Busch Lab

ZMP

si:ch211-46o5.1

Ensembl ID:
ENSDARG00000001559
ZFIN IDs:
ZDB-GENE-030616-39, ZDB-GENE-060503-890
Description:
Novel protein similar to vertebrate CUB and Sushi multiple domain containing protein family [Source:
Human Orthologue:
CSMD2
Human Description:
CUB and Sushi multiple domains 2 [Source:HGNC Symbol;Acc:19290]
Mouse Orthologue:
Csmd2
Mouse Description:
CUB and Sushi multiple domains 2 Gene [Source:MGI Symbol;Acc:MGI:2386401]

Alleles

There are 18 alleles of this gene:

Allele Name Consequence Status Availability
sa43322 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa8421 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa29241 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa36884 Nonsense Mutation detected in F1 DNA Not yet available
sa10968 Essential Splice Site Available for shipment Available now
sa9832 Nonsense Available for shipment Available now
sa45681 Nonsense Mutation detected in F1 DNA Not yet available
sa36883 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa11417 Essential Splice Site Available for shipment Available now
sa43321 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa44921 Nonsense Mutation detected in F1 DNA Not yet available
sa36882 Essential Splice Site Available for shipment Available now
sa15257 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa43322
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
ENSDART00000001805 Essential Splice Site 172 3604 4 70
ENSDART00000132471 Essential Splice Site 39 3456 2 68
Genomic Location (Zv9):
Chromosome 19 (position 38064716)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 36929236
GRCz11 19 36516356
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTCAATTACTTAATAAATAATAATTTTTTCTCTGTCACTTCATTTTA[G/T]CTCTTCCAAGCTACACATGTGGAAATCCAGGCCAGCTGCTCAACGGCATG
Long Flanking Sequence:
TTGATATATTGTAAAATGTTTCAGTTGGAGATAAATAAAACAAAATTGAGGTCAGAATTATTAGCCATCCTGCATTTTTAGCCCTCCCTGTTTATTTTCCCCCCATTTTTTTACAAAAAGATTTTTTAACACATTTATAAATATAATAACTGATTTATTTCATCTTTTTTATGATGACAGTAGATGATATTTCACTAGATATTTTTCAAGATACTAGTACTGACTATAAAATGTTTTTTTTTTTTTACTTTTATTCTAGCTGAAATAAAACAAGTAAGACTTTTTTCCAGAAGAAAAAATATTATTGCAAATAGTGTAAAAATGTCCTTGCTCTGTTAAATATAATTTGGAAAATTATGAAAATAATAATAAAATAAATTAAAGGGGGGCCAATAATTTTGACGTGTGTGTGTATGTATAACTTTTTGTAAATGCAATGTATTAAAAATCTGTTTCAATTACTTAATAAATAATAATTTTTTCTCTGTCACTTCATTTTA[G/T]CTCTTCCAAGCTACACATGTGGAAATCCAGGCCAGCTGCTCAACGGCATGCAGCAGGGATCCACCTTCAACATCGGGGACAAGATCCGCTACAGCTGCAACCAGGGATATGTTCTGGAGGGCCACACCGTGCTCTCCTGCCTGGCCACATCATCCGGCACCGCTGCCTGGGACTTCCCTCTGCCCTACTGCCGAGGTGAGTTTGGGTCCTCTGGTTGAATCATGTGGGATTTAGGATCCTTAAGAGAAGCTCAGGAAAAGGTTAAAGAGTGTCTTTATCAGGGCTGACAGATACCCCAGCATTTAGTAGCAGGTTGGATGCACAGTTCTGTTTTTCCTAGATGAGACACAGTAGAGCCCCTGAGCTGATACCTGCCGACATGTGAAAGCCACACAGACGTCTTGTGTGAGACAGCGAGGTCACGTGTTAGCCTGTAAGCTGTTGCCTAAGGGGAAACAATATCCAAATGCTTTTCGTCATAATGCTTTATAAACATCCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8421
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
ENSDART00000001805 Essential Splice Site 399 3604 8 70
ENSDART00000132471 Essential Splice Site 266 3456 6 68
Genomic Location (Zv9):
Chromosome 19 (position 37964211)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 36828731
GRCz11 19 36415851
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGATCCAGGAATCCCGGAGAGGGGCAAAAGAAAAGGCTCTGATTTCAGG[T/C]GAGAAATGAGTTTATGGATTACTTATTAAAATAGTCCACTGAGAGGACAC
Long Flanking Sequence:
ATGGCTTAGTTGCAGAAGGTTTCATTTTACTTTGAACAAAACATTTACTAAAACTATATTTATGTATTTATAACTAAGTTTTTGACCAACCATTAACCAACATCAGACAACCCTAAACAAGATTGCAACCCCTGAAAAATGCCAAGGTTTTGACTTGAAGTTTTCACTTAAATATTAATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTATTTATTTATTTATTTATTTATTTATTTTTTCATCATTTTATTGTATTTTTTGGGGGGAAAAAATCAGAGTGGCATAAAAGTTTAAACACCACCTACTCTTTCATACCCACCTGTTTCAATTGATACCAACCTTTCTTATCATTTTTGTCTTTTGCAGTGTCGCAGATGGGGGTGGCGCAAGGACACAACATGTGCCCAGATCCAGGAATCCCGGAGAGGGGCAAAAGAAAAGGCTCTGATTTCAGG[T/C]GAGAAATGAGTTTATGGATTACTTATTAAAATAGTCCACTGAGAGGACACAGAGGAGAGAGCAAAGAGGAGTGCAGTTAATTTAGTGTTTGTAATGCCAGGATGATGAATAGCAAGAGATGCAGGAGGTGGGCACCTGTTTAATTTCTCATTGGCCTTTTAATTCTCAGGGCTCATGGAGGATATTTGATCAGCATAAACATGGGCTGTGGGCTCCCAAAGGTCAAAGCGTGTGTGTGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGATGGAGAATGTGAGAGAGAGATTATTAATGTTGTATTGTATTTATACAAAATGGATGATTATGTAAATTAAAACAGCAGGCCAATGGGGTAAATTTAAGGGGAAAAAACACCAGGAGAAATTTGAAAATGACAATTAAAATAATAAAATATGACAAAAGTCCTAACAAAATTCATAAAACTAACCACATTATCTGCTTAATTCTGAATTTATTATAGTGAACAATAAATCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa29241
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
ENSDART00000001805 Essential Splice Site 441 3604 9 70
ENSDART00000132471 Essential Splice Site 308 3456 7 68
Genomic Location (Zv9):
Chromosome 19 (position 37957349)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 36821869
GRCz11 19 36408989
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTACAGACAGTTATGTTGGATGGAGTGATGACCGGCCGATCTGCAGAGG[T/C]AGGACTCTAAAAAAAAAAAAATCTTATTTTATTTTTAATTTGCAATAATT
Long Flanking Sequence:
ATATTTGTGTAAACATGGCTAATATTCTGTATAATCGATTATTATCAGTGGCCACCAATCTTCTGGGTTAGATTTATGTCTCTGTGGTCATTTTCTTTCTTACAAAATACAGTCATTTTAACTCTGATCGATATTTCGTGTTCATTAATTTATTTTTTTGCTTAGTAGCTGTCTGTTAAGTAGGATGAAATGCTGCCGGATGGTCATTATTGGAAAATAAACATCCACATTGGAGTCTTGATTACCCTGCCGGGATTTATTTTGCCATAATGACTGGCTGACTGTGTTGAATGTACGTAATGTAGAAAATATAGATGTATGATTTGTTATTCATGCAAAGTAATAATGTTTTTGTTTTTTTACTATTCTTGCAGACGGGGTGCTACTGTGCACTTTTCTTGTGATGAAGGATATGAGCTTCAGGGGTCTAAAAGCATCACCTGTTTGCGAGTTACAGACAGTTATGTTGGATGGAGTGATGACCGGCCGATCTGCAGAGG[T/C]AGGACTCTAAAAAAAAAAAAATCTTATTTTATTTTTAATTTGCAATAATTTTTTATTATTTTATTAGCTCAAACATACGACATGCGTGGCAACGTAGGTAGTGCTGTCGGCTCACAGCAAGAAGGTTGCTGGTTCGAGCCTCGGCTGGGTCAGTTGATGTTTCTGTGTGGAGTTTGCATGTTCTCCCCGTGTTCACATGAGTTTCTTCTGGGTGCTCCGGTTTCCCCCACAGTCCAAAAACTGTGTAGTATATGAGTGTGAATGAGTGTGTATGAATGTTTCCCAAAGATGGGTTGCTGCTGGAACAGCATCGCCTGCGTAAAACACATGCTGAATAAGTTGGCGATTCATTCAGCTGTGGCGACTCCAGATTAATAAAGGGACTAAGCCAAAAAGAAAATGAATGAATGAATAAATTAATAAATGAACATATAAAAAGCTTTCTCTCCCCTTTTTAATAGTATACTACTGTTTTATTTTATTTATTATATATATATATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36884
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
ENSDART00000001805 Nonsense 951 3604 18 70
ENSDART00000132471 Nonsense 818 3456 16 68
Genomic Location (Zv9):
Chromosome 19 (position 37911485)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 36776005
GRCz11 19 36363125
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGGATACACTCTCAGTGACCACGAGCCCCTCGAATGTGAACCAAACTTC[C/T]AGTGGAGTCGCCCCCTGCCCAGCTGCGATGGTACAGTCCACCCTTTACCA
Long Flanking Sequence:
TATGTGTATTTCAAAATAAATAATCTGTAATTATAAATATCAATAATTATGCAAAATTTCATAAGTTTAATTATTGAGTTAATGCCTGATCAGTGATAAGTAAAAATTATTAAATACATAAATAAATAAATAAATGACAACAAAACAAAAACTAAATAGTATATGTATTGCTTCCATATATTAGTTAAATGTTGGCATTTTACTTTGTATATTATTATTAGCATTATACAAGTTAATAATTCAATACAATTACAGTTAAAATACATTGTCTGCTAGGAAATCCTCTCATCTAAATCATCAGCTTTAATCCCACATTACCCTTTGTGTTTTTCTGTCTTGTAGCTCTGCAGCTTCAGTCGGACCACTGTGTTGATCCAGGAATCCCAGTCAATGGTCAGCGACACGGCAATGATTTCTACGTGGGAGCGCTGGTGACATTTAGCTGTGAAGCCGGATACACTCTCAGTGACCACGAGCCCCTCGAATGTGAACCAAACTTC[C/T]AGTGGAGTCGCCCCCTGCCCAGCTGCGATGGTACAGTCCACCCTTTACCACCCAAAAAACAGGCACTAGCAGGGAAAAGGACACATTAGAGACAGGTCATTTATTCAGTCGCTCCAAGACTCGAAAGGCCTTTACGGTTTGAAGCTCCACTTCTCCGTTTCCACCGGGCTTTGAATATTTAAGGCCATTATTGATTTTTCCCCTTGGGTAATGATAGGAATAATTCCGCCTCCATATGTTGATGTCCTTTAGAAGGGCACTTGGTGTAAAGTTGTTGGGCAGGATTGTGCTCAGCGGTTTGACGAATTGCCTTTATCTTTTTTTTTTTTCTTCTAGCGCTCTGTGGAGGGTTTATTCAGGGGAACAGCGGCACTATTCTGTCCCCTGGGTTTCCAGATTTCTACCCACATAACCTCAACTGCACCTGGATGATTGAGACTTCACATGGGAAAGGTGAGAGCGCCGGCTTCTGCTTTTGACAGTCTTCTTGAAGGGTTACG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10968
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
ENSDART00000001805 Essential Splice Site 961 3604 18 70
ENSDART00000132471 Essential Splice Site 828 3456 16 68
Genomic Location (Zv9):
Chromosome 19 (position 37911453)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 36775973
GRCz11 19 36363093
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAATGTGAACCAAACTTCCAGTGGAGTCGCCCCCTGCCCAGCTGCGATGG[T/C]ACAGTCCACYCTTTACCACCCAAAAAACAGGCACTAGCAGGGAAAAGGAC
Long Flanking Sequence:
ATAAATATCAATAATTATGCAAAATTTCATAAGTTTAATTATTGAGTTAATGCCTGATCAGTGATAAGTAAAAATTATTAAATACATAAATAAATAAATAAATGACAACAAAACAAAAACTAAATAGTATATGTATTGCTTCCATATATTAGTTAAATGTTGGCATTTTACTTTGTATATTATTATTAGCATTATACAAGTTAATAATTCAATACAATTACAGTTAAAATACATTGTCTGCTAGGAAATCCTCTCATCTAAATCATCAGCTTTAATCCCACATTACCCTTTGTGTTTTTCTGTCTTGTAGCTCTGCAGCTTCAGTCGGACCACTGTGTTGATCCAGGAATCCCAGTCAATGGTCAGCGACACGGCAATGATTTCTACGTGGGAGCGCTGGTGACATTTAGCTGTGAAGCCGGATACACTCTCAGTGACCACGAGCCCCTCGAATGTGAACCAAACTTCCAGTGGAGTCGCCCCCTGCCCAGCTGCGATGG[T/C]ACAGTCCACCCTTTACCACCCAAAAAACAGGCACTAGCAGGGAAAAGGACACATTAGAGACAGGTCATTTATTCAGTCGCTCCAAGACTCGAAAGGCCTTTACGGTTTGAAGCTCCACTTCTCCGTTTCCACCGGGCTTTGAATATTTAAGGCCATTATTGATTTTTCCCCTTGGGTAATGATAGGAATAATTCCGCCTCCATATGTTGATGTCCTTTAGAAGGGCACTTGGTGTAAAGTTGTTGGGCAGGATTGTGCTCAGCGGTTTGACGAATTGCCTTTATCTTTTTTTTTTTTCTTCTAGCGCTCTGTGGAGGGTTTATTCAGGGGAACAGCGGCACTATTCTGTCCCCTGGGTTTCCAGATTTCTACCCACATAACCTCAACTGCACCTGGATGATTGAGACTTCACATGGGAAAGGTGAGAGCGCCGGCTTCTGCTTTTGACAGTCTTCTTGAAGGGTTACGTTTATATGGAATTAAATATTCTTTTAGAAGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9832
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
ENSDART00000001805 Nonsense 1010 3604 20 70
ENSDART00000132471 Nonsense 877 3456 18 68
Genomic Location (Zv9):
Chromosome 19 (position 37904318)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 36768838
GRCz11 19 36355958
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTCCTCTCGATCTCCACAGGAGTYCAGTTTACCTTCCACACCTTTCACT[T/A]GGAGAGTCCTCACGACCACCTTTTAGTTACAGAAAATGGTAGTTTTTCTC
Long Flanking Sequence:
CTTGTTTACTAAAATAACCTTGTGCATAACATTGGTAAGGTTTTATTTTACAAACAAAGTACTTTTGCATTCACAACAAAACACACATCATCTGCACAACATGCTGGAGAAGGCAACAATAATTCAAAGTGTTGCAACTTCTTTGTATATAGTTTTGAGTGACAATCTTCTCAAAGACTGATCTCAATTTGGTGACATTCTCGAACAAAGTATAAGGCTTGGATGCATCTTATAAAACTTTCATAGACAATATATTTTTGTGTTTGGGTCTTTGATACAAAATCGCATCATACAACTATTTTAATATCATGTTGAAACAGGAACATGTCTGGCTGACCACTTCTAAACTAATCACTGAAAATGAATAAAAACACAAGCTTGAACCATTGTTTATGTGACTGAAGCTCTTTATGATCTCTTAAGCTGCTCATATATAACCAGTGTTCTTCTCTTCCTCTCGATCTCCACAGGAGTCCAGTTTACCTTCCACACCTTTCACT[T/A]GGAGAGTCCTCACGACCACCTTTTAGTTACAGAAAATGGTAGTTTTTCTCAACCCCTGTGGAGATTGACCGGCTCGACACTTCCTCCTCCTCTTAGCGCTGGACTCTTCGGCAACTACACCGCTCAGATCCGCTTCCTCTCTGACTTCTCTGTTTCCTACGAGGGCTTTAATATCACTTTTTCAGGTACAGGGCTTTCTGATTTTTATAACAACTAGATCAGATTTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTTTATTTATTTTTTATTTTATTTTTTATTTATTTATTTATTATCATATTTATTTATTATCATATTTTTATTTATTTATTATCATATTTTTATTTTTTTATTCTCATAGTAATTTATTTATTTTCATATTTATTTATTTATGTATTTATTTATTTATTATCATATTTATTTATGTATTTACTTATACTAATGTTTGTTTATTTAATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45681
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001805 Nonsense 1018 3604 20 70
ENSDART00000132471 Nonsense 885 3456 18 68
Genomic Location (Zv9):
Chromosome 19 (position 37904294)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 36768814
GRCz11 19 36355934
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGTTTACCTTCCACACCTTTCACTTGGAGAGTCCTCACGACCACCTTT[T/A]AGTTACAGAAAATGGTAGTTTTTCTCAACCCCTGTGGAGATTGACCGGCT
Long Flanking Sequence:
CATAACATTGGTAAGGTTTTATTTTACAAACAAAGTACTTTTGCATTCACAACAAAACACACATCATCTGCACAACATGCTGGAGAAGGCAACAATAATTCAAAGTGTTGCAACTTCTTTGTATATAGTTTTGAGTGACAATCTTCTCAAAGACTGATCTCAATTTGGTGACATTCTCGAACAAAGTATAAGGCTTGGATGCATCTTATAAAACTTTCATAGACAATATATTTTTGTGTTTGGGTCTTTGATACAAAATCGCATCATACAACTATTTTAATATCATGTTGAAACAGGAACATGTCTGGCTGACCACTTCTAAACTAATCACTGAAAATGAATAAAAACACAAGCTTGAACCATTGTTTATGTGACTGAAGCTCTTTATGATCTCTTAAGCTGCTCATATATAACCAGTGTTCTTCTCTTCCTCTCGATCTCCACAGGAGTCCAGTTTACCTTCCACACCTTTCACTTGGAGAGTCCTCACGACCACCTTT[T/A]AGTTACAGAAAATGGTAGTTTTTCTCAACCCCTGTGGAGATTGACCGGCTCGACACTTCCTCCTCCTCTTAGCGCTGGACTCTTCGGCAACTACACCGCTCAGATCCGCTTCCTCTCTGACTTCTCTGTTTCCTACGAGGGCTTTAATATCACTTTTTCAGGTACAGGGCTTTCTGATTTTTATAACAACTAGATCAGATTTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTTTATTTATTTTTTATTTTATTTTTTATTTATTTATTTATTATCATATTTATTTATTATCATATTTTTATTTATTTATTATCATATTTTTATTTTTTTATTCTCATAGTAATTTATTTATTTTCATATTTATTTATTTATGTATTTATTTATTTATTATCATATTTATTTATGTATTTACTTATACTAATGTTTGTTTATTTAATTATTAAAATCGTTGGGCTATTTATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36883
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
ENSDART00000001805 Essential Splice Site 1071 3604 20 70
ENSDART00000132471 Essential Splice Site 938 3456 18 68
Genomic Location (Zv9):
Chromosome 19 (position 37904132)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 36768652
GRCz11 19 36355772
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCTCTGACTTCTCTGTTTCCTACGAGGGCTTTAATATCACTTTTTCAG[G/A]TACAGGGCTTTCTGATTTTTATAACAACTAGATCAGATTTTATTTATTTA
Long Flanking Sequence:
ATTTGGTGACATTCTCGAACAAAGTATAAGGCTTGGATGCATCTTATAAAACTTTCATAGACAATATATTTTTGTGTTTGGGTCTTTGATACAAAATCGCATCATACAACTATTTTAATATCATGTTGAAACAGGAACATGTCTGGCTGACCACTTCTAAACTAATCACTGAAAATGAATAAAAACACAAGCTTGAACCATTGTTTATGTGACTGAAGCTCTTTATGATCTCTTAAGCTGCTCATATATAACCAGTGTTCTTCTCTTCCTCTCGATCTCCACAGGAGTCCAGTTTACCTTCCACACCTTTCACTTGGAGAGTCCTCACGACCACCTTTTAGTTACAGAAAATGGTAGTTTTTCTCAACCCCTGTGGAGATTGACCGGCTCGACACTTCCTCCTCCTCTTAGCGCTGGACTCTTCGGCAACTACACCGCTCAGATCCGCTTCCTCTCTGACTTCTCTGTTTCCTACGAGGGCTTTAATATCACTTTTTCAG[G/A]TACAGGGCTTTCTGATTTTTATAACAACTAGATCAGATTTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTTTATTTATTTTTTATTTTATTTTTTATTTATTTATTTATTATCATATTTATTTATTATCATATTTTTATTTATTTATTATCATATTTTTATTTTTTTATTCTCATAGTAATTTATTTATTTTCATATTTATTTATTTATGTATTTATTTATTTATTATCATATTTATTTATGTATTTACTTATACTAATGTTTGTTTATTTAATTATTAAAATCGTTGGGCTATTTATTTATTTATTTTTTACTAATGTTTATTTATTTATTATACTTATGTTTATTTATTTATTACAATATTTGGGTTATTTATTAATTTGTTCATTTATACTCATGTTTATTTTTTTATTTATTTTATTATTATACTGATGTATGTTTATTTAATTAATACATGTTTTG
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa4067
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001805 Nonsense 1073 3604 21 70
ENSDART00000132471 Nonsense 940 3456 19 68
Genomic Location (Zv9):
Chromosome 19 (position 37903135)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 36767655
GRCz11 19 36354775
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CRGAAAACAAGCTAAAGAATATCCATAATTCTCTTGTTCCTTATAGAATA[T/A]GACCTGGAGCCTTGCGAGGATCCTGGGATCCCCCCCTTCAGCACTCGTAA
Long Flanking Sequence:
TTTGTGTTATTTATTTATATATTTATTTATTTATTTATTCTAATGTATTTTTATTTATTTATTAATTAAAATTGTTGACTTATTTATGTATTTATTATTTATTTGCATTTCTTTGAACGTTTTTGCCGAAACACCCTAGCACTCTTTTGCAGCCCCTTAAAGGTCTTTGGAGCCCATTTTGAAAAGCCCTGTCACACAGTAATATATAACATCTCAGTAAAATTGCCTTGGAAAGATCTGTTTCATCTGGGGTTATTTTGGGGGTTATTCATAGTCTGCTAAAAGTAATTTATTATTTGTAATACTTTACCTTTAGATATTCAATTAACAAACTATGAGGTGAATAATGACGCCTCACTGTAACCACTTGTTTTTAAACACTTCACTAATCATTTACAGTTTTGTGAAGGCGTATTTACGCACAGCATCTAAGGGTAATGGGGAAAAAAGCGGAAAACAAGCTAAAGAATATCCATAATTCTCTTGTTCCTTATAGAATA[T/A]GACCTGGAGCCTTGCGAGGATCCTGGGATCCCCCCCTTCAGCACTCGTAAGGGTCTGCAGTTTGGGGTTGGGGATGCGCTCATCTTCTCCTGTTTTCCGGGGTATCGTCTTGAGGGGCCTGCGAGGGTGGTGTGTTTAGGGGGGCGTCGGAGGGTCTGGAGTTCCCCTCTGCCAAGGTGTGTTGGTAGGTGGTCACATGCTTTTCATTTTGCTTTCTTATAACATATTTTCCCCCATGTTCTCAGATACACTCTAGACAATTCTGAGTGCACTAAAACTTCAAATATCTGAATATAAGGCTGAAGTCTCATTATAACAATAGTGTACAACGCCTTAGTAATAGTCAGAAATAAAAAGGGCACCACTTTATAAAAAAAAAAGTGGATTTACATTAAAAAATACATGTTGTCTATTTAGTTCATATTGTATTAATAATAGTGCTGGAAAACTATTAATTACATCCAAAATAGTTACATTACTTTGTAATTACATTACAAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11417
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
ENSDART00000001805 Essential Splice Site 2177 3604 42 70
ENSDART00000132471 Essential Splice Site 2029 3456 40 68
Genomic Location (Zv9):
Chromosome 19 (position 37771389)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 36635909
GRCz11 19 36223029
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAACAYGGCACGACGCGCAACTGGGATCATYCGTTTCCTCGCTGTGAAGG[T/C]ACGACCCTCTTTATTTCSTCCCCCACTTCAGTAAACATCTGCTGTGCTTA
Long Flanking Sequence:
GCAGTTGGCTGCCTGTGTGAACATTGATCAACATATTGCATTTCCGTGAAGTTCAGACTTCCATCATTGAAATCTGAGAGGAAATGACAGCATCTTTCATTGCCGGAGCTTTGATTGCCTTTGCTTTGAATCAAATCCCAAAGCTTTGTTGGGGCACAGCAATCAGTTGATTCCATGGGTACGGTTTACGTTTAATATTCAGAGTCTAGGTTTGGATTGGATCTTGGAGCTCAGAGCAATCTCTTTTTTAAATGAAACATACATTTTCATCCTCTATGTATCATGCATCAAGTATGTCTGTCTCTTTCAGCATATGAACTCCAGGAGTGTCCTGATCCTGAACCCTTCCATAATGGTGTGGTGGTTGGTGCTGGTTATAACGTGGGTCAGTCCATCTCCTTCGAGTGCTATCCAGGGTATCATCTGACAGGACACTCCATTCTTACCTGTCAACACGGCACGACGCGCAACTGGGATCATCCGTTTCCTCGCTGTGAAGG[T/C]ACGACCCTCTTTATTTCCTCCCCCACTTCAGTAAACATCTGCTGTGCTTATTTGCATTGTGAGAGAATAGATTTATTCGGCATGCTAATTGACATTTTTAGCTTTTTAAAATTTAAAATTTTAATTTTTGATTATAATTGTCATCCTAATTAGCTTTTTACAGGTAAAATATAAAGTAATATTTTCTATTTTTCTATATATTTTATTCTTAAAAAGAGTAAAATTATGAATTAGGATGACAAATATGGTCATGCTTTACGATAAGGTTTCATTTGTGTATTTACTAACAACAACTAATTATAAACAATACACATACAGCATTTATTAATCAAAGTTCAACATTTACTAATGCATTATTAACATCTGTAATAACGTAACGCAATTATAATTTTATTTAATTATATGTTTTATTAAATCCAATGAGGACTTAGAGAAACTTGTTCATGCTTTTATCACCAGCAGGGTGGATTACTGTAACGGTCTGTTGACATGAAGTAGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43321
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
ENSDART00000001805 Essential Splice Site 2284 3604 44 70
ENSDART00000132471 Essential Splice Site 2136 3456 42 68
Genomic Location (Zv9):
Chromosome 19 (position 37766106)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 36630626
GRCz11 19 36217746
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCCGAAGCAGTTCTGAGAAAGGGGGGTTGTTCAAGATCAACTACCAAG[G/A]TAATTTGTTTAAAGGAAAGCTACCATTAGCATTTCAATTCATTCCAAAAG
Long Flanking Sequence:
TTGAGGACTGCAGAGATGGAGATAAGGAGATGTCCTTGTAGATGGTGGCTACGTTTTTACTATGTCATGACACACATTTAGGGTGAGTGTGAAGGAACCAGAGTGCAATATCTAAGAGAGTGTGAAAGGAGTCCCTGAAATTGGAGAGGTAATCAGTATGGCTGGGATAGTCTCTCAAATCAGTAAAGTAATCAATATTTAGAGAATCGTTCTGCAAATCAGCCGGGTGATCAATATGGATCTCACTTACTGTGCGTTTTCAGGCAACAAAGGCACGTGGTGTTCTCTTGTTGTATTGAATGCCCACTGTTAATGGGTTTTATACTCTGAATCCTAATGTTCTACCTTCAACAGGGATGGACCACAGGAAACAACTCGTAAACTTGGAGTGTTTACCGAGGGAGAGCCAAACAACCCACCGAGCAGCACATCTAATCAAGTTCTGATACGTTTCCGAAGCAGTTCTGAGAAAGGGGGGTTGTTCAAGATCAACTACCAAG[G/A]TAATTTGTTTAAAGGAAAGCTACCATTAGCATTTCAATTCATTCCAAAAGTACAAGTCCAGGTCGAGACTTGAGTAGGTTGAGTCAGAGTCAAGACTGAAATCAGAGAGTTGAGTTAAAGTCAGACTACGCTTTTAACACGGACAACAAAATATATCCACAGTACTTTAGACTAGTCTCGAGTTACTGTAAAATACCCATGACAAGACCAAGACCATTTAGGTATGGTTTGGTCTTAGAGTCAAGTGGATTTAAGATGCAAGTACTCCAACAAGGTTTTTCAATCCAGTGGAGGCACAGAAAACGACAGGTCACCACAGTTTATAGACTTTTTGGAATATTAGGTCTATTTCAGACATTGAAAGTCGGAGAATTATTATCATTTTGTCGAAGTCATGGATTATCAGGGATTTTTGTTTACCACTTTAAATGCTAGGTTCAATTTATCAATTACCATTTTTTATATTGCGCTGTTTCACTTCTGGTGTTATGGTTAAACTA
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa6564
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001805 Essential Splice Site 2413 3604 47 70
ENSDART00000132471 Essential Splice Site 2265 3456 45 68
Genomic Location (Zv9):
Chromosome 19 (position 37739678)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 36604198
GRCz11 19 36191318
KASP Assay ID:
554-5217.1 (used for ordering genotyping assays)
KASP Sequence:
GAACATTTTCAGACCAGCAGGCAGTTTGATGAGCTGGAAATATTTGATGG[T/G]GAGTGATCACCTYTAATTCATGCAATATTTATTTATTTATTTATTTATTT
Long Flanking Sequence:
TACATCTTCGGTTGAATTGCCTTTGAGTTGGTTTTCTCTTTTGGTGTGCTTGGTTTGGGCAGGTGTGAATGTAGAAAACAGACCCAACTAATCCCAATGGTACTGCACATTTTTTGGCATCATATTCTGTGATTTACAAGTGTTTTCCATTTATTCTTGGTTGTTAATTGGATTATGGAACCTTGATCTCAGCTTTGTTGACTTTTGATGTTGAAAATTGAACTGTACAGTTTGACAAAGTGACTTTAACTGACGTTTTAGTAGTTTGAAGTAATATAATGGCTAACTCTCTTGTCTGCTTTCCTCACAGTTACCTGTCCCATGAACGAGGTGCTGACGGCCTCTACAGGGGTGATCCTTAGTCAGTCTCCGGGCAGCAGCCTGCCACACTTTGAGTCCTGCTCCTGGTTGGTGAAGGTGGATTCGGGCTACAACATCACTTTCACTGTTGAACATTTTCAGACCAGCAGGCAGTTTGATGAGCTGGAAATATTTGATGG[T/G]GAGTGATCACCTCTAATTCATGCAATATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTAAAATTCAAATTTTCAAACATTTCAAAATCTATATATTTTTACTCTAAATACTATTATTACTTTTGCTGCCATTATTATTTTTTTATTTATTTTTTTATATTATTTATATTATATTTATTATTATTTAAATTTTCTATTTAAAATAAGCATTTAAAAATGTATACATTTTTACTCTGTATACTACTGTTACTGCTGCTGCTATTATTTAGTTATTTATTTTATTTTAACTTTAATTAAAATTACCTTTAATTTAACTTATATTTTATTTATTCATTATTTATTCATTTATTTAATTAAAATCAAAAATTTGATTTTAAATAAATTTTTAATTAATTAATTTATTTATTTATAATAATTTACTATTTAAAATGTTTACAATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44921
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
ENSDART00000001805 Nonsense 2571 3604 50 70
ENSDART00000132471 Nonsense 2423 3456 48 68
Genomic Location (Zv9):
Chromosome 19 (position 37720065)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 36584585
GRCz11 19 36171705
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAATCCTGGTTTCCGATTGGCCAACACTCAGCCAGTGTCAACACTTTGT[C/T]AAGAGTCTGGGAGGTGGAGCCCAATCGAGACCCGCCCTCGCTGCGTCCGT
Long Flanking Sequence:
TTTAAGTGTAGTTGAAGTGTTCAAATACACAGATATGGTTGTGTTTGTGTTCAGGATTCTCCTGACAGGTGTGCAGGATGCTATATAGTTCTCTCTGTATCCTACAGTCCATATGCAGATGTAATCTACATCCTAGATTGAGCCTGTTGCTTTCTGGCTGCTCTTGTTTACCGGCTTCAGAAGCGCTGCAAGCTTGTGTTTGCACAGTCGCATAACAGCTTTTGGTGTGTTCGCTCAGTGTGTTTACACTGAGTATTCTTTGAAGTATGACGGTGAAAAGAAATAGCCAGTTTCCTTGGGGTTTTTGAGAAAATACTCGAGTCTGCTTTTGAGGTCAGCATTCAATCTTTTTCTCCTTCACAGTCGTTTCCTGTGGGATGCCGATTGCTCCAGTCAATGGCACTGTCATCGGGCAGCACTTCACTCTCGGATCTAGAGTCACTTTCTCTTGTAATCCTGGTTTCCGATTGGCCAACACTCAGCCAGTGTCAACACTTTGT[C/T]AAGAGTCTGGGAGGTGGAGCCCAATCGAGACCCGCCCTCGCTGCGTCCGTGAGTTCTTTAGCACCAATATTGCTTGATGATTTTATTTGCTTAAATTTAAAATGTAAATATTTAACTGTATTTTAATATATATTTTAAATTTGTTCTAATCTAAATAGGCTTTCTTAAGGTTTTCCAATTTTGTATTTATTTAATTTAGTATTTTTAAAGTTATATTTAAATAAGACAAGATAAGATTTAGGTTTCATAAATATGTTAAGTTGAATGGTGATGGAACATTACTTCATTCCTATTTTGTCAATTTATTTATTTTGTTTAGATATTTGACATTTATTTATATGCATAAAAATATTAAGAACCATTTATATAATAAAAAGAAGTATATATAGCATTATTTTAGGTCTTACTAAAATAAGCTCATTTTGATCCTCCAGCTGTGAACTGCCCTGACATCGGCCACTCTGCAGTAGATCATGGGAGGTGGAGGCTTATTTATGGCA
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa4077
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001805 Essential Splice Site 2587 3604 50 70
ENSDART00000132471 Essential Splice Site 2439 3456 48 68
Genomic Location (Zv9):
Chromosome 19 (position 37720015)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 36584535
GRCz11 19 36171655
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAGAGTCTGGGAGGTGGAGCCCRATCGAGACCCGCCCTCGCTGCGTCCG[T/A]GAGTTCTTTAGCACCAATATTGCTTGATGATTTTATTTGCTTAAATTTAA
Long Flanking Sequence:
TCAGGATTCTCCTGACAGGTGTGCAGGATGCTATATAGTTCTCTCTGTATCCTACAGTCCATATGCAGATGTAATCTACATCCTAGATTGAGCCTGTTGCTTTCTGGCTGCTCTTGTTTACCGGCTTCAGAAGCGCTGCAAGCTTGTGTTTGCACAGTCGCATAACAGCTTTTGGTGTGTTCGCTCAGTGTGTTTACACTGAGTATTCTTTGAAGTATGACGGTGAAAAGAAATAGCCAGTTTCCTTGGGGTTTTTGAGAAAATACTCGAGTCTGCTTTTGAGGTCAGCATTCAATCTTTTTCTCCTTCACAGTCGTTTCCTGTGGGATGCCGATTGCTCCAGTCAATGGCACTGTCATCGGGCAGCACTTCACTCTCGGATCTAGAGTCACTTTCTCTTGTAATCCTGGTTTCCGATTGGCCAACACTCAGCCAGTGTCAACACTTTGTCAAGAGTCTGGGAGGTGGAGCCCAATCGAGACCCGCCCTCGCTGCGTCCG[T/A]GAGTTCTTTAGCACCAATATTGCTTGATGATTTTATTTGCTTAAATTTAAAATGTAAATATTTAACTGTATTTTAATATATATTTTAAATTTGTTCTAATCTAAATAGGCTTTCTTAAGGTTTTCCAATTTTGTATTTATTTAATTTAGTATTTTTAAAGTTATATTTAAATAAGACAAGATAAGATTTAGGTTTCATAAATATGTTAAGTTGAATGGTGATGGAACATTACTTCATTCCTATTTTGTCAATTTATTTATTTTGTTTAGATATTTGACATTTATTTATATGCATAAAAATATTAAGAACCATTTATATAATAAAAAGAAGTATATATAGCATTATTTTAGGTCTTACTAAAATAAGCTCATTTTGATCCTCCAGCTGTGAACTGCCCTGACATCGGCCACTCTGCAGTAGATCATGGGAGGTGGAGGCTTATTTATGGCATGCAGAATAAATATGAAGCTATGATGATGCTGACCTGTGACCCTGGATAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36882
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
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001805 Essential Splice Site 2768 3604 53 70
ENSDART00000132471 Essential Splice Site 2620 3456 51 68
Genomic Location (Zv9):
Chromosome 19 (position 37716245)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 36580765
GRCz11 19 36167885
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTGTGAGCAGGACCACCGCTGGTCCGGGAAGACTCCTGTCTGTATCCG[T/C]AAGTGTTGCTTAAGCAGCAACTCTCTTATCTGAGGTCTTTTGACAGTTTT
Long Flanking Sequence:
GAATATTTTTATGTAAAAACCATGACATCACATGAGTTGCACATGAATATCTTCCATAACCACACATTTTTACGTGTTCCACATATTTCAGATGTAATTTTAACATCACTGCACATGTGTAGCTTATGTCTATAAGGGACGAGGACCTGATCAAGATTTTAGTTATTTCAAAATTCATTAAAGCCTGCAAAAGCTAAATTAATTAAACCTAAAGTTATCAAGCAAATACATTTAAGAAATGGATGCAGTATTATTATTAATAATTCAGTCAATCACTCTTTTATGTGCTCTAAACAAGCATTTGCACCGTTTTTTTTTTCAACAGCTGGACACTGTGGCACACCAGAGCCTATAGTGAATGGTCAGATCATTGGAGAAAACTACAACTACAGAGGCAGTGTTGTTTACCAGTGTAATCCTGGATTCCGGCTCATCGGCGTGTCCGTTCGCATCTGTGAGCAGGACCACCGCTGGTCCGGGAAGACTCCTGTCTGTATCCG[T/C]AAGTGTTGCTTAAGCAGCAACTCTCTTATCTGAGGTCTTTTGACAGTTTTATGCCTCAGATGAATGAAATAATCATGTAAATGGCATTAACTTGTTTGCTGGTTTCTCCACAGCCATCACATGTGGACATCCAGGCACTCCTGCTAATGGTGTGACGCAAGGAACACAGTTTAACCTAAATGATATTGTGCGTTTCGCATGCAACCCTGGTTACGTTCTACAAGGTGCGCTCAAGTCTCAATGTCAATCCAACGGCCAATGGAGCAACGCTCTTCCCAGGTGTAAAAGTAAGTTATTTGGATTTATCTTCAGCGGCGCTCCTTTGGATGTCACTTGATAAGAGAGTGTGAATAGTATTTTATCAGGTTTAAATAGCTTGAGTGCTCTATTGAACTTTGCTTTATAACTTTATAACTGCTGGCGAATAAAAGTTTGTCTTCTAATAATAATGGAGGTAAGCATTTACATGAAAATACTTATAAAGACTTGGATGTGTTTAA
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa29240
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001805 Essential Splice Site 2825 3604 54 70
ENSDART00000132471 Essential Splice Site 2677 3456 52 68
Genomic Location (Zv9):
Chromosome 19 (position 37715957)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 36580477
GRCz11 19 36167597
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAATGTCAATCCAACGGCCAATGGAGCAACGCTCTTCCCAGGTGTAAAA[G/A]TAAGTTATTTGGATTTATCTTCAGCGGCGCTCCTTTGGATGTCACTTGAT
Long Flanking Sequence:
TCTAAACAAGCATTTGCACCGTTTTTTTTTTCAACAGCTGGACACTGTGGCACACCAGAGCCTATAGTGAATGGTCAGATCATTGGAGAAAACTACAACTACAGAGGCAGTGTTGTTTACCAGTGTAATCCTGGATTCCGGCTCATCGGCGTGTCCGTTCGCATCTGTGAGCAGGACCACCGCTGGTCCGGGAAGACTCCTGTCTGTATCCGTAAGTGTTGCTTAAGCAGCAACTCTCTTATCTGAGGTCTTTTGACAGTTTTATGCCTCAGATGAATGAAATAATCATGTAAATGGCATTAACTTGTTTGCTGGTTTCTCCACAGCCATCACATGTGGACATCCAGGCACTCCTGCTAATGGTGTGACGCAAGGAACACAGTTTAACCTAAATGATATTGTGCGTTTCGCATGCAACCCTGGTTACGTTCTACAAGGTGCGCTCAAGTCTCAATGTCAATCCAACGGCCAATGGAGCAACGCTCTTCCCAGGTGTAAAA[G/A]TAAGTTATTTGGATTTATCTTCAGCGGCGCTCCTTTGGATGTCACTTGATAAGAGAGTGTGAATAGTATTTTATCAGGTTTAAATAGCTTGAGTGCTCTATTGAACTTTGCTTTATAACTTTATAACTGCTGGCGAATAAAAGTTTGTCTTCTAATAATAATGGAGGTAAGCATTTACATGAAAATACTTATAAAGACTTGGATGTGTTTAAATATATACAACGTTAGAGTATTGTCACCCTCAGGCCAATCACTCAGAACTGTGAATTGTCAGACATAGACGATCACCAGATTGCAATACATTATTTTTTACACATTTTATACAACCTAACAAGTGCTGATTCAGCATGTTCAATTAATGAAAACAAGCTCTGACAGATGCCAACAGACACAGAAATAGGAAACACTGATCTGACAATGCCGAAAGTGTCTTTCTGCATATGTCTATTGAAAGGAAACCCATCGCACACATATATGTAAAAATATATATGTAAAAATTT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa7885
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001805 Essential Splice Site 3007 3604 57 70
ENSDART00000132471 Essential Splice Site 2859 3456 55 68
Genomic Location (Zv9):
Chromosome 19 (position 37701250)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 36565770
GRCz11 19 36152890
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACCTGTCTGGCTAACGGGAGCTGGGTGGRCATCCAGCCYGAATGCCACG[G/A]TAAGAAATATGAANCGCCATGCGCAGCTGAACGTACATGATTAATCGCTT
Long Flanking Sequence:
TCTTTGTATGTGTGTTTTGAATAAAATTTAATTAAAAAAATCACCAACAAAAAAAAAGAAAAAAAAAAAGAAAATTTCTGTGGTGAAGCAGGTTTACAAGTGTTGACTTTTTTATTAATTAATTAATTAATACAATTAATTTAATTTTGTTTATATTTATTTAAATTTATTTAATTTTCAAGGCCACACAAAAATACTTCTTTTATCTCTGTAAAAAACAGAAAGAAATTAGAATTTGTAAAATACAATGCATTCACATGAAACTAGTAATAAAGCAAAGCGTCCAAATAAATGCTGATAAATGTGTGCTGTTTCAGGGGATTCTGCTGGTCTGTGTGGAGATCCAGGCATTCCAGTACATGGGATCCGTCTGGGAGAAGAGTTCACCACAGGGAGTGTTGTCCGATTCAGCTGCGAGCCTGGATACCAGCTGAAGGGCTCCTCCGAGCGGACCTGTCTGGCTAACGGGAGCTGGGTGGGCATCCAGCCTGAATGCCACG[G/A]TAAGAAATATGAAACGCCATGCGCAGCTGAACGTACATGATTAATCGCTTCCACTTCCAGAAGATTCTGCTACAACCAGAACTGTAGCCTATGCAAATTTATCAGCCAGCAACTGATTTCAAAGCAGTTTGTGTCTAAACTTTGTGCAGTTGGCGCATTTCAGGTAGTCCATTGCAATATGAATCAATTCCAAGAGAATCAAGTTTCTATCAAGGGGAACACACAGTTGGAGTCAGATTTATTTTAACACCCTTTGATTTTTTTTGGTCTTTTTTTAAATATTAGGTTTAACAGGGCAAGGACATTTTCACAATATTTCTGATAATGTTTTTCCTTCTGGAGAAAGTCTTTTGTTTTATTTCAGCTAGAGTAAAAGCAGTTTTTATTTTTTTATGAGCCATTTTAAGGATAAAATGATTAGCCCTATGAAGCAATTTTTTTCCAATTGTCTACAGACCAAACCATCATTATACAATAACTTGCCTAATTACCCAAATCCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15257
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001805 Essential Splice Site 3008 3604 57 70
ENSDART00000132471 Essential Splice Site 2860 3456 55 68
Genomic Location (Zv9):
Chromosome 19 (position 37701249)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 36565769
GRCz11 19 36152889
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTGTCTGGCTAAYGGGAGCTGGGTGGRCATCCAGCCYGAATGCCACGR[T/A]AAGAAATATGAANCGCCATGCGCAGCTGAACGTACATGATTWATCGCTTC
Long Flanking Sequence:
CTTTGTATGTGTGTTTTGAATAAAATTTAATTAAAAAAATCACCAACAAAAAAAAAGAAAAAAAAAAAGAAAATTTCTGTGGTGAAGCAGGTTTACAAGTGTTGACTTTTTTATTAATTAATTAATTAATACAATTAATTTAATTTTGTTTATATTTATTTAAATTTATTTAATTTTCAAGGCCACACAAAAATACTTCTTTTATCTCTGTAAAAAACAGAAAGAAATTAGAATTTGTAAAATACAATGCATTCACATGAAACTAGTAATAAAGCAAAGCGTCCAAATAAATGCTGATAAATGTGTGCTGTTTCAGGGGATTCTGCTGGTCTGTGTGGAGATCCAGGCATTCCAGTACATGGGATCCGTCTGGGAGAAGAGTTCACCACAGGGAGTGTTGTCCGATTCAGCTGCGAGCCTGGATACCAGCTGAAGGGCTCCTCCGAGCGGACCTGTCTGGCTAACGGGAGCTGGGTGGGCATCCAGCCTGAATGCCACGG[T/A]AAGAAATATGAAACGCCATGCGCAGCTGAACGTACATGATTAATCGCTTCCACTTCCAGAAGATTCTGCTACAACCAGAACTGTAGCCTATGCAAATTTATCAGCCAGCAACTGATTTCAAAGCAGTTTGTGTCTAAACTTTGTGCAGTTGGCGCATTTCAGGTAGTCCATTGCAATATGAATCAATTCCAAGAGAATCAAGTTTCTATCAAGGGGAACACACAGTTGGAGTCAGATTTATTTTAACACCCTTTGATTTTTTTTGGTCTTTTTTTAAATATTAGGTTTAACAGGGCAAGGACATTTTCACAATATTTCTGATAATGTTTTTCCTTCTGGAGAAAGTCTTTTGTTTTATTTCAGCTAGAGTAAAAGCAGTTTTTATTTTTTTATGAGCCATTTTAAGGATAAAATGATTAGCCCTATGAAGCAATTTTTTTCCAATTGTCTACAGACCAAACCATCATTATACAATAACTTGCCTAATTACCCAAATCCGC
Associated Phenotype:
Not determined