Busch Lab

ZMP

Q32PV1_DANRE

Ensembl ID:
ENSDARG00000009341
Description:
NRAP protein [Source:UniProtKB/TrEMBL;Acc:Q32PV1]
Human Orthologue:
NRAP
Human Description:
nebulin-related anchoring protein [Source:HGNC Symbol;Acc:7988]
Mouse Orthologue:
Nrap
Mouse Description:
nebulin-related anchoring protein Gene [Source:MGI Symbol;Acc:MGI:1098765]

Alleles

There are 15 alleles of this gene:

Allele Name Consequence Status Availability
sa170 Nonsense Confirmed mutation in F2 line Not yet available
sa35320 Nonsense Available for shipment Available now
sa35321 Nonsense Mutation detected in F1 DNA Not yet available
sa42059 Nonsense Mutation detected in F1 DNA Not yet available
sa12190 Nonsense Available for shipment Available now
sa12645 Nonsense Available for shipment Available now
sa17073 Essential Splice Site Available for shipment Available now
sa35322 Nonsense Mutation detected in F1 DNA Not yet available
sa42060 Splice Site, Nonsense Mutation detected in F1 DNA Not yet available
sa22130 Nonsense Available for shipment Available now
sa6261 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa42061 Nonsense Mutation detected in F1 DNA Not yet available
sa42062 Nonsense Mutation detected in F1 DNA Not yet available
sa45465 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa170
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000124251 Nonsense 198 450 8 15
ENSDART00000124920 Nonsense 197 1861 7 43
ENSDART00000126984 None None 84 None 4
Genomic Location (Zv9):
Chromosome 12 (position 32256882)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 30477859
GRCz11 12 30592761
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTTTCAGTGTTTTCCTGCTGATTTTCAGGTGAAATACACAGAAGAATA[T/A]GAGCAGTCTAAAGGAAAAGGCAGTTTCCCAGCCATGATCACCCCAGGATA
Long Flanking Sequence:
CCAGAAGAAAAAATATTATCAGACATACAGTGAAAAATTCTCTGCCCTGGTAAACATCATTTGGGAAATATTTAAAAAATCCAAAGGGGGGAGGCTAATAATCCTGACTTTAACTGTATATTCAGATGATCCTGAAGCCATTTCTTTTATGTCATAAAAATTAAACTAAAATAATTCTGTTCATGATAAATGAAAAAAAAAATATTTAAAAGCTAATTTTTAATTACAAGCACATGTAAACCAACATTTGGGGCATTAAATCAACATAGAATAATTACTGAAAGTGACACTGAAGTACTGATAATGAAAGTCTACTTATAGCAATAAAATGGTTTTTTTTTTTATTCTTTGTAAAAATATGATTATACAATTTTGACTATTTTTCATTAGATAAATTCAGCCTTGGAGAACAGATCAGATCAGACTAGATACTACGTTATTGCACAAACTGTGTTTCAGTGTTTTCCTGCTGATTTTCAGGTGAAATACACAGAAGAATA[T/A]GAGCAGTCTAAAGGAAAAGGCAGTTTCCCAGCCATGATCACCCCAGGATATGAAATGGCAAAAAAAGCCAATACACTGGCTAGCAATGTAAGCGTAACCATTTCTTCAAATTGTACACTGATGTGAGTATGAGTGACATGTGATATGATTTATTATGTCTACTTTTCATTCAGTTGGAGTACAAGAAAGGCCATGAAGAACGAGTATCAAAATACACGACTGTGACAGATACTCCTGACGTACTTCTAGCTAAAACTCAAGGGAAGATCGTCAGTGATGTAAGGGAAAGAAATATGGATGTTCTTTGTAGCCACATTCTGTATTATACATACACCCTAACTGTGCATCATATTAAATAGCATGTCTACACTGAGGGCTATGAACAGCAGAGGGGCAAAGGCAGTTTCCCTGCCCACTTCACTCCAGGATACCAGGTGGCCAAAAAAGCAGGAGACATGGCCAGCAAAGTAAGCGTCCAATAATGTGTCAATTTCATGTGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35320
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000124251 Nonsense 357 450 12 15
ENSDART00000124920 Nonsense 356 1861 11 43
ENSDART00000126984 None None 84 None 4
Genomic Location (Zv9):
Chromosome 12 (position 32257994)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 30478971
GRCz11 12 30593873
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATATGAACAGCAGAGAGGCAAAGGGAGCTTTCCTGCTATGATTACCCCT[G/T]GATACCAGATGGCCAAGAAAGCACATGACATCGCCAGTGATGTAAGTGTC
Long Flanking Sequence:
ACAATTACACATATATAAATAAATGCATGTATACACACATACAATATAAAGGTATCAAATGGTATATTAAGAGCAGGTGATACAAGATACAAGTTATATGGACAAAAGATTTAGAGTTTTTTTTTTTTAGAGCTTTCTGTATTTATCCAATAACAAGCTGTTATAAGTTTTGCATGTAATAAACATGCAGAATCATAGTTAGCAGTGTTGCTTTTGTTCAGGTAAAATATCAACAGAAATACGAGCAGGAGATTAAAGGCAAGGCCAGCACTGAAGCAGGAGCTGCTGAATTTGCTTTGGCCAAAGAAAACGCAGAGCACTTCAGCCAGGTGACACAGAGCTCTTCTGTATATTGTATATTGTGTGTGTTTTTATTTTTTTTATTTTTACATCATATACATTTTAATCATTATATATGCCTCTAATTCCTTTAGCATGCCTATACTGAAGAATATGAACAGCAGAGAGGCAAAGGGAGCTTTCCTGCTATGATTACCCCT[G/T]GATACCAGATGGCCAAGAAAGCACATGACATCGCCAGTGATGTAAGTGTCCACACTGTTTGAGGGGTCTGTCATTTTAGAAGATCTACATTTCACAGTTAAAAGCATGTTCTGTCTCAGCTAGGATATAAACATACACTGTAAAAAATGCTTGGTTCCATTGGGACTTCATGAAGGATTTAAGTGGATTGAACGTAAAACAAGTAAGTTGTCCCAAAATAACACTAAAATTGTGCTGTATTAGCTCATTTTAAATAAGTAGTTTGAACACACAGCAAAAATAAATAAATAAATAAATAAATAAAAATAAAAATATATAGAGTTGAAGATAGAATTATCAGCCCCCTTTTGATTTTTGATTTTTTTTTCCCAAATGAAGTTTAACAGACCAAGGAAATTTTCACAGTATGTCTGATAATTTTTTTTTTAAATAAGACAAATTTAAATAAGACAAAACATATTTGTTTTATTTCATCTAGAATAAAAGCAGTTTTCAAGATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35321
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000124251 Nonsense 447 450 15 15
ENSDART00000124920 Nonsense 446 1861 14 43
ENSDART00000126984 None None 84 None 4
Genomic Location (Zv9):
Chromosome 12 (position 32262713)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 30483690
GRCz11 12 30598592
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAAGCTCATTTTTCAAAGCTTGCCTTTGCTTGTGTTTGCAGAATAAATA[T/G]AAAGAGAATTACACCAATCACATGAAGGGTCACTATGAAGGGGGCGGCAT
Long Flanking Sequence:
ACATCCCATGAGCCCTCCTACTGAGCCCAGCCGCACATGCACATAAACAAAAACCACATCATTGTTCTATTTTGACCCTCTCACATCTTTTTGGATGCCATGGTGTTTACCTAATAATACTACATCCTCATGCCTCCTGATTTACAAGCAAATGTCAATAGGGCACATGGTTTTCTACATGCAAAGTAAGTGATAGAGACTTAAAATTTCACAATATTATTGCCTACGTGGCCCAAATATTCCCCTATCATACAGGTTGAATACAAGAAGGACCTTGAAACCACCAAAGGCCACAGCATCAACTACTGCGAGACGCCACAGTTCAAGAATGTGTCAAAGATCGCCAAGTATACTAGTGATGTAAGTGCCTCATCAGTGATATGATGGCTAAGAATGACAGGCTGTTCTATATTTGTGCTGTTACTGTGCTGGGAACTTGTGCGGTCATGTGCAAGCTCATTTTTCAAAGCTTGCCTTTGCTTGTGTTTGCAGAATAAATA[T/G]AAAGAGAATTACACCAATCACATGAAGGGTCACTATGAAGGGGGCGGCATCGACAAGAAGACCATGCATGCCATGAATGTCAGAAAGCTTGCCAGTGATGTAAGACAAGAAAATATTTTTGGAACATTTTATTTTTCCTGTGTTTTTTGTTGCCTATGTTTAATTTGAATAAATTAATACAATTCACACAATTGAACGCAATTGAAGTAAATTCTGAGCATTCCATTACTTTTTTTATAAAAATTGCAAATGTTTTTTTTATTATTTTAATTTATTTTGGATACCTTTTTTATAGCAACAAGAATGCATTAAATAATCAAAAGTTGCTAAAGTTTTTATCTATTTATCAAAAATGTAAATACAAATATTACAATTTTAAGCACTTTAAGTGCAGTTTTTTAAATTTTTTTCAACATTTGATTTTAAAATCAAATGTTACTTGAGCAAAAAATATTATGAACACTGACTGGAGTAAACTTTGATTGGAATTATGTTTAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42059
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000124251 None None 450 None 15
ENSDART00000124920 Nonsense 702 1861 20 43
ENSDART00000126984 None None 84 None 4
Genomic Location (Zv9):
Chromosome 12 (position 32265168)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 30486145
GRCz11 12 30601047
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCAAGCTCTGGCCAGTGATCTGGAATATAGGAAGAAGTTACATGATTA[T/G]ACTCTCCTGTCTGATGACATGAAAGTGCAGCAAGCTAAAAAAGCCTACAA
Long Flanking Sequence:
AATCAAGGAATTTCGCTGTTGTGCCTTTTAATAAAGAAAGTGGAATGTTTTTTTAAAGTATACTTATAATGATATACATAAAACAAACAAAAAGTGCTTAGGGGTAGCTTAAATGTTTTGTCGGTGCTCTTTGGGTAAGGGAATTAACAAAAAAAATAATAAAAAACAACGAAAATCAGTCCAAGGCACTCGAAAAATTTGGAAACTTTAAAAAGCCTTTATTCAAATGGCTAATCCTTAAAAACCTATGTGTTTCTAAACAATAAAAAAGCTATCAATATGTACAAAAGTCTTACATAAAGCCCCTTAAACATCCAAAATACAAACCTATACAAAGCCTAACCAATTAAAATTTCTTTAAAATAGGTTGCTTATAAAAAGGATTCTAAGGAAACTCAATCCAAGTGCCACCTGCCTCAGGACATGGTGAATCTGAGTCATGCTAAGAAGGCTCAAGCTCTGGCCAGTGATCTGGAATATAGGAAGAAGTTACATGATTA[T/G]ACTCTCCTGTCTGATGACATGAAAGTGCAGCAAGCTAAAAAAGCCTACAAACTGCAGAGTGACGTAAGTAATGCAAGAACAGAGCGGAATGATACTCATAATGTAACTCTATGTGTTTGCTAAATACTCTAAATCAGTGTTTCCCAACCCTGTTGCTGAAGGCACACCAACAGTACACATTTTCAACCTCTTCCCAATCAAACACATCTGAATCAAGTCATCAGAACATTAGAAGAGACTCCAAAACCTGAAATTAATGGGCCAGATAAGGGAGACACCCAAAACATGTACTGTTGGTGTGCCTTCAGGAACACGGTTGGGAAACACTGCTCTAAATATTACTTTATATATACTATATACTACAGAACCAGTACAGATCAGACCTGAACTGGATGAAAGGAGTTGGATGGGAGGCCGATGGATGCCTAGATGTAGAACAGGCCAAGAAAGCAGGAGAACTCTTCAGTGAGGTTGGTGATCACAGGATTTGCATTACCAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12190
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000124251 None None 450 None 15
ENSDART00000124920 Nonsense 865 1861 25 43
ENSDART00000126984 None None 84 None 4
Genomic Location (Zv9):
Chromosome 12 (position 32266706)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 30487683
GRCz11 12 30602585
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATWCAATCTAAATGATCATTTYTGATGCTTTGTGTATGTAGGTGAAGTA[C/A]AAGCAAAAATMWGAAATGACAAAAGGGAAGATGATTGGCGTGAAGACTGT
Long Flanking Sequence:
AGTGTTACAGTATGTTGAATTATAATTTTTTTAATTATGCACACATTTCATTTATTTAAAAAAAGAGTAAACCCCTTGCCTTAAAATGTTTAAGTCAACTACAGTAATCCGTTCAAAAGCAACCGGTTTACTCCCTTTTTTAGTAAAGTCAACTGATCGCCTTTATAGTGGATACACTGTATTTTGTACCATTAACCTGCACAAGAACTAACAACCCACTTCTGCTTTTAATCAACACATTGGGTTTCTGGTTTTTAGAAAACATATAAGAGTAGTTGGGATGAACAGAGGGAGAAGGGCTTTGAGCTAGGCTTGGACACACTTTCGATTCTCTCTGCCAAAGCAACAAGAGATCTCGCCAGTGATGTGAGTGAACAAGCACCCTACTGAAAGCACATGACTCACTTGCCACTCAATGACACTGGAGCTTTAGGTTCTGTATGGTGACTTAATACAATCTAAATGATCATTTCTGATGCTTTGTGTATGTAGGTGAAGTA[C/A]AAGCAAAAATATGAAATGACAAAAGGGAAGATGATTGGCGTGAAGACTGTGGCAGACGATTCTCAAATGGCCCACTCGACCCATGCTACCAAACTCCACAGTGACCTCAACTACAAGAAACAGTATGAGGACACCAAGACCAAACACAGCGCCTCACTCGATATGTTGACCCTCACCCATGCCAAGAAAGCCCAGGAGCTGGCCACAGAGACAAACTACAAAACATTCTTGCACAAGTACACCATCCTGCCCAGTGATATGAAACTGGAATGGGCCAAGAAAGCCTACGGCTTGCAGAGTGATGTAAGTGTTTTCCCAGATCTCAATTTAATGAAGCGGAAACATGCTCATATATGCATTTGGTTGAAGTATTATGAAACAAACTTTGTTTTGATTGCAGAAAAAGTATCGCTCTGACCTGAACTGGATGAAAGGAGTGGGCTGGGAGACTACTGGATCCCTTGACATACGACAGGCTAGAAAAGCCACAGATTTAGCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12645
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
ENSDART00000124251 None None 450 None 15
ENSDART00000124920 Nonsense 869 1861 25 43
ENSDART00000126984 None None 84 None 4
Genomic Location (Zv9):
Chromosome 12 (position 32266718)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 30487695
GRCz11 12 30602597
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGATCATTTYTGATGCTTTGTGTATGTAGGTGAAGTAMAAGCAAAAATM[T/A]GAAATGACAAAAGGGAAGATGATTGGCGTGAAGACTGTGGCAGACGATTC
Long Flanking Sequence:
TGTTGAATTATAATTTTTTTAATTATGCACACATTTCATTTATTTAAAAAAAGAGTAAACCCCTTGCCTTAAAATGTTTAAGTCAACTACAGTAATCCGTTCAAAAGCAACCGGTTTACTCCCTTTTTTAGTAAAGTCAACTGATCGCCTTTATAGTGGATACACTGTATTTTGTACCATTAACCTGCACAAGAACTAACAACCCACTTCTGCTTTTAATCAACACATTGGGTTTCTGGTTTTTAGAAAACATATAAGAGTAGTTGGGATGAACAGAGGGAGAAGGGCTTTGAGCTAGGCTTGGACACACTTTCGATTCTCTCTGCCAAAGCAACAAGAGATCTCGCCAGTGATGTGAGTGAACAAGCACCCTACTGAAAGCACATGACTCACTTGCCACTCAATGACACTGGAGCTTTAGGTTCTGTATGGTGACTTAATACAATCTAAATGATCATTTCTGATGCTTTGTGTATGTAGGTGAAGTACAAGCAAAAATA[T/A]GAAATGACAAAAGGGAAGATGATTGGCGTGAAGACTGTGGCAGACGATTCTCAAATGGCCCACTCGACCCATGCTACCAAACTCCACAGTGACCTCAACTACAAGAAACAGTATGAGGACACCAAGACCAAACACAGCGCCTCACTCGATATGTTGACCCTCACCCATGCCAAGAAAGCCCAGGAGCTGGCCACAGAGACAAACTACAAAACATTCTTGCACAAGTACACCATCCTGCCCAGTGATATGAAACTGGAATGGGCCAAGAAAGCCTACGGCTTGCAGAGTGATGTAAGTGTTTTCCCAGATCTCAATTTAATGAAGCGGAAACATGCTCATATATGCATTTGGTTGAAGTATTATGAAACAAACTTTGTTTTGATTGCAGAAAAAGTATCGCTCTGACCTGAACTGGATGAAAGGAGTGGGCTGGGAGACTACTGGATCCCTTGACATACGACAGGCTAGAAAAGCCACAGATTTAGCCAGCGAGGTACATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17073
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
ENSDART00000124251 None None 450 None 15
ENSDART00000124920 Essential Splice Site 1106 1861 30 43
ENSDART00000126984 None None 84 None 4
Genomic Location (Zv9):
Chromosome 12 (position 32270148)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 30491125
GRCz11 12 30606027
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTGGWTATCTGTCTGACTATTCATTTGAYTGTACAAATATTTACCTTC[A/T]GCWAAAGTACAARGCGCAGTTTGAAAAGACAAAAGGGAAGATGATTGGGC
Long Flanking Sequence:
GCTCTTTCTATGAATCCATGCATTGAACTGGAAGAAAAAGAGAGATGTTTTTCATTGTAACATGCAAGTTATTATTAATGTTGACAGAGATTGTACAGAGAGAAAGGAGAGAATGAAATGCACAAGTATACAATGATTGGAGATATTCCAGAGCATGTGCAAGCTAAGCTCAACGCCATCAACCTCAGTGAGGTGAGAATCCATTTCACAGCCTCTGTTTCTACTTCAAAGCCTATTGAGCTCATACACAAATGATTGAGTTTCCATATTAAAATGTTAAAACTAAAATTGTTTTCTGTGAAGTCACATTATAAAGAGTCCTGGAAGAAGATCAGAGATGGTGGCTACAAGTTGCGCTTGGATGCTATTCCTTTCCAAGCAGCCAAATCTTCAGCTGAAATCCTCAGTGATGTGAGTGTTTCGCATGCATTTTGGATGAACTACAGTTTATTTTGGATATCTGTCTGACTATTCATTTGACTGTACAAATATTTACCTTC[A/T]GCAAAAGTACAAAGCGCAGTTTGAAAAGACAAAAGGGAAGATGATTGGGCTAAAGGGACTTCAGGATGACATAAACATGGCTCACTCTGTGCATGCCTCTAGCATTCAGAGTGATGTGAGTATTCCAGTGGTTTGATCATTAAAGATGCACGAATATGAGAATCACAGACCAAGTGATTGATCAATTTTCTGTCTTTTAGCTCAAATACAAAAAGGGCTCTTCTGAGGTTCATTCTCAGTTCCATCTACCAATGGATATGTTGGATGTGATCCATGCTAAGAAGGCTCAGTCTCTGGTTAGCGATCAGGACTACAGACATACATTGCACAAGTACACAACACTGCCTGATGACCTCAAAGTGCAGGCTGCAAAGAGAGCTTATGAACTGCAGAGTGAGGTAATAGCCTGTTATATCTGATTTGGTTATTGAATCTCATTGGCCTAGAGAATTCTTCTAAACTGTTGAGTCGACTAAAACGTAATGTGTGTTTGTACAACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35322
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000124251 None None 450 None 15
ENSDART00000124920 Nonsense 1108 1861 30 43
ENSDART00000126984 None None 84 None 4
Genomic Location (Zv9):
Chromosome 12 (position 32270158)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 30491135
GRCz11 12 30606037
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTCTGACTATTCATTTGACTGTACAAATATTTACCTTCAGCAAAAGTA[C/A]AAAGCGCAGTTTGAAAAGACAAAAGGGAAGATGATTGGGCTAAAGGGACT
Long Flanking Sequence:
TGAATCCATGCATTGAACTGGAAGAAAAAGAGAGATGTTTTTCATTGTAACATGCAAGTTATTATTAATGTTGACAGAGATTGTACAGAGAGAAAGGAGAGAATGAAATGCACAAGTATACAATGATTGGAGATATTCCAGAGCATGTGCAAGCTAAGCTCAACGCCATCAACCTCAGTGAGGTGAGAATCCATTTCACAGCCTCTGTTTCTACTTCAAAGCCTATTGAGCTCATACACAAATGATTGAGTTTCCATATTAAAATGTTAAAACTAAAATTGTTTTCTGTGAAGTCACATTATAAAGAGTCCTGGAAGAAGATCAGAGATGGTGGCTACAAGTTGCGCTTGGATGCTATTCCTTTCCAAGCAGCCAAATCTTCAGCTGAAATCCTCAGTGATGTGAGTGTTTCGCATGCATTTTGGATGAACTACAGTTTATTTTGGATATCTGTCTGACTATTCATTTGACTGTACAAATATTTACCTTCAGCAAAAGTA[C/A]AAAGCGCAGTTTGAAAAGACAAAAGGGAAGATGATTGGGCTAAAGGGACTTCAGGATGACATAAACATGGCTCACTCTGTGCATGCCTCTAGCATTCAGAGTGATGTGAGTATTCCAGTGGTTTGATCATTAAAGATGCACGAATATGAGAATCACAGACCAAGTGATTGATCAATTTTCTGTCTTTTAGCTCAAATACAAAAAGGGCTCTTCTGAGGTTCATTCTCAGTTCCATCTACCAATGGATATGTTGGATGTGATCCATGCTAAGAAGGCTCAGTCTCTGGTTAGCGATCAGGACTACAGACATACATTGCACAAGTACACAACACTGCCTGATGACCTCAAAGTGCAGGCTGCAAAGAGAGCTTATGAACTGCAGAGTGAGGTAATAGCCTGTTATATCTGATTTGGTTATTGAATCTCATTGGCCTAGAGAATTCTTCTAAACTGTTGAGTCGACTAAAACGTAATGTGTGTTTGTACAACAGAAAATCTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42060
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:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000124251 None None 450 None 15
ENSDART00000124920 Splice Site, Nonsense 1209 1861 31 43
ENSDART00000126984 None None 84 None 4
Genomic Location (Zv9):
Chromosome 12 (position 32270544)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 30491521
GRCz11 12 30606423
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGATGACCTCAAAGTGCAGGCTGCAAAGAGAGCTTATGAACTGCAGAGT[G/T]AGGTAATAGCCTGTTATATCTGATTTGGTTATTGAATCTCATTGGCCTAG
Long Flanking Sequence:
GAAATCCTCAGTGATGTGAGTGTTTCGCATGCATTTTGGATGAACTACAGTTTATTTTGGATATCTGTCTGACTATTCATTTGACTGTACAAATATTTACCTTCAGCAAAAGTACAAAGCGCAGTTTGAAAAGACAAAAGGGAAGATGATTGGGCTAAAGGGACTTCAGGATGACATAAACATGGCTCACTCTGTGCATGCCTCTAGCATTCAGAGTGATGTGAGTATTCCAGTGGTTTGATCATTAAAGATGCACGAATATGAGAATCACAGACCAAGTGATTGATCAATTTTCTGTCTTTTAGCTCAAATACAAAAAGGGCTCTTCTGAGGTTCATTCTCAGTTCCATCTACCAATGGATATGTTGGATGTGATCCATGCTAAGAAGGCTCAGTCTCTGGTTAGCGATCAGGACTACAGACATACATTGCACAAGTACACAACACTGCCTGATGACCTCAAAGTGCAGGCTGCAAAGAGAGCTTATGAACTGCAGAGT[G/T]AGGTAATAGCCTGTTATATCTGATTTGGTTATTGAATCTCATTGGCCTAGAGAATTCTTCTAAACTGTTGAGTCGACTAAAACGTAATGTGTGTTTGTACAACAGAAAATCTATCGCTCTGATTTGAATTACCTTCGTGGTGCGGCCTGGATCGCTACTGGTGCTCTACAGATTGAAGGATCCAGAAGGGCTACAGATCTAATTAGTGAGGTATGAGTGGCTATAAATTTCAACATTCCAGCTTGGTTGTCTAAAAATTTATAAAGCTTGGTGTCAGATACAGGCGAAATTAAAAAACAAGTTCAATTCAAGTGAAAACTAAATTTATTTCAGGGATTTGAAGCATCTTGCCAAATCAAACATTTCAGAAAAATGTGAGGCTCTGTCTACTTTAATGTGAAAATCTCTAACTACTTTCCTGTTTAGTCCATGGAGGTTAGATGTCCAGAGGTGGGGAAAGTTACTTTTGAAAGTAATGCATTACAATATCAACTAGTTGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22130
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000124251 None None 450 None 15
ENSDART00000124920 Nonsense 1327 1861 35 43
ENSDART00000126984 None None 84 None 4
Genomic Location (Zv9):
Chromosome 12 (position 32273251)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 30494228
GRCz11 12 30609130
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCAGGTTAAGTACAAGGAATCATGGAATGTGCTTCGAGCTCAGGGTTA[T/G]AAACTCACCATGAAGGATATCCCCTTCCAAGCTGCCAAAGCATCCACCAG
Long Flanking Sequence:
CACACATCTGTCACGGATTCTCCAGATATGGTTCATGCCAAGACCAGTAACAAGATCACTAATGAGGTAGGAGGACATCCCCAATTTCGTATCAATCAATATACTATTATACAGTGAAACTCATTCCAATGTTTTCTGCTTTTTAAATTATTTAGCGCTTATATAAAGAAAAGGGGGAGAACTTCAGGCACAACTACACCATTACTGCAGAGAGACCTGAAATCACCCAGGCCAAGATTAACGCTGCTAACTTCAGTGATGTAAGATGAGCCCTCCAAGTCTATTTTTGAGTTTATGGATATTGCTGCATCATAAAATGCACTATTCTAAACTATTCACAATTTATAGTATATTTTAAAAATATTCTTAAGAAGAAATGCTTAAAATGCATTGCAAAAAGTGCACTTGTATCCAAGACGATAGTTGCAAGCTTTTACATTTTCTGTTGTATTTCAGGTTAAGTACAAGGAATCATGGAATGTGCTTCGAGCTCAGGGTTA[T/G]AAACTCACCATGAAGGATATCCCCTTCCAAGCTGCCAAAGCATCCACCAGCATTGCTAGTGATGTAAGAATACCTCATCTAAATTTACACACATAAACATCTATGGGCAAAAACAGCTCTGATAAACGCAATAAGGATGGCTTGCAGTTTATACTTCTATTTGAATACGTTCACTTCCTTTGCCTTGTTAGGTCCAGTACAAGCACAGCCATGCATTAGAGAAGGGCAAGCACATTGGAGTCCGCAGCATTTTGGAGGACTCTCATCTAATGCACTGCCTGGAGATGGGCCGTCTGCAGAGCGACCAGCATTATCGTAAAGACGCCATGTGCACCAGTGGCCAGTATCAGCTGCCTTTAGACATGGTGAACCTGGTTCATGCCAAGAAAGCCCAGGCCTTAGCCAGCGATCAGGATTACAAGACTCAAATTCATTCTTACACAGTCCTGCCTGACGATATAAAGGTGCAGTGGGCCAAAAAGGCATATGAGCTGCAGAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6261
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000124251 None None 450 None 15
ENSDART00000124920 Essential Splice Site 1348 1861 35 43
ENSDART00000126984 None None 84 None 4
Genomic Location (Zv9):
Chromosome 12 (position 32273316)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 30494293
GRCz11 12 30609195
KASP Assay ID:
554-4223.1 (used for ordering genotyping assays)
KASP Sequence:
GGATATCCCCTTCCAAGCTGCCAAAGCATCCACCAGCATTGCTAGTGATG[T/A]AAGAATACCTCATCTAAATTTACACACATAAACATCTATGGGCAAAAACA
Long Flanking Sequence:
GGTAGGAGGACATCCCCAATTTCGTATCAATCAATATACTATTATACAGTGAAACTCATTCCAATGTTTTCTGCTTTTTAAATTATTTAGCGCTTATATAAAGAAAAGGGGGAGAACTTCAGGCACAACTACACCATTACTGCAGAGAGACCTGAAATCACCCAGGCCAAGATTAACGCTGCTAACTTCAGTGATGTAAGATGAGCCCTCCAAGTCTATTTTTGAGTTTATGGATATTGCTGCATCATAAAATGCACTATTCTAAACTATTCACAATTTATAGTATATTTTAAAAATATTCTTAAGAAGAAATGCTTAAAATGCATTGCAAAAAGTGCACTTGTATCCAAGACGATAGTTGCAAGCTTTTACATTTTCTGTTGTATTTCAGGTTAAGTACAAGGAATCATGGAATGTGCTTCGAGCTCAGGGTTATAAACTCACCATGAAGGATATCCCCTTCCAAGCTGCCAAAGCATCCACCAGCATTGCTAGTGATG[T/A]AAGAATACCTCATCTAAATTTACACACATAAACATCTATGGGCAAAAACAGCTCTGATAAACGCAATAAGGATGGCTTGCAGTTTATACTTCTATTTGAATACGTTCACTTCCTTTGCCTTGTTAGGTCCAGTACAAGCACAGCCATGCATTAGAGAAGGGCAAGCACATTGGAGTCCGCAGCATTTTGGAGGACTCTCATCTAATGCACTGCCTGGAGATGGGCCGTCTGCAGAGCGACCAGCATTATCGTAAAGACGCCATGTGCACCAGTGGCCAGTATCAGCTGCCTTTAGACATGGTGAACCTGGTTCATGCCAAGAAAGCCCAGGCCTTAGCCAGCGATCAGGATTACAAGACTCAAATTCATTCTTACACAGTCCTGCCTGACGATATAAAGGTGCAGTGGGCCAAAAAGGCATATGAGCTGCAGAGCCAGGTGAGAAAGAGCGAGATTGTAAAAGATGGTAAATATTATTCTTCATACACAAGAAAATGGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42061
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000124251 None None 450 None 15
ENSDART00000124920 Nonsense 1391 1861 36 43
ENSDART00000126984 None None 84 None 4
Genomic Location (Zv9):
Chromosome 12 (position 32273569)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 30494546
GRCz11 12 30609448
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATGCACTGCCTGGAGATGGGCCGTCTGCAGAGCGACCAGCATTATCGT[A/T]AAGACGCCATGTGCACCAGTGGCCAGTATCAGCTGCCTTTAGACATGGTG
Long Flanking Sequence:
GCACTATTCTAAACTATTCACAATTTATAGTATATTTTAAAAATATTCTTAAGAAGAAATGCTTAAAATGCATTGCAAAAAGTGCACTTGTATCCAAGACGATAGTTGCAAGCTTTTACATTTTCTGTTGTATTTCAGGTTAAGTACAAGGAATCATGGAATGTGCTTCGAGCTCAGGGTTATAAACTCACCATGAAGGATATCCCCTTCCAAGCTGCCAAAGCATCCACCAGCATTGCTAGTGATGTAAGAATACCTCATCTAAATTTACACACATAAACATCTATGGGCAAAAACAGCTCTGATAAACGCAATAAGGATGGCTTGCAGTTTATACTTCTATTTGAATACGTTCACTTCCTTTGCCTTGTTAGGTCCAGTACAAGCACAGCCATGCATTAGAGAAGGGCAAGCACATTGGAGTCCGCAGCATTTTGGAGGACTCTCATCTAATGCACTGCCTGGAGATGGGCCGTCTGCAGAGCGACCAGCATTATCGT[A/T]AAGACGCCATGTGCACCAGTGGCCAGTATCAGCTGCCTTTAGACATGGTGAACCTGGTTCATGCCAAGAAAGCCCAGGCCTTAGCCAGCGATCAGGATTACAAGACTCAAATTCATTCTTACACAGTCCTGCCTGACGATATAAAGGTGCAGTGGGCCAAAAAGGCATATGAGCTGCAGAGCCAGGTGAGAAAGAGCGAGATTGTAAAAGATGGTAAATATTATTCTTCATACACAAGAAAATGGACAGGTCAAAGCATCACAATACAATCCCTATAATTCTTTGTCTTTATACAGAATGTATACAAATCAGATCTGAACTTCATGAAAGGAGTGGCCTGGGATTCAGTCGGCGCACCTCAGCTAGAGTCTGCAAAGAAAGCTGGAGAGCTCATAAGTGATGTAAGTTGTGCTTAATTTCAAAAGTTTTAGGGGCTATATTGGATACTGGTGGTGTCCCATGAAATTAAAATAAAGTATTTAGATGTTAGTATCAGTAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42062
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000124251 None None 450 None 15
ENSDART00000124920 Nonsense 1523 1861 39 43
ENSDART00000126984 None None 84 None 4
Genomic Location (Zv9):
Chromosome 12 (position 32275441)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 30496418
GRCz11 12 30611320
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTTGGGTCATGCGAATAACAAAATTTTTATCTTCTTATAGAGGATGTA[T/G]AAGTCTGGGGACTCTGACTCCATGCACAAATACACATTGCATGCCGATCA
Long Flanking Sequence:
GAGTGTGTTTTTGACAGTGACGTGCAACCATGCTTAATGAGCACTTTGATATGTTAAAAAACAAAGAATACTTCAGTAGGTTTCTTCTCATATTTTGAGAAGGCGTATGTAATGAAACACCCTAAACATTTGTTAAAGAGCCTTTATTTACATTTATCCAGTGATTCTGATCTTATGCTATGTACATGTGTGTGAACATGCCCTCCATTTCTTATAGAACAGCTAGAATTCTGTGTATGCACATTCTGCTTTATCTCAGATGAATTGACTCTTCTTTGCTTTACTGTAACGTCCTGTAGAAGAAGTACCGTCAAAATCCAGACAGTCTGAAGTTCACTCAGGTTGCTGATTCACCTGATATCATCCATGCAAAGAACAGCTACATGCAATGTAGTGAGGTAAAAATCACCTAGCATACTTACTGAACATATAAGTGTGTAGCCAGTGATTGTTTTGGGTCATGCGAATAACAAAATTTTTATCTTCTTATAGAGGATGTA[T/G]AAGTCTGGGGACTCTGACTCCATGCACAAATACACATTGCATGCCGATCATCCTGACTTCATCAGAGCAAGGATCAACGCTCAGCAAATTAGCGATGTAAGCTTGCTGTTATTCTGTGCTCTTACTTTTAGATGAATTACAGTAGCTCCATTTATGTTCCACATCGGTTGAATATTTTGATTGTCAGTGTACATCCTTTAATATTGTCCATGCTCTTTTTCTCTCTCTTTCACTTTGTAGAAAGTGTATAAAACATCAGGTGAGCAGGTGAAGTCTGCAGGTTATGACCTCAGGTTAGATGCCATTCCCTTCCAGACAGCCAAGGCCTCCAGAGAAATTGCAAGTGATGTAAGTCAAAATCAAAACGTTTATCCAACAAACTGCATACCAAACCAATTTCATACTTTTAATTAAAAAGCTGGAGAGCGTGAAATTACCTCTCCTTAGCTTAAGCTTGTAATCATGCTTTTTAATTTTCGTGAGACATGCCATTCTCCATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45465
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000124251 None None 450 None 15
ENSDART00000124920 Nonsense 1698 1861 42 43
ENSDART00000126984 None None 84 None 4
Genomic Location (Zv9):
Chromosome 12 (position 32278783)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 30499760
GRCz11 12 30614662
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCCTCATAAAGCAGGGTTTATTGACTATCTCTGGTTGCAGGTGAACTA[C/A]AAATCAGATCTGAACTGGATTAAAGGTGTGGGCTGGACCCCACCAGGCTC
Long Flanking Sequence:
TTGGGACTTAACATTTGTTGTTCTTTTTTTTCCCCCTCAGTTCCGCTATAAGGAGGCATTTGTCAAAGACAAGGGCCATCAGGTGGGCCTCCTCAGTGTTGAGGACGACCCCAAGATGAGACACTCGCTGGCTGTAGGGAAGCTCCAGAGCAACAATGAGTACAAGAAGCAGTTCAAGGAGACGCGCTCTCAGTTTAAGATCAATGCTGACCTGCCTGAGTTCCAGCACGCTAAGAAGAGCCAAGCTCAGCTAAGCAACATCAACTACCGCCAGCAACTTCATGACTACACCTGCGATCCTAACCAGCTCAATGTCAAACATGCTAAACAAGCCTACCAGCTGCAGAGCGACGTGAGACTGAGCTTTAGATTTATTCTGTTACGCAGATTCTGTTAAATATGTGGAACTTAATTGACAAAATTTAAAAAAAATACATCTTGTTTGGGAATTTTCCTCATAAAGCAGGGTTTATTGACTATCTCTGGTTGCAGGTGAACTA[C/A]AAATCAGATCTGAACTGGATTAAAGGTGTGGGCTGGACCCCACCAGGCTCTCTGAAGGTAGAAATGGCCCGCCGAGCTGCAGAACTGGGCCTTGCCGAAGGAGTAACAACTGACGAGGCTATTGCGCAGTATCAGCAGCTTATGGTAGGAAAACTGTACATTATAACATCTAAATATCTGCACTGTTCCAAAACCTAGATAGCTGCCTTGTTAGTACCTTAGCAACCATAAATTAACAAACTAAACTGCTTTACATAGGCAGCAACTACACAAATAGCAACGGTGAAGTGACTTACAAATGATTTTAATTAAATAAGTGTTAGCACATTGCTAAGTTAACTGTACATTGATTAATTTTTTTTCAGCTTAGTCTCTTTATTAATCAGGGGTCGAACCGCCAACTTATCCAGCATATGTTTTATGCAGTGGATGCCCTTCTAGCTGCAACCATCACTGGGAAACACCTATACAGTACATTCTCATTTACAAACATACACTAC
Associated Phenotype:
Not determined