Busch Lab

ZMP

lrp2

Ensembl ID:
ENSDARG00000060649
ZFIN ID:
ZDB-GENE-050119-2
Description:
low-density lipoprotein receptor-related protein 2 [Source:RefSeq peptide;Acc:NP_001181916]
Human Orthologue:
LRP2
Human Description:
low density lipoprotein receptor-related protein 2 [Source:HGNC Symbol;Acc:6694]
Mouse Orthologue:
Lrp2
Mouse Description:
low density lipoprotein receptor-related protein 2 Gene [Source:MGI Symbol;Acc:MGI:95794]

Alleles

There are 17 alleles of this gene:

Allele Name Consequence Status Availability
sa41550 Nonsense Mutation detected in F1 DNA Not yet available
sa34763 Nonsense Mutation detected in F1 DNA Not yet available
sa25440 Nonsense Mutation detected in F1 DNA Not yet available
sa34764 Nonsense Mutation detected in F1 DNA Not yet available
sa38765 Nonsense Mutation detected in F1 DNA Not yet available
sa17023 Essential Splice Site Available for shipment Available now
sa25 Essential Splice Site Confirmed mutation in F2 line Not yet available
sa18967 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa21599 Nonsense Available for shipment Available now
sa34765 Nonsense Mutation detected in F1 DNA Not yet available
sa41551 Nonsense Mutation detected in F1 DNA Not yet available
sa34766 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa21600 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa41550
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085697 Nonsense 115 4632 3 77
ENSDART00000129237 None None 3092 None 50
Genomic Location (Zv9):
Chromosome 9 (position 49451970)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 48766588
GRCz11 9 48464073
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGAGGATACAGGTGTGACAGAGTGCCCGACTGTCTGGATGGAGCAGAC[G/T]AGAGGAACTGCTGTAAGTGTGCTCGTGACATCTGATCAAGCCTGTTTACA
Long Flanking Sequence:
GGGTATTCATAGTGGCTTAGGAATCGTCTGATTGGTGAATCATAAATTGAATAATGCGGGGCCGGCTGCAAGCAATCATAAGCACGTGATCCTCTTGAAATTAGTTCATAAATAACTTCACATATCAAGATATGAGATTTTGATCATGTCTCCATCCATCTCTTCCCTGCTTTCTGCCTCACTTTCAATTACCAGCTGAGGGCTCCGTTGATTCACAGTAATGCAATTTCCGTCATGTCAGAGAAAGAAACACGATAGCTCAGATGTCGAGTCTGAAACACAAAGGGAGAAGCGTGCACGTGTTGTAGAGAGAGTTTGTGCCGCTTTAGTGATGATGAAGACCACCCAGCGCTGGTCTATTATATTGATGTGTGTTTCTTTGATGTTTGCTGGCAGCTGGCAGGACGTGCTCCAGTTCACAGTTCACCTGCACCAACGGGGCCTGCATCCCTGGAGGATACAGGTGTGACAGAGTGCCCGACTGTCTGGATGGAGCAGAC[G/T]AGAGGAACTGCTGTAAGTGTGCTCGTGACATCTGATCAAGCCTGTTTACAGCTGCTCACTGCATGGTAGTGTGTGTGTGTCACTGTCTGTGTGCGTGTGTGCGCCCATGTGTTTGTGTGTGTGTCTGTCTGTGTGTCTGTCTGTCTGTGTGTTTTTCTGTCTGTCTATCGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTGTGTGTGTGTTTGTATGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTGTGTGTTTTTTCTGTCCGTCTGTGTTTGTGTGTGTGTGTGTTTGTCTGTCTGTCTGTGTGTGTGTGTTTCTGTCTGTCGGTGTGTGTGTGTGCGCCTCTCTCTCTGTGTATCTGTCTATGTGTGTGTGTGTGTGTGTGTGTCTGCCTCTGTGTGTGTTTCTGTCTGTCAGTGTGTGTGTGTGTGTGTGTGTGTTTGTGTTTGTCTGTTTGTGTGTGTCTCTCTGTGTGTGTGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34763
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
ENSDART00000085697 Nonsense 191 4632 5 77
ENSDART00000129237 None None 3092 None 50
ENSDART00000085697 Nonsense 191 4632 5 77
ENSDART00000129237 None None 3092 None 50
Genomic Location (Zv9):
Chromosome 9 (position 49457146)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 48771764
GRCz11 9 48469249
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGCTACATCTGCGATCATGATGACGATTGCGGAGACAGAAGTGATGAA[C/T]AAAACTGCAGTACGTACATTTCATTTATTCATTCATTTTCTTTTGCCCCA
Long Flanking Sequence:
TCAGGGCAGGTACTATTTGAGAGTTTGGTCATTTATTTCATTTGGTCATTTATTTTGATTTGGTAACCGTCAAACGTCATCAGGGAAACGGTTAAAATTTCTGCTTAGTAAAAAAAACATTAGTGCTCCATTTGGAACGACACTACATACATGTACTATGCTGTTTAGTGTGTAAGTGCATAAGTACATAGTACATAGTGCAAAGTGTATAGTGTGTCATTTGGGAAGCAGCTAGTGTCACATAAACACTGCAACATTGATGTGCGTATCCGCAGCTCTATCCTATCTAGACTTTACCCTTATTTTTGATTGGTGTATTTTTTTAAATGTGTTGTTTTTACAGTGTTTCATTTATTGGTGAGATCACACATTGTTCTTTTCCTTGGTTGTGTTCAGCCCAGCGGTGCAGCAGTGGTCAGTTTCAGTGCAGTAATGGAGAGTGTATTCCTCGAGGCTACATCTGCGATCATGATGACGATTGCGGAGACAGAAGTGATGAA[C/T]AAAACTGCAGTACGTACATTTCATTTATTCATTCATTTTCTTTTGCCCCAGTGTCTATTTCAGAGGTCGCCACAGCTGAATGAACTGCCAACTATTTCAGCATATTTTTACGCACGGATGCCCTTCCAGCTTTTTTTATTTATATTGTTTTATTGTTTTTAATCTTTCTAAAAAAATGTATATATATATATATATACATATATATGTGTATATATATATATATATATATATATATACACACACACACACACACACACACACACACGCACACACACACACACACACACACACACACACACACATACACACACACACACATTATAACAACCCAGGCTCATTCTGAAAACGTAGTCCCGTGGATGTTTCTGGAGACCGTGAACTATGTAGCCGGAGGTATGATGACTGCATTAATTTTTTTAAGCGAATGATACGGGACGGTATGACGCCGTTCCTTTTCGCGCTTACCAGCTGACCGCTTACCTTCATGTGGAGGGCTTTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25440
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
ENSDART00000085697 Nonsense 191 4632 5 77
ENSDART00000129237 None None 3092 None 50
ENSDART00000085697 Nonsense 191 4632 5 77
ENSDART00000129237 None None 3092 None 50
Genomic Location (Zv9):
Chromosome 9 (position 49457146)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 48771764
GRCz11 9 48469249
KASP Assay ID:
554-7650.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGCTACATCTGCGATCATGATGACGATTGCGGAGACAGAAGTGATGAA[C/T]AAAACTGCAGTACGTACATTTCATTTATTCATTCATTTTCTTTTGCCCCA
Long Flanking Sequence:
TCAGGGCAGGTACTATTTGAGAGTTTGGTCATTTATTTCATTTGGTCATTTATTTTGATTTGGTAACCGTCAAACGTCATCAGGGAAACGGTTAAAATTTCTGCTTAGTAAAAAAAACATTAGTGCTCCATTTGGAACGACACTACATACATGTACTATGCTGTTTAGTGTGTAAGTGCATAAGTACATAGTACATAGTGCAAAGTGTATAGTGTGTCATTTGGGAAGCAGCTAGTGTCACATAAACACTGCAACATTGATGTGCGTATCCGCAGCTCTATCCTATCTAGACTTTACCCTTATTTTTGATTGGTGTATTTTTTTAAATGTGTTGTTTTTACAGTGTTTCATTTATTGGTGAGATCACACATTGTTCTTTTCCTTGGTTGTGTTCAGCCCAGCGGTGCAGCAGTGGTCAGTTTCAGTGCAGTAATGGAGAGTGTATTCCTCGAGGCTACATCTGCGATCATGATGACGATTGCGGAGACAGAAGTGATGAA[C/T]AAAACTGCAGTACGTACATTTCATTTATTCATTCATTTTCTTTTGCCCCAGTGTCTATTTCAGAGGTCGCCACAGCTGAATGAACTGCCAACTATTTCAGCATATTTTTACGCACGGATGCCCTTCCAGCTTTTTTTATTTATATTGTTTTATTGTTTTTAATCTTTCTAAAAAAATGTATATATATATATATATACATATATATGTGTATATATATATATATATATATATATATACACACACACACACACACACACACACACACGCACACACACACACACACACACACACACACACACACATACACACACACACACATTATAACAACCCAGGCTCATTCTGAAAACGTAGTCCCGTGGATGTTTCTGGAGACCGTGAACTATGTAGCCGGAGGTATGATGACTGCATTAATTTTTTTAAGCGAATGATACGGGACGGTATGACGCCGTTCCTTTTCGCGCTTACCAGCTGACCGCTTACCTTCATGTGGAGGGCTTTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34764
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085697 Nonsense 766 4632 16 77
ENSDART00000129237 None None 3092 None 50
Genomic Location (Zv9):
Chromosome 9 (position 49492966)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 48807584
GRCz11 9 48505069
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTTTTGGCAGCCAATCGGGTGGACGGAGTGGAAGATCTGGCATATGATT[G/A]GATATCGAAGAACTTATACTGGACGGATCCACGTTACAGGAGTATTTCTG
Long Flanking Sequence:
AGCCTCATAAAAGTGATTAAAGTAATTTAGATTTAATCATAACTCTTGCTCTGACATGCCTCTAACTATACTTAAATGGATAGTTTACCCAAAAATGAAAATTCTGCCAAATTCTGAAAAAAATCCAACCTTTGAGTTTCTTTCTTCTGATAAATAAAAGCAAAAATATACTGAAGAATGCTGGAAAAAGCAGCCATTGACTTTCATAGTGTTTAGTTACAGCTATGGATGTCAATGGCTGCCTTTTTTTAATATTCTTCAGAATATCTTGTATTGTGTCCAGTAGAAGTTTAGAACCGCTTGAGTAAATGATGACGAAAGATTATTATGGTGAACTATTCCTTTTAAATGATCAGGGTCAAGTGATCAGGGTCTACATGTTATTTTTTGTCATTATTATTATTTGAGTCTCATCTTTGTCTTCTTTACTGTATTCGCTACAGGTCGAGAGGTTTTGGCAGCCAATCGGGTGGACGGAGTGGAAGATCTGGCATATGATT[G/A]GATATCGAAGAACTTATACTGGACGGATCCACGTTACAGGAGTATTTCTGTGATGAAGGTGGTGGATAAATCCAGACGAGCCATCGTACGCAACCTTAACAACCCCAGATCCATAGTGGTCCATCCAGTGGCTGGGTGAGTCAGAATTATTAAAGAAAGCTTGGGTGGCTCAGTGGTTAACACTGTCACCTCACACCAAGAAGGTCGCTGGTTGGAGTCCCAGCTGGGTCAGTTGGCAATTCTGTGTCGAGTTTGCATGTTTTCCACGTGTTGGCGTGGGTTTTCTCCAGGGGCTCCGGTTTCCCCCACAGTCCAAAGACATGCGATATAGGTGAATTGAATTAACTAAAACAAGAATGTATGGGTGTTTCCCAGTACTGGGTTGCGGCTGGAAGGGCATCCGCTGCATAAAACATGGCAGAATAGTTGCCGGTTTATTCCACTGTGGCAACCCCTGATAAATAAGGGACTAAGCCGAAGAAAAATAAATGAATTAATTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38765
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
ENSDART00000085697 Nonsense 1053 4632 21 77
ENSDART00000129237 None None 3092 None 50
Genomic Location (Zv9):
Chromosome 9 (position 49507919)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 48822537
GRCz11 9 48520022
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTCACAGATAACACTTGCTCGCCCCTTGCCTTCACCTGTGCCAATCAG[C/T]GATGTGTGCCCAGAAGCTGGCACTGCGACGGACACAATGACTGTTTTGAT
Long Flanking Sequence:
TGAGCCCTATGTGTGCACGTGCTTTTGGACTGTGGGTGAAACCGGAGCACCCACACCAATCATAAAGCACTGTTTGTTTATTTATTTTTGATTGTAATTTATTATAATAATGCCGATCCACTGCATAAAAAAGGAATAGACCATCCCAGTCGAAAGGTATAGGCTTGAATACTGTTAGACTCCCCAAAAAACCATATAGCACTGTTTATTTGCACTCATGGAAAATGACTTGATTGTCCCAGCTGATCTAAATTAATGAAATCTTTCCAAATAGAGTTATTCAAATCATCTGGTGAAATTATATTCATATCGCAATTTACCCTGCAGCAAAAACAAAATATCGAAATGTCAGATTTTTCCCAATATCATGCGGCCTTGTAAAAATATCAAAGCTTTTTAATTAGTCTTTTTTATTTACAGTGAAACTAAACCTAACTCCCTTTCTATACTGGCTCACAGATAACACTTGCTCGCCCCTTGCCTTCACCTGTGCCAATCAG[C/T]GATGTGTGCCCAGAAGCTGGCACTGCGACGGACACAATGACTGTTTTGATGGCAGTGACGAGAGGGACTGTCCCACTCAGACCCCTGGCACATGTCCGGCAGACCAGTTCATCTGTGCCAACCATTACTGCATCCCTCGCACTTGGCTCTGTGACACCGACAACGACTGCGGAGATGGATCAGACGAAAACAACTGCGGTGAGGCCTCACACACTCTTACGTTTTAAAGTGTGCATTTTAATTCTTGTATACAGTACATTTTGATACACACATCTTTGGAAACAATTAAAAGAATGCTTTAGGGTTTTACACATTATAGTTATGTGTTTGAGTAAAACTTAATTTTAGTTTTTCTTTCTATAAAATATTATAGCATTTCTTCCAAAGTTAAAATAAAGAGTTGTTTTGTAGTAATAGTACTAACAAAGGTTAGGTTCAATTGACTTATAGCGCATGTGTTTGGACTGTGGAGGAAATTCACGCCAACATGAGGAGAGCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17023
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085697 Essential Splice Site 3366 4632 50 77
ENSDART00000129237 Essential Splice Site 1826 3092 23 50
Genomic Location (Zv9):
Chromosome 9 (position 49660743)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 48915939
GRCz11 9 48613424
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACACCAACGACAAACTCTACTGGTCTGAYGCTCATCTCAACTACATTGAG[T/C]AAGACTCGCTCAGGYTTATATTCTGGGTGATTTAGTTAAATTCAATTYAT
Long Flanking Sequence:
GACTAAGCTGAAGGAAAATGAATGAATGAATGAATTGTTAAGTACAGTAAGGACTTTCATAACACTACGTACAGTATGCTGGGATATAAATTACAAATGTGCTTTATCTGAAATGAAAGGTGCTTTAAAAAGTGCTTGAGAGTCCTGTTCATGAAAGAGTGGGAGCCCTGCTTTTAGTAGCGATTGTTTAGTAAGTGATATGATCATTAATACTTGTTTTAATTTTTTTTAATACTGTTTTAGGTTATGGGCTTGCCAATGTAATTTCAGCTTATCTGTTTTCATGTCTAATGTAATGTACTGTACATCTTATGTCCTATTTGTGCAGGTATGTGTACTGGACTGACTGGGGAGAAAGAGCGTTCATTGGTCGTGTTGGAATGGATGGAAATAACAAGTCTGCCATCATCACTACCAAGATCGAGTGGCCAAATGGTCTGACCATCGACTACACCAACGACAAACTCTACTGGTCTGATGCTCATCTCAACTACATTGAG[T/C]AAGACTCGCTCAGGCTTATATTCTGGGTGATTTAGTTAAATTCAATTTATTTACATTGATTACATTGAATCTGACAATGACTTGGTTGTTGATTTGCATTTGTCTCTTCAAGTTGTTGTTTTGATCATTTTAAAACATGAAACATTATATAAACCTTAAAGTTTTGATTATGATTTTAATGTAAAATTTTGTATGAATTATAGAGAAAATTGATAAGAATGTAATACATTTCAGCGCCAATAGCCTAGTGGTTAAGTGTGTCGACATATAGAACCGTGGTGCTCAGTGACCCGATTCTCGGCTTGAGGTCCTTTGCTGACCCTTCCCCTCTCTCTGCTCCCAATACTTTCCTGTCTGTCACCTCCACTGTCCTATCCCAATTAATGGTGAAGAAATGTAATTTAATACATTTATATTTTGTATGATATTTATATTTAAAGATGTATGTTAAGTTTATATTTATTAATTGAGTTGCATGTTTTTAAAGTTTTTATTATCAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25
Status:
Confirmed mutation in F2 line
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
ENSDART00000085697 Essential Splice Site 3565 4632 53 77
ENSDART00000129237 Essential Splice Site 2025 3092 26 50
Genomic Location (Zv9):
Chromosome 9 (position 49669867)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 48925063
GRCz11 9 48622548
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCAATCAGGACTGTCCCGACGGCTCCGATGAGGACACTGTGCTCTGTG[G/A]TACGGAACAATATAATGATATATAATTTTCCACAAATTGATGTGATTTAT
Long Flanking Sequence:
TCATGTGAAAAGGATCTATTAGGAAAATCATTGTATAACGATGGTTTTTTCTGTAAACAATCAGAAAAAAATATATATTGCTTCGAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAAATATTATCAGACATACTGTGAAAATTGCCTTGCTCTGTTAAACATCATTTGGGAAATATTTGAGTTAAAAAAATTATAATTCGTGAAAAAATATTCACAAGATGGCGAATAACTCTGACTTCAACTGTATGTCTGAATCCTTGAGTAATGGAGCATCCTAACATTATTTCTCACTCCATGCAGTTGTATCCCGATCTGGTGGAAGTGTGACGGTCAGCGGGACTGTAGAGACGGGTCAGATGAACCCTCCACGTGTCCCGTCCGGCACTGCAGGCTCGGTCAGTTCCAGTGTAATGATGGAAACTGCACCAGTCCACACTTCCTCTGCAACTCCAATCAGGACTGTCCCGACGGCTCCGATGAGGACACTGTGCTCTGTG[G/A]TACGGAACAATATAATGATATATAATTTTCCACAAATTGATGTGATTTATCGTCTTTAAAGTGAACAATCAGTGAATCGTTTCTTAATTAATCGTTAATATGTATAATCCAACATATTTACACTCAAAACACAAGCATCCCCATCCATAGTAATGAAAAGCTAGTGGATTTTGTAAAAAAAAAAAAAATCATTTTAAATGAACCATTATACAGGCTCCCACGGATTTTAGTTTTTTTGGTAACACTTTAGAATAAATATACATTATAACTAGTCAATAGATCATTAACAAACTGTTAGTTAATGGGTTATAAATGGCTTGTAAACTGCATTTTAATGATTTATAACTATACCTAATAAATTAGTAATAGATCATGAACAAGCTGTTAGTAAATTACTCACTAAAGACTTGTTAAGTATTAGTTAGGGTTAAGGTTATAACCCATTAACTAACAGTTAATTAATGGTCTATTAACTGGTTATAATGGATAGTTATAAATAA
Associated Phenotype:
Normal
Stage Entity Quality Tag
Larval:Day 5
ZFS:0000037		 whole organism
ZFA:0001094		 quality
PATO:0000001		 normal
PATO:0000461

Mutation Details

Allele Name:
sa18967
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085697 Essential Splice Site 3648 4632 55 77
ENSDART00000129237 Essential Splice Site 2108 3092 28 50
Genomic Location (Zv9):
Chromosome 9 (position 49675097)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 48930293
GRCz11 9 48627778
KASP Assay ID:
2260-2531.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTTCAGGGTGACTTTAAGTGTAATGCAGTATTTTTCTCTGTTGTTTGC[A/T]GTGGGTCCGGCGTACAGATGTGACAATCACACAGAGTTTGACTGCAGGAC
Long Flanking Sequence:
TGTTTAGAATTCTTAAGTGCATGGCATTCTGGTGTGCGACCTGCTTTATGGTTGCTGTTCTGAGTTATCCAGAGCTGTAGGACTTCACAAATCTTGAATACCACAATATTATTTGATATTAAAGTTAAACTAATATCAACAGCAAGACTCTCGCAAAAACCCAGCTGATTCATTCATTGCCTTGCGAATTAAATTACAGACATTTAATTTTGTTTTTTGGAGTATTTATCCGGTATCAATAATATGTCCCTGTAAATGTTTGAGATTGTAAACAAAAGTTATTGGCATCATTTTACCCAGAAACGGCATGCAAATGTATGCCAAGACACATATTGGCAGTTTCCCAATAAAGTAGCCCTGGGCACATATTCCCAATGAGTCTGTGTTGCTAATCACTCTCAGTTAGAGAAGGAAGACATAGGTTTGCAGTATGAAGTTGTACTGTATGTTGATTTCAGGGTGACTTTAAGTGTAATGCAGTATTTTTCTCTGTTGTTTGC[A/T]GTGGGTCCGGCGTACAGATGTGACAATCACACAGAGTTTGACTGCAGGACGAACTACCGCTGTGTTCCTCTGTGGGCCGTGTGTAATGGACACAACGACTGCAGAGACAACAGTGATGAACAGAACTGCGGTGAGCAATGTTGGGGAGGTTTACTTTAAAAAAAAAAAAGTTATAGTAAAAAAGTAAAAGTAATAGTTACTTTTTTGCTGGAGTTACTTTTGATGGAAAGTAATGCGTTACATTCCTCTTGAGATACTTTCGCAACACTGGTCGTGAGACTTCACACATTGCCCTTATTCCCAACAACCAGTGCATATGAAAATGAATATATTCATGAATAAAACATATATGGGTCATTCTTCAACTATGGGCACTTTTAGCCTTGTGAAGTTTTTGTCTAGTTTTAAGATTTTGAAGAAGAAACATTTTTTTTCCATCTTGAATTGAATAAATGTCAATTCCACCACATCTCAATATACAGCTTATTTCAAAATGAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21599
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085697 Nonsense 3825 4632 59 77
ENSDART00000129237 Nonsense 2285 3092 32 50
Genomic Location (Zv9):
Chromosome 9 (position 49688919)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 48944115
GRCz11 9 48641600
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCACACGCTACCCGAACAGCACCTACTGTCCACCCTTCCTGTTTGAGTG[T/A]AAGAACCATGTGTGTGTGCAGCAGCACTGGATATGTGATGGAGATAATGA
Long Flanking Sequence:
TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTCATGTATCCGATTGGTATGTCATGTCATATACTGTATGTATGTAATTTTTTATTCATGTCTCCTCATAACTTTCAGTCAAAATACCTTCCCCTCCACCGTTTCAACATTATCTCTTTTCTGATAAACCTCATATCACTCATGTGAGATCCACTAATAGCGAACCACAATCATTTAATTAATTCGCCACAGAATTGCTTCATTTTTTATCTTTTTTGAGAAGCCATTCAGATATACAGCCCATTATCATAAACATCAGATTCTTGATTGCAGTGTTGGTCGCTTTTGTATGTTAAGTTTGATAAGCAAGTTTGTGCTGAGTTTGAGATGCTTGTGTTTATTTTTCAGCCACACGCTACCCGAACAGCACCTACTGTCCACCCTTCCTGTTTGAGTG[T/A]AAGAACCATGTGTGTGTGCAGCAGCACTGGATATGTGATGGAGATAATGACTGCGGGGACAATTCAGATGAGGAGCTGCATCTCTGCTGTGAGAAAAACACAGTCATCCGTCTATCCATCTATCCATTCAACTATTTATCCACCCATCTCTGATTACATTCACCTACCTGTACATTCATTCACCCATCCATTTATTTACCCACCCACCATCCATTCATCTGCTCATCCACCTTTTCACCAGCCACCATACATCCATCCATATTCACCACACATCCTTTCATTCATCTATTAATACATCCATCTCTCATTTACCCACTTATTCATAGATGATTCCATTCATCCATCCATCCACCTCTCCTTCCATCTTTACCTCATTCTATCCATCAATACATCCACGTATTCACCTGTCTGTCATTTCCATTCCCCAGTCCATGCATTCATCCACCCACCCACCGTCCATACATCCATTGAGCCTTCTCTCCATCCACCCATACATCCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34765
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085697 Nonsense 4263 4632 68 77
ENSDART00000129237 Nonsense 2723 3092 41 50
Genomic Location (Zv9):
Chromosome 9 (position 49703559)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 48958755
GRCz11 9 48656240
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACATCGGCCACCCCTACAGTCTGGATGTGTTCGAGGGCCACGTTTACTG[G/A]ACGACTAAAGAGAAGGGAGAAGTGTGGAAGAAAGATAAGTTCGGGAAAGG
Long Flanking Sequence:
TGTGAATGCAGGCCATGATGGGTTTTGTAGTCCGATTCAGTGGCAGATGTGATGTGTTGAGTGCCCTCTAGTGTGTCTGGTGAGGACTCTACTTGATGACTGTGACAGGCGACTAAAAATCACACATCCTATTTGTGCCTAGGCAAACTTCTTCAGACTTTTTCTTCTTTTTACTTTTACATAAAATTATTCATAAAAAAATGCTTTTTTTGATTTCCCAGTATTTTATTACAACCAAATTAAATATCTGTAAGATTTGTCTCAATTTAAATTCCCTTCTTTTAATTATGCAAAAAAAAAAATAATAATAAATTTTAAAAAACGTAAAAGTGTTTTTTTTTTTGTAAAACAAGCCCAAATTAGATTTCTATTTAAAATCATTCAAGAAATTGATTGATGTATATTTGGTACGTAAAGGGTTGAGCTGTGCTGATGTTTGTTGTGTTTGCAGACATCGGCCACCCCTACAGTCTGGATGTGTTCGAGGGCCACGTTTACTG[G/A]ACGACTAAAGAGAAGGGAGAAGTGTGGAAGAAAGATAAGTTCGGGAAAGGAGACAAGGTGAAAGTGTTGACTATAAACCCCTGGCTGACCCAAGTGAGAATCTACCAGGAGCATCGACACAACCACTCAGGTAAAGCAATAGAAATGCATATCTAGCTAGCAACATGATGTTTTATGTCCTAAAGACATCTGATTGCAAAAAAAAGTCTCATTTTCATTTCGTTTAACTTGATGTACTAAATAATTCAAATAAAAACTAGTCTAGTTTTCTTTAGTTTTTCTCTAGTTTTTTCTTGAAAATCATTAATTATTAATTTCAATTAGTTTTAAAGAACCATCAAATAACACATTGAATTTTGTATAAAATTGTACTTTTAATTCAGGTGTTTTCTTGTAAAACATAGTCTAGTAAACTACATAAACTAAATACAATATTTTTTTTTATAAAATTATATTTAGATAATTAAATTAATTTTGTTTTTAAACCTACTTTGCATTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41551
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085697 Nonsense 4363 4632 70 77
ENSDART00000129237 Nonsense 2823 3092 43 50
Genomic Location (Zv9):
Chromosome 9 (position 49707614)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 48962810
GRCz11 9 48660295
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCCATTGAGGCCGAGGTGTCCATGCCGCTTGCATGCAGATGCATGAAT[G/T]GAGGAACGTGCTTCACTGATGAAGGAGGCCTGCCCAAGTGCAAGTGAGTC
Long Flanking Sequence:
AATTGGCTATTGATTGCAATCAGACGATAATCGATTCGTAAAAGTCAGTCTTCAATTTTACTATATACATTTGTGAACTAAATTATGAACCATCCTGTGAAACTTTTATACTTTTAAAAATATTTCCCAAGTGATGTTTCAGATTTTTTTCCCAACACATTTTAAACATAAGAATTTTAATAATCAGTTTCTAATAACTAATATACTTTGTCTTTGCCATGATGGCAGTTTATAATGTATATAGTATATAATGTTTTACTAGATATTTTACAAGTTAGGGTTATTTGTTCTAAAAATTCACGTTAAAATGCATTTTAACCAGTGTTTTCAGCTCATAAATCATGAACGGAGCACTGTTAGACTGGAGTGCTGTGGAAATGTGTGGTGTTGTGGTCTGACATTGTGGCTGTGTTACATTGCTGTTGTGGTGTTTGACCATCCGCTGCACCGCAGCCATTGAGGCCGAGGTGTCCATGCCGCTTGCATGCAGATGCATGAAT[G/T]GAGGAACGTGCTTCACTGATGAAGGAGGCCTGCCCAAGTGCAAGTGAGTCTGAACGCTAGTCAAGAGCTGCTGTTCACGCTCTACAATTCCTTACAAGGATTATCCATAATGGGGAATCACATTTTTATTGGTTTTATGATATCTGCTCCATTAAGTTAAAATATTGGATGCATATATGGATGGAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGACGGACGGACGGACGGACGGACGGACGGACGGACGGACGGACGGACGGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGATAGAATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGAAAGATAGAAATAAGGGGAGATAGATCGGGACATGGATGGATGGAAGGATGGATGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34766
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085697 Essential Splice Site 4481 4632 73 77
ENSDART00000129237 Essential Splice Site 2941 3092 46 50
Genomic Location (Zv9):
Chromosome 9 (position 49712087)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 48967283
GRCz11 9 48664768
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGCCGCAGACTCTCGGGGTGTCCTTCATTGACAGGGCTATGCAGCTG[G/T]TAAATCTCCATCATTTCACGCTAACTGTTTAGTCGGGGAGGAATGGGGGG
Long Flanking Sequence:
TTGGTTCTTTTCAACTGGTTCGAACCAAAGCAATCAGTGTGGTGTAAAAACGACCCTAAGCTGCAGAAAATGCTACAATGTATCATTTATTTCCCTTGGTCTGGACCAAGTAATGTGTAAAATGGGATCATGAAGGAAACATTCAAAAAGCAACTCATGCAAACACCTTAATCTTATTATTGTCTTAATCAGATTAAGGCAAATAATTTGATTACCGATGTCCATGTAAACATACTCATTGTTAGCATTAATATAAAATTTGGTAGTCAGCTGTTGACTAAAACCATTCATTTTGACTTGCATTATCCACTTGTCATAATGCAAATGTTAGTTTTCGAGTGCTTGAGATGTGATGAGTGTGTGTTTTTTGCAGTCTGAGCAGTCTGGTGAAGTCTGGAGATACGGGGAATGGAGTGTCCTTTCATTCGGGTGATAATGTGACCATGGATCTGGAGCCGCAGACTCTCGGGGTGTCCTTCATTGACAGGGCTATGCAGCTG[G/T]TAAATCTCCATCATTTCACGCTAACTGTTTAGTCGGGGAGGAATGGGGGGGTTCAAACTACTCATCTAAAATGAGCTGAAATAACGCAATTCAAAAACAGCACAACTTAATTGTTTTATGTTCAGCCCTCTTAAATTTTAGTTAACTTAATCAATTTGTGTTGGGACAACATGAATGATTTGTGTGGAACCCTGCATTTTTTAAAGTCTATCCAGGAGTGTATTTAGTAATTTGGGGCCCCGAAGCAATTCCAGCCATAGGGCCCAGAAGACTTAATATGCCCCCTTTGTATTTATTTATTTGTTTGTTTTGCTGTCTTTTTCTTATATTAATTAATAAATGTATTTATCGATTTTTATTATATAAATTATTTTATATTTATTAAAATATATACACTTATGCATATATATATTTATATATATATATATATATATATATATGTATGTTTATATATATGTTCATATAGAAATATATATGCAAATTAGCATGTTTAATTAAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21600
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085697 Nonsense 4536 4632 75 77
ENSDART00000129237 Nonsense 2996 3092 48 50
Genomic Location (Zv9):
Chromosome 9 (position 49712960)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 48968156
GRCz11 9 48665641
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGAACGTCAGTGCGGACCAGGTGGACAATAACTTCTCAAACCCCACATA[T/A]CAGCAGGCAGTGGAGGTGAAGAGCGAACAAGTAGAGGAGAAAAACACACA
Long Flanking Sequence:
TTATATTTATTAAAATATATACACTTATGCATATATATATTTATATATATATATATATATATATATATGTATGTTTATATATATGTTCATATAGAAATATATATGCAAATTAGCATGTTTAATTAAACATATGCTATCAACTAGACATGTTTATTTGCTGTTTAAAGTACCCAATTATTGACCGCTGCAATTCACTAATAAATATCATTCAATATTTACATTTTTTTATCTTGTTTCTCTGTTATTTATTATTAGGATGAGAATTTTGCAGACCCTGGACGACAGCCAATTACGTTTGAAAATCCTCTGTACTCGACTGCAGCCGCTCCGTCCAGTGATCCTGCAGTAATACACGCTACACAGGTATTGTTACCGCTACAGAACTCTCTAGAAATGGCTAACAGGTGCGGGTCTTTAGTTTTGTGTTTCTGTGCTTCACTAAAGGTCACTGTGAACGTCAGTGCGGACCAGGTGGACAATAACTTCTCAAACCCCACATA[T/A]CAGCAGGCAGTGGAGGTGAAGAGCGAACAAGTAGAGGAGAAAAACACACAGGTAAATAAAGTGACCACATTCATCATTTTAGCCATTATGTTAACACACTATTTTGTTTTGTTTTATTATGTTTTTAAAGATTTATTCATTATTTTATATTCATAATATATTTTCTTTTTAATTTTAATCTAAATTTGATTTCATTTATTTAATATTATTATTTGTTGTTTTATTTTGTTTTTATTTATTTTAGTATATTTTATAATTAATATTTTAATTTATATTATTTATTTTACATTTATACTTATTTATTGTTTATTTTTATTGTAATATTAGTTACAATTTGTACTTTATTTTATTATTTAGACTATCTAATTTTATAATTTGTTGTTTTATTATTTTTATAAAATATTTTATTTTATTTTATTTATTTTACATTTGATTTTAATTTTATTTAAAAATATATTTTATTTTATTATATAGATTATGTTTTAATTTATTTTTATGTT
Associated Phenotype:
Not determined