ZMP
ttnb
Ensembl ID:
ZFIN ID:
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.
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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.
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.
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.
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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.
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.
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.
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