Busch Lab

ZMP

dnah7l

Ensembl ID:
ENSDARG00000000606
ZFIN ID:
ZDB-GENE-030616-623
Human Orthologue:
DNAH6
Human Description:
dynein, axonemal, heavy chain 6 [Source:HGNC Symbol;Acc:2951]
Mouse Orthologue:
Dnahc6
Mouse Description:
dynein, axonemal, heavy chain 6 Gene [Source:MGI Symbol;Acc:MGI:107744]

Alleles

There are 21 alleles of this gene:

Allele Name Consequence Status Availability
sa19487 Essential Splice Site Available for shipment Available now
sa5936 Nonsense Mutation detected in F1 DNA Not yet available
sa14187 Essential Splice Site Available for shipment Available now
sa15767 Essential Splice Site Available for shipment Available now
sa25565 Nonsense Mutation detected in F1 DNA Not yet available
sa479 Essential Splice Site Confirmed mutation in F2 line Not yet available
sa19488 Nonsense Available for shipment Available now
sa19489 Nonsense Available for shipment Available now
sa25566 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa32658 Nonsense Mutation detected in F1 DNA Not yet available
sa19490 Essential Splice Site Available for shipment Available now
sa32659 Nonsense Mutation detected in F1 DNA Not yet available
sa32660 Nonsense Mutation detected in F1 DNA Not yet available
sa18694 Nonsense Mutation detected in F1 DNA Not yet available
sa6581 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa32661 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa19487
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000054388 Essential Splice Site 50 3802 None 73
ENSDART00000137429 None None 84 None 4
ENSDART00000141317 Essential Splice Site 240 3966 None 75
Genomic Location (Zv9):
Chromosome 1 (position 20841815)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 21313911
GRCz11 1 22006848
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTCTTCAGTACCTAAATCATCAATTAACTTTGACACATATAACCTCAAG[T/A]AAGAAATGCAGTATTTGTACACTACCATTTCAAACTCATTTATTTTATTT
Long Flanking Sequence:
TATGAAACCGTACAACAACCAGAAGCTGACTCCTAAGATGCCCTTTCAATTTGATGAGGTCCAGTCTATTGATTCTTCTACAGAGAGAGGACCCTCCGTATTACAGCTTCCCAAAATTCCACACTACATCAAAGATAGACAGGTTTGACTTTAAACTTCTCTGTTCATAGATGTCTGTTGTAACATTAGTAAAACTGTACATGCTTTTTATGTGATCCTTTTAGGTGCAGTTGACTCAGGGCTCACTCAGGATACCCTCCCCACCTAAAAGAGTAAAAAGCTCCTCCAAAAGTTGCCCAGTTCCATCTCTGAGCTACACTCCCTCTCCACCGCTTTCTGGTTCACTGCTGTTTGACTCAGTGGATGAATTAATACGTGCTAAGATTTGCTCCCCACCCCACATCGTCCAAGCCATCCGGACTAACCCTCACCTGGGATTCTTCTATTTGACGTCTTCAGTACCTAAATCATCAATTAACTTTGACACATATAACCTCAAG[T/A]AAGAAATGCAGTATTTGTACACTACCATTTCAAACTCATTTATTTTATTTGATATTTTATTTCATATTTCATTGATGCATCAAAAAAAAAAAAAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTAAATTGTTGTAAAATTGTTACTTTTTTGTTTTAAATAAACAATGTTCTTTTAAAGTTCATCAAAGATTTTTTTTTAACAACATCAGCATATTTGAAGGATTTATATGGTCATGTCATACTGAAGACTAAAGTAATGTAATAAATTAGTTAATTAAAGTATATTACAATACTGAAATATATGTAAAACATCAAATCAAAACATTTAATTTACAAATACAAAAATCTATTTTTGATTTTAAATATTCATATTAAGTCTTGTTTTTACATATTTCATTAGATCAAGTTTAATATTGAGTGATTTTAATTTGTATTTTGAATGTTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5936
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
ENSDART00000054388 Nonsense 625 3802 14 73
ENSDART00000137429 None None 84 None 4
ENSDART00000141317 Nonsense 806 3966 16 75
Genomic Location (Zv9):
Chromosome 1 (position 20853381)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 21325477
GRCz11 1 22018414
KASP Assay ID:
554-3940.1 (used for ordering genotyping assays)
KASP Sequence:
CACCATGCATAACTGCTGTAAGAAACACCATCGACAAGGCAGTGGGAGAG[C/T]GAGACTCTTATGTGGACAAATTTTGCCAACATCTCCAGCAAGACATCGGY
Long Flanking Sequence:
ACATTTAATGGCAGAAACAAGCTTCCACTGTGTCCTTGCCTTACTCTGCCTGATACATATTTGATCTCCTTCTCTAGGCTATTAATGATATTCTACCTCGGCTGGCAAAGAAAAAGATGGATGACATCATTGCAGAGGCTCAGGATGCCCAGTTCAAACTGGACTTTGTTCCAACTGTAACCACTGAATATGTTGACTCCCTCAACTTCCTGGATGAAATTCAGAAAAGGGTAAGTTTGTGAGAGTTTTTCTGTAAAAACAAAAAATCCACTAGGCAATTAGATATTTGACAAAGGTTTGCTCAGATGTACTACTCTTATCTTTCAATCTTTTTCTGTCAGATCGAGGTGCTTGAAAAGGAGACTGTGACCGTCAGTGAGATGTACAAGTTGATTGAGTGTTACTCTGTCCCCACACCTCCCGAAGATATTGCAGTGTATGCCACGTTGCCACCATGCATAACTGCTGTAAGAAACACCATCGACAAGGCAGTGGGAGAG[C/T]GAGACTCTTATGTGGACAAATTTTGCCAACATCTCCAGCAAGACATCGGCCAACTGAACAATACAGTACAGGAAGTGAAAGCGGAGGCAGAGGTAAACACACCACAATAATGTGGTAGGGTTGTTAGAGTGTATTTTTATTTATAATTAATGCATCAGGTAACACTTTACTTGAAGAGGGTGTTCATAAGAGGGTGTTCATGCCCTCCAGGAAGTTTGGTGACCCCTGTTCTAGGCATAAAGATAGCATTATTTGAGATGTCTTCATCAAGACAACTTGACATAAACAAATACATTACAACCTGCCTTTGTCTTGACATTTCCAAGATAAAAATACTGTCAGTGTCTTTGTTGTGACAACTTGACTTTACCAAGACAATATAACTTGTTATAAATCTCATAAGCATGATTGTCTTGAGGCCACTGAAATTGTGCTATGAAATGTATAGAACAGCATCACTGTTATTTATTTTTTTACCTCCACTACAGTGATACAAATAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14187
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000054388 Essential Splice Site 737 3802 17 73
ENSDART00000137429 None None 84 None 4
ENSDART00000141317 Essential Splice Site 918 3966 19 75
Genomic Location (Zv9):
Chromosome 1 (position 20857660)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 21329756
GRCz11 1 22022693
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGAATTACGGTGTCCTCTAAATGTCACATGGTCAATTATCTCTTTTATAT[A/T]GGATAAGTTKGATGAGCTGGACCCAGAACTGCTGAGCAAGCAGGTGAACA
Long Flanking Sequence:
AGTGGGCAAAAACAGCCACAAACATAATGAAAGAGTAGCCAATTTGCCCAAAGTGTTGAATTTTTTTTTACATTTGCCAAAAGTTTTTCTATAATATTGTGAACATAAGATTTGTTGTCATTTGCTGAAATACTGAAAGTTGTGGCCAAATTAAGACTCAAAATGACCCCAGAGTGGATGAAAACATCCCTAACAGCACACAAGAATTAAAGGTGTATCTAATAAAGTTGCCAGTGCTTGTAAATCTCCTCAGAGGGTCAGCTAGTGCTTAAATTCTTAACCTGAAGGTTGAAGGCTAGTTATTCTGTACTGAGGAGCAGAAATAAAACAGCTAAAGTGTTACTGAGAGACACAGCTAAACTTGTCATAGGTACGTCCTTGAGCAAGGCACTTCACACTAGATAACTTTGGATGAAGTGACTTTGCAAATGGGTATGCTGGAAGCCATTTCGAATTACGGTGTCCTCTAAATGTCACATGGTCAATTATCTCTTTTATAT[A/T]GGATAAGTTTGATGAGCTGGACCCAGAACTGCTGAGCAAGCAGGTGAACAGGTTTGTCAAATATGTCAGCCAGCTGGAGAAGGGACTGCCACCAAACAATGTGGTGCCCTTCCTCAAAGCAAAAGTGGAGAGCATGAGAGAAAAGGTGGGTGAGGTTCACACTAATGAATGCATGTAATTGCCTGAGGTTGACGACAGTATTTTACATTTGCCCATGGAAAAAAAGATGTCTCAAAGCCATAAAACTTGTAGTAGGCCTACTAGGCATAGAGTACTCTTCTAAATGTACAGTGCATACGAAAAGTATTCTTCAGTTTTTCCACATTTGTTTATGTTACAGCCTTACTCCAAAGTGGATTAAATAGATTTATTTCCTCAAAATTCTATACACAATATGTTGCAAATGTATTACAAATAAAAAACCTGGAAATCACATGTATGTAAATATTCATGGCCTTTGCCGTGAAGCTCTAAATTGAGCTCAGGTACATTCTGTTTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15767
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000054388 Essential Splice Site 853 3802 19 73
ENSDART00000137429 None None 84 None 4
ENSDART00000141317 Essential Splice Site 1034 3966 21 75
Genomic Location (Zv9):
Chromosome 1 (position 20863650)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 21335746
GRCz11 1 22028683
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCTGGACAAGCCTCAGGAGAAGCATCTCTGGAGAACATTCTSAGAAAG[G/A]TGATGCCTACATTTATTATTGTCTTTTAACATTATACATACACGTCTYTR
Long Flanking Sequence:
ACACACACACACACACACGCACACACACACACACACACACACACACATTACCCTCTTCCACGGAACGTAAACAAAGCGGGTCGCAGGTTTCAAATCTCCCGGGTTTGCGCGTGCGCGGTAATAACTTCGTTATTACGTCATAGCGAAACACCTAATGACTCGTTATCAAGACGACTCGTTTGAAGCACTATGAGTCGACTCTTTTATAGGTGAATCAACAGTTTTAAACACTGTACATTTACAGATTTAAGCCTTAGCTGGATATTTCACTTCACTTAGAGCTGTGTTACACAATACATGGAAGGGCATTTTCATAATATGGGCTCTTTAACACTCACTGATGTACTAAAAACTCTAGGTTTGAGCCACAACCTAACAGGAAGGCGTAAATCAGCATATAGGAACTACAAATTCATTCTTTAACCGGATGTATCCTGTCAAATTTTCAGGTGTCTGGACAAGCCTCAGGAGAAGCATCTCTGGAGAACATTCTGAGAAAG[G/A]TGATGCCTACATTTATTATTGTCTTTTAACATTATACATACACGTCTCTATGTTGAGCTTCACACATGCACACTGTTGATAGATTGAGGATTCCTGGAAGACGACAGAGTTTATAGTGCTGCCTCATCGGGACACTAAGGATGTGTTTATTCTTGGTGGAACCGATGACATTCAGGTAAATTAAATTTAGATGTAACTCTCATTCTTTCCAGAATTGAATGAAGAACATACAGTTTTTTTTAATATAAGTAATATTTGTATTTTGCCTGTGTGAATTTTGTAGGTGCTTCTTGATGACAGTATAGTCAACGTTGCGACTGTTGCATCATCCCGTTATGCAGGCCCAATCAAGGCCAGAGTTGACAAATGGCAGAGACAGCTTTTGCTGTTCAACCAGACCTTGGTAATCCAAACTAGAGTTATGAACTTCAAAAAAATACATTTTATGTCAAATGTTGGCGTGGGTTTCCCCGGGTGCTCCAGTTTCCCCAACAGTCCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25565
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
ENSDART00000054388 Nonsense 1287 3802 29 73
ENSDART00000137429 None None 84 None 4
ENSDART00000141317 Nonsense 1479 3966 31 75
Genomic Location (Zv9):
Chromosome 1 (position 20882426)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 21354522
GRCz11 1 22047459
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCATTTTTATCATAGGATCGCTGTTACCTCTGCCTAATGGGAGCGCTG[C/T]AGCTGGATCTCGGAGGAGCTCCTGCAGGTCCAGCAGGCACAGGCAAAACT
Long Flanking Sequence:
AGTAATCACTCCACTGACGGTACACATTCATTTAAATTTTTTTTTCCTTATGATGGTAAGGGATTTGTCAAATGCATTATATAAAATACATTTATATTTTAGTCTGTATAAAAAAATTTGCAATCTGAAGAATAATGGTTTGGCATAAAGTAAAAAAAAAAGTTAACATACTGAATGGTTGTCCATTCAAGCAATTCACTTCTTGTTGATTAATAGAATAAATATCTTGGTTTGTTTTTCAGTTTATTGATCATTTTCTGATAATCCAAATCCAGATTCTGATATTGGATCTTATATTTTTACGTCATGCATAAGAACTGTTTAACTACATATACTAAAACTTAAAAACTACTAAAAAACTAAGTTAAAACTACATATATTAAAGTGCATATCAGTGTATGGATAATCTATATTAATGTAGTGTGCATTTGCATTATCATTGTTATGTTTACTCATTTTTATCATAGGATCGCTGTTACCTCTGCCTAATGGGAGCGCTG[C/T]AGCTGGATCTCGGAGGAGCTCCTGCAGGTCCAGCAGGCACAGGCAAAACTGAGACCACAAAAGACCTTGCAAAGGCTCTGGCAATCCAATGTGTGGTGTTTAACTGCTCAGATGGACTTGACTATAAGGTGCCTCTCTGTCTTCATGATGAATTTGTTAAGCAACTAGACACTAAAACAAGATTTTCCTGTTCAGTGTAAACATTTGTGTTATTACACTGAAATGAACTAAACTGAACTGTGAAAACTGGACCGAAGCAGTTTACTAGAATGTCATTTATGTTAAGCTGCTTTGACACAATCTACATTGCAAAAGTGCTATAGAAATAATGATGAAATGAAAATATGAACCCTACCGTACTAGAGTGAAAAAATTCCTCTGTCACTAGGAGGCAGCACAGCCCCAACTGAATTCTTTCTACATTACATGAAACCCACTGTAGATCTCAATTCTGAGAGTTTTACCTTGCATGCTGTCCTTATTTATGGCCAGTGTTTAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa479
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
ENSDART00000054388 Essential Splice Site 1375 3802 30 73
ENSDART00000137429 None None 84 None 4
ENSDART00000141317 Essential Splice Site 1567 3966 32 75
Genomic Location (Zv9):
Chromosome 1 (position 20884934)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 21357030
GRCz11 1 22049967
KASP Assay ID:
554-0300.1 (used for ordering genotyping assays)
KASP Sequence:
CAGTCATTGCTCAACAACTTATCACTATTAGAAATGCCAAGGCAGCCAAG[G/A]TAAAGCACTTCCACACACACGTGCATGTTTAAACCCCATATGCTGCTCAC
Long Flanking Sequence:
TATTAGTTTAAGCTTTATGTTTCATTCTTTGAAAAATATAAGGAAAATAGTTGAGAATGTAGGCAAAATAAATGAATGTTGTTTTTATTACACTACACTGCCTGAGGTTGCTATATTCAATTGGCAAGATTAAACTTTAGGTAAGTTTTAAATAAAGATTCGCTATTCATATGCGCTAGTAGCACACTGAGGACATCTGCTGGTTACAGGGTGGTAATGCCGAATTAAAAGCATTGTGTGTGTGGATGCAAATATATTTATATTTCAATAGATACTTATAGTTATTGTGCTTGGTATGAAAGTCATTTAGAGTGTTAAGTATTCAGCTTGGTTAAAGTTTTAAATGGTAATTGTGTGTTTAGATGATGGGGACATTCTTCAGCGGTTTGGCTCAGTCAGGTGCCTGGTGCTGCTTTGATGAGTTCAATCGCATTAACATCGAAGTGCTGTCAGTCATTGCTCAACAACTTATCACTATTAGAAATGCCAAGGCAGCCAAG[G/A]TAAAGCACTTCCACACACACGTGCATGTTTAAACCCCATATGCTGCTCACACCAAATAATTTCCACCTGATTTTTCTTAATGTGTTTGTGTTCTTCAGCTGAGTCGATTCATGTTTGAGGGGAGAGAGATAAAATTGGTGATGACATGTGCAGCTTTCATCACCATGAACCCTGGTTACGCTGGCAGAACTGAACTCCCTGACAACCTGAAAGCTCTTTTCCGACCTATCGCCATGATGGTGCCCAACTATGCACTCATCGCTGAGGTGTGTAATTAAACCAGCAGATCTGATCGCAGAAATGATGATAAAACACACTAGGTGAGAGACAGAGAGGTCAGAGATAGTGCGGCTCATGTGTGCTCTTATTAAAAGCTATTTTCTGGTCATGTGTGTGTTAAGGCTACTCCACACTGCACTGACCGATGCTGAACAATGCCAACAGACAAATTTGATGGGTTTGGTTACAGTAGATCATTGCCTCTTTTGGCAGTGAACTGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19488
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
ENSDART00000054388 Nonsense 1870 3802 38 73
ENSDART00000137429 None None 84 None 4
ENSDART00000141317 Nonsense 2062 3966 40 75
Genomic Location (Zv9):
Chromosome 1 (position 20908922)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 21381018
GRCz11 1 22073955
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCAGCGTAGGTGATTTATGGAGCGTCTATATGAACTTTGATATTAAATG[T/A]TTGGAGCCATGGGAAAGGATCATTCCCGTCTTCAGTTATAACAGTGAGAT
Long Flanking Sequence:
AGATCTTAAAATCGTGAATTACTGCTGAAAACAAGTCAAATCTGCAGAAGCTTTTTAAAAAATAAAATATTGTGCAGAACTTTAAGCATTTTTCTGACTGCCCATGACAAATAAGTTCCATAAACAACTATCACATGACAAAACTAAAAATAACAGATCATCTACAGCAGGTAATTACACATAGTTTTCAGGGCATGTTAATTTTTGTATAGCACAATTTTTTATGAATTCAGTTGTTTGTGAGCATATGTAAACATATGTTATGTGAACTAGCCTAATTATGTTTTTTGGAGATTACAGTAGGTAACACATTTTGTAAATAGGGTAAATTGGGACAGAAATATCGTGGAGTACATAAAATGCCATAAATTAGAAGAAACAAAAACAGATGCTCAATGGCAGCCAAGAAAAAGTCTTAATAGTTAAATAAACTCTGTCTTTTTACAGTTGTCCAGCGTAGGTGATTTATGGAGCGTCTATATGAACTTTGATATTAAATG[T/A]TTGGAGCCATGGGAAAGGATCATTCCCGTCTTCAGTTATAACAGTGAGATACCCTTCTTTGAGATGCTGGTACCCACCACAGACACAGTGAGGTACGGATACCTGATGGAAAAACTGCTGTCTGTCAATCACTCTGTCCTCTTCACTGGCATCACTGGTGTGGGAAAGGTAAGACGGTGTGTGCTTAATATAATGTACAGTAAATGTTTGTGAAGTAGAGTTTAACTTCAATAAGACATTGTTTAAGAGGACAAAATTCTTTTCTAGAATTTCAATTCTTACATTTTACCTCTTAAATGACCTCTTCATTTACTCTCCCTCATGTGGTTGTTAATACAAAAGATTTTGAAGAATGTTGTTGCTGGGACCCATCGGCTTCCATAGTAGGAAAAAAAAGCTATGGAAGTCAATGGGTCCTAGCAACCAGAAAGTTTTAAATCAATATTGTTTGTATTTGATTTGATTTATTTATTTAGAGTAGAACATCATACACTTAAAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19489
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
ENSDART00000054388 Nonsense 2161 3802 43 73
ENSDART00000137429 None None 84 None 4
ENSDART00000141317 Nonsense 2352 3966 45 75
Genomic Location (Zv9):
Chromosome 1 (position 20919700)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 21391796
GRCz11 1 22084733
KASP Assay ID:
2259-0521.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCATATCTTCCGTTTGTTCTGTCATGAGTGTCAACGTGTCTTCCACGAT[C/T]GACTCATAAACAACGAAGACAAAAGCTACTTCAATACCATGATCTCTGAG
Long Flanking Sequence:
ATCTGTTGTACCAAAATCCACCAAAGGCTTTTAATCAGCTTTCTTTGTTTAAGAGCTCTCAAATGACAAATACAAATGCTCTCTCTTAATTTGAAATGCACTTTGGGGGGCTGTTAAAACGTTGGCTTAGGACTCATCCACAGGCCAAATTATAGACTCTCAATAGGAGATACTGTCTATCTAAGCTAAAGCACAACCCCCATCTGATTATGTTTTCATTTTTAGTGAAAGGTCACAGGCAAGTTTATCTTTTACTGATATTGATCTGTAGACACAGTATTGATTGTTTGCCAGCAGTAAGTCTTGCTATAAAGATATATATTAAAGAATCTAATCTGTGTAAACGTTGAACAAAATTTCTTTTCATTATTTGTCTTTGAATGTGTGTGTGTGTGTTTGTTTTCTGTGTAGGTATGCTGCAGTGTGAGCCAACTACGGTTAGAGATCAAACCCATATCTTCCGTTTGTTCTGTCATGAGTGTCAACGTGTCTTCCACGAT[C/T]GACTCATAAACAACGAAGACAAAAGCTACTTCAATACCATGATCTCTGAGATGGCCAGTAAGCACATGACCCTCAAATCCCCTTCAGTGTTAATCTCTCTAGTCCAGACATCTGTTAAGGTGTATATTATAGGGCTTTTCTCTATTAAAATAATTAACACTGGGTCATTCTAAACATAGGATAAATTGAATCCTGGGTTATCTTCACTTTTCACACACTCACTCTTTTTTTCATATCATTTTTTATTATTATTCATTCATTCATTCATTTTCTTGTCGGCTTAGTCCCTTTATTAATCTGGGGTCGCCACAGCGGAATAAACCACTGAACTTATCCAGCAAGTTTTTACGCAGCGGATGCCCTTCCAGCCGCAACCCATCTCTGGGAAACATCCACACATACACACACACACACACTCATACACTACGGACAATTTAGCTTACCCAATTCACCTGAACTGCATGTCTTTGGACTGTGGGGGAAACCGGAGCACCCGGGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25566
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
ENSDART00000054388 Essential Splice Site 2256 3802 45 73
ENSDART00000137429 None None 84 None 4
ENSDART00000141317 Essential Splice Site 2439 3966 47 75
Genomic Location (Zv9):
Chromosome 1 (position 20924508)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 21396604
GRCz11 1 22089541
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGGAAACCAAGCTGGTTTTCTTTCAAGATGCCATTGAACACGTGTCTAG[G/A]TAAACAAGCAGCTTGCCTTTTCGTCTGGTGTTCACAAAAGCAGGTGTTCA
Long Flanking Sequence:
TCTAACCTATTATTAATGTTTTATGACGTGTGTCTGCTGGGATTGTACTAATGATGCCATACAACCTTGCTTACAGATTATACATAACAGAACCCTAAAATGTCACTCATTTGTCATCAGCAATTGCTTCAACTGTCTAGTTTCGATTTGATGGCTTTCAGCCTTACTCTGCTTTATATTACCATGATAATAAGTTTTACTTTAACTCATTTTGTCATGTCATCATGAAAATATGCCTTTGTGTGGTGTTAATATGTGTCCACCAGTGGCAAAAAATACACATTTCACCTTTAATGACAGGGTTTAGTTAATGTTTTGTAATTAAACAATTTAATTCAATTTTAGGTTGGAGCAGACAAGGCTGATCGTGTCTATGAGGATCTAACTGACATGGACAAGATTCGCCAGGTGCTTCAGGACTACCTGGATGACTACAACACAACCTTTGCAAAGGAAACCAAGCTGGTTTTCTTTCAAGATGCCATTGAACACGTGTCTAG[G/A]TAAACAAGCAGCTTGCCTTTTCGTCTGGTGTTCACAAAAGCAGGTGTTCAGATGACCCTGTCATTTAGCCTGCACGTCTGGATCAGTTTACTAATGGAATGCTTTGTTCATCCACCCAGTTGACCTTCCTTTCTTATCGTTCATCTGTTCCTCTGTCCACAGAATTGCCCGCATGATTCGCCAAGAGCGTGGCAATGCCCTGTTGGTTGGTGTGGGTGGCACAGGAAAGCAATCTCTGACACGTCTGGCTGCTCACATGTGTGGTTACCGTTGCTTTCAGATTGAGTTGAGCCGTGGTTATAATTACGACAGCTTCCATGAAGACCTGCGTAAACTTTACAGAATGGCAGGTGTGGAAGGCCAGGACATGGTCTTCCTCTTCACGGACACTCAGGTACAGCCTAGGAGAAATCTGATAATAAATGATATTAAAAGTGTGTGTTTTTTTATAATTAAAAAGTATTAAAAACAAATAATTATTTTAAATAGGTTGAGTGGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32658
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
ENSDART00000054388 Nonsense 2263 3802 46 73
ENSDART00000137429 None None 84 None 4
ENSDART00000141317 Nonsense 2446 3966 48 75
Genomic Location (Zv9):
Chromosome 1 (position 20924690)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 21396786
GRCz11 1 22089723
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTATCGTTCATCTGTTCCTCTGTCCACAGAATTGCCCGCATGATTCGC[C/T]AAGAGCGTGGCAATGCCCTGTTGGTTGGTGTGGGTGGCACAGGAAAGCAA
Long Flanking Sequence:
CATGATAATAAGTTTTACTTTAACTCATTTTGTCATGTCATCATGAAAATATGCCTTTGTGTGGTGTTAATATGTGTCCACCAGTGGCAAAAAATACACATTTCACCTTTAATGACAGGGTTTAGTTAATGTTTTGTAATTAAACAATTTAATTCAATTTTAGGTTGGAGCAGACAAGGCTGATCGTGTCTATGAGGATCTAACTGACATGGACAAGATTCGCCAGGTGCTTCAGGACTACCTGGATGACTACAACACAACCTTTGCAAAGGAAACCAAGCTGGTTTTCTTTCAAGATGCCATTGAACACGTGTCTAGGTAAACAAGCAGCTTGCCTTTTCGTCTGGTGTTCACAAAAGCAGGTGTTCAGATGACCCTGTCATTTAGCCTGCACGTCTGGATCAGTTTACTAATGGAATGCTTTGTTCATCCACCCAGTTGACCTTCCTTTCTTATCGTTCATCTGTTCCTCTGTCCACAGAATTGCCCGCATGATTCGC[C/T]AAGAGCGTGGCAATGCCCTGTTGGTTGGTGTGGGTGGCACAGGAAAGCAATCTCTGACACGTCTGGCTGCTCACATGTGTGGTTACCGTTGCTTTCAGATTGAGTTGAGCCGTGGTTATAATTACGACAGCTTCCATGAAGACCTGCGTAAACTTTACAGAATGGCAGGTGTGGAAGGCCAGGACATGGTCTTCCTCTTCACGGACACTCAGGTACAGCCTAGGAGAAATCTGATAATAAATGATATTAAAAGTGTGTGTTTTTTTATAATTAAAAAGTATTAAAAACAAATAATTATTTTAAATAGGTTGAGTGGATTTAATTCATTACAATAATCATATTGCCAGGCACAGTAAGATGGAAGTAACTACATATTTATATTAAAACGTGTTGTATAATAGAATTGTACCAAGAGTAATATCCAATGATGCAAGCTAGTTAGTTTTTTGCCACTTTTTTTACTTTTTAAACAGAACACAAAGAGCCATTTATGTTTATGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19490
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000054388 Essential Splice Site 2432 3802 49 73
ENSDART00000137429 None None 84 None 4
ENSDART00000141317 Essential Splice Site 2615 3966 51 75
Genomic Location (Zv9):
Chromosome 1 (position 20937366)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 21409462
GRCz11 1 22102399
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTGTGTTTGTTACATTGCAGTCATTTTCTGTTTCTTGGGTTTATTTTTC[A/T]GTGGCCCCGTGAAGCTCTGCTATCTGTGTCTCAGACCTTCTTCCAGAATG
Long Flanking Sequence:
AGGTCTGTAAAGTCTAAGAAGGGAAGTATTGGTCGTATTAGTATTTTTTTTTATTTTTTTTTGGTACAGTTAGTGTGATATTCAGAGAGGCAATTGCAGATTAGGAGGTGTAGTGGAGACTAAATAGTTGAGTTTTTAGTCGTTAGTCGTTAGTAGTCAGTGCGGCAAGAACAGTCTCAAACATAATAAAAGGGTAGTAAGTTTGTCCAGAGTGAATTGAGTTTTTGAAGGTTTTCAAAGCATTGTGTTAACACAAATGATGTGTTAAAATAAGATTTTTCATCAAAAATGATTGCATTTGCTGAAACACAGAGAAAGTTGTGTACAAATTAAGACTCAAAATCACTCCAGAGTGGATGACAACATCCTCAACAGCACACAAGGGTTAAATAAAAAATACTTTCAGTATTATGCTAATGATAAACAATTGATATGTGCTTTTTACTATGTGTTGTGTTTGTTACATTGCAGTCATTTTCTGTTTCTTGGGTTTATTTTTC[A/T]GTGGCCCCGTGAAGCTCTGCTATCTGTGTCTCAGACCTTCTTCCAGAATGTGGAGTTTGGCAGTGAGGAGATGAAGCAGTGCTTTTCAGAGATGTGTGTGGAGATTCATGTTAGTGTGACTGACATGGCTGAGCGTTTTTACTCAGAACTAAGGAGACACTACTACACCACACCGACCTCCTATTTGGAGCTCATTAACCTGTACCTGGGCATGCTGGGAGAAAAGAGACAACAGCTGCAGGCGGTGAGGATGAGTGATGGATAATGCATTAGTCTCTTATGTTGTTACACCGTTACTTAAAGGGGCTATATGTAGAAATGTTCTTGTATTAGCTGTTATTAATGGACAAAGTGTGAACCGCTTGCAATACAACATTTTATAAACGAGACCTCCTTTTTTTCAGGATAACAAACAAGTTTTTAAGATTTCTGTATTCCCCAAACTATTTAGATAAGACTTGGTTTTGAATGAACTGCCCAGAGATGTTGCAAATGTTGGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32659
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
ENSDART00000054388 Nonsense 2831 3802 54 73
ENSDART00000137429 None None 84 None 4
ENSDART00000141317 Nonsense 3014 3966 56 75
Genomic Location (Zv9):
Chromosome 1 (position 20959594)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 21431690
GRCz11 1 22124627
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAACGTCATTGGAAATGTGTTCATCGCTGCAGCTTGTGTGGCTTATTA[T/A]GGGGCCTTTACCTCCCATTACAGACAACTGGTAGTGTATTATTAAATCAC
Long Flanking Sequence:
ATGTCGGTCTTACACTATCTTGAGATGATGCTATCTTCTAGTTTAGTCAATAAAAATCCAGCATCTCTGCTGTGCTCTATGAATCTGAGCACAGTTGTGGAATTATGTATGTGCAACTTTCTAGATATATATTTTCATTTATGTTAATTAGGGATGTATAAACTAAATATTTATGTGTAAAATTGACACGTCAATGACTAAAGTCTACACATTTTTTACAGTTATACAGTGAGCTGTTTTTAATGTTGCAAACTGCATACTTTTTGGCCTTCTACTTTCACGCATGTTTATACTTATGTGTATAAGTTTATGTGTGTTTGTTTTGTGATTGTAGCCAAAACCATGGCTTTGACTGAAGCACGTCTGGGACGGTCAGGAAAGTTAACATCTGCTCTGGGTGATGAGCAGGTGCGATGGCAAGAAAGCATTACTCTGTTTGAGCAGGAGATCCACAACGTCATTGGAAATGTGTTCATCGCTGCAGCTTGTGTGGCTTATTA[T/A]GGGGCCTTTACCTCCCATTACAGACAACTGGTAGTGTATTATTAAATCACAATCTTCATTATGTATATTAAATAAATATAAAAAAAAACACTTGAGTATATTACATTATCTAGTTATTATTTCAGTTGGCCGCCCTATGACACATCAAAAATAGTCTCCCTTTTTAGCCTCGCACCCCATCACCCTGCATATTGTTCAAGTCTGTCCTATTTAAAGTCACCATAAAACAGAAGGTAAGATTGCCCTTTTTTGATCTATCCATTTGAAACATGGTACATCCACTTAAAACTGTCCTGAAATTAAAAAGAAGAAAAGAAAAATAAATTAGGACAGTGCATGATTTTGTCCTTTGGGAACCGATTGGATTGTTGGAAGATGAGTTTTAATAACAAATGTAAAACAGACATGCCCTGGCTGATAGCCTGCCCTCAAGGCATGACTAAAAGAAAACGTTCTTTTAGATTGTAGAGAAAGTTATTGTACATGATTAAAGTTTCTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32660
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
ENSDART00000054388 Nonsense 3083 3802 59 73
ENSDART00000137429 None None 84 None 4
ENSDART00000141317 Nonsense 3266 3966 61 75
Genomic Location (Zv9):
Chromosome 1 (position 21017216)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 21489312
GRCz11 1 22182249
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTGCTCTTCACTTCTGAGGGAAACATACTGGACAATGAGGAGCTTGTA[C/T]AAACCTTACAAGAGTCAAAGGTCAGTGGCAGAATTTAAAAGAGTTCAGTC
Long Flanking Sequence:
GCCTAAAGTCCTTCAAAAGGTCCAAAATATTCCCTTGGGGGATAGAGCCTGAGTTTTTTTTTCTATATTTTTGTTCTTTAAAATATATAGATTTTCAAGACTTTACTTTTTATATTATGAGCCATGGATATCAATAAGTTGCTGTACAGTTACATAGTCATTATACTGTAGGAGTTAAATCAAGGTTGACTGATATTAACATAAATCAGATGCAAATGGATTTCTTGACAAAAGCTGTTGTTTGATGATAACTAACCAATTATTTTCTCGCAATATGGTTTTAATTTGGTTTTAATTTACGTGGTGTTTATTTATTTATCTACTTTATGTCTGTGCCTAGTGATGTAGTCCGTCTGGAGCGTCCTGACTTGGAAGAACAGAGAAGCCAGCTGATAGTCCGCATAAACGCAGACCGAAACCAACTGAAAGCCATTGAGGACCGAATCCTCAAACTGCTCTTCACTTCTGAGGGAAACATACTGGACAATGAGGAGCTTGTA[C/T]AAACCTTACAAGAGTCAAAGGTCAGTGGCAGAATTTAAAAGAGTTCAGTCTTCAGTTTGCTGATTTGGGGCACAGAAAACATTATATTGAAACAATATCATAACTATTTGTTTGCACGATTCTTTGTTGTATAAATGCATGTGCAAAGAATAATATTAAAGCCTTTACTGTATATCGAATATTTTATCGAATTAATGTAACATTGTATAAATTTGATTTAAAGGGCACCTATGCTGAAAATCAACTTTTGTAAGCTGTTTGGACAGAACTGTGTGTACAGTATGTTTAGTGTCCACAGTCATATTGGAGTCATAGAAACACAATAAATCACACCGATCAGGCTTTTTCATTGAGATGCACCTTTTTAAAAATTATTTTCTAATGGCCGCGTGCTTTTTGCGTGCTGCTTGTGTGCCCTACGCACCTCACATTTTAACCGCCCACTGCGCCTCATGTTTTTGCCCTTGCGTGGTGTTCGCTCGCAGTAAAAAAAAAAGTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18694
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
ENSDART00000054388 Nonsense 3141 3802 60 73
ENSDART00000137429 None None 84 None 4
ENSDART00000141317 Nonsense 3324 3966 62 75
Genomic Location (Zv9):
Chromosome 1 (position 21022276)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 21494372
GRCz11 1 22187309
KASP Assay ID:
2259-0526.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATCATGTACTTTGTCATTGCCAGCCTGTCTGAGATTGACCCCATGTAT[C/T]AGTTCTCACTAAAGTACTTTAAACAGGTAATTTTAGTGTACAACAGCCAT
Long Flanking Sequence:
GCACGTCACTGTCTGCCACTCTTCTGCCACCCACAGAGAGTAATGAAGGGCTGAATGGGAAGTACAGATAGAAAGACAGATGAACGAAAGGTTGGCCCGGCAATGAACGAAATATCTGTCTTGAAAACCAAAAACAGATCTGTCTCTGTCTGACGCTTTTGCTACAGTCTCATGTATTTCTGTGACATAGATACCGCTGTCAGTGTGGACAGCTTTACAGCTCCTTCTGCATTTTTAGAGCTCTTTACAAACACATCAAGCTGTCGAGTCATTACATTTGTCTCTGTTTGGAATACAACGCTTATACAGGACAAGAAACTGATTTTCTAACAATTTCTCCTATGCAGGTGACATCTCAGGCCATTAAGTCTCGGCTGGTGGAGGCGGAGACGACAGAGGAGATGATCAACAGAGCTAGAGAGAAGTATCGCCCTGTTGCCACACGTGGCTCCATCATGTACTTTGTCATTGCCAGCCTGTCTGAGATTGACCCCATGTAT[C/T]AGTTCTCACTAAAGTACTTTAAACAGGTAATTTTAGTGTACAACAGCCATTGTATAATGTATTTTTTTTTCTGATTGTAATTTATTTAAATGTAACCCAGCTAAATGCTTTTTACATAGTATAATAAGGTTTAAATGTTTTGGTTTAGTATTTTTTACACACAAAGTCTGCATTTAAACAAAAATGTTGTGAAATTATGATTTATAATGACTATTTTCAGTTTCAATATGTTTTCAAATATATTATATTTTACATTTTAGCCCAACAGACTCTCTAGAAAATCTGGCATTACTCACTACTTAAGACAATATGTATCTTTGCTGTAATTTCATGCACTGCACATTCAGAAGAAAAACACAACAGCAGTATTGTGTAGTTTTACTAAGTAATTTCGGGAGGGTCATGTGATATGATTGATGGCCTCTCATCCTTAATCAGCAATAATCCAATCAGATTGATTCAAGCTTACCATAAATAGATCGAATTCGCCCTGCTACCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6581
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
ENSDART00000054388 Essential Splice Site 3572 3802 68 73
ENSDART00000137429 None None 84 None 4
ENSDART00000141317 Essential Splice Site 3755 3966 70 75
Genomic Location (Zv9):
Chromosome 1 (position 21046599)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 21518695
GRCz11 1 22211632
KASP Assay ID:
554-4778.1 (used for ordering genotyping assays)
KASP Sequence:
CTACTGCCAGACAGGACATATACCTTGGGAWGCTCTTACATACATCACAG[G/A]TACAGTATTCGAGTGTTTATTGTAGAAGTATAGCATCACTCRTTGATATT
Long Flanking Sequence:
GTTCCAGTCAGTACTAAATAATAAAAATAGCTTGTCTTATTTTGGTAAAATAATTTAGCATGCACTGCAAGCTATATGCAAATATTTGACTTCAAATGTAGATACCTTAAAAATACAATACAGTATACAGTATATTTATTTCAGTTTTTAATAATTGTTTTCATTCCCATGATTGCAAGTGCAAATTGTTAGCAGTCATTACTCTCAGCTTCTCAAGATCTTTCATTTATTTGAAAAGAAATACTTTAACTCAGTCTAATGCAAATATTTTGAAATATGCAGAGGTTCAAGGGCAGCTTTATAATTATCACTGCTTCTAAATCCTTCACTTTTATTTCTGATTGCATTGATGTATGTACAGGAGCGGAAGAAGTTTGGTCCTCTGGGCTGGAACATCCGTTACGAATTCAATGACAGCGACAGAGAGTGTGCTCTGCTCAACCTAAACCTCTACTGCCAGACAGGACATATACCTTGGGATGCTCTTACATACATCACAG[G/A]TACAGTATTCGAGTGTTTATTGTAGAAGTATAGCATCACTCGTTGATATTTACCTCTATTATTATTGTGTCCATTGTACTTGCATACATTTCAGTGTATGAGTATAAATAGATTGAATGAAACTGTTTATGTAACATTATTGAACTTTCCATTTCATTAGAATTTCCATAATGTTTTTAAATGTTATGAATGAATGCAATGCTCTAAGTAGACTTCATTTCACAGACCATCAGCTGGTGACAATAAATGTTATTAAATTTGCAGCATCTGGTTTGTGCAGGGAATGTTCCAGTAAATGAAAGGCTTTGGGAAAGACTCATTAAGAAAGCTTCACAGAATGTCAAACTGTCTCATTAATTTTTGGCAAGGTGTCAGTCAGTCATGCATTGAGCAGAAATGTTTATGTGAATGTGTTTTATCGTCTCTGTAGGTGAGATTACGTATGGAGGCAGGGTGACAGATGCCTGGGATCAGCGATGCTTGCGCACCATACTCAAGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32661
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
ENSDART00000054388 Nonsense 3760 3802 73 73
ENSDART00000137429 None None 84 None 4
ENSDART00000141317 Nonsense 3943 3966 75 75
Genomic Location (Zv9):
Chromosome 1 (position 21057368)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 21529464
GRCz11 1 22222401
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTACTCTGCAGAAGGCGATAGCAGGTCTGGTGGTGATGTCAGAAGAAATG[G/T]AGAAGATTTATAACAGTTTCCTGAATAACCAGGTTCCTGATCACTGGTCT
Long Flanking Sequence:
AGCAAAGATTCCTGGTCAGTTTTAAACCCCTGCAGTTCCCTGGACAAGTCGAGAGTCAGTCCACTGGTCTTATAATGAGATTTCGACCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCGTGTCTGTGTGTGTGTGTGTGTGTATGACATGCATCTGAGCAGATAAACTAGATATGGATGCAGCAGTGGAGAGTCTGTTCTTGCAAGACCCCAAAGGTAGAGTTAACTCTCTCACCACTGTGCTTGGACAGGAAGTAGACCGCTTTAACTTCCTGCTGCGTGTGCTCAAAGTAAGCAATGATAGATTGATTACAGTAGCTATTTAAACAGGAATGAATGAAATATTAATCGTACTAATCTGTGTGTTGTTGATTGTGTTTGTATTTCTCTGCAGACTTCACTATGTACTCTGCAGAAGGCGATAGCAGGTCTGGTGGTGATGTCAGAAGAAATG[G/T]AGAAGATTTATAACAGTTTCCTGAATAACCAGGTTCCTGATCACTGGTCTAATGCTGCTTATCCATCTCTCAAACCTCTTGGCAGCTGGGTTAGAGACCTCAACCTGCGCACAGCATTTATAGAGGTATGTGTGTAGAGTCAAAATCAGAGCACTAGTTGGGCTCTGGGATTTTTTGCGATGTGGAAAACATGGACAGAATCAAGGAATTCTTTAAAAAAAAAAAAAAAAAAAAAACTGACCCTAAACTTTTGATCGGTAGAGTATGGAATTTTTATACTGTATACTGTATTGTAATATATCATATTTCTTTGTGATATAGAAAAAGTGCATGCCATTCTGTCTTTGTTACCTGTTGTACAGCAGAATATCTGGTGTCCAAATCTGATTGGATGGGAACCGGAGGGTCTGGACACCAGGATAGTTATCCGGGTTCCAGCTCAGATAGACATCTGTCCATCCCTGAAAACACAAAACATACATCAGATTCACCTTCTTTTA
Associated Phenotype:
Not determined