Busch Lab

ZMP

si:ch211-1c4.1

Ensembl ID:
ENSDARG00000003403
ZFIN ID:
ZDB-GENE-060531-26
Description:
Novel protein similar to vertebrate odz, odd Oz/ten-m (Drosophila) family [Source:UniProtKB/TrEMBL;A
Human Orthologue:
ODZ1
Human Description:
odz, odd Oz/ten-m homolog 1(Drosophila) [Source:HGNC Symbol;Acc:8117]
Mouse Orthologue:
Odz1
Mouse Description:
odd Oz/ten-m homolog 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1345185]

Alleles

There are 17 alleles of this gene:

Allele Name Consequence Status Availability
sa45197 Nonsense Mutation detected in F1 DNA Not yet available
sa40401 Nonsense Mutation detected in F1 DNA Not yet available
sa14203 Nonsense Available for shipment Available now
sa5812 Essential Splice Site F2 line generated Not yet available
sa2238 Essential Splice Site F2 line generated Not yet available
sa33576 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa31428 Essential Splice Site, Splice Site Available for shipment Available now
sa2239 Essential Splice Site F2 line generated Not yet available
sa11851 Nonsense Available for shipment Available now
sa38462 Nonsense Mutation detected in F1 DNA Not yet available
sa16414 Nonsense Available for shipment Available now
sa16472 Nonsense Available for shipment Available now
sa25295 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa20387 Nonsense Available for shipment Available now
sa20386 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa45197
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000040184 Nonsense 1 2571 1 29
ENSDART00000144198 None None 2389 None 25
Genomic Location (Zv9):
Chromosome 5 (position 23254862)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 20967734
GRCz11 5 21471534
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACTATCATTAAATATTATAATTACATCTCTCCTTTTCTCTTTCCCTTT[C/T]AAGATCTCCCTTCCAGCCCTGTGGCTCAGTTTACATTTCGACCTCTGCCC
Long Flanking Sequence:
ATACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATAAAAACTTGCTCCCCATTTGCTTACTGTGCGTTGCTTCTTACAGCAGTGCCTACTCATAAATGCATCTTTAAAAACTATAATGCTGTATAATGGGCTTGATAACATTGCATAACTCTGGAAGCGGAATGCTGATGGTGTGTTTTAATGCATTATACTTATATATATATAATACATGAGGCCATACAAATGATTACAAGCTGTGGGACATTAATGCATAAAGAATAGCTTTTCAAATTCATAATACATACATGCTGCAAGTGAAGCGTTTCCTACTGTTCATTGAGTTTGACAAGAAAATAGAAGCTGTAAGAGAAACAAGGGCAATGTGATTTTTAAAAGGGGCCCATTTCTCACTCAGGAAATGGACACTTTGAAGACTATCATTAAATATTATAATTACATCTCTCCTTTTCTCTTTCCCTTT[C/T]AAGATCTCCCTTCCAGCCCTGTGGCTCAGTTTACATTTCGACCTCTGCCCCCTCCTCCTCCTCCGCCTCATGCTTGTACCTGTGCCCGTCCTGCACCAGCTCCCCTTCCAGAGGTGGTGCAGAGGAGCACGCTGCCTGCCCGATGCCAACCGCTGGACTCTGGGAACAAAGCTGGACAGGATGACAATGGGCAGACGCACAATACCTGGGCCCTGAACAGCAACATACCACTAGAGACCAGGTGAAATACAAGCACACACACACTTGTTTTTCTGTTATAGTGGGGTATCCCATTGACTTCTATTGTTTTATATATAAGTTAAGTTTTTTTTCTGCAACATATCTCCAAACCTAAACCTTTGTGCATTTGATTTCTCTTTGTTTGGTGGTCCTCCATAGACATTCTATTGACCAAAGGCTGAATTATACTTCAGCGTCGAGTGATCGCCGGCGCATGCCTTGCGCTTAGCTGTGCATTTATACTTGTGCATTCTGTTTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40401
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000040184 Nonsense 209 2571 3 29
ENSDART00000144198 Nonsense 49 2389 1 25
Genomic Location (Zv9):
Chromosome 5 (position 23205575)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 20918447
GRCz11 5 21422247
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCTGATTTCACCTTCACTCCTGTCCACCTGCCAGGACTCAACACCACA[C/T]AGCCGGGTATGTATGTGTGTGTTACTTCAGTCATCACATAAGGTTTCTAT
Long Flanking Sequence:
TGTGTCATTCTATATCTTTCATGTCATCAGTCTGTTGTTCTGTCTGTCATTCTGTCTATCGGTTGTTCTGTCTGTCTGTTATTCTATCAGTCTAGCTGTCTTTCATTCTTTCTTTTGTTCTGTCTGTCATTCTGACAATCTGTCTTTCATTTTATTTGTTGGTTGATCTGTCAATATATTTTACATTCTGTGTCTGTGTGTCGGTCTGTTAACCTGTTTTTGTATATTTCCGTCTGTCATTCTTTTTCTGTTTTTTTCTGCCGCTACCGTACATGTATGTCTATCTTTGTACTGTATGTTTCTATGCTTCTACTCTTGCTGTATTGTTGTATTTACTGTATCTATATCTCTCTGCAGTTGTTCATCTGCTGGGTTTACCATGGCATCTGAAGCGAGTGGAAGGAGAGCTATATGAGAATGGTATGAGTAAAGAAGATCAGCCTCTACCGGGAGCTGATTTCACCTTCACTCCTGTCCACCTGCCAGGACTCAACACCACA[C/T]AGCCGGGTATGTATGTGTGTGTTACTTCAGTCATCACATAAGGTTTCTATATAGTGTGAATTCAATTCTGCATTTGACACAATGTGACCAAATGTCAAGTCTTTGCCTGCAGCAGGAGCAAAGAGAGAGGATTTGTGTGTTTTCATTGGGTTTATTTGCCATTTAATTAATGTCAGTAAACAGCAGTAAATTATTTTCTCTCAGATAACCCCTGAAATGATGAGGTCATTTTATAAGTGTGAGGTAGGATTCTATCTGTGCAGGCCTGTAGAGTTTGATAACATTCAAATTAGATTTAGTTTGCAATGTTTTTGGAATGTAAAGGAGTAAAATAGAATAGAGTATTGATCCACACAGTGCAACCTAGCGATAGGAAACAGTGTCTAAATGGAAAATGTGGCTGTGCTAAGTTTCAAAAAGTGACACCATGCTGCCCCTTTTCAAAAACAGAAAGTTGTTAATCATGTATACCTTACAGATTTTTGGGGTCAGTGAGATTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14203
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000040184 Nonsense 551 2571 9 29
ENSDART00000144198 Nonsense 388 2389 7 25
Genomic Location (Zv9):
Chromosome 5 (position 23176780)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 20889652
GRCz11 5 21393452
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGRCGTTGTCAGTGCGAGGAAGGGTGGGAGGGAACCACTTGTGACAAA[C/T]AGCCCTGCCATCCAATCTGTGAAGAGCATGGAGAATGCAGGGACGGGCAG
Long Flanking Sequence:
ATAGAGGAAAAGAAGCTGGGGCTTCAAGCACAGATTGTGAACACACACCACTAAATTCCTCCATCCAATGCATAACCCCAGCAGGAAGAGAGCAGTCTCGTCATGGTACAGTGCCGCAACCAGCTGTGTATCAGCATGAACCACCAACAACACACAGAAAATCACCGCCACTCAGTTCAAAAATGCCCATATACTGCATGTTTGCTGCAAAATGGAGGAAAACAATGCATAAACTGCTTTTGACGTGCAGCAGCGCTACTTAGTAAACACACACTGATTCATGCATCCAGTCAGTATGAAATCTAAGACTTTGTTTGAAGGGAAACTTTTTGAGTGCACTTCTAAAGAGATGGTTTGATGATAGATGGCAATGAAAGGTAACAAAACTCTGTCATTTTTTTTTTTCAGAGGTTTGCCCTGTTCCTTGCAGTCCACATAGTGTGTGTGTTGCTGGGCGTTGTCAGTGCGAGGAAGGGTGGGAGGGAACCACTTGTGACAAA[C/T]AGCCCTGCCATCCAATCTGTGAAGAGCATGGAGAATGCAGGGACGGGCAGTGTGTCTGTCAGCCTGGTTGGGAGGGAGAGCACTGCACTATTGGTAAGTTCTTATAAGTTAATGCACACTGACAATAAGACATTTGCATTAAATCAGCATACAACAATGATTTCTGACACGAGACTGCACTAATGACTCCTGAATATTCCAATAGTATTTGGATGAAGCCTTTATTATGCACTCAATACATACACAGTGCACTCAATGAAGCTAGTGACATCACTGTGATCATTGCATGCAGCTCAGATTGCAAGTGCACCAGGTCTTTGCCAGCATGTCCTGGAAAATTCGGAAAAGTCCCATTGACTTCCATTTGACTTTCCACCAGGCTGTCATACAGACTTACAGTTGAGCTCATTTAACTCAGACTACCAATCTGCCAATCACTGATGATCTTTCAGCCACACGCTAGCAACCACTTACAGCACCCTAGCAACTGTCCCATAGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5812
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000040184 Essential Splice Site 582 2571 9 29
ENSDART00000144198 Essential Splice Site 419 2389 7 25
ENSDART00000040184 Essential Splice Site 582 2571 None 29
ENSDART00000144198 Essential Splice Site 419 2389 None 25
Genomic Location (Zv9):
Chromosome 5 (position 23176685)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 20889557
GRCz11 5 21393357
KASP Assay ID:
554-3059.1 (used for ordering genotyping assays)
KASP Sequence:
GGGCAGTGTGTCTGTCAGCCTGGTTGGGAGGGAGAGCACTGCACTATTGG[T/C]AAGTTCTTATAAGTTAATGCACACTGACAATAAGACATTTGCATTAAATC
Long Flanking Sequence:
TCTCGTCATGGTACAGTGCCGCAACCAGCTGTGTATCAGCATGAACCACCAACAACACACAGAAAATCACCGCCACTCAGTTCAAAAATGCCCATATACTGCATGTTTGCTGCAAAATGGAGGAAAACAATGCATAAACTGCTTTTGACGTGCAGCAGCGCTACTTAGTAAACACACACTGATTCATGCATCCAGTCAGTATGAAATCTAAGACTTTGTTTGAAGGGAAACTTTTTGAGTGCACTTCTAAAGAGATGGTTTGATGATAGATGGCAATGAAAGGTAACAAAACTCTGTCATTTTTTTTTTTCAGAGGTTTGCCCTGTTCCTTGCAGTCCACATAGTGTGTGTGTTGCTGGGCGTTGTCAGTGCGAGGAAGGGTGGGAGGGAACCACTTGTGACAAACAGCCCTGCCATCCAATCTGTGAAGAGCATGGAGAATGCAGGGACGGGCAGTGTGTCTGTCAGCCTGGTTGGGAGGGAGAGCACTGCACTATTGG[T/C]AAGTTCTTATAAGTTAATGCACACTGACAATAAGACATTTGCATTAAATCAGCATACAACAATGATTTCTGACACGAGACTGCACTAATGACTCCTGAATATTCCAATAGTATTTGGATGAAGCCTTTATTATGCACTCAATACATACACAGTGCACTCAATGAAGCTAGTGACATCACTGTGATCATTGCATGCAGCTCAGATTGCAAGTGCACCAGGTCTTTGCCAGCATGTCCTGGAAAATTCGGAAAAGTCCCATTGACTTCCATTTGACTTTCCACCAGGCTGTCATACAGACTTACAGTTGAGCTCATTTAACTCAGACTACCAATCTGCCAATCACTGATGATCTTTCAGCCACACGCTAGCAACCACTTACAGCACCCTAGCAACTGTCCCATAGACATCCATCATAAAAAAAACTGCTATTGACTTTACATTGGACATACAAACAACATACTGATCATATTAGCAACATGGAAATTCATACTAAAAACATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2238
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000040184 Essential Splice Site 582 2571 9 29
ENSDART00000144198 Essential Splice Site 419 2389 7 25
ENSDART00000040184 Essential Splice Site 582 2571 None 29
ENSDART00000144198 Essential Splice Site 419 2389 None 25
Genomic Location (Zv9):
Chromosome 5 (position 23176685)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 20889557
GRCz11 5 21393357
KASP Assay ID:
554-3059.1 (used for ordering genotyping assays)
KASP Sequence:
GGGCAGTGTGTCTGTCAGCCTGGTTGGGAGGGAGAGCACTGCACTATTGG[T/C]AAGTTCTTATAAGTTAATGCACACTGACAATAAGACATTTGCATTAAATC
Long Flanking Sequence:
TCTCGTCATGGTACAGTGCCGCAACCAGCTGTGTATCAGCATGAACCACCAACAACACACAGAAAATCACCGCCACTCAGTTCAAAAATGCCCATATACTGCATGTTTGCTGCAAAATGGAGGAAAACAATGCATAAACTGCTTTTGACGTGCAGCAGCGCTACTTAGTAAACACACACTGATTCATGCATCCAGTCAGTATGAAATCTAAGACTTTGTTTGAAGGGAAACTTTTTGAGTGCACTTCTAAAGAGATGGTTTGATGATAGATGGCAATGAAAGGTAACAAAACTCTGTCATTTTTTTTTTTCAGAGGTTTGCCCTGTTCCTTGCAGTCCACATAGTGTGTGTGTTGCTGGGCGTTGTCAGTGCGAGGAAGGGTGGGAGGGAACCACTTGTGACAAACAGCCCTGCCATCCAATCTGTGAAGAGCATGGAGAATGCAGGGACGGGCAGTGTGTCTGTCAGCCTGGTTGGGAGGGAGAGCACTGCACTATTGG[T/C]AAGTTCTTATAAGTTAATGCACACTGACAATAAGACATTTGCATTAAATCAGCATACAACAATGATTTCTGACACGAGACTGCACTAATGACTCCTGAATATTCCAATAGTATTTGGATGAAGCCTTTATTATGCACTCAATACATACACAGTGCACTCAATGAAGCTAGTGACATCACTGTGATCATTGCATGCAGCTCAGATTGCAAGTGCACCAGGTCTTTGCCAGCATGTCCTGGAAAATTCGGAAAAGTCCCATTGACTTCCATTTGACTTTCCACCAGGCTGTCATACAGACTTACAGTTGAGCTCATTTAACTCAGACTACCAATCTGCCAATCACTGATGATCTTTCAGCCACACGCTAGCAACCACTTACAGCACCCTAGCAACTGTCCCATAGACATCCATCATAAAAAAAACTGCTATTGACTTTACATTGGACATACAAACAACATACTGATCATATTAGCAACATGGAAATTCATACTAAAAACATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33576
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000040184 Essential Splice Site 641 2571 11 29
ENSDART00000144198 Essential Splice Site 468 2389 8 25
Genomic Location (Zv9):
Chromosome 5 (position 23170841)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 20883713
GRCz11 5 21387513
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACGTCGTCATGGAAACCGAGTGCAATGACAGTAAAGATAATGACAGCGG[T/C]AAAGAACTCTATAGGAGATGAGCTGTGTGAATGAATGAAGCTTTAGGTTA
Long Flanking Sequence:
TGTGGCGCTCATGATGAGAACAGTCTGTGAAGCTCAGGGGACAAATATACGCTTAAGGCAGTAAACGACAGGGACACTTTAAAAAAAAACACCAGTGCACATTCACACACAGAGCTCCTCTGAAGTATGTCTCCAATGTAATTTCTCCTCTTTATTCTCTCCATCTTTCATTTTGTAACTCTTTCAGCCGCACATTACCTGGATCTGTTTGATAAAGGTAAGTGTGTGCGCGTTAGAGTGAATGAAGAAATGAATAGATGTCTTTGTGATGTCTTTTATGTGAACAGCTTTATTCCGAGTCTGAAGAAGTAATGACATGATTAATGGTATTTTGTCGTTTTTCCTCCCCCAGATGCCTGCCCAGGGTTGTGTAACGGTAATGGACGCTGCACGCTGGAGCAGAGCGGTTGGCATTGTGTGTGCCAGTCTGGATGGAGCGGGCCGGGCTGTAACGTCGTCATGGAAACCGAGTGCAATGACAGTAAAGATAATGACAGCGG[T/C]AAAGAACTCTATAGGAGATGAGCTGTGTGAATGAATGAAGCTTTAGGTTAACTCTTACAAAGAAACTGTTCATACATGACCATTCAAAGAGGGTTTTTAGAGAAATGATTATGTATTTATTCAGCAAGGATTCTGTGAATTAAACAGAAGTGACAGTAAAGACTTTTATAATATTAGAAAAGATTTCTATTGCAGATAAAAACTCTTCTTTAGAGCTTCTGAACCATTTTACAAATATATGAGAGTTTTCAAAAGAAAATTCATCAGCACAACTGTTTTCAATGTTAATGATTATAATAAGAACTGTGCATATAACAATCATTTCTGCATGATCATGCGCCACAGGACACTGTAGTAATGGCTGCTGACAATGTACCAAGAATAATGTAGATTTTAAAATATTAAAATAGAAATAGTTCATTTAAGTTGTGTTACAGTTTCACAAAATAACTGCCTTTATTAGTGTAAGAGAAAACTCTGAAAAATCTTGCCTACCGCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31428
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > C
Consequence:
Essential Splice Site, Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000040184 Essential Splice Site 641 2571 12 29
ENSDART00000144198 Splice Site None 2389 None 25
Genomic Location (Zv9):
Chromosome 5 (position 23167554)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 20880426
GRCz11 5 21384226
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCATCAAGGCTACATGTCTCATGTAAAGTGTGTGTGTGTGTGTGTTTT[T/C]CAGATGGTCTCATGGACTGTGTCGACCCAGACTGTTGTAGTCAGCAGGTG
Long Flanking Sequence:
ACTAAACTAAAAATAAACTGCAAAAAAAAATCGTAGCTCCTGAGACATGTTTCGCTCTCTCTTCAAAAATGTATACTGGGATACATGTCCATAATGAGCCTGGGTTGATTATAATGGGCAAAAAATGCATAAAACATGTATGTAAGGTGATTTGCGATTAACAAAAATATACTTTGTAAAAGGCATGTCCATGCAAAACAATATATATTTCAGAGATTTATTTGAGTAATTAGCGATTGAAACCAGCTTCAAATTAAACAGTGAAAGTCTGTAATAGGCATGTCCTTTTTTAAAGGCATCTAAGTAAACATATGTGTGAGTGTGTGTGAGAGGTTTCTGGGTTATTCTCTCTGAGACTCTCTCCTGTGGGAGGGTAAAAGCACAGATCCCCTTTAATGGAGCTGACAAATGAGATCATGTGCACACAGACACACGCTGAGCAAGGGCAACCTGCATCAAGGCTACATGTCTCATGTAAAGTGTGTGTGTGTGTGTGTTTT[T/C]CAGATGGTCTCATGGACTGTGTCGACCCAGACTGTTGTAGTCAGCAGGTGTGTGCGAGCGCCCCACTGTGCCAAGGCTCTCCTGACCCTCGTGACATCATTCAGCAGAGCCACACCTCTTATGAAACTCGCCCTTCGCGTCAGTTTTTCGAGCGTGTGCGATTCCTCATCGGACGGGACAGCACACACATACTACCAGGAGACCTGCCATTTGACAGCAGGTGAAAAACAAACGCTTGTAAATATTTGCACTCTCAAATGCACACAAAGTCTTTTTTTTTACAGGTGAAGCAGCATTTTTATATTTATTTTGGTCGTAAGATTAGCTTTTTTTTACCATACACATCATATTCCAGTGAAATCACTCTTCTGCTTTTGTATTTTTATGACTGCTGTGCAATACAGCAGAGATTCTGTGTAGAAGCAAAAGCAGATGCTGCTGTTTTATTAGGTCAGACACTGACAGACATCTTCGCTCAGACTTTGGTCACGATCTGACAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2239
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000040184 Essential Splice Site 714 2571 12 29
ENSDART00000144198 Essential Splice Site 540 2389 9 25
Genomic Location (Zv9):
Chromosome 5 (position 23167332)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 20880204
GRCz11 5 21384004
KASP Assay ID:
554-3082.1 (used for ordering genotyping assays)
KASP Sequence:
GACGGGACAGCACACACATACTACCAGGAGACCTGCCATTTGACAGCAGG[T/C]GAAAAACAAACGCTTGTAAATATTTGCACTCTCAAATGCACACAAAGTCT
Long Flanking Sequence:
TGAGTAATTAGCGATTGAAACCAGCTTCAAATTAAACAGTGAAAGTCTGTAATAGGCATGTCCTTTTTTAAAGGCATCTAAGTAAACATATGTGTGAGTGTGTGTGAGAGGTTTCTGGGTTATTCTCTCTGAGACTCTCTCCTGTGGGAGGGTAAAAGCACAGATCCCCTTTAATGGAGCTGACAAATGAGATCATGTGCACACAGACACACGCTGAGCAAGGGCAACCTGCATCAAGGCTACATGTCTCATGTAAAGTGTGTGTGTGTGTGTGTTTTTCAGATGGTCTCATGGACTGTGTCGACCCAGACTGTTGTAGTCAGCAGGTGTGTGCGAGCGCCCCACTGTGCCAAGGCTCTCCTGACCCTCGTGACATCATTCAGCAGAGCCACACCTCTTATGAAACTCGCCCTTCGCGTCAGTTTTTCGAGCGTGTGCGATTCCTCATCGGACGGGACAGCACACACATACTACCAGGAGACCTGCCATTTGACAGCAGG[T/C]GAAAAACAAACGCTTGTAAATATTTGCACTCTCAAATGCACACAAAGTCTTTTTTTTTACAGGTGAAGCAGCATTTTTATATTTATTTTGGTCGTAAGATTAGCTTTTTTTTACCATACACATCATATTCCAGTGAAATCACTCTTCTGCTTTTGTATTTTTATGACTGCTGTGCAATACAGCAGAGATTCTGTGTAGAAGCAAAAGCAGATGCTGCTGTTTTATTAGGTCAGACACTGACAGACATCTTCGCTCAGACTTTGGTCACGATCTGACACTTTTTATCTTATCTGTAAGATCCTTTGATTACTGTTAACTTTAATTAATTTCAGTGTACTACCTAGTAATTATGAAGCATATTAATAATAGACTCATTCATTTATTTATTTGCTTATTTGTTAACCTATTTTATTCATTTATACATTCTCTTTTCGACTTAGTCCCTTTATTAATCAGGGGTCGCCACAGCGGAATGAACTTATGCAGAATATATTTTTACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11851
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000040184 Nonsense 746 2571 13 29
ENSDART00000144198 Nonsense 572 2389 10 25
Genomic Location (Zv9):
Chromosome 5 (position 23162797)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 20875669
GRCz11 5 21379469
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTCTCGTTGGCGTGAACGTCACGYTTCAGCATAACCCTGAGTATGGGTA[C/A]ACACTCAGCCGGCAAGACGGCAGGTAACACACACTCTAAWGCACTTTGCA
Long Flanking Sequence:
GAAAAAACCTTAACAGATCCAAAAATGCATTATGAATATTGTGATGTTTTGTAAATACATCCACACACCACTGAAAGTGTTTGGTTAGCACATGCGAAGTGAACTCGCCTCTGGCTTTCCTATGCTGATCCAATACCAGCTTGTGCTTTGAGCAGTGTGACTCACCCCAAAAATAATCTCCCAAAATGATTTTTGCCATCATCGTCTAGTTTGAGGAAGTATGCGATCGATTGAAGCATGTATTGTATTTTTCTCTGATTACTGGAAAGAGAGTGCTGCTCTCCCAGCTTCGATCTCTCCTGACAGATCCTGGTTTCTCTTGCAGTGGCTGCACTCATTCTTTCCCTCTCTTTCCCTCCCTCTCTCTCTACCTCCCGTCTCTCTCTCTCTCTCTCTCTGTGCAGTCGAGTGTGTGTAATTCGAGGTCAGGTTTTGGCCTCTGATGGAACTCCTCTCGTTGGCGTGAACGTCACGTTTCAGCATAACCCTGAGTATGGGTA[C/A]ACACTCAGCCGGCAAGACGGCAGGTAACACACACTCTAATGCACTTTGCAAAGAAAGACATATAACAGAACACACACTGTTATAATCTCTCGTGAACATTCCTCTTTATTTATGCAGTGCATTCAGTATCTTCTGCTTGTTGTGTAGGTCCTGCATACTGTATCTACTCCATTCTATGCATACAGTGGGAGGCAAAAGTCAGCTAGTTGAATACAAAAAAAAAAAAAATAAATGGATTGGATATTTTACAAGAATTTCTTATTCTTTTGCTAACACCTACACTTCTGTTGCATGAAATTCAAGTTTGCAGTTATTCTTTGTTTGAGATTGTTGCCATTCCTCATTTTAAACAATGATTTTATAATATTGCAGAATGTCTTTCTTATTCATACTTCCATATATTATAAAATATAATTAACTGCAAAATGCAACGCTTTCAAATATCAGTACAGTAACTAAACAAGCGTATGGACAAGTTGTATAAAAACATTTTGGTGCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38462
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000040184 Nonsense 771 2571 14 29
ENSDART00000144198 Nonsense 597 2389 11 25
Genomic Location (Zv9):
Chromosome 5 (position 23160404)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 20873276
GRCz11 5 21377076
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTTGATCTTCTGGCAGTGGGTGGAATCTCAGTGTCTCTTGTATTCCAG[C/T]GAGCCCCATTTTTGTCCCAGATTCGGTCGGTCTGGCTTCCTTGGAACCAG
Long Flanking Sequence:
TGTAAGAGTTGCAGAGAGCTAGCTGCCGGCAATGCTGAATACTATGTACTATGTACTAATGCTGAAATATCTAGTAAAAAATAAAAGCCAAAGATAAAAGAAATCTGTTAATAGAAATTAGTTATTAAAACTCTTACATTTAGAAATGTGTAAAAAAAAAAACATCTGTTAAAAAGAAATTCTGAAAAAATATATAAAAGAATTTAAATTTAACACACTGAAAAAATGATGTCTGCAAAACTGTTGCAAACAATTTATATGGGGTTCAATTTAGTTTTGTTCAAATTAATTTGTTTGTTTTAATTCAGCCTTTTTGTAAGCTTAAATTTTGTAAATCTAAGGATGTTTTTCAGTGCAGCAGGGCTAATAAATCTGACTTCAAATGTATATATTGAATAGAAAATCTATAAAGCTTTGTTTCTAATTATGTTTGTGTTTTCTTTCCTGCCAGCTTTGATCTTCTGGCAGTGGGTGGAATCTCAGTGTCTCTTGTATTCCAG[C/T]GAGCCCCATTTTTGTCCCAGATTCGGTCGGTCTGGCTTCCTTGGAACCAGTTCATGGTCTTGGACCGAGTTTTTATGGAAAGAACTGAATCCAAAACACCTGTCTGTGATCTGAAAAACCTTATCAGCCCTCATGCCGTTGTTCTGTCTGCTCCCCTTCCACGCTTTGCTGCTGACTGTGAAGAGAGAGGAGCAGTCCTACCTGAGCTACAGGTAAAAGACTAATATAATGATAACTTAGGTCATCATATAGTCACATACTACTGACTACCAGTCACTCGTATATTAGTAAATGTTATGGCAGTATCTGCTTGCACTTTATTTTAACAGTTTCCCCAACGGACATTTAGTTACAGTGGGGTAAATAAGTATTAAACATGTCCCTATTTTCCTCAGAAAGCATATTTCTATAGGGGCTGTTGACTTGAAAACTTCATCAGATGTTGATAGTGATCAAAGAAGTCCATGTATGCAAAGAAAACAAATCTAATTAAGCCTGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16414
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000040184 Nonsense 1333 2571 22 29
ENSDART00000144198 Nonsense 1151 2389 18 25
ENSDART00000040184 Nonsense 1333 2571 22 29
ENSDART00000144198 Nonsense 1151 2389 18 25
Genomic Location (Zv9):
Chromosome 5 (position 23115135)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 20828007
GRCz11 5 21331807
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATGAATGTGTCCCCAGGTGACGGAGGTTACGCTCGCGATGCCAAGCTG[A/T]AGTCTCCCTCATCTCTAGCGGTTTCTCCTAATGGCTCCCTCTGCATCGCT
Long Flanking Sequence:
AAAAACTACATATACAGTATATAGTCAGTATATGTAGGCTATATACACAGAAAATTATACTACTGACATCTTTCAAAGGTACATAGTGTATATTTCTATTGCATATTGTTACATATTACAGGTCTTATACAGTACTTGCATTTTGTTACTGCATTTGATCCAAAATGGTCTGCGGTGTGCCATTAGGCAACTATGCTGTGTGACTCTGTCATGCTGGGAGATTCAATTTGTGAATATTTTCCTGCCAGACTTGTTGGTATGACACATTTAAGAGTCCTGGCTGCTGCTGTATGCAGGTTTAATTAGAGAAAAATCTTTATTATTTAACTGCCATAGACAAGTGTTGCAGTTTTACTGCAGCGGGTCTCTGAGGGTTAATCGTTAAGCCCAACACTGAATGCCTAATGAACTAGACTTCCCTTTTTCCACTTCTTCTCCCTCTCATTCTCTCCATGAATGTGTCCCCAGGTGACGGAGGTTACGCTCGCGATGCCAAGCTG[A/T]AGTCTCCCTCATCTCTAGCGGTTTCTCCTAATGGCTCCCTCTGCATCGCTGACCTGGGGAATGTGCGCATTCGCCGGCTCACCGCTAACCATCCGCAGCTCAATCCCGAGGGGCTGTACGAGCTCGCCTCCGTGGCCGATCAAGAGCTCTATCTGTTCAGTCCAAACGGCACTCACCTGTTCACCCGCAGCCTGGTGACAGGGGACTACCTGCTTAACTTCACATACACCCCAGAGGGCCACCTGAGCAGCATAGCAAACAGGGAAGGCACCATAGCGCAGTTGCGGCGGGATGCTAATGGCGTGCCCCTGTGGCTCGTAGCCCCGGGCGGCCAGGTGTACTGGCTGACCATCAGTAACGCCGGGATGCTGAAGCGCATTTCGGCTCTGGCGCACGACCTGGCGCAGCTCAGTTATTACGGCAACACGGGGCTGCTCGCCACCATCAGCAACGAGAACGGCTGGACAAGCGTCTACGAGTAAGTGCTGTCCTTCGTCTGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16472
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000040184 Nonsense 1333 2571 22 29
ENSDART00000144198 Nonsense 1151 2389 18 25
ENSDART00000040184 Nonsense 1333 2571 22 29
ENSDART00000144198 Nonsense 1151 2389 18 25
Genomic Location (Zv9):
Chromosome 5 (position 23115135)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 20828007
GRCz11 5 21331807
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATGAATGTGTCCCCAGGTGACGGAGGTTACGCTCGCGATGCCAAGCTG[A/T]AGTCTCCCTCATCTCTAGCGGTTTCTCCTAATGGCTCCCTCTGCATCGCT
Long Flanking Sequence:
AAAAACTACATATACAGTATATAGTCAGTATATGTAGGCTATATACACAGAAAATTATACTACTGACATCTTTCAAAGGTACATAGTGTATATTTCTATTGCATATTGTTACATATTACAGGTCTTATACAGTACTTGCATTTTGTTACTGCATTTGATCCAAAATGGTCTGCGGTGTGCCATTAGGCAACTATGCTGTGTGACTCTGTCATGCTGGGAGATTCAATTTGTGAATATTTTCCTGCCAGACTTGTTGGTATGACACATTTAAGAGTCCTGGCTGCTGCTGTATGCAGGTTTAATTAGAGAAAAATCTTTATTATTTAACTGCCATAGACAAGTGTTGCAGTTTTACTGCAGCGGGTCTCTGAGGGTTAATCGTTAAGCCCAACACTGAATGCCTAATGAACTAGACTTCCCTTTTTCCACTTCTTCTCCCTCTCATTCTCTCCATGAATGTGTCCCCAGGTGACGGAGGTTACGCTCGCGATGCCAAGCTG[A/T]AGTCTCCCTCATCTCTAGCGGTTTCTCCTAATGGCTCCCTCTGCATCGCTGACCTGGGGAATGTGCGCATTCGCCGGCTCACCGCTAACCATCCGCAGCTCAATCCCGAGGGGCTGTACGAGCTCGCCTCCGTGGCCGATCAAGAGCTCTATCTGTTCAGTCCAAACGGCACTCACCTGTTCACCCGCAGCCTGGTGACAGGGGACTACCTGCTTAACTTCACATACACCCCAGAGGGCCACCTGAGCAGCATAGCAAACAGGGAAGGCACCATAGCGCAGTTGCGGCGGGATGCTAATGGCGTGCCCCTGTGGCTCGTAGCCCCGGGCGGCCAGGTGTACTGGCTGACCATCAGTAACGCCGGGATGCTGAAGCGCATTTCGGCTCTGGCGCACGACCTGGCGCAGCTCAGTTATTACGGCAACACGGGGCTGCTCGCCACCATCAGCAACGAGAACGGCTGGACAAGCGTCTACGAGTAAGTGCTGTCCTTCGTCTGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25295
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000040184 Essential Splice Site 1863 2571 26 29
ENSDART00000144198 Essential Splice Site 1681 2389 22 25
Genomic Location (Zv9):
Chromosome 5 (position 23090698)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 20803570
GRCz11 5 21307370
KASP Assay ID:
554-7664.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACCTGATGCACGAAGGATTCGTTTGCACCATACGCTACAGACAGACAG[G/A]TAAAAACAACACACTGACAATAAGTCATAGTGCATTAATCTTTCATAAGC
Long Flanking Sequence:
TCACAAATATAAGTACTGTTATGGCTATCTTTATAGTTTTCATTCCTGATGTGAACGGGCCTTTAGTCTTATCTAATTAGCTTCTCCATGTTCTTCTTCTTCTTTTCAGTCTGTCCAGCTGTTGTTACACAGTCAGCGGCGCTATACGTTCGAGTACGATCAGACAGACTGTCTCCTATCAGTGACCCTTCCCAGTATGGTGAGGCACAGCTTGCAGACCTCTCTATCTGTGGGATACTACCGAAACACCTACACCCCTCCCGACTCGCCCACGTCCAGCTTCACGCAAGACTACGCTCATGATGGGCGCCTGCTGCAGAGCCTATATCTGGGCACGGGCAGACGGGTCATCTACAAATACAGCCGCGTCGCCCGGCTGGCTGAGATCCTCTATGACTCAACACTTGTTACCTTCACTTACGATGAGGCGACAGGAGCTGTTAAAACCATCCACCTGATGCACGAAGGATTCGTTTGCACCATACGCTACAGACAGACAG[G/A]TAAAAACAACACACTGACAATAAGTCATAGTGCATTAATCTTTCATAAGCCTTTTAGTGAATCACACACCGTTTCCAGGGATTTTAGTGCAGCGAGTTATCAGTGACGTTTAATTCATAAACAAAGCACTACTGCGATTGACTGAGAAAAGCGTACTGTAGTTCACCCAAAAATGACAATTCTGCAGTCATTTATTTACCCTTGACTTGTTCCAAACCAGTTTTTTTTTCTGTTGAACCCAAAAGAAGATATTTTGAAAAATGTTACGATTAATGGTTTTTGTTTTCCCTGCTATGGAAGTCAGTGGTTACAGGTTTCCAGTATGTTCATGTGTTCTTACTAGCTTGGAACAAGTCAAGGGTGAGTAAATGATGCCAGAATTTTTGGGTGAACTATCCTTTTAATTACTTCCTCATACTACAATGTAAAAACTATAACAATTACCTTACTATCTATTAATAAGTAGTAAGTTGGATTTATTGAGACAAACATTCATTCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20387
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000040184 Nonsense 1930 2571 27 29
ENSDART00000144198 Nonsense 1748 2389 23 25
Genomic Location (Zv9):
Chromosome 5 (position 23085328)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 20798200
GRCz11 5 21302000
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACGTGTCTGGACGTATCGAGCAATTCGGGAAGTTCAGTGTCATCAACTA[C/A]GACTTGAACCAGGTCATCACCACACATGCCATGAAGCACACTAAAATCTT
Long Flanking Sequence:
AATGGGTGAGGTGATAATCCTGTGAGACAGAGAGACGAGTAAGACGGCTGAGCGGTCAGACAGGTAAACAGGTTATACTCTTCCACCAATAAACATACAGGCTGACATTTAATCTTCCTTTTGTCACTTGGCTTGCACTCCCCTCCTGCTTGGCTGATCTAAAAGCGCTTTGAATCACAATCAGCCGTCTGACAGTGGCGGAGTTCATCCTATCTCACACTGTGGCAAAACTGACTCGTGTTTTACCTCACCTCTGTCTGGCTTTCTGCTAACTTCTTTCCACTCTGTTTCTCGCATTCAGGTCCTCTGGTGAGCAGACAAATATACCGTTTCAGCGAAGAAGGATTGGTTAACGCTCGCTTTGACTACAGCTACAACAACTTCAGGGTCACCAGCATGCAAGCTATGATCAACGAAACACCTCTTCCTATTGACCTCTACCGATATGTGGACGTGTCTGGACGTATCGAGCAATTCGGGAAGTTCAGTGTCATCAACTA[C/A]GACTTGAACCAGGTCATCACCACACATGCCATGAAGCACACTAAAATCTTCAATCCCAATGGGCAAGTGATCGAGGTTCAGTATGAGATTCTGAAATCCATCGCCTACTGGATGACGCTGCAGTACGACAGCATGGGACGCGTCACAAACTGCGATATTCGCATTGGTGTGGACAGCAACATCACACGGTACGCATATGAGTATGATGCCGATGGCCAATTGCAGACGGTTGCCATTAATGACCGCCCACAGTGGCGTTACAGCTACGACCTGAATGGAAACATCAATTTACTGAGTCACGGCAACAGTGCGCGATTGACACCATTGCGTTACGATCTTCGAGATCGTATCACGCGGCTTGGAGAAATCCAGTATCGCACTGATGAAGATGGGTTCTTGCGTCTTCGAGGCAACTTACTCTTTGATTACGGTTCGAATGGACTGCTAATGGGTGCCTATGATCGGGACAGTGAGCAGAGAGTGTGGTACCGTTACGATGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20386
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000040184 Nonsense 2044 2571 27 29
ENSDART00000144198 Nonsense 1862 2389 23 25
Genomic Location (Zv9):
Chromosome 5 (position 23084988)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 20797860
GRCz11 5 21301660
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACTGAGTCACGGCAACAGTGCGCGATTGACACCATTGCGTTACGATCTT[C/T]GAGATCGTATCACGCGGCTTGGAGAAATCCAGTATCGCACTGATGAAGAT
Long Flanking Sequence:
AAGGATTGGTTAACGCTCGCTTTGACTACAGCTACAACAACTTCAGGGTCACCAGCATGCAAGCTATGATCAACGAAACACCTCTTCCTATTGACCTCTACCGATATGTGGACGTGTCTGGACGTATCGAGCAATTCGGGAAGTTCAGTGTCATCAACTACGACTTGAACCAGGTCATCACCACACATGCCATGAAGCACACTAAAATCTTCAATCCCAATGGGCAAGTGATCGAGGTTCAGTATGAGATTCTGAAATCCATCGCCTACTGGATGACGCTGCAGTACGACAGCATGGGACGCGTCACAAACTGCGATATTCGCATTGGTGTGGACAGCAACATCACACGGTACGCATATGAGTATGATGCCGATGGCCAATTGCAGACGGTTGCCATTAATGACCGCCCACAGTGGCGTTACAGCTACGACCTGAATGGAAACATCAATTTACTGAGTCACGGCAACAGTGCGCGATTGACACCATTGCGTTACGATCTT[C/T]GAGATCGTATCACGCGGCTTGGAGAAATCCAGTATCGCACTGATGAAGATGGGTTCTTGCGTCTTCGAGGCAACTTACTCTTTGATTACGGTTCGAATGGACTGCTAATGGGTGCCTATGATCGGGACAGTGAGCAGAGAGTGTGGTACCGTTACGATGGGCTTGGGAGGAGAGTGGCCAGTCGCTCTAGTGACGGAGCACAGCTGCAGTTCTTTTATGCCGATCTGATGGAACCAACGCGGGTGACGCACCTTTACAACCACAGCAGCGCAGAGATCACCTCCCTCTATTATGACCTACAGGGACATCTCATCGCAATGGAAATGAGCAGCGGCGAAGAATTCTACATAGCATGTGACAATGCTGGAACTCCACTTGCGGTTTTCAGTAGCCGTGGCCATGTAGTGAAGGAAGTTCGGTACACACCGTATGGAGATGTTTACCGGGACTCCAATCCTACCTTTTCTCTGATCTTCGGATTTCAGGGCGGCCTCTATGAC
Associated Phenotype:
Not determined