Busch Lab

ZMP

NBEAL1

Ensembl ID:
ENSDARG00000012524
Description:
neurobeachin-like 1 [Source:HGNC Symbol;Acc:20681]
Human Orthologue:
NBEAL1
Human Description:
neurobeachin-like 1 [Source:HGNC Symbol;Acc:20681]
Mouse Orthologue:
Nbeal1
Mouse Description:
neurobeachin like 1 Gene [Source:MGI Symbol;Acc:MGI:2444343]

Alleles

There are 12 alleles of this gene:

Allele Name Consequence Status Availability
sa38536 Nonsense Mutation detected in F1 DNA Not yet available
sa40626 Nonsense Mutation detected in F1 DNA Not yet available
sa26667 Nonsense Mutation detected in F1 DNA Not yet available
sa45241 Nonsense Mutation detected in F1 DNA Not yet available
sa16584 Nonsense Available for shipment Available now
sa40627 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa25327 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa18594 Nonsense Available for shipment Available now
sa16324 Nonsense Available for shipment Available now
sa26669 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa38536
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
ENSDART00000006221 Nonsense 160 2723 5 53
Genomic Location (Zv9):
Chromosome 6 (position 4155504)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 4124048
GRCz11 6 4284634
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGCAGAAGAGTTTGTCCGTCACGCTCTGGCCTTCTGCGAGAGTCTGTA[T/A]GATCCCTACCACAACTGGAGGCATCGCATTCATGGGTGAGAAAAGCACCG
Long Flanking Sequence:
TCATTTTCTTGTCTTCCTTTTTTCTTTATTTAATTTCTCTTTAAATGTTTTTGTTTTCTTGTCCTTTTTGTTTTCTCCTTATTTTCCTTTTTTATTAATTATATTTTTACTCCTTTATTTTCCTATTTGCACTCCTCTTCCACTTTGTTTTACCATCGTTTCCCTTCTTCTTCTTTTACTTTTTTTTCTTTCCTTTCTTTTTTTTGTTCCTCTCTGTTTCAGGTTTTTCTCTTTCTATTTTCCATTTCCTCTACCTATTTCTTTTCCTTTCTTGTTTTAATTTCTTTTTTTACACCTTTCCCTTTAATTTTCTTCTTATTTCTTCCTCTTTTCCCTTCATTCTTCAGTGTTCTTTTCCTTTTCTTCAGTCATGATGTAGATCCACAACTCGTTTTCCCCTCTCTTTAGCTGAAGAGTAAGACAAAAGAGAAGGAGCTGGCCGATCAGACACAAGCAGAAGAGTTTGTCCGTCACGCTCTGGCCTTCTGCGAGAGTCTGTA[T/A]GATCCCTACCACAACTGGAGGCATCGCATTCATGGGTGAGAAAAGCACCGACAATTAATCCCACAGCTCCGCTTTTCACAAATATCTCCAGAAGTCCTCTTTGACAGAATAAGCTAATAAGCTGAACATCTAATGCATATAGCGCACTCTTATGGAAGCACTTCAGCAGGTCGTCCTCTGATTGGTAACACCACACAGAAACGCCAACTGACCCAGCTGGGACTTGAACCAGCGACCTTCTTGCTGTGAGGTGACAGTGCTAACCACTGAGCCACTGTGTTGCCTCCGGAAGCACTGTTAATCTCTTTGTTAAAGCATGTGCTAATCCAGAAGTTTCCTCATGCATGCCGAATTGAACATTCTTAGGCTGCTAATCTAGAATAAACTGCTGTTGTTTGTGGAGCTTGTTGAATTTGGAAATCAAAATCATTTACTGAGGAGTGAATCATTGACTTTTTTTTAACAAGTAATACATGGTTCTGCTGTAAATGATTTGTCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40626
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
ENSDART00000006221 Nonsense 586 2723 13 53
Genomic Location (Zv9):
Chromosome 6 (position 4173709)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 4143115
GRCz11 6 4303212
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCTTCTGAGGCTCCTGCGTCAGGACGAGCCGGGCCGCGCTCACCCGTA[T/A]GTGGGACCGGTGCTGTGTTCACTGCTGGGGATGGTGCGCAAACAGGGTTT
Long Flanking Sequence:
ATGAAATTGCTGGTTTCCACGTGGTATTAGCAGACTTTTATAACTCTGATAACATGTCAGCCACAGTATGCAATAGCATTTTTGTCATTCTCAGTGGACATCTCACCATCAGACTTTCTCTCTCTTCATCCTCATGTTCATCAGGCTGTTGAAGGAGAGCATTCGTCTGTCGGCCTGCTGGGCATCAGTAACGTGGATCCTCTGCTGCTCCTGATCCAGTGGCTCCCAGAGCTGGACTCTGCCGAGCTGCAGATCTTCACCGCCGACTGGCTCCGGCGTATCTGCGGTCTGAACCGGCGCACGCGAGCCACCTGCGTCAACTCCTGCATGACTGCTGTGGTGCTGTCGGCTCTGGAGAGACACCAGCGGCTGCACCGGGCCTGTGCCGAGAGTCTGGTGGCTCTGCTGGGCTCTCTGGGCAGTCAGTCGCTCAGTTCCTCCGAGCTCCAGCTTCTTCTGAGGCTCCTGCGTCAGGACGAGCCGGGCCGCGCTCACCCGTA[T/A]GTGGGACCGGTGCTGTGTTCACTGCTGGGGATGGTGCGCAAACAGGGTTTGGAAAGTGCCATGCAGTATTTTGATCTGTCACCACCCATGGCTGGCATCGCGGTGCCTACTATCCTCCGCTGGCCAGGCTCCGCCTTCAGCTTTTTTGCTTGGCTGTCATTGGACCAAGATCAGCTGGGCCCGCCCAGCAAAGGAGAAAAGAGGAAGCAGCTGTATAGGTGAGGGTGGAAATCAGCGTTTTAATCTGTATATTCCATGTGTGTATATAAGCTAATGCTAATAAAATACTTGGGTAGTTACTAGGGTAATACTAAGGTAAAGATGCAGTTTTTAAAAACGCTTTATTAGTTTGATAATAATTAAAAAAACATCAAACAGTTGAAAACAGTTGTGCTGCATCATATTTTGTAGAACCTGACCAGTTTTTTTATGAAAGTATAGCAGTATTTATTTAGTTATTTGATTTTTTAATTATAAAAAAAAGCTATTAAATAATTATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26667
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
ENSDART00000006221 Nonsense 830 2723 16 53
Genomic Location (Zv9):
Chromosome 6 (position 4178468)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 4147633
GRCz11 6 4307730
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGTCCCACATCACTGCAGGGCCAGCTGGGCAGTGTTATGGTCTTCCAC[G/T]AGCCGCTGCAGGCCACTCATGTCAAAGCCCTCTGTAGCGCAGGACCAAAC
Long Flanking Sequence:
TGATACTAATGCACACTGTGCGTCTGAAATGGCATACTTCCCTATTATGTAGTATGTAAAAGCAGTTTGTGAGCTGGATTTTACTATCTTTAACATGCAGTGAGTTTGCAGGCTTTAACATACTGCTGTATGAAGTAGGGAAGTATGACAGATCACTTGACAATTGCATATTAATGTAGGGTGAAATATTGCATCAATCACGTTTCTTTCAGTGTTGATGTGTAGATGTTTCCATCTCTCAGGCCTTTACGTCATGCTGTATCGGTTCAGCGGGTCACCGCACCACCACCCCTCCTCCATCTCAGATCCCCGATCCTCCGTTTTCCGGAGCTCATCCATCCGGACGCTCATCCTTCGGCGCCATTCTCCCGGGATGGGGTGGACTGCTGGGCACCAAACCCGAGTCTGTCACCAAACTGATCTCTGCCGGGACGCAGGACAGCGAGTGGGGCAGTCCCACATCACTGCAGGGCCAGCTGGGCAGTGTTATGGTCTTCCAC[G/T]AGCCGCTGCAGGCCACTCATGTCAAAGCCCTCTGTAGCGCAGGACCAAACTGCATCTCGGCCTTCAGGAGTCAGGAGGCGGAGCTGGGAGAGCTGGCACCCAAACTCCTGCTGCACTACTCTCCAAAGGTGATCAGTTTAGCAATAGTGAGCATAAGAAACTTCTTTCAAAAACAGCTGACCACAAAGCTTTGAACTGCAGTGTATATACATGTAAAAATAAAGGGACGGAAATATAAAAATAATAGTTTTATTAACTCTTTCTAATAGCTGGTTTATTTTATCTTTGCCATGATGACAGGACATAATATTTCACGAAATATTTTTCAAGACACTAATATTCATCTTAAAGGTATATTAAGTGTGTTTACACTAGCACGTTTGGTCCGCACCCTGGTTCGTTTGACATCAGAGCACGGTACATTTAGCTAGTCTGAACGTTGTCTTCTGATCTCGGGTGCTTCTGATTTATTTGACCATAGCCTTGCTCTTTTTATTCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45241
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
ENSDART00000006221 Nonsense 879 2723 17 53
Genomic Location (Zv9):
Chromosome 6 (position 4180222)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 4151275
GRCz11 6 4311372
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACTCATCACTGTGCTCTTTAATTCTCAGGCGTGCAGGAACCCCATTTG[T/A]CTGGATTTGTCCCCTAATTTGCTGCACGGTCGCCTGACGGGAAATAAAGT
Long Flanking Sequence:
CTTAACATGTAAATCACTAGCGCTTGACGCGCGTTCCGCATCTGGTGTGAACGCAGCATAACAGCGCCATTGTGCTCCAGTGGTCAGCATGTTGCGTTACGACGTTGTCGATCCATGTTCGATCCTCACCCGAGCAATTCTTTTCTTTTTTTTTTTTCTTTTTATTGTTAAGGCATATAAAACTGTAAGGTTGTTGAACATTTGAATTTCTAAAGGGGGCTAATAATATTGTTTAAATGGTTTTAAAAACAATTCAAATCTGCTTTTATTCTAGCCCAAATAAAACAAATAAGGCCTTTATCCAGAAGAAAAAAATACTATAGAAAATACTCTGAAACCTTCCTTGCTTTGTTAAACATCATTTAAGAAATATTTGAATGGAATTGACAGGAGAGTTAATAATTTAGATGTCAACTCTATATTAGTTACATGTTGGGCGGTTTTAACATTTGACTCATCACTGTGCTCTTTAATTCTCAGGCGTGCAGGAACCCCATTTG[T/A]CTGGATTTGTCCCCTAATTTGCTGCACGGTCGCCTGACGGGAAATAAAGTGGTCAACTGGGATATTAAAGTATGTGTGCTGTTTCCCTGATTTATTTATGATGTCTTTATCTGTCAGATGGTCCAACAGCTGCTCTCAGCGTCTCTCTCTCTCTCTCTGCAGGACATGATTAACTGTGTTGGAGGGATCCCTGTGCTTCTTCCAGTCCTGGAGCAGTTGACCTTATTAAACCCAGATTCAAATCCTGTGGAGCCGTCAGGGTCGGAGTTCATCAGCCCTGACTCCGCAACACCCGCTGATGGAGACTGGGTCATACTGCCCTCCAACAGGGCCTCAGGTGGGCACTGTCACACAAGACAATCCGTGGTTACTGCCATTATTAATAATAAAATTAACTTTTTTTATATATGATTTAAGATTTTATCATATTATAAGGCATTTAAGTTTTGTTATATTTTGATAATGTTGATGCATTGTTTTTATTTGGGGCATTGCTGAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16584
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
ENSDART00000006221 Nonsense 1114 2723 22 53
Genomic Location (Zv9):
Chromosome 6 (position 4183349)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 4154502
GRCz11 6 4314599
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATGCAGATCTGAGTGAGGACGACATCAAGACAATYAGAGCTTCMCTTTA[C/A]GGCCTCCTCAAGTATTACATCAGCAAGGGAACCACTCAAGAGGAGATCCA
Long Flanking Sequence:
TTTAATTTTATTTTATTTTATAAATTATTTATTTATTTAATTTAATTATTATTTAGGTTTAATTTAATTTATTTAAATTTGTTTAGATTTATTTTATTTTTATTTGTTTTATTTAATTATTAATAAATTTTAATTTGATTTAATTTATTTACATTTATTTTATGTTGTTGTTGTTTTTTTGCTGTGAGTTTGAGGATTTGGTTTGCAGTTTGAATGTTTGTGATGTGATTTTTTTTGTTTGTCGTACTGAAGGCCACATCCAGTACACCTCCACCGTCATCAAAGACAGCAGGAAGCAGTTCAGGAAGAAATACGGAGTGCAGTTCCTCCTGGACACAATTCGCCTGTACTATGGGTAAGACTACATCTCCTATAATCCCTCTCTGTGTTCTCTCTTCTACCTATTTCTCTTAACACCTCGTCTCTCTTCATTCCAGTTCAGGAAGTAAAGATGCAGATCTGAGTGAGGACGACATCAAGACAATCAGAGCTTCCCTTTA[C/A]GGCCTCCTCAAGTATTACATCAGCAAGGGAACCACTCAAGAGGAGATCCAGAGCATTCTGGGATACATTGCTGCTATTGGAGATGAAGAACAGGTGAGGTCCAAACTGAACAATCTTGCTTATCTCAAACTTTTGAACAGTCAAATCAAATAGAGTCCATCTGTTAAAATAGAGTTAATACGTTTTCTGCGTCGCACAAAGACACAGTGGTTGGAATCAAAGATCTCAAAATTGGACTCATCAGACCAAATCGCAGTTTTCCATTGGTCTAATGTCCATTCCTTGTGCTCTTAAGCCCAAACAAGTCTCTTCTGCTTGTTGCCTGTCCTTAGCAGTGGATTCCTAGCAAAAACCCTACCATGAAGGCCTGATTCACACAGTCTCCTCTTAACAGTTGTTCTGGAGATGTGTCTGCTGCTTGAACTCTGTGTGGCATTGACCTGAGCTGCTGTTAACCTGTGATTTCTGAGGCTGGTGACTCGGATGAACTTATCCTCCGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40627
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000006221 Essential Splice Site 1145 2723 22 53
Genomic Location (Zv9):
Chromosome 6 (position 4183444)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 4154597
GRCz11 6 4314694
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATCCAGAGCATTCTGGGATACATTGCTGCTATTGGAGATGAAGAACAGG[T/G]GAGGTCCAAACTGAACAATCTTGCTTATCTCAAACTTTTGAACAGTCAAA
Long Flanking Sequence:
ATTTTTATTTGTTTTATTTAATTATTAATAAATTTTAATTTGATTTAATTTATTTACATTTATTTTATGTTGTTGTTGTTTTTTTGCTGTGAGTTTGAGGATTTGGTTTGCAGTTTGAATGTTTGTGATGTGATTTTTTTTGTTTGTCGTACTGAAGGCCACATCCAGTACACCTCCACCGTCATCAAAGACAGCAGGAAGCAGTTCAGGAAGAAATACGGAGTGCAGTTCCTCCTGGACACAATTCGCCTGTACTATGGGTAAGACTACATCTCCTATAATCCCTCTCTGTGTTCTCTCTTCTACCTATTTCTCTTAACACCTCGTCTCTCTTCATTCCAGTTCAGGAAGTAAAGATGCAGATCTGAGTGAGGACGACATCAAGACAATCAGAGCTTCCCTTTACGGCCTCCTCAAGTATTACATCAGCAAGGGAACCACTCAAGAGGAGATCCAGAGCATTCTGGGATACATTGCTGCTATTGGAGATGAAGAACAGG[T/G]GAGGTCCAAACTGAACAATCTTGCTTATCTCAAACTTTTGAACAGTCAAATCAAATAGAGTCCATCTGTTAAAATAGAGTTAATACGTTTTCTGCGTCGCACAAAGACACAGTGGTTGGAATCAAAGATCTCAAAATTGGACTCATCAGACCAAATCGCAGTTTTCCATTGGTCTAATGTCCATTCCTTGTGCTCTTAAGCCCAAACAAGTCTCTTCTGCTTGTTGCCTGTCCTTAGCAGTGGATTCCTAGCAAAAACCCTACCATGAAGGCCTGATTCACACAGTCTCCTCTTAACAGTTGTTCTGGAGATGTGTCTGCTGCTTGAACTCTGTGTGGCATTGACCTGAGCTGCTGTTAACCTGTGATTTCTGAGGCTGGTGACTCGGATGAACTTATCCTCCGCAGCAGAGGTGACTCTTGGTCTTCCTTTTCTAGAGCAGTCCGCATGTTAACCAGTTTCTTTGTAGCGCTTGGTTTTTTTGTGACTGCACTTGGGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25327
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
ENSDART00000006221 Essential Splice Site 1252 2723 24 53
Genomic Location (Zv9):
Chromosome 6 (position 4191209)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 4159405
GRCz11 6 4319502
KASP Assay ID:
554-7780.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCACCTCCACCCTCATCAAGTGCCTCCTTCACCAAGTGCTGTCTACTGG[T/C]CAGTCTCATTCACACTTTAACACTTTAAACCACCCATGTTAGCAATCCCT
Long Flanking Sequence:
TTATAGCACAATGGTGTTCAATGCTGAATACACAAGTGAAGATGCACCTGGCATTGCCTTGATTTTATATTTTTGCATTCTTTAACATTGATTGGACAGATTTCATTTCAGTTGCTTTTTTTGTAGCTCAAAAATTAAACAAAATGTTACGTTAAAATTAGAAATGTTCATCACTGTTGAAGGCATTTGCCCCAACCTTTCCATCATTCTCCCTCTCTTCTCAGATGGGACGGTGGCCCAACTTAAAGGTTGCCATAGGCCAACTTCGGCCTGCTGGCTCTAGTTTGGCCATCTCTGCATTAGGGTGAATCTAGTCCCTCTGTCTTTCTGTCTGTGCAGTTATTTGAGCGGATGCTGAAGTGTGATCGTGTGTACGAGAAGAGCAAGCAGCGGCTGCGATTGAGGGATGTGGGATATTCAGGCCTCAGTCTGCTGTTCTCCGACCTGCACCTCACCTCCACCCTCATCAAGTGCCTCCTTCACCAAGTGCTGTCTACTGG[T/C]CAGTCTCATTCACACTTTAACACTTTAAACCACCCATGTTAGCAATCCCTCTTTTTCGCACAAACCTTTACTAGTACTGATCGATATTGATGTTCATTTTAAGAATTTTGATAACTTTTGAAAGCAGTTTTATGTTTGGCATATACAAATATCATCAAGCGCATACTGCTTTTGCAGAGAACACTGTTTGGTGATAGAGTCACAGTGAATTTGTGAAGTGTTTTTCTCTTTGTCTTGCAGATACTGTGGTGAACTATAAAGATCTGATGGCTGTGGTTCAGCTCACACATAAAGCCGGGCCCAGTGTTCGCCTGACTGTATGCAAGAGGGTAAAAGCATCTTCATTATCATTATCATGTGCACATCACAGCTATTAGTAAAATCAATTAATAAACAAAAGGGTTCTCAGCGTTATTGCAAAAACAAGTCCTGCAAAAAAAAAAGGCAAAATTCTAAGCAAATTTCCAGTTTCCAAGTTCCATGGAATGAACACACACACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18594
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000006221 Nonsense 1437 2723 26 53
Genomic Location (Zv9):
Chromosome 6 (position 4194628)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 4162746
GRCz11 6 4322843
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAGTATGCAGAGCACGCCATMGCCTCTGGAGAACGCCAAACCRTTCCCT[G/T]GAGCTTCCTCTCTCAACGATGACAACTTCCTGTTCAGTGACAACGTGTCC
Long Flanking Sequence:
TATAATTAAATCCTGCATGTTTTATTATTGCGCAGCTGTACACACTGCTTCAGTCTCAGCCGGACGCAGTGCTGCAGATCTCCAAGCAGGTGTGTTGGCAGGGAACTCTGATGCGGCTGTTTGTCCGGAGCCCCGGGAGTGACGGAGGTTCAGGTCGTGGTGACGCTGCCAGTCTGGGGAGTTTGGAACTGAGCCGCAGCAGCGGAGGAAACCGCCTGGAGCCGCCTCTGGAGCGCAGGCCTCTGGGAGACAGCGTAAACCGGCTGAACGAAGAGCGGGACAGTGTTTCAGACAGCAGGTCTATAGACAGCCTGGATAACGGAGAGCTCATGTCTCTGTCTGACACGCCGGTGGAAGCACACACACCTAAAACCTGGCCAGGGAAAGCAGGAGTGCTGAGTCTGGATCTGTCCCAGCTGGATCGCGGGGATAGCGGCAGTCAGACTCCTGGCAGTATGCAGAGCACGCCATCGCCTCTGGAGAACGCCAAACCGTTCCCT[G/T]GAGCTTCCTCTCTCAACGATGACAACTTCCTGTTCAGTGACAACGTGTCCCTGGGGGAGTCGTTTAACAGCGAGGTGAGTCTGGAGAACTGGTTGTGATGCGTCACTTAATACAATTACTGTTTTGTAGGATTTTACACCATTTAACTCAAAGTAACTAATAATGGAGTAGTGAATTTCTATAGTTGTAAAGAAAATTATTAGCCCTCTGAGTTTTAATTATTTATCAAATCTTTCCCAAGTGCTTATTAACAGAGATCCATTTTAATCCAAAACACTTTAAAAGCTAGTGCTGTCAAAAGAATACTCACAATTAATCAAATCCAAAAGAAAAGCTTGTATTTATTAAAATAAATAAATTAATTATATACAGTTTATATAATATAACATAATCGTAAGAGCAACAAATAATACTCCTAGTTGATCATTTGGAAAGTGGCAGAAGGTGGATTTTTCTGATGAATCATCTGTTGATCTTCATTCCAATCATCACAAATACGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16324
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
ENSDART00000006221 Nonsense 2237 2723 42 53
Genomic Location (Zv9):
Chromosome 6 (position 4222282)
KASP Assay ID:
2259-7066.1 (used for ordering genotyping assays)
KASP Sequence:
GTGTGTGTGTGTGTGCGTGTGCGTGTGCGTGTGTGTGTGTGTTTAGGAAT[C/A]AGAGTTYGTGTCRGCTCATCTGCATGAGTGGATCGATCTGAKCTTCGGTT
Long Flanking Sequence:
ACTGCAGTTAACCATACAGGGAGCAGATGGCACTCTAGGCTAGTTTTTAAACAGCCAATGGTGCTCTAGGTGAGTTTATACCAGCAGCGAGCACTCTACACTAGCTTTTACTGCAAATGACGCTGTAGCCTAGTTTTTAACTGTACGCTTCTATAGTTAATAGCATTTGTGTGTTTGGCTGACTCATGTAAGTTGGCTTTTATGTCACGTGATTAATGTAAACGCAGCTCACTGTTAATAATTTTGTAATTCACGTAAACCTTTCCCAACTTCCTTAATGATTATTTTATGTTCAAGTGTATTTGTAAGGGGTTGTATGCAAGCGGTGTACGGCTGTTTGTAAAGTAAAGCCTACTGCACAATCTGATATCCTGGATGTGTCTAATGTGTGCGTGTGTGTGCGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGCGTGTGCGTGTGTGTGTGTGTTTAGGAAT[C/A]AGAGTTTGTGTCGGCTCATCTGCATGAGTGGATCGATCTGATCTTCGGTTATAAACAGCGGGGCCCGGCGGCAGTGGAGGCCCTTAATGTCTTCTACTACTGCACATATGAAGGTATAAGAAGTCTGTCACAGTCATAAACATACAGGTCTTAGGAAATTGCTTGGTTTTGGTGACACATTTGTTTTACAGTGTTTCTTTAAGTTGTAATAACTAATTTATTTTATTCTAGCCATGATGACTGTACATAATATTCTTATAGTCTTCATCTATAAATGAGAGCGTCTGTGGTTGTTTTAGGGGCTGTTGATCTGGATGCCATCACAGATGAGAAGGAGAGGAAAGCTGTAGAAGGCATGATCAGTAACTTCGGACAGACGCCGTGCCAATTACTGAAGGTACCACACTCTCATCTATCTCCAACATAAACATCTACAGTACACTTTAATTTAATAAAAAAAAAGAGTTCATATATATATATATATTTACATACAATCCTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26669
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
ENSDART00000006221 Essential Splice Site 2690 2723 52 53
Genomic Location (Zv9):
Chromosome 6 (position 4233037)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 4200042
GRCz11 6 4360139
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGGAGGACGGCAAGCTGATCGTGGTGGGCGTCGGGAAACCAGCGGAGG[T/C]AAAAAACTCCTTCAGGAACTACATCACCCAGCGGATGGAGGGCTCGCCTC
Long Flanking Sequence:
GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTCAGGATAAGAACGCTCTGCACCTGTACTCTGTGAACGGAAAGCACCTATGCAGCTCTTCTCTGAAGGAGCAGGTGACGGACATGTGTGTTTCAGGAGAGCATGTGGTCATCGGCAGCGAGCAGGGCTTTCTCTCCGTCAGAGATCTCTACAGGTAATCTCACACAACACACTAAAATCAGCAGATTCATTCCCTGAAGCCAGATGGATATGTGCTGTTAATACAAAGATTGTCTGACAAATAACATTGAGGGAGGTGTGTTCTCTCCTCATGTCAGCCTGAGTCTGTGTGTGTCACCGATGGCCATGCGGGTGCCCATTCGCTGCGTCTCTGTGACCAAGGAGCAGTCTCACGTGCTTGTGGGACTGGAGGACGGCAAGCTGATCGTGGTGGGCGTCGGGAAACCAGCGGAGG[T/C]AAAAAACTCCTTCAGGAACTACATCACCCAGCGGATGGAGGGCTCGCCTCTTATGAACACGCTGCGGGTGCGATCGCCCGCACGCCTGCTACATCTCCGAGACCAGAACACATTCAGCCCTGACTTCATCTGACACAAACACACACACACACTTATCTGATTTAAGCTAAGGTTAATTTACCTAAATGGGCACTACTTATTTGAACTTAAAAAAATAACTCCCGTTAACCAAATAAGTAAAGAACAAATGCATATTTAGATTAAAAGAACTTCTATTTTGCTTATTTATTTTTTTGAAGACCATACATTCAGATTAAATCAGATTTAGCTAAACACACACACACACACACACACACACACACACAAACATGTTAACGTAATAACAAAATAATTATGAAAACGATTTTTCTTTTTAAACTTGGGCATTCGTTGTATAATCAGTGGTAATTGTGTGACGTCTAAATGTTGTTTACTATACTATGTTTGCTGTTTTTTTTTAA
Associated Phenotype:
Not determined