Busch Lab

ZMP

syne2b

Ensembl ID:
ENSDARG00000053484
ZFIN ID:
ZDB-GENE-071218-5
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
sa11835 Essential Splice Site Available for shipment Available now
sa13694 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
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Availability:
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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.
Availability:
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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.
Availability:
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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.
Availability:
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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.
Availability:
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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:
sa11835
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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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:
sa13694
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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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.
Availability:
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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.
Availability:
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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.
Availability:
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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.
Availability:
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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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
Availability:
Order Allele From ZIRC
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.
Availability:
Order Allele From ZIRC
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