Busch Lab

ZMP

ttnb

Ensembl ID:
ENSDARG00000091908
ZFIN ID:
ZDB-GENE-030616-413
Description:
Novel protein similar to H.sapiens TTN, titin (TTN) [Source:UniProtKB/TrEMBL;Acc:B0S6Y0]
Human Orthologue:
TTN
Human Description:
titin [Source:HGNC Symbol;Acc:12403]
Mouse Orthologue:
Ttn
Mouse Description:
titin Gene [Source:MGI Symbol;Acc:MGI:98864]

Alleles

There are 23 alleles of this gene:

Allele Name Consequence Status Availability
sa41523 Nonsense Mutation detected in F1 DNA Not yet available
sa16157 Essential Splice Site Available for shipment Available now
sa34739 Nonsense Mutation detected in F1 DNA Not yet available
sa14252 Essential Splice Site Available for shipment Available now
sa529 Nonsense Confirmed mutation in F2 line Not yet available
sa11847 Nonsense Available for shipment Available now
sa17611 Nonsense Available for shipment Available now
sa41522 Nonsense Mutation detected in F1 DNA Not yet available
sa15669 Nonsense Available for shipment Available now
sa41521 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa16201 Essential Splice Site Available for shipment Available now
sa41520 Nonsense Mutation detected in F1 DNA Not yet available
sa2520 Nonsense F2 line generated Not yet available
sa9015 Nonsense Mutation detected in F1 DNA Not yet available
sa44712 Nonsense Mutation detected in F1 DNA Not yet available
sa21570 Nonsense Available for shipment Available now
sa41519 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa7211 Nonsense Confirmed mutation in F2 line Not yet available
sa34738 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa41523
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
ENSDART00000000908 Nonsense 196 5618 4 53
ENSDART00000141122 Nonsense 196 5618 5 54
ENSDART00000144779 None None 497 None 8
Genomic Location (Zv9):
Chromosome 9 (position 43943850)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 43069020
GRCz11 9 42870807
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACATATTCAATTTCTATATGTTTATTGTTACTTTCTTTTCATTTCAGGT[G/T]AGGAAGTTGCAGTGCCTGCAAAGAAGACTAAGACTTTTGTTTCAACTTCT
Long Flanking Sequence:
GCTGAACTGCTGGCTACAGGTAAGCAGCCGTTTAATAAAGTAAATCTGTGTACTTTTCTGCCAGTTTCTATCATGCAAACGCTATTTCTTTGCTTGCCTCACAGCGGAAACTGCTCCACCAAACTTCATTCAGAGACTTCAGAGTGTAACTGTTACACAAGGGAGCCAAGTGAGATTGGATGTTCGAGTTACAGGAATCCCTACACCTGTGGTGAAGTTCTACAGAGAGGGAGCCGAGATTCAGAGCTCCGCTGACTTTCAGATTGTTCAAGATGGAGACCTTTACAGTTTGTTGATTGCTGAGGCCTTTCCAGAGGATTCTGGAACCTATTCTGTCAGTGCTTCTAACAGCAGCGGACGCACTACCTCTAACGCTGAACTTCTGGTTCAAGGTTTGATTTGGTTTCACCCAAATTTCACTTGTCATTTTATAATAAAGTTCATAATATAAACATATTCAATTTCTATATGTTTATTGTTACTTTCTTTTCATTTCAGGT[G/T]AGGAAGTTGCAGTGCCTGCAAAGAAGACTAAGACTTTTGTTTCAACTTCTGAAATTTCACAGACTCGCCAGGCTAGGGTTGAAAAGGTAGTCAACATCCACACACAATTACACTTGAAACTGACAGCCAAAGACCATGGTTACTTAGTTTAATGTGTTCTTCACAGAGAGTGGAGGCCTCCTTTGAGTCCACAACCTCAATGGAAATGCTGATAGAGGATGGTGATTTGGCTCATAAGGCACCACCTCGTGTGCCTCCAAAGCCAACCTCCAAGTCCCCAACTCCACCAATAGGAGTGTCAAAGGTCGCAGCTCCACGCCATCAGTCACCCTCTCCTGTGAGGCCTGTTAAAGCTCCTGCTCACACACCTCACAGGTGAAGTATATTTTTCATTGTGAATACAATTTATTAGTTGATACCTTAAGCTACCAAGACTTGCACGAGTGCACATTTTGCAAATAAGAAAAAGTATTGATAATGGAGAGTAATATCTTTCTTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16157
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
ENSDART00000000908 Essential Splice Site 483 5618 8 53
ENSDART00000141122 Essential Splice Site 483 5618 9 54
ENSDART00000144779 None None 497 None 8
Genomic Location (Zv9):
Chromosome 9 (position 43939505)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 43064675
GRCz11 9 42866462
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACAAGTGAGGCTGGAACTATCAGCACCTCCTGCTACCTGCTYGTCAAAG[G/A]TAACAAATCATAAAATATGATTTGGCTTTAAACAAAACTATCTCTGCAAT
Long Flanking Sequence:
TGCTATACAGTTTGAGACTGCAGCAATCCCATCTATCACAAAAGAGCAAGTGATGCCGCCAACTATAGTAGCTGTGAGTAAATTATCACTATTTCCTCATTCATTTACTACACATAAAATGTGTTGTTTCAAAGATTTGCAAATTACAGAGTACTCTTTCAGTATTTACTATTTGTAATAGATCTCAGATATCCTGCAAGTAATTTCCTTGCATTTTGAAATTATTTTCTGCTTTGTCCAGGCTTTGAAGAATGTGACTGTCACAGAGGGGGAAACTGTTGCTCTGGAATGCCAGATTTCAGGTTACCCCACTCCAGCCATTATGTGGTTCAGAGAAGATTACAGAATCGAGAACTCCATTGACTTCCAGATCACTTATGAAAAAAGTTATGCCCGCTTGATGATTCGTGAGGCCTTTGCTGAAGATAGTGGCCGCTTCACTTGCACTGCTACAAGTGAGGCTGGAACTATCAGCACCTCCTGCTACCTGCTTGTCAAAG[G/A]TAACAAATCATAAAATATGATTTGGCTTTAAACAAAACTATCTCTGCAATTACAGATTAATTTTTTTTACCTATTTTCATCTTCAGTCTCAGAAGAAATTGAAAGTCGTGAAGATTTCTCTAATGTCCCTGAGCACGTTGAAATGTCTGCTCAACAAAGACAGTAAGTTGATCAAATTCTTGGTATTGTAGTATTATAATAATTAATATAGGAATTTGCAATCTTACGTATTGATGTTTAACAAACAGGGGTGCAATTGAAGCCAAAGAGGAGACCATGTCTGAAATAAGTGCTGTCTCTGAACCTGTGGAGGCTGGTGCTGGTGCTGCTCCATTCTTTGTGAAGAAACCCACAGTGCAAAAGCTTGTGGAGGGAGATAGAGTAGTCTTTGATTGCCAGGTCGGAGGTACCCCTAAGCCTCATATTTACTGGAAAAAGAGTGGAATTCCTCTTACTACTGGATACAGGTACGTTTTATATAGTACATATTTTGCACATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34739
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
ENSDART00000000908 Nonsense 686 5618 12 53
ENSDART00000141122 Nonsense 686 5618 13 54
ENSDART00000144779 None None 497 None 8
Genomic Location (Zv9):
Chromosome 9 (position 43937705)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 43062875
GRCz11 9 42864662
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCAGAGATTCATCCAAGAAGTTGAGTTTCACCTACTCAAGATTACCTA[T/A]CAGGAGCTGGTGACTGAGGATGGGGAACAGCTGGATATGAGTGTTCCTGA
Long Flanking Sequence:
CAGGAGAGTACACCGTTTTTGCTAGAAACCCACTTGGAGAATCCTCTGCTTCAGCCATACTGCTTGATGAAGGTTGTATTTTTTTGGTGATCAATGTTTTGAGACATTAGAAGAATAGAAATGTTAATGTATGTATTCTTTTCGAAATGTTTAGAGTCATATGACCAATATGTGAAGAAACAGGAAGATCATTTCAAGACAGAAGTGCCTACTATTGCAGAGGAGCCAAAAGTTGCTGATGTACCTGCTGCTTTTGAAACAGTAACCGAGAAAGACCAATTGCTCATGCAGAGGAGAATGGCTCAACAAACCCAGATGATGCAGTCTTTCATTTCAGAACAGGTATGAAATTCTTTAAGCTGCTCAACCTCCTGTTAAAATGTTAAATTGAAAAGATTTATATGAGCCTTACAATGGCTTTTCTTGAAGGAGTTACAGATGTCTAGCTTGGAGCAGAGATTCATCCAAGAAGTTGAGTTTCACCTACTCAAGATTACCTA[T/A]CAGGAGCTGGTGACTGAGGATGGGGAACAGCTGGATATGAGTGTTCCTGAACATGATGCTGTTTCTCCTGTCTTTAATACTCCGGTTAAAGGTTACAGACTTAGGGAGGGAATGAGTGCAACATTCCATTGTAGGATGTCAGGAACCCCCCTACCTAAGGTAAGCTTGAATCATGATATATTTACATTTATTAAAATCATCAATACTTGGCCAAACCAATTAGCAAACCTGACCTATCATTATATTATTTGAACAATAGATTGTGTGGTACAAAGATGGCAAGCGCATCATACATGGAGGCCGCTATCAGATGGAGGTTCTGCGGGATGGTAGAGCCAGTCTGCGCCTTCCTACTGTGCTTGCAGAAGATGAGGCTGTCTACACTGCTTTGATCAGTAACATAAAGGGTAATGCTGTCAGCTCTGGAAAGCTGTATGTGGAGTCAGCTGGTGTAGCACAAACACAGCTTTCTCAGCCAGGGGCAGTTCAAAGAATCAGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14252
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
ENSDART00000000908 Essential Splice Site 889 5618 15 53
ENSDART00000141122 Essential Splice Site 889 5618 16 54
ENSDART00000144779 None None 497 None 8
ENSDART00000000908 Essential Splice Site 889 5618 15 53
ENSDART00000141122 Essential Splice Site 889 5618 16 54
ENSDART00000144779 None None 497 None 8
Genomic Location (Zv9):
Chromosome 9 (position 43936834)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 43062004
GRCz11 9 42863791
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATTACAATTTTATTGCAATATAGTGGCAACTATATATATTTTTCATTTC[A/T]GGACAACAAGTGGTCAATGACTACACTCACAAGATYGTGGTMAAGGAGGA
Long Flanking Sequence:
GAGGCTGTCTACACTGCTTTGATCAGTAACATAAAGGGTAATGCTGTCAGCTCTGGAAAGCTGTATGTGGAGTCAGCTGGTGTAGCACAAACACAGCTTTCTCAGCCAGGGGCAGTTCAAAGAATCAGGTAGGTTCTGAAAAATATTAGGTATATTAATATTAGGTTGCAATACTGCCACAGCAAATTTTATTCTGTTGCTCTTCTCAGGTCTACATCACCACGCTCCACAAGTCGTTCTCCTGGCCGTTCTCCTTCTCGTAGGCTTGACGAGACAGATGAGGCGCAGCTAGAAAGACTCTACAAGCCAGTGTTTGTACAGAAGCCCTCATCCGTTAAGTGCTCTGAGGGACAGACAGCAAGATTTGATCTGAAAGTAGTTGGAAGACCCATGCCAGAAACTTACTGGTTCCACAATGGTTAGTGTTCTGCAACTCAGTTTTTTTAGCTGCATTACAATTTTATTGCAATATAGTGGCAACTATATATATTTTTCATTTC[A/T]GGACAACAAGTGGTCAATGACTACACTCACAAGATCGTGGTCAAGGAGGATGGAACTCAGTCAATGATTGTGGTTCCTGCCATGCCTCTGGACTCTGGAGAATGGACAGTTGTTGCTCAAAACAGAGCTGGAAAGACAACTGTTTCTATGACTCTCACTGTTGAAGGTATTGTTTAGTTTGAAGAATAATGTTTTGTGTGACAGTCACTTCAGGCAAATGTGATGAAATAATTCTAATTAAATCTTACATTGTTGTAATTTTCAGCCAAGGAAAACTTGGTGAGACCACAGTTTGTTGAGAAGCTACGAAACATCAGCGTTAAAGAGGGTACTTTGGTTGAGCTAGCTGTTAAAGCCATTGGCAATCCTCTTCCTGACATTGTTTGGCTGAAGAATAGTGATATCATCTCCCCACACAAACATCCACATATTAGGTATGTTTTCAGTCATTAAAATAAACAGGTTTATGATAAATATTGCTCCCAGTAATGAAAAACTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa529
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000000908 Nonsense 1206 5618 17 53
ENSDART00000141122 Nonsense 1206 5618 18 54
ENSDART00000144779 None None 497 None 8
Genomic Location (Zv9):
Chromosome 9 (position 43935677)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 43060847
GRCz11 9 42862634
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAAGATGAGAAAAGCCTTGTTGAGGAAACTCAATTGCCAGAGGGAAGG[C/T]GAGGGCAAAGAATAGATGAAATAGAGCGTATTGCTCATGAGGGTGGTCCT
Long Flanking Sequence:
GAGTTAATGTTGAGGTGGATGCAGTAAAGCCTCAGCCTGAGAAAAAGCTTGTCATTCCAAAGGGAACCTACAAGGCTAAAGAAATTGCTGCACCAGAATTAGAACCACTACATCTTCGCTATGGTCAGGAACAGTGGGAAGACGGTGACCTCTATGATAAGGAGAAGCAACAGAAGCCACACTTCAAAAAGAAGCTTACATCAGTCAGGCTGAAGCGATTTGGACCTGCACACTTTGAGTGTAGATTGACCCCTATTGGTGACCCGACCATGATTGTTGAGTGGCTGCATGATGGCAAGCCATTGGCAGCTGCTAACAGGCTACGCATGGTCAATGAGTTTGGCTATTGCAGTCTTGATTATGAAGCTGCTTATTCAAGAGATAGTGGTGTCATCACTTGCAGAGCCACCAATAAGTTTGGAGTTGACCAGACCTCTGCTACACTAATTGTTAAAGATGAGAAAAGCCTTGTTGAGGAAACTCAATTGCCAGAGGGAAGG[C/T]GAGGGCAAAGAATAGATGAAATAGAGCGTATTGCTCATGAGGGTGGTCCTTCTGGAGTCACTGGAGATGATAACCTTGAGAAGACTAAACCAGAAATTGTGTTACTTCCAGAACCAGTAAGAGTTATGGAGGGGGAGACAGCTAAATTCCGCTGTAGGGTGACTGGATACCCTACTCCGAAAGTCAACTGGTATCTCAATGGACTGCTTATCCGCAAAAGTAAAAGATTTAGGCTTCAATTTGATGGTATTCACTACTTGGAAATTGTAGACACCAAGTCTTATGATTCAGGAGATGTCAAAGTTTCTGCTGAAAACCCTGAAGGGGTTACTGAGCATGTTGTGAAATTTGAGATCCAGCAGAAAGAGGACTTCAGATCAATCCTGCGCCGTGCTCCTGAATTTAAAGCTCCTGCTCCTGCACCATCACAAGAGCATGGTAGAGTTTCATTTGAGGTTGTCAAAGCTGAGAAATCAGCTGACACCTCTAAAGAACCCAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11847
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000000908 Nonsense 1570 5618 18 53
ENSDART00000141122 Nonsense 1570 5618 19 54
ENSDART00000144779 None None 497 None 8
Genomic Location (Zv9):
Chromosome 9 (position 43934500)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 43059670
GRCz11 9 42861457
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCCTRSATRGATTTCAGTCATTATTTTTTNCTTCTGTTTTTTAGGCAAA[C/T]AAGTTGTTACATTCACACAACTTTTAGAAGATCAGAGTGCTAAAGAGAAG
Long Flanking Sequence:
GAGAAAAGAAAAACTTCTCCATCACACCAAAGAACTTGGTCCCGAAGCTGAGAAGAAGAAAGAGGAGGAGGCTAAACTCTCTATTTCCAAACCCAAACCAGAGAAAATTGTGCTCTCTCCAAGCATGGAAGCTCCAAAGATCATTGAACGGATCCAGAGCCAGACAGTTGGTCTTGGAGATGAAGTACACTTTCGTTGTAGAGTCACTGGTAAACCAGACCCTGAATGTCAATGGTTTAAGAATGGTATTCTATTGGAGAAGTCAGACCGGGTTTACTGGTATTGGCCAGAGGACCATGTCTGTGAATTAGTAATCAAAAATGTCTTAGCTGAGGATTCTGCTAGTGTAATGGTCAAAGCCATGAACATTGTTGGAGAGACCTCAAGCCATGCTTTCTTGCTGGTTCAAGGTAAAAGCTTTTTCTTACTTGTTGTTTGTATAGTATTTGTGTCCTACATAGATTTCAGTCATTATTTTTTTCTTCTGTTTTTTAGGCAAA[C/T]AAGTTGTTACATTCACACAACTTTTAGAAGATCAGAGTGCTAAAGAGAAGGACACCATGGTGACTTTTGAGTGTGAGACAAACGAACCATTTGTCAAGGTCAAATGGATGAAGAACAACGCAGAGATTTTCTCTGGTGACAAATACAGAATGCACTCCGACCGAAAGGTGCACTTCCTGTCAGTGCTGATTATTACTATGAATGACGAAGCAGAATACAGTTGTGTGGTTGTTGATGATGACCAAATAAGAACCAGTGCGTCACTCTATGTTGAAGGTTTGTACAACACATACACTACAATGTTGTAACTTCTTGGTTATCTGGTAAAGAGACACATACTTAATTATTTGGTCATTTGATGTTTTAATCAGGTGCACCACTTGAAATAGTAAAGAATCTTGAGAATACAGAAGTACCTGAGACATACTCTGGAGAGTTTGAATGTGTATTGTCCCGCGAGGATGCTGAAGGCACCTGGTATTTTGAGAACAAAGAAATCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17611
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000000908 Nonsense 1849 5618 21 53
ENSDART00000141122 Nonsense 1849 5618 22 54
ENSDART00000144779 None None 497 None 8

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 43933247)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 43058417
GRCz11 9 42860204
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTTAGTAATCACTTTGTTTCATACACAGCTWTTGGCTTCTTGACACCAT[T/G]AAAAGATGTATCCACTGTGGAAGGGACTAAAGCTGTCCTTGAGGCTAAAA
Long Flanking Sequence:
TGGATAATCAACGCAAATAGTTTAATATTACAAGTCATTTTAATCTTATTTGCATGTTTTTCTATCACTCCAGTGCGTCCTGTTACTCTGCTGCAAGGTCTTTCTGACTTGACAATCTGTGAGGGTGATATCGCACAACTTGAGGTGCGATTCTCTCAGGAAAATGTTGAGGGCTCATGGATGAAGAATGGTCAGGCCATCTCTGCTTCCAATAAGATTCACATGGTCATTGACAAAGTTACCCATAAGCTTCTCATTGAGGATGCTACTAAGGATGATGGAGGAATGTACTCATTTGTTGTTCCTGCTCAGGACATTTCTACAAACGGAAAACTGATAGTTCAGAGTAAGCCAGCTTTACATCTATCAATGAATATTCAATGGATTTTTAAAGTTTATTTTGAATTCTTACATTTTTAAAGTACATGCTACATTGTGAGGACAGTGACTGGTTAGTAATCACTTTGTTTCATACACAGCTATTGGCTTCTTGACACCAT[T/G]AAAAGATGTATCCACTGTGGAAGGGACTAAAGCTGTCCTTGAGGCTAAAATCTCTGCAACTGATATCACTTCAATAAAATGGTTCCAAAATGACAAGCTGGTGACAGCTAGTGATAGAGTCCAGATGGTTGTCAAAGGATCCAAACAGAGACTGGCCATTAATCGAACTTATGCATCAGATGAAGGACAGTATAAACTGATTGCTGGAAAAGTAGACTCAACATGTAAACTTTCTGTCGAGCGTGAGTATCATTTCAAAATACTTGCATTTCCTTAGTTTTGGTTAAATGAATTTTAAAATGGGTGGTAATGATTGTATTGTTAATTATGTTTTATAGCTGTAGCTATCATTAAGCACATGGAAGACTGCGTTTGCACTGAGACCCAGAATGTGACTTTTGAAGTAGAGGTTTCTCATCCTGGCATTGACGCTCTCTGGACTTTCAAGGGTCAAGCTTTAAAGGCAGGCCCAAAATACAAGATCGAGAGCAAAGGTACAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41522
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
ENSDART00000000908 Nonsense 1908 5618 21 53
ENSDART00000141122 Nonsense 1908 5618 22 54
ENSDART00000144779 None None 497 None 8

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 43933070)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 43058240
GRCz11 9 42860027
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTTGTCAAAGGATCCAAACAGAGACTGGCCATTAATCGAACTTATGCAT[C/A]AGATGAAGGACAGTATAAACTGATTGCTGGAAAAGTAGACTCAACATGTA
Long Flanking Sequence:
TGGATGAAGAATGGTCAGGCCATCTCTGCTTCCAATAAGATTCACATGGTCATTGACAAAGTTACCCATAAGCTTCTCATTGAGGATGCTACTAAGGATGATGGAGGAATGTACTCATTTGTTGTTCCTGCTCAGGACATTTCTACAAACGGAAAACTGATAGTTCAGAGTAAGCCAGCTTTACATCTATCAATGAATATTCAATGGATTTTTAAAGTTTATTTTGAATTCTTACATTTTTAAAGTACATGCTACATTGTGAGGACAGTGACTGGTTAGTAATCACTTTGTTTCATACACAGCTATTGGCTTCTTGACACCATTAAAAGATGTATCCACTGTGGAAGGGACTAAAGCTGTCCTTGAGGCTAAAATCTCTGCAACTGATATCACTTCAATAAAATGGTTCCAAAATGACAAGCTGGTGACAGCTAGTGATAGAGTCCAGATGGTTGTCAAAGGATCCAAACAGAGACTGGCCATTAATCGAACTTATGCAT[C/A]AGATGAAGGACAGTATAAACTGATTGCTGGAAAAGTAGACTCAACATGTAAACTTTCTGTCGAGCGTGAGTATCATTTCAAAATACTTGCATTTCCTTAGTTTTGGTTAAATGAATTTTAAAATGGGTGGTAATGATTGTATTGTTAATTATGTTTTATAGCTGTAGCTATCATTAAGCACATGGAAGACTGCGTTTGCACTGAGACCCAGAATGTGACTTTTGAAGTAGAGGTTTCTCATCCTGGCATTGACGCTCTCTGGACTTTCAAGGGTCAAGCTTTAAAGGCAGGCCCAAAATACAAGATCGAGAGCAAAGGTACACACTATAGTCTTACTGTTTTGAATGCCATGAAGGATGAAGAAGGGGAGTACGTGTTTATGGCTGGTGAGAAGGAATCCAGAGCAAGGCTGATTGTATCAGGTAAGCAGGCATTCAAACTTAATTTTAACACCAAAGTACTTTCTGTTTTTCCATGCATAATATGGGAATCATGTCACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15669
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
ENSDART00000000908 Nonsense 1929 5618 21 53
ENSDART00000141122 Nonsense 1929 5618 22 54
ENSDART00000144779 None None 497 None 8

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 43933008)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 43058178
GRCz11 9 42859965
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTATAAACTGATTGCTGGAAAAGTAGACTCAACATGTAAACTTTCTGTC[G/T]AGCGTGAGTATCWTTTMAAAATACTTGCMTTTCCTTAGTTTTGGTTAAAT
Long Flanking Sequence:
TACCCATAAGCTTCTCATTGAGGATGCTACTAAGGATGATGGAGGAATGTACTCATTTGTTGTTCCTGCTCAGGACATTTCTACAAACGGAAAACTGATAGTTCAGAGTAAGCCAGCTTTACATCTATCAATGAATATTCAATGGATTTTTAAAGTTTATTTTGAATTCTTACATTTTTAAAGTACATGCTACATTGTGAGGACAGTGACTGGTTAGTAATCACTTTGTTTCATACACAGCTATTGGCTTCTTGACACCATTAAAAGATGTATCCACTGTGGAAGGGACTAAAGCTGTCCTTGAGGCTAAAATCTCTGCAACTGATATCACTTCAATAAAATGGTTCCAAAATGACAAGCTGGTGACAGCTAGTGATAGAGTCCAGATGGTTGTCAAAGGATCCAAACAGAGACTGGCCATTAATCGAACTTATGCATCAGATGAAGGACAGTATAAACTGATTGCTGGAAAAGTAGACTCAACATGTAAACTTTCTGTC[G/T]AGCGTGAGTATCATTTCAAAATACTTGCATTTCCTTAGTTTTGGTTAAATGAATTTTAAAATGGGTGGTAATGATTGTATTGTTAATTATGTTTTATAGCTGTAGCTATCATTAAGCACATGGAAGACTGCGTTTGCACTGAGACCCAGAATGTGACTTTTGAAGTAGAGGTTTCTCATCCTGGCATTGACGCTCTCTGGACTTTCAAGGGTCAAGCTTTAAAGGCAGGCCCAAAATACAAGATCGAGAGCAAAGGTACACACTATAGTCTTACTGTTTTGAATGCCATGAAGGATGAAGAAGGGGAGTACGTGTTTATGGCTGGTGAGAAGGAATCCAGAGCAAGGCTGATTGTATCAGGTAAGCAGGCATTCAAACTTAATTTTAACACCAAAGTACTTTCTGTTTTTCCATGCATAATATGGGAATCATGTCACAGACTGGAGTTTTTATGTTGAATTTTCTTTGCTCCACTAGGCGGTGCTATAAACAGGCCACTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41521
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
ENSDART00000000908 Essential Splice Site 2103 5618 23 53
ENSDART00000141122 Essential Splice Site 2103 5618 24 54
ENSDART00000144779 None None 497 None 8

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 43932269)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 43057439
GRCz11 9 42859226
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCTACCAGGTGGCAAATTCCAAGACATCTGGCAATCTGAAGGTTGAAG[G/A]TAAACTGCTTGGCCTTTGCAAAAAGATTTATCTTCCTCACTTATTAGAGG
Long Flanking Sequence:
CAAGATCGAGAGCAAAGGTACACACTATAGTCTTACTGTTTTGAATGCCATGAAGGATGAAGAAGGGGAGTACGTGTTTATGGCTGGTGAGAAGGAATCCAGAGCAAGGCTGATTGTATCAGGTAAGCAGGCATTCAAACTTAATTTTAACACCAAAGTACTTTCTGTTTTTCCATGCATAATATGGGAATCATGTCACAGACTGGAGTTTTTATGTTGAATTTTCTTTGCTCCACTAGGCGGTGCTATAAACAGGCCACTTCATGATGTGACAGTAGCCGAATCCCAGACTTCTGTTCTGGAATGTGAAGTTGCTAATCCTACAACAGAAGGCAAATGGCTTAAAGATGGCAACCCTGTTGACTTCAGCGATAATATCCTAAGTGAAAATAATGGTGCTGTCAGACAGCTTGTGATTGTCATCACCAGGCCACAGGATGTTGGAGAGTACACCTACCAGGTGGCAAATTCCAAGACATCTGGCAATCTGAAGGTTGAAG[G/A]TAAACTGCTTGGCCTTTGCAAAAAGATTTATCTTCCTCACTTATTAGAGGTGTAGATATTAATTTGTAATTTTGTTTTCAAGCTGTGAAAATCAGGAAGACAATGAAGAACCAAACCGTGACTGAGACCCAGGAGGCAGTATTCAGTATTGAACTCACCCATTCAGATGTAAAAGGATCCCAATGGATCAAGAATGGTGTTGAGATTCATCCAAGTGACAAATTTGATATAACAATCGATGGCATGGTTCACACCTTGAAGATCAAGAACTGCAACACTCAAGATGAATCAGTTTATGGGTTTAAACTTGGAAAACTCTCTGCTAACGCCAGACTGAATGTTGAAAGTATGTTTTAATTTATCTGTCAAATATATAGTTACATAAATTTGTTTCTTTTTATTAGATGCATATTAATACTCTCTTACCTTTTTTTGTAGCTATCAAAATTGTGAAGAAACCAAAGGATGTGACTTCTCTGCTGGGTGCCACTGCCTCATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16201
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
ENSDART00000000908 Essential Splice Site 2192 5618 None 53
ENSDART00000141122 Essential Splice Site 2192 5618 None 54
ENSDART00000144779 None None 497 None 8

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 43931921)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 43057091
GRCz11 9 42858878
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGTTTAAACTTGGAAAACTCTCTGCTAACGCCAGACTGAATGTTGAAAG[T/A]ATGTTTTAATTTATCTGTCAAATATATAGTTACATAAATTTGTTTCTTTT
Long Flanking Sequence:
TGGCAACCCTGTTGACTTCAGCGATAATATCCTAAGTGAAAATAATGGTGCTGTCAGACAGCTTGTGATTGTCATCACCAGGCCACAGGATGTTGGAGAGTACACCTACCAGGTGGCAAATTCCAAGACATCTGGCAATCTGAAGGTTGAAGGTAAACTGCTTGGCCTTTGCAAAAAGATTTATCTTCCTCACTTATTAGAGGTGTAGATATTAATTTGTAATTTTGTTTTCAAGCTGTGAAAATCAGGAAGACAATGAAGAACCAAACCGTGACTGAGACCCAGGAGGCAGTATTCAGTATTGAACTCACCCATTCAGATGTAAAAGGATCCCAATGGATCAAGAATGGTGTTGAGATTCATCCAAGTGACAAATTTGATATAACAATCGATGGCATGGTTCACACCTTGAAGATCAAGAACTGCAACACTCAAGATGAATCAGTTTATGGGTTTAAACTTGGAAAACTCTCTGCTAACGCCAGACTGAATGTTGAAAG[T/A]ATGTTTTAATTTATCTGTCAAATATATAGTTACATAAATTTGTTTCTTTTTATTAGATGCATATTAATACTCTCTTACCTTTTTTTGTAGCTATCAAAATTGTGAAGAAACCAAAGGATGTGACTTCTCTGCTGGGTGCCACTGCCTCATTTGAGCTCAGTTTGTCCCACGATGACATTCCAGTTAAATGGATGTTAAACAATCAGGAGCTCACAACAAGTTCAAATATTAAAATACTGTCTGAGAGAAAAGCCCACAAACTTATTATTCAGAGTGTTGAAAGTGACTTGGCAGGTGAATACATTGCTGTGATTGGACACCTGCAGTGCAGTGCACATCTTCAAGTTGAACGTAAGTATAAGCAACCTTTTTAAGTAGTGTTGACCTAAATTTGACTTTCTAAAGTGGTGTAATCTCTCTCGCATTCAGATCTGAGAGTCACCAGACCTCTGAAGAACATTGAGGTTCCAGAGACCCATGTGGCCACGTTTGAGTGTGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41520
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
ENSDART00000000908 Nonsense 2227 5618 25 53
ENSDART00000141122 Nonsense 2227 5618 26 54
ENSDART00000144779 None None 497 None 8

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 43931725)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 43056895
GRCz11 9 42858682
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCATTTGAGCTCAGTTTGTCCCACGATGACATTCCAGTTAAATGGATGT[T/G]AAACAATCAGGAGCTCACAACAAGTTCAAATATTAAAATACTGTCTGAGA
Long Flanking Sequence:
TTAGAGGTGTAGATATTAATTTGTAATTTTGTTTTCAAGCTGTGAAAATCAGGAAGACAATGAAGAACCAAACCGTGACTGAGACCCAGGAGGCAGTATTCAGTATTGAACTCACCCATTCAGATGTAAAAGGATCCCAATGGATCAAGAATGGTGTTGAGATTCATCCAAGTGACAAATTTGATATAACAATCGATGGCATGGTTCACACCTTGAAGATCAAGAACTGCAACACTCAAGATGAATCAGTTTATGGGTTTAAACTTGGAAAACTCTCTGCTAACGCCAGACTGAATGTTGAAAGTATGTTTTAATTTATCTGTCAAATATATAGTTACATAAATTTGTTTCTTTTTATTAGATGCATATTAATACTCTCTTACCTTTTTTTGTAGCTATCAAAATTGTGAAGAAACCAAAGGATGTGACTTCTCTGCTGGGTGCCACTGCCTCATTTGAGCTCAGTTTGTCCCACGATGACATTCCAGTTAAATGGATGT[T/G]AAACAATCAGGAGCTCACAACAAGTTCAAATATTAAAATACTGTCTGAGAGAAAAGCCCACAAACTTATTATTCAGAGTGTTGAAAGTGACTTGGCAGGTGAATACATTGCTGTGATTGGACACCTGCAGTGCAGTGCACATCTTCAAGTTGAACGTAAGTATAAGCAACCTTTTTAAGTAGTGTTGACCTAAATTTGACTTTCTAAAGTGGTGTAATCTCTCTCGCATTCAGATCTGAGAGTCACCAGACCTCTGAAGAACATTGAGGTTCCAGAGACCCATGTGGCCACGTTTGAGTGTGAAGTTTCACATTTCAATGTTCCATCTGCCTGGCTGAAAAATGGAGTTGAGATTGAGATGAGCGAGAAGTTTGGAATTGTGGTGCAGGGCAAAATTCATCAGCTGAAAGTCATGAACGTCAGCCAGGAGGATGTTTCAGAATACACATTTATATGTGGAAATGACAAAGTTTCTGCTAATCTGACTGTAAAACGTAAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2520
Status:
F2 line generated
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
ENSDART00000000908 Nonsense 3632 5618 36 53
ENSDART00000141122 Nonsense 3632 5618 37 54
ENSDART00000144779 None None 497 None 8
ENSDART00000000908 Nonsense 3632 5618 36 53
ENSDART00000141122 Nonsense 3632 5618 37 54
ENSDART00000144779 None None 497 None 8

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 43923879)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 43049049
GRCz11 9 42850836
KASP Assay ID:
554-3282.1 (used for ordering genotyping assays)
KASP Sequence:
CTTCAGAGCTAGCAACCGTGAATTCCACTCAATGTTTGGTAGAAAAGGAA[C/T]AAACCAAACCAGTGCTTGCATCAGTCAGTGATACTAAGCACACTCTTTTA
Long Flanking Sequence:
ATGTAAAACCTGCCTCTGCACAGACAACACCAACATTGGCAACTTCTCTAAAACAGCTGCATATGACTGCAATGACCTCTGCCGTTCAAGAAAACCAAGGATTTACTGAACAGCACTGTTATAGGATCGCTAGTCCAGAAGTCAGGCAGCTCGAATTGAGTGTTGAGGAGTCCTCAAATCTTATGTCTGCCGTTTCAGAAAGTATTACACCTCTTTGTATAGTAAAATCTGAGGATCTGATAAAAAGTGAGAAAGAAAAGCTGCACGCAACTTTTGAGCAGGAGGTTATAGTTAGTGGTCCTCAAGTTGAAATGAAGTTGCCAATTCCACAAGAGCAATGCATACAAATTAAAAGTCCCGAAGAGGAGAAAAGCTACAGTGTCACCGAAGGAGTTAAGTTATTATATACTGCAACCTCGTCAGAGAATGTAGTGCTTGCAGAAGTTCATACTTCAGAGCTAGCAACCGTGAATTCCACTCAATGTTTGGTAGAAAAGGAA[C/T]AAACCAAACCAGTGCTTGCATCAGTCAGTGATACTAAGCACACTCTTTTAAAAGAGGAAATCTTTGAAATGCATAGACCAGTAGAGGAAACTGCTAAGCTATCTAAAGATCCAATAATAAAATCAGCTCTGATTTCTCAAGAAAATAAAGAGTTTCAAGCTGACAAAGCCACTGAAATACCTGTCCTGGAGCAACCAATCTCAGTCTGTTCCCAGAAGCAATTGAATCAGGTACTTCATTTACAGCTTATCAGTGACCAAGAGACTTTTCTGTCTGAGGGAAGATTTACAAGTGAGAAGCTTGGATTGGAGCATACAGATGTCAGAAAAGTGGCACTTCATTTGCACGCAGTTTCCACTGATGACCAGAAAACCGCTAGTTGTGAACATGTAACACAGTTTGCATCCAATGATAGCACAATGGTTGGAATGCCCAAGGAAGAGCTTCCTGCACAATTACATCTTCCCTTTGCACAGTCAAAAATAATGTTAAGTAAAGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9015
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
ENSDART00000000908 Nonsense 3828 5618 36 53
ENSDART00000141122 Nonsense 3828 5618 37 54
ENSDART00000144779 None None 497 None 8

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 43923291)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 43048461
GRCz11 9 42850248
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATCCAGAGACAAGAAAAAGACCGTAAATGTCTAGCAATCAAAGAAGAG[C/T]GAGTAGAACTAACTTCAGATCATRTCAAAGACCTTGATATGAWGGTAGAA
Long Flanking Sequence:
AAACTGCTAAGCTATCTAAAGATCCAATAATAAAATCAGCTCTGATTTCTCAAGAAAATAAAGAGTTTCAAGCTGACAAAGCCACTGAAATACCTGTCCTGGAGCAACCAATCTCAGTCTGTTCCCAGAAGCAATTGAATCAGGTACTTCATTTACAGCTTATCAGTGACCAAGAGACTTTTCTGTCTGAGGGAAGATTTACAAGTGAGAAGCTTGGATTGGAGCATACAGATGTCAGAAAAGTGGCACTTCATTTGCACGCAGTTTCCACTGATGACCAGAAAACCGCTAGTTGTGAACATGTAACACAGTTTGCATCCAATGATAGCACAATGGTTGGAATGCCCAAGGAAGAGCTTCCTGCACAATTACATCTTCCCTTTGCACAGTCAAAAATAATGTTAAGTAAAGAGGGGATACTTTCAATTGAAAAGCCAGATGAACGGAAAGCCATCCAGAGACAAGAAAAAGACCGTAAATGTCTAGCAATCAAAGAAGAG[C/T]GAGTAGAACTAACTTCAGATCATGTCAAAGACCTTGATATGATGGTAGAAGGTCTTAAGATTGATCACAAAACAGAAGCTAAACCCTTGAGTGTTCTTCAGGTTGTCTCGCAGCCTGTTTTGCTCTTAAAGGAAAGCCCTATTGTCAGTAAAGTCAAACCGCATAGTGCAGTTGTGCAGAAAGAGGATTGGTGGAATAACATGCATGCAGCATCTATGTCTGTGTCTCATGCTATAGAAGAGGGTCTTACAGACAGTTTCCAAGCAGTTGATAAATTCAATTGTATGGCAGATGTAGAGCCAAAAATACCGGTTCAGCCTATTCATGTAGAAGAAAAAGCCATTTCAACAGAAAGTTGTCTTGCTCTTGAGGCTGCAGAGCAAGACTTTGCAGTTCAGATTCAAGAAGGTCAATCTGTAAGGCAGTCAATACATGTGGAGGAAAAACATACCCTGACAGGTGAAACGTCTCAGGGATTTACCAGATCAGAGGAGGGTAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44712
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
ENSDART00000000908 Nonsense 4038 5618 36 53
ENSDART00000141122 Nonsense 4038 5617 37 54
ENSDART00000144779 None None 497 None 8

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 43922660)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 43047830
GRCz11 9 42849617
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTGTAATTCCTGCACCAAAATCTCACAGCTTGGACATCAAACAACAGT[T/A]GAAAATGACGCTTAAGTCTGCCGTAGCTTGTGATCAGCCTTTAATTTTGG
Long Flanking Sequence:
GGAAAGCCCTATTGTCAGTAAAGTCAAACCGCATAGTGCAGTTGTGCAGAAAGAGGATTGGTGGAATAACATGCATGCAGCATCTATGTCTGTGTCTCATGCTATAGAAGAGGGTCTTACAGACAGTTTCCAAGCAGTTGATAAATTCAATTGTATGGCAGATGTAGAGCCAAAAATACCGGTTCAGCCTATTCATGTAGAAGAAAAAGCCATTTCAACAGAAAGTTGTCTTGCTCTTGAGGCTGCAGAGCAAGACTTTGCAGTTCAGATTCAAGAAGGTCAATCTGTAAGGCAGTCAATACATGTGGAGGAAAAACATACCCTGACAGGTGAAACGTCTCAGGGATTTACCAGATCAGAGGAGGGTAAAATAAACATTACAAGTCAGCCATTAGAACCTATTTTGGTAAGCGAATCTCAGGAAAGCAGAACTCTTCCAAAGGAGCTTACTTTTGTAATTCCTGCACCAAAATCTCACAGCTTGGACATCAAACAACAGT[T/A]GAAAATGACGCTTAAGTCTGCCGTAGCTTGTGATCAGCCTTTAATTTTGGCAGATGTTGTGCAAAGTTTAGGAGTTGTTGAAGTAATGGAGGTCAAGGTGCGGATGGAATTGAAATCTATGATGTTCACTTACCTTATCACAACAGCTGGCCCACCCATGGAAATTACAATTGCCTTGGAGGGAGAATACCCTCAGATGGCAACTCTTAAAAATGAGCTTCATGCTGCATTTTACTCTATGCTTAATGAAGAGAGGCCCATCTTCATGTCTGAAGATTCAAACATCTTAACACTTGACAGACCTGAGAGACTGCATGTTAACAAAGCATCTTCATATCCTTTATCCTCAGCTGTTATATCAGAGAAGGTAGAAGTATTTGCAACACCGAAGATGCAATCTGCTGTTCTACAAACAGAATCTGAAATATTGTCCCAATCTGCATTGGTTCAAAAGCCTACTTCTATTATTGAGTCAAGTCACCATGAAACTCAGAAGACTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21570
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
ENSDART00000000908 Nonsense 4222 5618 36 53
ENSDART00000141122 Nonsense 4222 5618 37 54
ENSDART00000144779 None None 497 None 8

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 43922109)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 43047279
GRCz11 9 42849066
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAATCCAAAATGGAGAGCTACAGTATCATTGAAACTGAACATAAAAGT[G/T]AAATGAAATTAGGATCAGTCGAATATTTTAAGAGAGATGTGTGTGTTTCA
Long Flanking Sequence:
CAGATGTTGTGCAAAGTTTAGGAGTTGTTGAAGTAATGGAGGTCAAGGTGCGGATGGAATTGAAATCTATGATGTTCACTTACCTTATCACAACAGCTGGCCCACCCATGGAAATTACAATTGCCTTGGAGGGAGAATACCCTCAGATGGCAACTCTTAAAAATGAGCTTCATGCTGCATTTTACTCTATGCTTAATGAAGAGAGGCCCATCTTCATGTCTGAAGATTCAAACATCTTAACACTTGACAGACCTGAGAGACTGCATGTTAACAAAGCATCTTCATATCCTTTATCCTCAGCTGTTATATCAGAGAAGGTAGAAGTATTTGCAACACCGAAGATGCAATCTGCTGTTCTACAAACAGAATCTGAAATATTGTCCCAATCTGCATTGGTTCAAAAGCCTACTTCTATTATTGAGTCAAGTCACCATGAAACTCAGAAGACTGCTGAATCCAAAATGGAGAGCTACAGTATCATTGAAACTGAACATAAAAGT[G/T]AAATGAAATTAGGATCAGTCGAATATTTTAAGAGAGATGTGTGTGTTTCAGATTTAACAGTTGATGTTCATCCCAGTCAGATCACTGTTGAAGAGTCAATAAATGTTCTTGATCAGGAAGACAAAGGAGGATGGGGTTTAACAGAGGATGTTTCAATTAAGCAACAACCTAAAGAGCTGTTTTTTGAAAAAACATTAAACAACATTACCGCAGAGGAGAATTCGAAGGTTACATTTTCTGTAAGAATAAAAGGTGTAAAAAGTGTGAACTGGCTTTTCAATGGAGTATTAATCAAGTCTGGCAAAGAGTTCAAATGTTTAAAGGACAATGACTCTTACACACTCGTAATCAACAAAGTTATAAGGACAAAACATGAAGGCGAATATACCTGTGAAGCTGTGAGTGAAGCTGGCAAGATTTCATCATCATCAAGGCTCACGGTTTTCTCAAGAGGTTGGACTGTGTGGATTTTGTCATATTTGACACGATAAATAATTCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41519
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
ENSDART00000000908 Essential Splice Site 4566 5618 39 53
ENSDART00000141122 Essential Splice Site 4566 5618 40 54
ENSDART00000144779 None None 497 None 8

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 43916977)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 43042147
GRCz11 9 42843934
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATGCCTTCGGAAGAGAAATTTGCCATGCTACTGTGACTGCAGTGACTG[G/A]TTTGTATACTAGGATTTCGGTAATGCTGTATATATTTTATTTGATGATTC
Long Flanking Sequence:
ATGTCAGTGTTCTTCAAAAAAAAAAAACTGTCATCCTTTAAATCACATGATGGTTACTTTGTTGAACATGCATTTCTGTAATCATGACCTTGCATTGAAATACTTTAGGCTCATTATGGTGAACAGATATAATGCCTTCGGAAACAAAATTTTATATCTTCAATCTCCCATTTTTAGAAATATAACCTCAGCTGTACTGTTTCTCACAGCATCAGAACCAGCCCGCTTTTTGAGGAAACTGAGCAACATTTCCATCCCAATGAGCCAAAAGTTGAGACTTGAGTGCAAATTCACTGGAGACCGGAAATTGTTTGTGACCTGGTACAAAGATGGCAAACAACTCTATGCATCGTACAGATACAATACAACAGTCACAGATAACTCCTGCACACTGGAAAGCCTTCAAGAATGTGACAACACCACCACAGGGATATATTCGTGTGAAGTTTCAAATGCCTTCGGAAGAGAAATTTGCCATGCTACTGTGACTGCAGTGACTG[G/A]TTTGTATACTAGGATTTCGGTAATGCTGTATATATTTTATTTGATGATTCTTTAGGTAATTATTTTGAGCTTTTCAATTTTAAAGAAAGTTATTAGTAATTATAACCTCAAAAATGGAAATCAGACTGTAAATGAAACAGAAACAGGGTTGTAAATTATTTCCTAGACTAAAGCCTCTTAATCCTCTTCACTTCAGAACCTGCCCGCTTTGTGAAGAAGTTGACAGATTTATCTATTCCAATGAGCCAAAAACTAAGGCTTGAATGCACATTCACTGGAGCTCCAAAATTGTTTGTTACTTGGTACAAGGATGGCAAACAGCTCTATGCATCCTATCGATACAACACCAGAGTTACAGCAAACTCCTGCATCCTGGAGTGTCTTCATGAGTGCAACAATGAGACTACAGGAAGATACTCATGTGAAATTTCAAACATTTATGGAACGGATAAATGTGATGCTCAAGTAGTGGCAGTCACAGGTTTGTAATTATGCTGCAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7211
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
ENSDART00000000908 Nonsense 4990 5618 44 53
ENSDART00000141122 Nonsense 4990 5618 45 54
ENSDART00000144779 None None 497 None 8

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 43913682)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 43038852
GRCz11 9 42840639
KASP Assay ID:
554-5183.1 (used for ordering genotyping assays)
KASP Sequence:
GGAATTGGAAAAATCTTTGTMACWTGGTACAAGGATGGCAAACAGGCCTA[T/A]GCTTCATATAGATGCAACACAAAAGTTATCGGAAACACTTGCGTTTTGGA
Long Flanking Sequence:
AGTCGCCATGAGCAAAAACCTGAAGCTTGAGTGCACATTTACCGGAGCTCCTAAAATTTTTGTCACCTGGTACAAGGATGGCAAACAACTCTATGCCTCTTATAGATATAATACTACAGTTGTTGGAAACACCTGCACTCTAGAGTGTCTACATGAATGCACTAAAGAAACTCCTGGAAAATACTCATGCGAGGTGTCTAATTCTTATGGAAAGGATATTTGTCATGCTGAAGTGACCACTTTTTCCGGTTAGTACATTTTTAAAAGGCTCTTTATCCAAAAAGATAATTAGTGTTGGACGGTTTCATGTTGTTTCCTTAAAAGAAGGCAGTATTTTGCAAGGATGTTCATATGGTGTTGTTCCTCTTAGGACCTGCTCGTTTTGTGAAGACACTCACTGACCAGAGTCTTCAGCAGGGACAAAAGCTGAGGCTTGAGGCCTCCTTCAAAGGAATTGGAAAAATCTTTGTCACTTGGTACAAGGATGGCAAACAGGCCTA[T/A]GCTTCATATAGATGCAACACAAAAGTTATCGGAAACACTTGCGTTTTGGAATATCTTCATGAGTGTGATGAGAATACTCCTGGAAAATACTCTTGTGAGGTTATGAATGAAGATGGTTCGGATATTTGTCATGCGCTGGTTACCCTTGGGACAGGTTCGTTGGATGCTATTAATTTGAGTGTTTGCAAATCAGTAATCAGTTTTTCTATTTTTTACCATAACTTTCTAGATGCTCCGTTTCGTCCTCAAAGACTTCTTTAATCCCATAAAGAAATTTTTTTTCTAGATGTAAAATCCAAATGAAACACTGGAGTCATTAACAGAGGAAATCATTCCAAATGAATGAAAACATTTAATATTTGGTTAATAATATTATCATATTTTTTTATAACTAATATTTATCCATACTGAATTAGCTTAGTTTTTATTTATTTATTTATTTTTCATTTTTATTGTTTTACATTTTAACTAATTTTCAAAGCAGCACTTGCTCACTTAAG
Associated Phenotype:
This allele has been associated with this phenotype by genetic linkage analysis and may not be causal.
See FAQs for more info.
Stage Entity Quality Tag
Larval:Day 4
ZFS:0000036		 larval locomotory behavior
GO:0008345		 disrupted
PATO:0001507		 abnormal
PATO:0000460

Mutation Details

Allele Name:
sa34738
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
ENSDART00000000908 None None 5618 None 53
ENSDART00000141122 None None 5618 None 54
ENSDART00000144779 Nonsense 363 497 3 8

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 43903412)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 43028582
GRCz11 9 42830369
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCCCTCAGACATCACCGGTAGTGATGCCAAAGGAAACTGAAACAAAGT[T/A]GAAGGAAGAGCGTAACGCACTTGAAAGAGGTAAAGATTATAATCTTCAGC
Long Flanking Sequence:
TGTAGAAGACATGCCTTCTCAACTTGAGGATTTATTTTTTCATCATGAGCATGTTGTAAAGGTGGATGCAAGTCATCACAGTACAGAATCACCATCTGACAATTTGAGGATAGTTGAAACAGAGCTTCGCCAGAAGCCAGAACCTTCTTTTGAACTAATAAAAACAGAAGAGATTTCTGAGATGAAACAGACCAAACAAGAAATCCTCATTGAGAAAAAGGAAAGGAAATTAGAGACATCTACTATTGAAACCTCTCCAGAAACTGTGGTGAAACCCAACATTAAGGCACCATTAAAAAAGCATGACACTGTGGCAGATAAAAAGAAAATGGCTAAAAATGTCTCTTTGCAAAACATAGACGATAGCCCAAGAAAAGAAATGGCCATTCAGAGAGAAATAGAAGTTCATATGCAAGAATATGTTCATGAAAACAAGAGATACCAGGAAGAAACCCCTCAGACATCACCGGTAGTGATGCCAAAGGAAACTGAAACAAAGT[T/A]GAAGGAAGAGCGTAACGCACTTGAAAGAGGTAAAGATTATAATCTTCAGCAAATGCCTCAAATGGTATATTGCAGTCTTTACTTGATTTTATTTGCCTTCAGGTATTTGCCGAATAGGCAATTGTGATTTAGTTTTATCTGTCTTTATACATTGCACTTGCATTAGCAAGTTCTTCTTTAGTGTCTTTTATCTTAAATATGTCAAAATTCTTAATTAGATGAGAAGACCCAGGCTGTGTCAGAACTTGTTTCAGAAGTTGTATCAGCTAAAAAAGGTACATAACGGAGGGCTGTGAGAATTGGTGCTATTTCTCTTTAGTTCTTAAATCAGTGTGTGATAATGTGTTTGTAAAATTATCTATACATTTTATTTCTTGATTGTGACCATGGTTTACTTATTTTATTTAAAGAATCAGAAATAGTGAGGAAACCTGAACCAGATGTTCTTAAGCCAGCTGTGGCTCCAGTTGAACAGAACACATCACTCCCACAAAAAGGTA
Associated Phenotype:
Not determined