [Source:UniProtKB/TrEMBL;Ac
Human Orthologue:
PCNXL2
Human Description:
pecanex-like 2 (Drosophila) [Source:HGNC Symbol;Acc:8736]
Mouse Orthologue:
Pcnxl2
Mouse Description:
pecanex-like 2 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2445010]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11440 | Nonsense | Available for shipment | Available now |
sa31929 | Essential Splice Site | Available for shipment | Available now |
sa22287 | Nonsense | Available for shipment | Available now |
sa17666 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11440
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078079 | Nonsense | 943 | 2005 | 16 | 34 |
ENSDART00000134973 | None | None | 203 | None | 5 |
ENSDART00000144215 | Nonsense | 372 | 1437 | 10 | 28 |
Genomic Location (Zv9):
Chromosome 13 (position 23908977)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23554637 |
GRCz11 | 13 | 23685087 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTCCAGCTCTTTTCTCTGGTTTCTGTGCTCTGCTAGTGGTCGTCTCCTA[T/A]CATCTKAGCCGACAAAGCAGTGATCCATCAGTGTTATTGTAAGAACATTG
Long Flanking Sequence:
AAATAATATTTTACTAGATATATTTCATGACACTTCTATAAAGCTTTAAGTTTCATTTAAATACTTAAATGCATTTAGGTGACATTTAAATAGTAGGTTAATTAGGTCAACTAAGCAGGTTAGGGTAATTAGGCAAGTTATTGTATATTGATGGTTTGTTCTGTAGACTATCAAAAAATATAGCTTAAAGGGGCTAATAATTTTGACCTTAAAATGGTTGTTAAAAATTTAAAAACTGGTTTTATTCTGGCTGAAATAAAACAAATAGGAAGTTATCTGGATGAAAAAATATTGTAAAATGTCCTTGCTCTGTTAAACATCATTTGAGAAATATTTTAAAAAGAACAAACTTCAAAGGGGGGCTAATAATTCTGACTTCAACTGTAGATTTTAGATGTGCAATGGCAATATTTGATATCTTGTGTGCAGGAGCCTTGGGATGAACAGCATATTCCAGCTCTTTTCTCTGGTTTCTGTGCTCTGCTAGTGGTCGTCTCCTA[T/A]CATCTTAGCCGACAAAGCAGTGATCCATCAGTGTTATTGTAAGAACATTGTGCCCTTTTCATTGATCATTTAGTTTTGAACATCTGCCACAGATTTAAGCACTAGAAGAGAACTCACACCAATGCTCAGAACCAAATACTGTTTGTAAGCACATTGTTTTTGTCTCAGCTCATTGATTAAGTCCAAGCTGATGCCTTCACTTGGCCATGGTGAGGAAGAAGAAGAGGAATCAGCTGAAAACACAGACCCTCTTCCAGAGAAACTCAGAGGCTCTGTGGTGGGTGCCTTTCATTTATTAGTGGATATTCAGATCCAGCATCTTTTATTTTGCCTGAGCTTTCATCACAAGGATCAGATTTGTTTGTTATGATTAAAAAAATGCATGAGGCTGCATTTACTTGCTAAAAAAATATAAAACATTATTATTGTAGAATATTATAACATTTTCAAATAAACTCTGTTTTTAATTTAACATAGTTAAGATCAAAAGTTGTGTTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31929
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078079 | Essential Splice Site | 1023 | 2005 | 18 | 34 |
ENSDART00000134973 | None | None | 203 | None | 5 |
ENSDART00000144215 | Essential Splice Site | 450 | 1437 | 12 | 28 |
Genomic Location (Zv9):
Chromosome 13 (position 23910030)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23555690 |
GRCz11 | 13 | 23686140 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTTTTGACCTTTGCAATTACTGCCAGCACGGTTTTCCTGTCTCTAAGA[G/T]TGAGTTTCTCTTACTTGTTACATTTCTTACACACAACCTCTTCATAATCT
Long Flanking Sequence:
CGCTGATTTAGTACTTAAGAAGCATTTGTTGATGAATGTATGAAAATAGTTCTAAATATGAAAATAGTTTGTTATGGAAACTATCATACATATTTTTCATGATGATCTCCTTGATGAATAAACAGTTCAAAAGAAGACATTTTACTTGAATTATACATTTGTAATATTATTGAAAATATATTTACTGTCAAGTTCATCAATTTAAATGATTAAATTGTGCCTGTTAAATTAAAGTACTAATTTCTTAAATCCAATAAACTATTATGTACCAGACAGCTGAAATAAAGAGCATTTATCTAAAATTTAAATATTTAGTGTAAAATAAGTGTATTTACTGTCACTTCTGATCAATATAATGCATTCTTTTCTAAATTATATTTTAAAATCAATGTATTTTGTTGTTACAGAAAGAGATTTTACTGTCAGATCTGGTTGTTTGCAGTCTGGCCTCAGTTTTGACCTTTGCAATTACTGCCAGCACGGTTTTCCTGTCTCTAAGA[G/T]TGAGTTTCTCTTACTTGTTACATTTCTTACACACAACCTCTTCATAATCTAAATCAAATCAGAGTTATCATAGAGACATAATATCTACATTATACCTACCTACAGTTGAAACCAGAAGCTTACTTACACTGTATAGAAAGGCACATAACCATTTTTTTTTAAGTCAGATGTTAATGTGACTAAACTTTTTTCTCTTTGAGTTAAGTTTGGAATATCAAATTTGTTTCTGTTATGCTTAATAGCAGAATAATGAGAACAATATATATATATTTTTTTTACATACAATAAGATTATTATGATTCTAAAAAAGCTCAGAAGATGGTGTCAAGGTTTTGTAAGTTTCTGATTGGTTAAATTTGAGTTAATTAGAGGCACAACTGTAGAAGAGTATTTAAGGAAAACCTCAAACACACTGCTTCCTTGTGTGACAACATGGGGAAATTAACAAGCCAGAATCAACACAAAAGCCAGATTACAATTTGCTAAATTACACTGGGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22287
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 |
---|---|---|---|---|---|
ENSDART00000078079 | Nonsense | 1537 | 2005 | 28 | 34 |
ENSDART00000134973 | None | None | 203 | None | 5 |
ENSDART00000144215 | Nonsense | 964 | 1437 | 22 | 28 |
Genomic Location (Zv9):
Chromosome 13 (position 23928705)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23574365 |
GRCz11 | 13 | 23704815 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGATTCTCCCCTGGTTACTCTGTGTTTCGCTCTGTCTGTGCTTGGCCGC[A/T]GATCCCTCAGTACAGCAGCACACAACAGATCCAACAGGTACAACATTCAA
Long Flanking Sequence:
AATGGCAAGGTTTTGCATTCAGATGACAATGATTTCAAAATGACACCCAAAATCACATGGATCCACAAAAACAACTATGCTATAATATGCATGCTAGGCCAATAGTTGGTGACTTTATTCAGCACAAACACTTTCCTTAATACCACAATAATTGTTTTGATTGTCAAACAGTTACACAAGACTGTAAACTAAATGTATGATGGCACTTATTTCCACAAATCTTAATTAAAAATTTTAAAGTTTAAAGATTTTATTCGAAAATAAGTAAAAAAAAAAAAATCTTTAAAATGGTATTGAAATGTAAATCAATGGGTTTCAAAGCTTTTCAAAGTTTCATTTTTTTGTGAACTAATCCTTTAAATTTAAAATTTAAAACCCCCGCAGATACAGTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTTTTTGTCCTCAGCCAGTGGACAGTGATGAAGATTCTCCCCTGGTTACTCTGTGTTTCGCTCTGTCTGTGCTTGGCCGC[A/T]GATCCCTCAGTACAGCAGCACACAACAGATCCAACAGGTACAACATTCAAAATCAGCCATAAGTAATATGACTCAACAGTTAAATCATGTAAAGACAACATAATAAAGAACAGCTAGTTTGAAAGATTCCAGTCAGAATCAATGATACTGTATTGATAATGTATAATGCATTAGATAATGTATATTTTTACCGGTCTCCTCTACAGTCTGGAGTCCTTCCTCTATGGCTTCAACACACTGTTTAAAGGAGATTTCCGCATCGCTGCTAAGGATGAATGGGTCTTTGCTGACATGGACCTTCTGCAGATGGTTGTGGCCCCAGCCGTGAGAATGAGTCTGAAACTTCACCAGGTGAGATGAACACTCTCCTTTTCTTTTCGGCTTAGTCCCTTTAATAATCTTGGGTCGCCACCGCGGAATGAACCGGCAACTTATCCAGCAAGTTTTTAGGCAGCGGATGCCCTTCCAGCTGCAACCCATCTCTGGGAAACACTCATAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17666
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078079 | Essential Splice Site | 1597 | 2005 | 29 | 34 |
ENSDART00000134973 | None | None | 203 | None | 5 |
ENSDART00000144215 | Essential Splice Site | 1024 | 1437 | 23 | 28 |
Genomic Location (Zv9):
Chromosome 13 (position 23929058)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23574718 |
GRCz11 | 13 | 23705168 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAGATGGTTGTGGCCCCAGCCGTGAGAATGAGTCTGAAACTTCACCAGG[T/C]GAGATGAACACTCTCCTTTTSTTTTCRGCTTAGWCCCTTTAATAATCTKG
Long Flanking Sequence:
CCTTTAAATTTAAAATTTAAAACCCCCGCAGATACAGTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTTTTTGTCCTCAGCCAGTGGACAGTGATGAAGATTCTCCCCTGGTTACTCTGTGTTTCGCTCTGTCTGTGCTTGGCCGCAGATCCCTCAGTACAGCAGCACACAACAGATCCAACAGGTACAACATTCAAAATCAGCCATAAGTAATATGACTCAACAGTTAAATCATGTAAAGACAACATAATAAAGAACAGCTAGTTTGAAAGATTCCAGTCAGAATCAATGATACTGTATTGATAATGTATAATGCATTAGATAATGTATATTTTTACCGGTCTCCTCTACAGTCTGGAGTCCTTCCTCTATGGCTTCAACACACTGTTTAAAGGAGATTTCCGCATCGCTGCTAAGGATGAATGGGTCTTTGCTGACATGGACCTTCTGCAGATGGTTGTGGCCCCAGCCGTGAGAATGAGTCTGAAACTTCACCAGG[T/C]GAGATGAACACTCTCCTTTTCTTTTCGGCTTAGTCCCTTTAATAATCTTGGGTCGCCACCGCGGAATGAACCGGCAACTTATCCAGCAAGTTTTTAGGCAGCGGATGCCCTTCCAGCTGCAACCCATCTCTGGGAAACACTCATAGACATTCACACTCATACACTACGAACAATATAGCCTACCCAATTCACCTGTACCGCATGTCTTTGGACTGTGCGGGAAACCGGAGCACCCGGAGTAAATCCCACACGAACGCAGGGAGAACATGCAAACTCTACACAGAAACCCCAACTAAGCCGAGGCTCGAACCAGCTACCCAGTAACCTTCTTGCTGTAAGGTAACAGCACTACCTACTGCGCCACTGCTTCGCCCTAATTGGTACATATTAAACATTTTTAATATTATTAAAGTCTCCATGAAGGGAAACCTGCAATCGTTATTTGTGTTTGTATTGTGATCCAGTCACCAAACGGAATATTAAATGAAAAAACAGTGGGC
Associated Phenotype:
Not determined