ZMP
syne2b
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens SYNE1, spectrin repeat containing, nuclear envelope 1 (SYNE1) [So
Human Orthologue:
SYNE2
Human Description:
spectrin repeat containing, nuclear envelope 2 [Source:HGNC Symbol;Acc:17084]
Mouse Orthologue:
Syne2
Mouse Description:
synaptic nuclear envelope 2 Gene [Source:MGI Symbol;Acc:MGI:2449316]
Alleles
There are 48 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22358 | Nonsense | Available for shipment | Available now |
sa31955 | Essential Splice Site | Available for shipment | Available now |
sa31954 | Nonsense | Available for shipment | Available now |
sa22357 | Nonsense | Available for shipment | Available now |
sa16388 | Nonsense | Available for shipment | Available now |
sa13694 | Essential Splice Site | Available for shipment | Available now |
sa11835 | Essential Splice Site | Available for shipment | Available now |
sa16245 | Nonsense | Available for shipment | Available now |
sa22356 | Nonsense | Available for shipment | Available now |
sa9847 | Nonsense | Available for shipment | Available now |
sa16713 | Nonsense | Available for shipment | Available now |
sa11394 | Essential Splice Site | Available for shipment | Available now |
sa22354 | Nonsense | Available for shipment | Available now |
sa22353 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22358
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 242 | 9778 | 8 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | Nonsense | 213 | 281 | 6 | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37646582)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37123394 |
GRCz11 | 13 | 37249284 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCGATACTTCATGCTCTAAGGCCAAATATAGTTGACCTAACCAGAGCT[C/T]GAACAAGAACAAACAGACAAAACCTGGAGGAAGCCTTCCACATTGCTGAG
Long Flanking Sequence:
AATATTAAGATTTCATTATTTATAAATACAAACACTCATGGTGAGTAATTGTCAGTTTTGGTGTTTGATTTTTCTGCTGTGTCTTCTATATTGTTTAGATTGAAGAATTGGCCAGCACATTGTCCTTCAGCTCCCGTCAGTCTTCTCTGGAGTCGCTGGCGAGTTTGGACACTCGTTCGACCAACAGCAGTGCCCGCAGCAGTCCAGTGCCACCCCGTGGTTCACCCTTACATGCCCGTTTTCGCGTATCAGCCAAGAAAGCCCTGCTGCTGTGGGTCAGAGAGCAGTGCCAGCGGTGAGGAACAATCTGCTTCAATAAATTGATGGGAACGGACAAATTCTGAACCTGTACTGTGAAACCTATCATCTCATGTTTGTTTTTTCTCAGGGCTGGATGTACTCTGAATGTGAAGGATTTCAAGGTGAGCTGGAGGAGTGGAGTTGTGTTTTTGGCGATACTTCATGCTCTAAGGCCAAATATAGTTGACCTAACCAGAGCT[C/T]GAACAAGAACAAACAGACAAAACCTGGAGGAAGCCTTCCACATTGCTGAGAGAGAACTTCATATACCCAGACTGCTAGATCCAGCAGGTAAGTCTGTTAGGCCTTGAAAATGTATGCTTTGTATATGCAGTATATCAATCAAACAGCAGTTGTATATTTGTATTTCAGATGTTGATGTTAGAGATCCTGATGAAAAGTCTATCATGACTTACGTTGCTCAGTTCCTGCAGTATTCTAAAGATGCTTCAGTTTCTGATGAAGAAATGCAGGTTAGATACACACACACGTTTTATTGGTGGTTTACGAAGACTTTGCATAGGCATAATGTATTTTATGCCATAAAAACATCTTGTTATATGGCCTTACCTCACCCCTACCCCTAAACCTAAAATGACAGGAAACCTGAGGCAAAATTTGAATGTGAAAAGACACCATTAAGTATTTAAGCATTTTGAATTATGAGGACACAAGGCATGTCCTCGTAAATCACCTTAATGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31955
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Essential Splice Site | 270 | 9778 | 8 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | Essential Splice Site | 241 | 281 | 6 | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37646494)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37123306 |
GRCz11 | 13 | 37249196 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACATTGCTGAGAGAGAACTTCATATACCCAGACTGCTAGATCCAGCAG[G/A]TAAGTCTGTTAGGCCTTGAAAATGTATGCTTTGTATATGCAGTATATCAA
Long Flanking Sequence:
TATTGTTTAGATTGAAGAATTGGCCAGCACATTGTCCTTCAGCTCCCGTCAGTCTTCTCTGGAGTCGCTGGCGAGTTTGGACACTCGTTCGACCAACAGCAGTGCCCGCAGCAGTCCAGTGCCACCCCGTGGTTCACCCTTACATGCCCGTTTTCGCGTATCAGCCAAGAAAGCCCTGCTGCTGTGGGTCAGAGAGCAGTGCCAGCGGTGAGGAACAATCTGCTTCAATAAATTGATGGGAACGGACAAATTCTGAACCTGTACTGTGAAACCTATCATCTCATGTTTGTTTTTTCTCAGGGCTGGATGTACTCTGAATGTGAAGGATTTCAAGGTGAGCTGGAGGAGTGGAGTTGTGTTTTTGGCGATACTTCATGCTCTAAGGCCAAATATAGTTGACCTAACCAGAGCTCGAACAAGAACAAACAGACAAAACCTGGAGGAAGCCTTCCACATTGCTGAGAGAGAACTTCATATACCCAGACTGCTAGATCCAGCAG[G/A]TAAGTCTGTTAGGCCTTGAAAATGTATGCTTTGTATATGCAGTATATCAATCAAACAGCAGTTGTATATTTGTATTTCAGATGTTGATGTTAGAGATCCTGATGAAAAGTCTATCATGACTTACGTTGCTCAGTTCCTGCAGTATTCTAAAGATGCTTCAGTTTCTGATGAAGAAATGCAGGTTAGATACACACACACGTTTTATTGGTGGTTTACGAAGACTTTGCATAGGCATAATGTATTTTATGCCATAAAAACATCTTGTTATATGGCCTTACCTCACCCCTACCCCTAAACCTAAAATGACAGGAAACCTGAGGCAAAATTTGAATGTGAAAAGACACCATTAAGTATTTAAGCATTTTGAATTATGAGGACACAAGGCATGTCCTCGTAAATCACCTTAATGGAGTACAACTAGGTAATACCTTGGTCATTATACAAATTTCTGTCCTTGTAAACCACCAAAACCAGTACACACACACAGACACTGACACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31954
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 1010 | 9778 | 23 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37632201)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37109013 |
GRCz11 | 13 | 37234903 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTATGATTGTTGTACAAGACTATGAAGCGGAGAAAGGTAGCCCACAAT[C/A]ACAAATACACCCCTGTGAGCAGGAAAAAGACTGTCAGTCCATTGAGCTTA
Long Flanking Sequence:
GCTGCTGTTGAAAAGTCACAGGTCTGTCAATTATTTATAGATGAAAATGGTTGCATCAAATAAAGAAAATGTACAACGCTGAAACTACCAAAAACTAATCACTAAGTAATTAGCAATCAGGATGTATTATCTAAGCATAACTAACCTTGTTTTAGAATTGTGTGCAAATGCATTATAATTTTTAAATTATGTTAAATTTTACCAGGAAGCTGTAGGGATGCTCAGCTCTTTGGGGTCTTGCAGAGACAGAAGCCCTTCCAGAGACCAGCCCCCTTCAAAGATATTTGTCCTGTATCAAGAGGCCGAGAAAGAGTCCCAAACCTCTCAATCGGGAGCCACTAGCCAACCAGAAACCCAGCCCACAGTTAGGGCAAAAGTCCCAATATCTTCTCAGATGCCCTCAGAGGTACCTTCTGTAGTCCTCAAGACCCAGCAGTGTAGTCAGCCTGTACCTATGATTGTTGTACAAGACTATGAAGCGGAGAAAGGTAGCCCACAAT[C/A]ACAAATACACCCCTGTGAGCAGGAAAAAGACTGTCAGTCCATTGAGCTTAAGTCACAAAAAGTTGTCGAAGCTCAAGCAAAAAGTCACATAGTCAAAGAACATTGTGTAGAAAGTCAGACAACACAACAGCTGGCAGAAAACCAGAGACAGGTGCAAGCTCCAATACCCAGCCAACCTTCACAAAATCAACAAAAAGTAGCATCTCAAGGTCATCATGAACAACAACTAACAACACAGGCACATGTGCAGATCCAACAACAAGATAAAACTCAATCTTCAAAACAGCAAATGGTTCAAGGATTAATGTCAACACAGCCACAACTTCAGGACCAATTAGAAGCACAACCACAGAAAGACATTACAGGTCAAAATCAAGCTCCAAAGCAGAAGAGGAAATCTAAAAAGTCCCAGGCAAATCTGCAGAACAGGCCTTGGCTACAACAGAGGAGTCAATTGGAAAACGTTACCCCCAAAACAGCTCAAGAGGTCCCACAGTCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22357
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 1362 | 9778 | 23 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37631146)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37107958 |
GRCz11 | 13 | 37233848 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAACCACAAAGATTTACAGTGGCCCAAGCAATGCCCCAAGGTATTTCC[A/T]GACCAGTCCAGCAGTACCCAACACCTCCCATGCAACCACAAATGATTATG
Long Flanking Sequence:
TAGTTGCTGTTAGCCCTACAGAAGCTCAGGGACCTCCTCAAAGCAGTGTGACAGCACAGCCAAAATATGTTGTTGAGAGTGATGAGAAGTGCCTGAAGCAAAATCAACCTGTTGCACAGGAGAAGGTGACACAAAGACTAGCTCAAACTGAGCCAGTAGTACCCGCACAACCAATGACACAAAAACAACCACAACAGTCAATGACTGTTACAAATCATCAAGTTCTAAGCCAACCTCAACCTGCTATATTAACTCAAGCCCAAGCAGCTTTAAAAACCGCACATGCTGCACCTATTCAACAACAAAAACAACCTCACATGGTGAAATCACAGCAACCTGATGTGATGATCCCAAAACAAGCACAACCTCAATTCATGACTCCCATGCAGCCACAAGTTATGCCCCAATGGCAGCCTCAACAGACCATCCTTCAGTCTCACCCTGCAGTACCACAACCACAAAGATTTACAGTGGCCCAAGCAATGCCCCAAGGTATTTCC[A/T]GACCAGTCCAGCAGTACCCAACACCTCCCATGCAACCACAAATGATTATGCCGAGGCAACAGTCACCACATGGAGCAGTGCAAACTCAGTCACAAATACTCCACAGTCCGACGGTACTTGCCCCTCAATCCAAAGGTGCATCCCCCATACAACCCAGAATCATCTCTATGCCTCAGTCTCAGATGCCTGTTCAAACTCAGACCCAACCTCAGCTGAAAGCACAGGGAAGTGCTCCACTTATGACTCAACCTGAAGGGCAACCACTGTGGTGTCCACCCCGAGATGCCACCCAAAATTACCCCAAAATTCAAGGACCAGTTTCTGCCCAAATGCAGCCTCTGGCTCATTTCCAAACTCATCCCCAACCTCAAAGCTTCCCTCCAGCCCAACCTCAGCAATGGTCACCAACAAGACCAGGCATTGTAGCCCAGACCTATCCCACTGTTCCAGGTCAGGCAGTACAACCCCAACCTCAATTATCTGTTTATCCTAAAACCCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16388
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 1452 | 9778 | 23 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37630874)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37107686 |
GRCz11 | 13 | 37233576 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGGGAAGTGCTCCACTTATGACTCAACCTGAAGGGCAACCACTGYGGTG[T/A]CCACCCMGAGATGCCACCCAAAATTAYCCYAAAATTCAAGGACCAGTTTC
Long Flanking Sequence:
AAAACCGCACATGCTGCACCTATTCAACAACAAAAACAACCTCACATGGTGAAATCACAGCAACCTGATGTGATGATCCCAAAACAAGCACAACCTCAATTCATGACTCCCATGCAGCCACAAGTTATGCCCCAATGGCAGCCTCAACAGACCATCCTTCAGTCTCACCCTGCAGTACCACAACCACAAAGATTTACAGTGGCCCAAGCAATGCCCCAAGGTATTTCCAGACCAGTCCAGCAGTACCCAACACCTCCCATGCAACCACAAATGATTATGCCGAGGCAACAGTCACCACATGGAGCAGTGCAAACTCAGTCACAAATACTCCACAGTCCGACGGTACTTGCCCCTCAATCCAAAGGTGCATCCCCCATACAACCCAGAATCATCTCTATGCCTCAGTCTCAGATGCCTGTTCAAACTCAGACCCAACCTCAGCTGAAAGCACAGGGAAGTGCTCCACTTATGACTCAACCTGAAGGGCAACCACTGTGGTG[T/A]CCACCCCGAGATGCCACCCAAAATTACCCCAAAATTCAAGGACCAGTTTCTGCCCAAATGCAGCCTCTGGCTCATTTCCAAACTCATCCCCAACCTCAAAGCTTCCCTCCAGCCCAACCTCAGCAATGGTCACCAACAAGACCAGGCATTGTAGCCCAGACCTATCCCACTGTTCCAGGTCAGGCAGTACAACCCCAACCTCAATTATCTGTTTATCCTAAAACCCAGCCACAACCACAGCCTCAGCAATGGCTCTCTCCAAGACCTGAATCACCTTGGGGTCAATCACAGATAAGACCTCAAGGTCCAGTTCAGCCTTGGAGGCCAGTCAGTCCAGAGAGTGTCAGCCCAGTATACCCCAGGGCTGAAACTCAAGGGCAAGGACTACATCCTCAGTCCCAATATCAACCCCTACCAAGGCCACAAAGCCCTCAACGGCAGTGGGGTCCAGTCAGGACAGAACATCAGTTTCAAGTTTCTTCCCAGACTACATTACATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13694
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Essential Splice Site | 1926 | 9778 | 27 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37626660)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37103472 |
GRCz11 | 13 | 37229362 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTGYGGAGAAGAGAGAGATAGTGAAACAAACGAGTACAGAAGAGGACAG[G/A]TATGGATTTAAAAAGAAAWCAGCTTTATATGTTACTATATTCAGTACGAT
Long Flanking Sequence:
TAGCTTTCATCAAAATATATTGTTTCAAGATCAATAGAATAAAGAAACTCATAATGGCTTTGAACCACTTAATGATGAGTTAATAGTTAGTGCGTTCTCCTTTTTCGGTAAACTAACCTTTAAATGTTTCTTTTTATTAACCAATAGTTCACAAACTGAGCAAGCAAAAGAGCCACAAACTCAGAAAGCACCGACAATCCCACCACCTGTTGAGAAGCCCAAAGAGGTTAATATCCCTGAGGTAAAACTTTATGAATATTTTATATCACCTGTATATTATGTATTTTAGAACCTATTAAATTTACAAACAGAAAAGTTACCTTTTGTTATTGTATCTACTGTAGATAAGCATGCAGTGAACTGACTGTTTTACTAGGACTGAATGAAAGATGTTGAGCACTTGTGATGTTGTTTTAGGGTGTTATACCAGTTAGCCCCCAGCGACCGAGAACTGTGGAGAAGAGAGAGATAGTGAAACAAACGAGTACAGAAGAGGACAG[G/A]TATGGATTTAAAAAGAAAACAGCTTTATATGTTACTATATTCAGTACGATTTAATTTTGTGTGTGGATCTTATGGTCTACCTCTTTTTTCCTTGCACCACTCAGGTACCGTAGCTCCAGATTCGCATTACAGGGTCAGCTAAATAGAAATGAACAATGCATGCTGGGAGATCATCCCTCAGAATCAGTCACTCCTACAGACCTGCAGAAACGACTGAGAGAATTAAAGGTAATAGTTTTAAGTTAGTCATTTCAGAATAATACTTTAGAATAATGGTCCATTAGTGAATGTTAGTTACTTTATTTACTAACATTTAGTATGAACAATCTTACTAACAGTAACTAATGCATCATTAAATTCCAATGTTATGCTTGTTAACATTAATTAATGCACTCCGAGTTAACATGAACTAACGTTATTTAACTTAAATATCATGATGAATACAGATATTCAGAATTAACAGAGAATACAGATGAATAAATCCCATAATAAACAACATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11835
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Essential Splice Site | 1926 | 9778 | 27 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37626660)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37103472 |
GRCz11 | 13 | 37229362 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTGYGGAGAAGAGAGAGATAGTGAAACAAACGAGTACAGAAGAGGACAG[G/A]TATGGATTTAAAAAGAAAWCAGCTTTATATGTTACTATATTCAGTACGAT
Long Flanking Sequence:
TAGCTTTCATCAAAATATATTGTTTCAAGATCAATAGAATAAAGAAACTCATAATGGCTTTGAACCACTTAATGATGAGTTAATAGTTAGTGCGTTCTCCTTTTTCGGTAAACTAACCTTTAAATGTTTCTTTTTATTAACCAATAGTTCACAAACTGAGCAAGCAAAAGAGCCACAAACTCAGAAAGCACCGACAATCCCACCACCTGTTGAGAAGCCCAAAGAGGTTAATATCCCTGAGGTAAAACTTTATGAATATTTTATATCACCTGTATATTATGTATTTTAGAACCTATTAAATTTACAAACAGAAAAGTTACCTTTTGTTATTGTATCTACTGTAGATAAGCATGCAGTGAACTGACTGTTTTACTAGGACTGAATGAAAGATGTTGAGCACTTGTGATGTTGTTTTAGGGTGTTATACCAGTTAGCCCCCAGCGACCGAGAACTGTGGAGAAGAGAGAGATAGTGAAACAAACGAGTACAGAAGAGGACAG[G/A]TATGGATTTAAAAAGAAAACAGCTTTATATGTTACTATATTCAGTACGATTTAATTTTGTGTGTGGATCTTATGGTCTACCTCTTTTTTCCTTGCACCACTCAGGTACCGTAGCTCCAGATTCGCATTACAGGGTCAGCTAAATAGAAATGAACAATGCATGCTGGGAGATCATCCCTCAGAATCAGTCACTCCTACAGACCTGCAGAAACGACTGAGAGAATTAAAGGTAATAGTTTTAAGTTAGTCATTTCAGAATAATACTTTAGAATAATGGTCCATTAGTGAATGTTAGTTACTTTATTTACTAACATTTAGTATGAACAATCTTACTAACAGTAACTAATGCATCATTAAATTCCAATGTTATGCTTGTTAACATTAATTAATGCACTCCGAGTTAACATGAACTAACGTTATTTAACTTAAATATCATGATGAATACAGATATTCAGAATTAACAGAGAATACAGATGAATAAATCCCATAATAAACAACATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16245
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 2783 | 9778 | 41 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37611451)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37088263 |
GRCz11 | 13 | 37214153 |
KASP Assay ID:
2260-6784.1 (used for ordering genotyping assays)
KASP Sequence:
AGGACTGGCTTCAGCAGAGGGAACAAGTGCCAGAACAGAGAGAAAAACTA[C/T]GACAAATCCAAGAGGAGTTTCTTAAAGAAAGGTAACACTTGCTTTTCTAA
Long Flanking Sequence:
AAGCTTTGTTCTCCACGTGGCATCAGGAACAGGAAGGAGAACTGGCCACACTGAGAGCACACTGTCAGGGACGCCATAAACAGCTAGATGACATCCTCTACAACCTCAACAGGTACACAGACTGAGCTCTTGTCATAGATTTTTGCTGTTGCTGTTGATTGAGCCAATTATTTAAATTAATGTTTTTAATCCAATTCGTCTTTTTTTCTATAGCGCTTTTACAATGTAGATTGTGTCAAAGCTGCTTAACATAGAAAGAGAAGAGAGAATAAAAAGCCATAACAATATTTTAGATGGGAACATTCCAGGCAGACTGGGGAGTAGTGGTGGAATGCTGGTGTAGTTCTAGTTAGATTAAACTGTTTTAGTTCAATTTAATGACACTATTGAAGTTCAGTTCAGTTGTGTGTCTTTATGTGTTTAGCTTGCAAGAGGAACACAATCATTTAAAGGACTGGCTTCAGCAGAGGGAACAAGTGCCAGAACAGAGAGAAAAACTA[C/T]GACAAATCCAAGAGGAGTTTCTTAAAGAAAGGTAACACTTGCTTTTCTAAATGTAAAGTTTGTTTTAAACATTTTTTGTTTTTTCAAACAATAATTTCAGTAATTAAATAACACATTCACAGCATATTTACTTGGTATTCCTAATTATAATTTTATACATAATAATAATAAGAGCAATACGATACTATTATTATATATACACTCACTGGCCACTTTATTAGGTACACCTTACTAGTTAGACCTACTTTTGCCTTCAGAACTGCCTTAATTCTTTATGGCATAGATTCAACAAGGTACTGGAAATATTAATCAGCAAATTTGCTCCATATTCACATGATAGCATCACGCAGTTGCTGCACATCCATGATGCAAATCTCCCTTTCCACCACATCCCAGAGGTGTTCTATTGGTTTGAGATCTGGTGACTGTGGAGGCCATTTGACTACAGTGAACTCATTATCATGTTCAAGAAACCAGTCTGAGATAATTCGTGCTTTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22356
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 3017 | 9778 | 44 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37608805)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37085617 |
GRCz11 | 13 | 37211507 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTTGCTGATGAAGCTGATTCCAGATTGGCCAGTTTACAGAGGCAAGGA[C/T]AGAGTTTATGTTCTTATAAAGAGCTTGACACTGAGAGGAGGAGTCACATT
Long Flanking Sequence:
TTTAAGGCTGTTCTTAATCAAAGCTCTGATGGTGACGCTAAACTGGTGGCTCTGAAAGGTGAGGGTGTTGCTTTATGTACACATGAGATTTTGGAGGAGACCAGAAGACAAGAACTTGTTCACACACTTAAAAACATCGAGGATGAATGGAAAAGAGTTCTGGATTTGGCCCAACTCCTAAAACATCAGGCAGAACTCCAAGACACTCTTCACAGGGAACTAGAAAATCTACAGGCCCAAGAAGAGAGTACCCAATCCTGGGTGAGAGAGCAGCTGCAGATGCTACGCTCCTTGGAGAAGGAACTTCAACCCCAGGAAAAACTCAACAAATTACTGGTAAGCACAAAGAAAAATTATATTTTGACTGCAAAACCCTTTTTAGAACTCTCTAGTAATTCTTACCTTGGTTGATTGGTTTATAACATGTATATATTCTCTAGGCTGTCTTAGACCTTGCTGATGAAGCTGATTCCAGATTGGCCAGTTTACAGAGGCAAGGA[C/T]AGAGTTTATGTTCTTATAAAGAGCTTGACACTGAGAGGAGGAGTCACATTGACCAAACCCATAGAGCAATAGAGGAGGAGTGGAGGAAAGTGCTGCAACTTGCTCAGGAGCTTAAGAACCAGGTCAAGCATGAGGAATCTCTCAACAGAGAGTTACAAAGCTTTTGTGATCAGGGAGAAGAGACTCAATCCTGGGTTAGACAGCTCAGAGAGACCTTGGAGACCCTTCATATGACATCTTCTATTCAAGAGAAGCTCAGTGGTGTTGAGGTAATGGAGAGTATTTTAGGGCAATTTATTGCTTGTTAAAGAAACAAGGCAATGTTTCCTGAAACAGTAAATATACACTGAAAACCAGTAAAAAATGTAAACAAAAGCATGATATCTTGGTTTTGTGTTTTTTTTAGGCAGTACTTGCTCATAGATCTGAGGGGGACTATAAACTTAGTGACCTAAAGATGAAGGGAGAGAGTCTATGTTCCTATGAAGATCTACAGGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9847
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 3786 | 9778 | 53 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
ENSDART00000075522 | Nonsense | 3786 | 9778 | 53 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37603919)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37080731 |
GRCz11 | 13 | 37206621 |
KASP Assay ID:
2260-6779.1 (used for ordering genotyping assays)
KASP Sequence:
CGTAAAAGCCTRCAGGTGGCACTGTCTCATAAAGAACTGCTGAGGGACTG[T/A]CTAGGCCCTGACTTGGCTGGAAAGCTTGAAAGAGATGGCCTAAAAACACT
Long Flanking Sequence:
AGGTAAGTGTGTTAAAGCAGGATTGGAACTAAACTGTGCAAGGCTGCAGCTCCAGGAATTGGCTTTGACACCTGTGATGTATCACAATTATAGTGTAATGCTGCTTTAATTTAGAGTTAAATATTTATTGGAAAATTATTGATTTCCTTCAGTCTGCGATCGAAACTATCAGAGAGGCAGAATGACTGCGCAGACAGCACTGTGCAGTGTGTGAGACAGGCCTTACAAAACATTCAGTCATGGAACCAGATGGCAAATGCAAATCCTCCAACCAGCTCAGCCACATCCATGCAGGTGTGTTTGTGTCTTAATTTGCATGCAGTATATGAATACATAACAACACAACACACCTGCCTTATACATATATATATTTGATAGTAAGGTTGTTGTCACCTTGTGAACTGTAACATTTTTACTTCTTAGACTGCAATTGAGGAAGGAGCAAAACTGCGTAAAAGCCTACAGGTGGCACTGTCTCATAAAGAACTGCTGAGGGACTG[T/A]CTAGGCCCTGACTTGGCTGGAAAGCTTGAAAGAGATGGCCTAAAAACACTAAGTGAAGCAGACGCTTACATGAATGACATCAAACAGGAACTTAGGGTAAGTACATCTCATTTCTGTAGGATGATGTGATGACTGAACAAAATTTCTAGTGAGGTAAACAGAGGAGTTTGTGTTTCAGAATCTTCAGGAGAAGGTTGAGCAGGAGGCTCTGAGGTTGTCATTAGAGGCTCAAAACATTCAGGTTCACTCACAGGTACACATTTTAAAAAATGAAAGTGTATTTCTAGACTTTTAAAGTATTATTATGTGCAGCACTAATGTATGTTAAAAACAATTTGAAGGTTTCAACTGTGACACCATCAACAAAGGAGTCTGATCAATTGGAATTAGTTTCTTTTTCATCTTTTATTAATGAAAGCTGCAAAACAACGGATTACAGCGAACAGGCTAAGGTACAGCTATCTGAAAGCCTTGACAGCAATATACCTACATGTGTTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16713
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 4380 | 9778 | 55 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37601969)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37078781 |
GRCz11 | 13 | 37204671 |
KASP Assay ID:
2260-6777.1 (used for ordering genotyping assays)
KASP Sequence:
AGGCCATTGATGTCATTTTAGRAGCAGASACAATGGCTTCATCAGGTGGT[A/T]AAGCAAAATCCACAGTWATTGAACCTAAACTRACACCTCTGTTTCAGCAA
Long Flanking Sequence:
AGCGTCGATATATTATTCTAGACTTGCCTGAGGGGGTGGAAATGCAGAGACATCACGCTCATGAAGGTACATCTTTAAGTGGATCCAGCGAGACACAGATTCAGGGATCAGGACATTCAGTAGCAGAAAGAATGGAGACAGAAGATGAGGCAGAATCTGCTGAAACTGAAACAGGTGCTTTAGTCAGCACAAACACAGTTTTGGAAGCACCAGAACAACATAAAACAATTGAAGCAGACCAAAACCTATCAACAAGGCAAGTTGAAGAAGATATGCATGTAATTCTAGATAAAGACACAAGAAAGACCCCATCAATGGATAAAGAACGATTTATAGAAACTGATTCTAAACTTAAACCTTCAGTCAAACAACCAAATGAGGGAGAAACTGAGGTTCAAACAAACAAGGTGGATATCTCCGTAACACCTGAAATGAAACCTGAAGGTAATAAGGCCATTGATGTCATTTTAGAAGCAGACACAATGGCTTCATCAGGTGGT[A/T]AAGCAAAATCCACAGTTATTGAACCTAAACTAACACCTCTGTTTCAGCAACTGACTGACAGGGACACTGAGATACAGTCCAAAAGAATGAATGTCATAATGACACCAGAAGAGACAAACAAGGCCCCATTAGTTGATGAAGCACAAATCATGGAATCGATACCTAAACTGATGCCTCCTGTCAAACGACAGGATAGTAAAACTGATGTCCAGTCAAACAAGATAAATGCATCAATGCAAGAGGAAAAAGCTGAAAATGAAAAAGGGATGGAAGTCATAAAACAAGAGACCTCATCAGGTGTAAAAGCACAGTCCATAAAAGTTAAACCTACAGTCATGCAATGGAATGATCAGGAAACTGAGATCCAGTCAAAACAGTTGTATGTTTCACAAGATGGAAAGGCTAAAGATGAACAAACTATTCAGATTGCTGAGGAAAAAGATATGTATATGACTCCATTATGTGAAAAGACTCATTCCATAGAAGCCGAACCTAGACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11394
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075522 | Essential Splice Site | 7162 | 9778 | 79 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37555972)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37032784 |
GRCz11 | 13 | 37158674 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTGGTGACGGTCCAGTTACAGCTGCAGGACAGACACAGCAACCATCAGG[T/C]ACACACGCACACTCTAATGCACAAAAYTTACTTCGCTTGCAAGAGMAGTT
Long Flanking Sequence:
TAAAAAAAAATTTTAAAAAGTAAAAACCACTGCTGTTGGATGTTCAAGTCAACAAACACTAATCGATCTCAATCTAAAGTCTGTCTGTTGGATTATTAATGAGATTTTTGTTCATATTTGTTTTTCTAAGACTGAGTCTTGGTTGAATGGAGCAGCATCTGTCAGCATCTTTAGTGCTTATTACTTTCCATTGTATCCTATTGTACCATGAACACCAGTAAGCATTTCTGTTTGCTTGACTGTATTCCTGCTGATTGCATTGGTTGTGTTGGAGTGATGCAGAGATGTTGTAGTTAGATGTTAATTGTGTGTTTGTTTTTTTTCATGAATCTAGACGACTCTGGTGGAGATCGAGCAGAGGATCTCCAGTCTTCCTCCATGTGGACTGAAAGAACAGGAGCAACACGAGGCTGAATCACTCAACACCAAACTCCAGCTCCTGAAGAACAGACTGGTGACGGTCCAGTTACAGCTGCAGGACAGACACAGCAACCATCAGG[T/C]ACACACGCACACTCTAATGCACAAAACTTACTTCGCTTGCAAGAGCAGTTCCTATACAATATGTTTCAGTAACAATTCATGCTACCTTTGTATATATACATATATATACAATTGAAGTTTAAGTTTAACGGAGATAAGATTTTTTCCGACACATTTCTAATATAATAAAAACATAATGCAATTCTAAGTATAATTGTTTGAGCTTTGACATGATGACAGTAAATAATATTTTACTAGATATTTTTCAAGACACTTCTATACAGCTTAAAATGACATTTAAAGGCTTAACAAGGTTAATTAGGTTAACTAGGCAGGTTAGGGTAATTAGGCTATTTATTGTATAACTATGGTTTGTTCTGACTATTGAAAAAATAGCTTAAAGGGGCTAATAATTTTGTTCTTTAAATGGTGTTTAAAAAATGAGTAACTGCTTTTATTCTAGCTGAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAAATATTGTCAGACTTATTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22354
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 9301 | 9778 | 118 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | Nonsense | 648 | 1153 | 12 | 22 |
ENSDART00000135935 | Nonsense | 64 | 207 | 2 | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | Nonsense | 33 | 252 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37499725)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 36976537 |
GRCz11 | 13 | 37102427 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCTGCCATGGGCTGTGATGTGTCGTTAACTGTACGTCAGGCTGTTTCA[C/T]AGCTATTACCGCCTGCTTTGGAGCGCTCAGGCCGTGAGACGCCTGTCAGT
Long Flanking Sequence:
TATAAATGAAAATAGAAGTTATATATACAAACATAAAAAAAACATAGAAGTATTCCTAAAAAAATGCCTGGTGCATTATGACAGGAAGAGTGATGTCCTACGGGTGGTTTGTCAAGCCCACTCACCTACATGGAGCACACTCATGCATCCTACAGTTAGGTGATGCATTGTATATATGTTTACTAAAGAAAACTAGATCTTTAATTTAGTTTTGAACAGAGAGAATGTGTCTGAGCCTCAGAAGCTATCAGGAAGGCTATTCCAGAGTTTAGGAGCCGTATATAAGAAAGCTCGACCTCCTTTAGTGGACTTTGAATACTGATTTACCTCTTTAATCTCTTGGTTTTTTACAGGTTCTTGAAGAGGAGCGTGAGTTCTCGGACAGAGACACAGATCCGGAGGACTCTGCTGATTTCGGTGGGGTGTGGGAGAGGGAAAGAGAGGAAGAGGAGGCTGCCATGGGCTGTGATGTGTCGTTAACTGTACGTCAGGCTGTTTCA[C/T]AGCTATTACCGCCTGCTTTGGAGCGCTCAGGCCGTGAGACGCCTGTCAGTGTGGATTCAATTCCGCTGGAGTGGGATCACACTGTGGATGTGGGAGGATCTTCTTCTCCGGAGGAGGATGAGGAGTTGACCTACTACAGCGCTCTGTCAGGTAACGCTTTACTGACTGATCTCTGACAATACTTTTCTTAGATCTCTCTGCGTGATGTATGAATAATACTGCATTTTAGAATACATTTTCACCTCTTGTGAAATTTGAATTCTTTAAAAATATTTCCCAAGTGCTGTTTAACAGAGAATATTTGTTCAACACATTATTAAACACAATAGTTTTAATAACTTATTTCTAATAGCTACTTTCTTTTGTTTTTTAATTTGATGACAGTATTTTAGTAGTTATTTTGCAAGGTACTAGCATTCAGCTTAAAGTGTTGCACTCACTTTTGGGGTTTACACTTACTTGAATTTAAATAGTAATTGTTCTTGAGCCCAGTGAGCTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22353
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 9396 | 9778 | 120 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | Nonsense | 766 | 1153 | 15 | 22 |
ENSDART00000135935 | Nonsense | 159 | 207 | 4 | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | Nonsense | 128 | 252 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37490962)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 36967774 |
GRCz11 | 13 | 37093664 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCACTACTCCACACAGACAGTATAATGTTGTACTTTGTCTCTCCAGGAT[A/T]AACTGATGTCCGAGTGTGCGGGCAGTATAGACAGTATAAAGCGAGTCAAG
Long Flanking Sequence:
TTTTTGTTTGAAAATGTAGTCCATGCCTATTTTCTAACCCTAAACCCAACCAAAACTGTAAATTATTCCCAAGATCAGAAGTGAATAATAGTTGGATAACAATTGTGTAGAAGTGTATAAACCTAACTATAAGCCTAAACTTAACATAAATGGTAAACATATCCCTTAATTCTGATTGGCTGATTGGAATGTTGTTCCAGGATCAACATAGATCTTAAACCAGGAACTTGTCCTACTTGGTGAAATCTGTTTGGCTAAAGTCAACAAATCACTTTAACAGCAACAGGTTTACTCATTTTTTTCAAGTACAGTCAACAAATCACTTTTTTCCAGTGTACATTATTGTTTCTTTCCATTTATTTGCACTACATATTCATTAATGATGTCAAAAACTATCCTCAAATGCAGTTAACCATTTGTGTACAATCTCCCAATTTTTATGCTGGGTAAAGCACTACTCCACACAGACAGTATAATGTTGTACTTTGTCTCTCCAGGAT[A/T]AACTGATGTCCGAGTGTGCGGGCAGTATAGACAGTATAAAGCGAGTCAAGCTGATTCTGAATGAGGATGAACAGCTGGAGGATCAGGGTCTGACGGGCTTCAGTGCAGCAGATAACACAGGTACTGCTGATTACATCAAGCACACACACACACACACACACACATAAGCAAACACACACCTTTACAGAGATTTATGGGCTAATTTTTTAAAGATGGTCTGTGTTCAGGTGTGATCGAGCGGTGGGAGCTGCTTCAGGTGCAGTCGTCTCGCGTCCCGCAGGATCTTCAGCACTGGCACAGACTGAACTCTGACCTCTCTGACATTATGGTATGGCTGAACGCTGTGATGCCTGAACTGGAGACATTGCAGACTCTAGAGGCCAAAATCACCATCAGAGACATGGAGAGCAAGATCCACAAACTGAAGGTATATCAAGACATTAAAGTTCATTAAGCAAAAAGAAGCCATTCAGGCTCAGCTATTGTATTGAGTGCTTTTC
Associated Phenotype:
Not determined