ZMP
pion
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q5TYU4]
Human Orthologue:
PION
Human Description:
pigeon homolog (Drosophila) [Source:HGNC Symbol;Acc:28042]
Mouse Orthologue:
Pion
Mouse Description:
pigeon homolog (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2442259]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20267 | Essential Splice Site | Available for shipment | Available now |
sa40284 | Missense, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33458 | Missense, Nonsense | Available for shipment | Available now |
sa33457 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa20267
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 |
---|---|---|---|---|---|
ENSDART00000066891 | Essential Splice Site | 48 | 872 | None | 32 |
ENSDART00000132464 | Essential Splice Site | 28 | 664 | None | 23 |
Genomic Location (Zv9):
Chromosome 4 (position 19157441)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 20500776 |
GRCz11 | 4 | 20221751 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGATGTTGTGTCAAGCATTTTGGCCAAGGAGGAAAGGGCGAATATAGG[T/C]AAGCAGACTTATAGTGTAATTTAGGCTATATTAATCATCGTTTTAACTGT
Long Flanking Sequence:
TCAGCAGTGTTTGGGATCCGCCTACGTGTTCTTATGACAAATCTGTAAACACCGCAAGTGATGTCGGGATTGGTGAATTCAGTGACTTTCGGTTTGTTGCGGGTAGAATATTATTGATCGTGATGCTTTTTAGTTTACCGGGTCTATCACTCTTGTCATTACAAGCTCCTAAAGTTCGCTTCAGTACGTCCGAATCGTTTTAAAACGCCGGTTTCAGCAAAGGGAGTTATTCACTAATAGATGTCTGATGGTGTTCAGCGTACTGACGGTGTTCGGCTCGTCGATAAACTGTAGGAATACATTTAATATGTTACGCTATAGAAGTCAGTGTGTTCAGTCATAAAGTTTGCGTGGAGTTCTCTGTCCTGAACGCGTGAAATCAGGCCACTTCTGCTAAATCTCTGCAGGACAAGACACATGTTGAGATTAAACCCCACCTTCGACATTCAAAGAGATGTTGTGTCAAGCATTTTGGCCAAGGAGGAAAGGGCGAATATAGG[T/C]AAGCAGACTTATAGTGTAATTTAGGCTATATTAATCATCGTTTTAACTGTCATATGAACTACTAATAATAATTATATAATTTCACTATCGTTTTGATTGTACTGTAGTCTATATATGAGCATGCACGAGTTATGCACTGTGTTTAATGTGTGCAGGTGTTCTTGAGCCTCGAATTCTGAGTGTGGAGAGAGATGGAGGAGTCGTGTACTCATGGAGAGTAAGTTTGACTTTAGTTTGTGTGTCTCTTTAATTTGACAGGTCATGTGCTCGACGTGCCGTTCATAGCAGCGCAAATGACTATCGCAGGAACAATCCGCCGACAGTACAGCAAACGAGCTCTGCGTGCCATACATACAATACACACTTGTACATGGCTTACATTCAGTCCAGAAATTAATGTGTGGACCCTGGTGAAAAAGGGTACAACTCTCATGCTCAAGTAAATGGATTTTACTGTATATATGAGATAAATTGAATTGCATTTTTACAATAATAATCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40284
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > G
Consequence:
Missense, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066891 | Nonsense | 130 | 872 | 7 | 32 |
ENSDART00000132464 | Missense | 80 | 664 | 5 | 23 |
Genomic Location (Zv9):
Chromosome 4 (position 19153252)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 20496587 |
GRCz11 | 4 | 20217562 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAACTCCTGATATGACTCTGTTTGCTTTCTACTTTAGTGTCAAAATGTT[T/G]AACGCTTCTCATCGAGATTCACCCAATCAACAACACAAAGGTCCTAAAGG
Long Flanking Sequence:
CCTTTAAACTGCATATTGTTTGTAGATTATTCCATGCAAAAAGTGCTGCGTATTTAAAAGCCTTTTTTCACCATCTCAGTTCGCACTTTAGGGACAGACAGTAAATAAATATTCTTTGAGCGAAGGCCATAGCTGAGGACAGGCTTATTACAAATGTAAGTATAGAGATATGATGGTAGTAAACCCAATATAGATTTGTAAAAAAATATATGCCAATGCTTGAGTCTACAAATGGACAAAGCAGACAAACCTACCCTAGTATTCAACACACAATGATGAGTAAGGGATTTAAATGTATATATGAATGTATTTATAACAGTGGCATATTCACAAATGTATACACATTTTCTCACATTCATTAAACAGAATCTAAGGGATTTAGAAAGATGAAATTACAGAAATCAAGGTGCAGTTAAACGTGCATAGGAATCCCGCTATTGCGGTTATCCTTTAACTCCTGATATGACTCTGTTTGCTTTCTACTTTAGTGTCAAAATGTT[T/G]AACGCTTCTCATCGAGATTCACCCAATCAACAACACAAAGGTCCTAAAGGCAGTCGATTGCAAGGTCAAAGTGCAGGTACTGAACAGCTGGTCATGTGAATCTTTGATTATTTTTTTTCTTGAAGGTCTACTGTAAATCTAATTGAAATTAACCCATGACATCCTTCCTAGTTTCTCTATCCCAAGACATGCCGGAGCACTGTACTAGAGAGCCATTTGCTGTTGGCATCAGAGGATGGCTGTATGTATTGTGGAAAAGTTGAAGATTTCATTAATATGCTTTATGAATTGCAGTCTATCGTGTTTTATAGAAGTCACTCACACAAATCCAGAATTGAACATAAGTTGCAGACTGTTCTGTATACCTGAGTAAAACATTAAATAATATAGGGTGGGACTTTATGTCTTTTTTCTTTTGGAATTGTTTGGATGGTGGGATAAGTGTGGTTTCCTAATGTTCTGCACTTGCTTTAGTAAAAACATCATCAACAAAACATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33458
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:
Missense, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066891 | Missense | 241 | 872 | 11 | 32 |
ENSDART00000132464 | Nonsense | 134 | 664 | 6 | 23 |
Genomic Location (Zv9):
Chromosome 4 (position 19152206)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 20495541 |
GRCz11 | 4 | 20216516 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTTTTTCCACACTGTAGGAGAAACACACATTGAAGTGTGTACAGTTT[T/A]ACGCCGATCGCAATTTCGAAACTGTGGTAAACTTTTTGTGCACATGACAG
Long Flanking Sequence:
AATAAATAAATAAAAATAAGCACTGTACTATTTTATTTAGAAATAGAAGCTGTTCGTTTTAACTTCATGCTGACTTTGTATATTTATTGTAAGTGTATGTGAATGATAATTTTTATTCTGCAGATGTTGATCAGTACCACATAGCTCTGACCAGACAGGAAGGGTACAGAGTGGTAAGAGAAATTCTTTTTCATGGTCTAAATCTATGAATACTCATATGCATTTTGGAGAGTCATGTATTTGTGTTTTCTGAAACAGGTGATGCAGAATTCAGAGCGTCTGAGCAGAGAGAGAGTGGCAGAGGAGTTCATATGGGTCCAGTGGGACTCAGACACTCAAAGAATATTCTACCTTACTGCACGGGTCAGAATCACTTTTCTTTTTACTTGCGCTAAAAATGTATATTTTTTTTTAAGAAGAAAATGTTCATCTTCCAGTGTATGTCAGTGTTGTTTTTTTCCACACTGTAGGAGAAACACACATTGAAGTGTGTACAGTTT[T/A]ACGCCGATCGCAATTTCGAAACTGTGGTAAACTTTTTGTGCACATGACAGTTAAATACTTTTAAATAATATTTAAAACTTGTTAATTGAAATACAAACACTTATGTTTGACAGTTTGAGCTTCCATTGGAGATGCCCAACATTGTCACTTCTCCTGTGAGGTGAGGGAGTGTTTTCTAGTAAAATACATGCAAAACAACTTAATTATGGGAGTGTGATATTGGCACAAACAGTATACCTTCATATTTTGGGTGATTTATTTATTTTTTTTTCAATAACAGTGTGTGGTTTAAGCTTGTCATGGATAAATTATTATCATACTAAAACTTCTAGAAGTTTATTGCAAATCCCCTGTTTTATGAGTGATTCATTGAAACATTAATTCAGTTGATTCATTCAAAACAGCTAATTCTGTCTTTATTTATTGATCACTGAATCGTATACTTTGTTCAAAAACAACAACGACATGCCACAGTGTTGCTCTGAGACACAATTGTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33457
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066891 | Essential Splice Site | 604 | 872 | 23 | 32 |
ENSDART00000132464 | Essential Splice Site | 429 | 664 | 15 | 23 |
Genomic Location (Zv9):
Chromosome 4 (position 19146650)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 20489985 |
GRCz11 | 4 | 20210960 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTTTCTCATGTGCAGAGTTTTATCCATGGTGGACACTTGGCGTTTGGG[T/A]GAGCTAAACTTACTTTAAATGGTCAGTCGTGTCAGCGAAAGGACACTTGT
Long Flanking Sequence:
ATCAAGAATACACACATACATTATCATATATATCATCTAGCACTGTGCTGTAATTATGTATTAAAATGTCTTGATATGTTGATATTCCTGCAGAACTCGGAGAAGAAGAAATCCCCCCGCAGTCATCACTACATTGAAGAGAACACCAAAAAGTGGGTGGATTTTGGCAAATGCTGTGTGTGTGTCTGTGTGTGCAGGGGAGCATGCTACACTTTCAAAACAGCATTAGTTATTTCTCACAGTAAACTAACCATTTATGAAGAGCTAAAAGATCTTTAAAACAACAGCATATTTGCTTTTTTAACAGTAGATCTAATTACTGTTGAATGTAAAATGTGCTACAAAAAGTTTTTTTTAATAATAAAGTGTCTGGTTGTGATTGATATTTGATGAAGCTTTGGAGTAAAGCAACTGTAACATCTTGATGTAATTAAAATGTCTCCTTTCTGTTTGTTTCTCATGTGCAGAGTTTTATCCATGGTGGACACTTGGCGTTTGGG[T/A]GAGCTAAACTTACTTTAAATGGTCAGTCGTGTCAGCGAAAGGACACTTGTGAGAATATTTTATCCCTGATCAAATCCTGGAAGTATTTCAGGCTTTTTTGGAAAGTCCCAGCGACTGGAGCTTCAGGGTCACATTCTCTGTTGTGAATGTAATCTGTCTCTAGGTTTATGTGTAGTTAATCAAGCACCTCATTAGATACGAGGGAAATGGGAGTAGGAATTCGGTAGTGTTATATAAGAATGATTACAGTACCTCCTCCTTACTCAGAAAACACACACAGTCACACACACAGATCTGTTATCGCACGTGAGTCAAAAGAGCTGGACGTTTCACTAAGCTTGCTTATTTTCTGCTCCTAACATGATTTATTACAAATTATTATGGTATGATTATTAAGGATTTTTTATCCAAAAAATTAAAATCTGTGAAATTTTACTTCATGCCCTCCTGTTGTTTCAAACCTGGCATTCTTTCTTTTGTAGAACGTAAAAGAAGATATT
Associated Phenotype:
Not determined