ZMP
zgc:152900
Ensembl ID:
ZFIN ID:
Description:
dipeptidyl peptidase 9 [Source:RefSeq peptide;Acc:NP_001070781]
Human Orthologue:
DPP9
Human Description:
dipeptidyl-peptidase 9 [Source:HGNC Symbol;Acc:18648]
Mouse Orthologue:
Dpp9
Mouse Description:
dipeptidylpeptidase 9 Gene [Source:MGI Symbol;Acc:MGI:2443967]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16756 | Essential Splice Site | Available for shipment | Available now |
sa41296 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31680 | Nonsense | Available for shipment | Available now |
sa21384 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16756
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 |
---|---|---|---|---|---|
ENSDART00000074495 | Essential Splice Site | 194 | 885 | 5 | 21 |
ENSDART00000123254 | Essential Splice Site | 170 | 861 | 5 | 21 |
Genomic Location (Zv9):
Chromosome 8 (position 49847564)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 47699541 |
GRCz11 | 8 | 47688533 |
KASP Assay ID:
2260-1117.1 (used for ordering genotyping assays)
KASP Sequence:
AAGCAACAGCCTTTTCTACTGCCGTGATGGCGGCCATAACGGCTTCAYTG[T/C]GAGTCTAGTTTTTTGCTTTATTTTCCTGTGNNTYTTAGTTTTTACAYTTT
Long Flanking Sequence:
AAAATCAAATTATGTTTTGTTTGTCGCATATAGGTTACTCTTTATGCTTTTTATCTTTATTTATTTATTTATTTATTATTACCTATATAATATCTTGCATATATTTATTTCTACATTTATTTATCACAGCATATATTTATTTGTGTGTTATTTATTACTGTACATATTTATTTTTGTATTTAGTTTCATATTTTCTTATTTTTGGCTTTGATTTATTTTTACTTTTCAGTCTGTAACAAGGATTTGGGTGATTCGGTTCTTGCATATATTTGGCGCATTATTGACAACATATAAATTCTGACATTAATTTGTGTGCTTCCTGCAGGCCACTCCACATCATGGAGTGTATTCTCGGGAGGAGGAGCTTCTCCGCGAGCGGAAGCGTTTGGGGGTTTTCGGCATCACGTCCTATGACTATCACGCACAAAGCGGCCTTTTCCTCTTTCAAGCAAGCAACAGCCTTTTCTACTGCCGTGATGGCGGCCATAACGGCTTCATTG[T/C]GAGTCTAGTTTTTTGCTTTATTTTCCTGTGTCTCTTAGTTTTTACACTTTGTTGCATAACTGTGTCTCCCCATGCCTGAAAGTAATGTGATGTTTAGCAGGCTGCCCCAATGAAGCCTATGGAAATAAAGACTCAGTGCTCAGGGATACGAATGGACCCCAAGATCTCGCCCGGTGATCCCAGTTTCATTGCCTTCATAAATAATAACGACCTGTGGGTTACCAATATCGAAACGGCAGAGGAGCGAAGACTTACTTTCTGTCATAAAGGTTAGTTGATGGGCTTGTATACTGTAGCAGGTTGTGTTGTGTACCATTAAATAGGGGTGTGCCAGATCACGGTCGAGTTGTGATTTGTTTGGATCACAACCCATGATTCGGAACACACATGACCTACGGATTATTACATTTTATTTATTTTTTTGCTTGTGGATTAATCCTTAATTTGTAACTATCGCCTTGCAGAGAGCACCTTTTGTATAATTCAAATCACATGTATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41296
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074495 | Essential Splice Site | 289 | 885 | 7 | 21 |
ENSDART00000123254 | Essential Splice Site | 265 | 861 | 7 | 21 |
Genomic Location (Zv9):
Chromosome 8 (position 49851344)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 47703321 |
GRCz11 | 8 | 47692313 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTTTGATCGCTTCACTGGATACTGGTGGTCTCCGGCTGCTACTGAAGG[T/G]TTGTTGAACGCCTAAACAGTCCATGTTGTCAGCATTTGAAGGTGGGTGGA
Long Flanking Sequence:
CGTCTATTTACGCGTGAATGAAGAGGTTTTGACACGCGAATAAAGTGGATTTGATGCGCGAATAGGTCGAGTAAACTCAATGTTCACACATCTATTTACATGCGAATGAAGCGGATTTAATTTACGAATAAAGGGGATTTGCATGATACACATTTTACTATCAGAACTTTCAGGAAATTATTTGAGCAATAAATTGACTAATTACAATTAAAGACATTTACTAAATTATCATGCAGTATAACAATAAACTCTAGTCTTTTGACTGGATTTTTATACTACGTATTGGTAAATATTTAAACATTCCTCCCTATTGGCAGTATGTCAGATTACATTGAAAATGTTAAAGGTTTCTGCACACTGTAATGTGCCTCCTCCTACCTCTGTTCAGGATTGAATAATGTCAAAGAAGACCCAAAATCTGCTGGTGTTGCAACCTTTGTGATTCAGGAGGAGTTTGATCGCTTCACTGGATACTGGTGGTCTCCGGCTGCTACTGAAGG[T/G]TTGTTGAACGCCTAAACAGTCCATGTTGTCAGCATTTGAAGGTGGGTGGATGTATAGATAGTACAATCAAAATCTATAATCGTTGTATCCCCAGTGCTGTTTTTATATGGAGATTCCAGTGTAGCTGCTATAAAGGCCCATTGCTTGTTTTGCCTGCGAGCCTCCATGAGGTCATGTGACTGAAAACTGTCAAATCTAAACCACCCCCTAATCATGGTGTTTGTGTTTGCATGCAGACGCAGATGGAGGCAAAACACTTCAACTGCTCTATGAGGAGGTGGACGAATCGGAAGTAGAGATTATTCATGTGCCATCACCGGCTTTGGAGGAGCGGAAGGCCGATGTGTACAGATACCCCCGCACTGGTAATAACAATCACACACACACTAGACAAATTCTACTATTAGTCTGCTGTTCTGCTATTAACTTTAGTCATTAGCAAAGTCAAGTTTTGTCGAAACCAGAATTTGTGTTGTAAGAATGCGGCTCTTCTTTTTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31680
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 |
---|---|---|---|---|---|
ENSDART00000074495 | Nonsense | 678 | 885 | 17 | 21 |
ENSDART00000123254 | Nonsense | 654 | 861 | 17 | 21 |
Genomic Location (Zv9):
Chromosome 8 (position 49866151)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 47718128 |
GRCz11 | 8 | 47707120 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTTGCTTTGTTATTTAAAATATAGGTGCAGTTAGTAAACAACTCTTA[C/A]AAGGGTGTGAAGTATCTGCGTCTGAACACGTTAGCATCTCTGGGTTATGC
Long Flanking Sequence:
GATGTGATAAACCGCAATACCAGCCCTAGATTTATCTCTTTCAGATGAAAATTCGGTGCATTCCTATGTTACCTACATGTTACCTAAACTAAAAACATGACCTCTAACCTTATAACAGAGAGTTACAGTATTAACATTCATTTGACTGATCTTGTCAGTAACTGGAAACTTAATTGATCTAGTTCCCAAGTATATTTAACTAATTCAGATATATGGATTCAGCAGGTCACGGGCCATTGAAAGAAAACCATTGAATACCTTTCTTGCTTTTATATTGTGTTGTCTGTAATATGTTGCTTTTGTTTTTTTTCTTTGTTTTTTTTTTGTAAGCTTTAAACATACATTTTTCGGTGTGATATTGAATATGTGATATAACTATTCATTTAGTTAAATCCATTTAACGGTTGCATCCCAAGTCCTGTATGTCTTCTAACATTTTTCCATTGTTTTTTTTTTGCTTTGTTATTTAAAATATAGGTGCAGTTAGTAAACAACTCTTA[C/A]AAGGGTGTGAAGTATCTGCGTCTGAACACGTTAGCATCTCTGGGTTATGCAGTGGTGGTCATTGACGGAAGAGGATCCTGCCAAAGAGGCCTCAAGTTTGAGGGGGCTCTTAAAAACAAAATGGTAAATACAGTTCACTGTCTAATCTCTGACTTTATGCATAAAAATCTAAATTTTTAACAAAGAACTGCCGATATCAGGCATACCCAGGCCCGGATTGGCTAATTGGGAGAACCGGGAGAATTCCCGGTGGGCCGGTCCGTTTTTTTGGCCGTGAGGGCTGGTGTACATATCTGCATGCACTCTCAGCAGTCACATTTTTTTTCATTTATTTATTTATTTGACCATAGCCTCACTTTTTTTTTCATTATTTTGCCGCAGCTCTGCTTTTTTTATATATTTTTTTTTCTCGCAGCCCCGTGAGCTTGCAGCCTGCAGGTTAACTAACGTTAATGATGATGTAACTATAATTATTCGACCCCAAACAGCGGCACCTTAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21384
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074495 | Nonsense | 721 | 885 | 18 | 21 |
ENSDART00000123254 | Nonsense | 697 | 861 | 18 | 21 |
Genomic Location (Zv9):
Chromosome 8 (position 49873782)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 47725759 |
GRCz11 | 8 | 47714751 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTAAAAATAATAATAGAAGTATTGTTATGTTCTTCTCAACCCTCAGGGG[C/T]AGGTGGAGATCGAAGATCAAGTGGAGGGGCTTCAGTTTGTGGCTGAGAAG
Long Flanking Sequence:
GTGAGCATGGAACAGCGCAACAGCACCACCTGTGTCTCATTATTGTAATTGTCACAGACCTAATATTGAAAGTGAGCACGGGCCACTTGGACTTCATTACCAAAACATGTTGTCGGGCCTGATTGAATGTTTTTGACGGGCCGCATTTGGTCCGCGGGCCTTGTAATTGACACATGTGTCTTAAGTGATGCTCAACCCACACACACAAATCTATTAAAACCTCAATAAAGTACTCGAGGGTTTCTTAAACTTTTAAACAGAAAATGGAAAAAATAAATAATAATAATAAATGAAAAAAAAAATATATATATATATATATATATACAGGGGGTTAATATTTTTGACTTCAACTGTATATTTTATTAGTATTTCATATGGTTGTAGGTAAAAAAAACATTAAATAGGCTTTAAGTGAGGTTTAAAATATTAATATTATAATATTAAAATATTATTAAAAATAATAATAGAAGTATTGTTATGTTCTTCTCAACCCTCAGGGG[C/T]AGGTGGAGATCGAAGATCAAGTGGAGGGGCTTCAGTTTGTGGCTGAGAAGTACAAGTTCATAGATTTGAGTCGAGTTGCGATCCATGGTTGGTCTTACGGTGGATTCCTCTCTCTCATGGGCCTCATTCACCGACCAAACATCTTCAAGGTGAGATTTGCACTACTTGTCTATTAGCTTGCATGTTGACTGCTAATAGTAAAACGCATATTAATGGAGCATTCCACTATTTTGTCCCCTACAGGTAATTAAACTTAGGTTTGACCTTTTTTTAATCCATTTAGCTGATCTCCATGTGTGGTGGGAGGACTTTTAGCTTAGCTTAGCATAAAACATTGAATGAAATTAGACCATTATCTTCTTACTCAAAAAAAAAAGTAGTTTCTTGCCAAATCTGCCCTGAAATAGCAACTTTTTTGTCGGTCTTTGTGCCTGATGTAACTACAGAAGAGTCCAGCTTTAAATAGGAAAATTATCAAAGCTTTTTTTTTTTATCAGTCT
Associated Phenotype:
Not determined