Busch Lab

ZMP

neb

Ensembl ID:
ENSDARG00000032630
ZFIN ID:
ZDB-GENE-041111-216
Description:
Novel protein similar to vertebrate nebulin (NEB) [Source:UniProtKB/TrEMBL;Acc:B0UY60]
Human Orthologue:
NEB
Human Description:
nebulin [Source:HGNC Symbol;Acc:7720]

Alleles

There are 25 alleles of this gene:

Allele Name Consequence Status Availability
sa906 Nonsense Available for shipment Available now
sa10635 Nonsense Available for shipment Available now
sa15371 Nonsense Available for shipment Available now
sa15997 Nonsense Available for shipment Available now
sa16506 Nonsense Available for shipment Available now
sa21476 Essential Splice Site Available for shipment Available now
sa34626 Nonsense Available for shipment Available now
sa11973 Nonsense Available for shipment Available now
sa11545 Essential Splice Site Available for shipment Available now
sa21475 Essential Splice Site Available for shipment Available now
sa18354 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa906
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
ENSDART00000032130 None None 334 None 8
ENSDART00000061293 Nonsense 1288 6235 30 134
ENSDART00000101711 None None 610 None 17
ENSDART00000142020 None None 175 None 6
ENSDART00000142585 None None 564 None 15
ENSDART00000143888 Nonsense 1311 6177 33 135
ENSDART00000146486 None None 388 None 11

The following transcripts of ENSDARG00000032630 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 23895131)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 23050917
GRCz11 9 22861786
KASP Assay ID:
554-0813.1 (used for ordering genotyping assays)
KASP Sequence:
ACGTTGGCTTCCGTAGCATCCAGGACGATCCCTTGCTGGTGCACTACATG[C/T]AGGTGGCAAAGATGCAGAGCGAGAGGAACTACAAGAAAGATTACCACAAG
Long Flanking Sequence:
TTTCGAAATATACGGTCTAATTATAGTGATAATTTACCAATTTTATATTTTTATAGTTATTTTTTCATGTCAAGATTCATTTATTGAATTTTATTTAGTTAAATGCTTTTACATTTGATTTCTTTGCTATTTATTATTACAAATTAATTACTAAAATTATGTAGATATTAAGAGAAAGGCTTCTTTTTTTACAGTCACACTACAAGGCTCAGTGGATTGCGGACATTGCCAAGGGTTATGACATGAAAGCTGATGCTATTCCCATTCTTGCTGCTAAACAAGGAAGGCACATTGCCAGCAATGTAAGTGCATAATGTATATAGCATTCAAATACTGAAAGAACTGTTAATAAGATCCAAATGAAATGTAATGAATTTATTTGATTACAATTTATTGTTCTTTAATCACAGTATCAATACAAAAAAGCATATGAGAAAACCAGAGGCCACCACGTTGGCTTCCGTAGCATCCAGGACGATCCCTTGCTGGTGCACTACATG[C/T]AGGTGGCAAAGATGCAGAGCGAGAGGAACTACAAGAAAGATTACCACAAGTCCAAGCTCAAATACCACACCCCTGTGGACATGCTGAGTGTTGTACAGGCCAAAATCGCCTCAAAGGTCCAGACAAATGCAGGATACAAGCAGCAGTTCCATCATTACAACCTGCTGCCTGATGCCATGAACCTGACGTTAGCTCGCTCTATGAACATCACCTCCAGTGATGTGAGTCCATCATTTCTAAGATTCATGCATTCAAAATTCAATGAGTAGATTATGATTTGTTGATTCCTCATTAGTGTTAAATTAATTTTTCAAAGAATCAACAAAACTTATGTTTATTTTCTCCCAGTATGAGTACAAGAGTGAGTACAACAGCACCATGAAGGGTATGGGATGGGTGCCCATTGGCTCCCTGGCTGTAGAGACTGCAAAGATTGGAGGAAAGATCCAGAGTGAGCACAACTACCGCACTCACCCTTCCAACTTCAAGTTCCACAAACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10635
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
ENSDART00000032130 None None 334 None 8
ENSDART00000061293 Nonsense 1929 6235 40 134
ENSDART00000101711 None None 610 None 17
ENSDART00000142020 None None 175 None 6
ENSDART00000142585 None None 564 None 15
ENSDART00000143888 Nonsense 1934 6177 43 135
ENSDART00000146486 None None 388 None 11

The following transcripts of ENSDARG00000032630 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 23891300)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 23047086
GRCz11 9 22857955
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCYCAGTATGTTTTTGAAGATTTTAAAACTGGCTTTGTTTTTCCTTCAG[C/T]AAAAGTACATTTCYGCATGGGAAAAGGACAAAACCACAATCCACATTATG
Long Flanking Sequence:
AAGTTCTGCCTGATGCCATGAACCTGCAGCTAGCCCGCAACATGCAAGCAATTGCAAGTGATGTAAGGAAGGATTGTGTCGTTGTATTTTAAACATTTTCCATGTTTTAATGTCTTTGATTGAAAGCCGTTGTTTCATTTTATGGTGAATGTGATGACATTCTGCCTCTTTTTGCAGAATCTCTACAAATCCGAATACAACAATTACATCAAAGGAATTGGATGGATTCCCATTGGATCTCTGGATGTGGAGAAAGCAAAGATTGCTAGCCGGATAGGCAGCGAAAAACAGTACCGCACACACCCCAGTAACTTCAAGTTCACCAAAGACATGGGGTCTATGGACCTGGTTCTTGCTGCAGCCAACAATGATATTAATAACAAGGTGAAAATCTAAATCATTTGACTTTACACTGTGTTTTGGTTTTTATTTTCTTGGTCTTTTTTGTTTGTCTCAGTATGTTTTTGAAGATTTTAAAACTGGCTTTGTTTTTCCTTCAG[C/T]AAAAGTACATTTCTGCATGGGAAAAGGACAAAACCACAATCCACATTATGCCAGATGCAATGGACGTGGCTCTTGCTCGTCAAAATAAAGTTATTTACAGTGAGGTTGGTGATGCCATCAGATACACAACTGTTGACCGATTGCATGACTGTTTTCACACTATGTAAATAATCCTCTCACTATCTTCTTTAGAAACTATACAAACTTGCCAATGAACAAGCAAAGAAGAAGGGATACGATCTACGTGCTGACGCTATCTCAATTCAAGCTGCTAAAGCTTCATGTGCCATTGCCAGTAATGTAAGTTTTTTAACCTTATTATAATCCTGCAAATAATTACTGGGTACTGTGAAAGTGATTAATGTTTTAATGAACTTATCGCAGTACAAGTACAAAGCTGGGTATCGTAAGCAAGTCGGTCACCACATTGGAGCTCGCAGTGTCCAGGATGATCCTCTGCTCATGCTGGCTTTGAACTCAGCTAAAATTGCTAGTGATGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15371
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
ENSDART00000032130 None None 334 None 8
ENSDART00000061293 Nonsense 2002 6235 42 134
ENSDART00000101711 None None 610 None 17
ENSDART00000142020 None None 175 None 6
ENSDART00000142585 None None 564 None 15
ENSDART00000143888 Nonsense 2007 6177 45 135
ENSDART00000146486 None None 388 None 11

The following transcripts of ENSDARG00000032630 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 23890907)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 23046693
GRCz11 9 22857562
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTAYTGTGAAAGTGATTAATGTTTTAATGAACTTATCGCAGTACAAGTA[C/A]AAAGCYGGGTATCGTAAGCAAGTCGGTCACCACATTGGAGCTCGCAGTRT
Long Flanking Sequence:
TAAATCATTTGACTTTACACTGTGTTTTGGTTTTTATTTTCTTGGTCTTTTTTGTTTGTCTCAGTATGTTTTTGAAGATTTTAAAACTGGCTTTGTTTTTCCTTCAGCAAAAGTACATTTCTGCATGGGAAAAGGACAAAACCACAATCCACATTATGCCAGATGCAATGGACGTGGCTCTTGCTCGTCAAAATAAAGTTATTTACAGTGAGGTTGGTGATGCCATCAGATACACAACTGTTGACCGATTGCATGACTGTTTTCACACTATGTAAATAATCCTCTCACTATCTTCTTTAGAAACTATACAAACTTGCCAATGAACAAGCAAAGAAGAAGGGATACGATCTACGTGCTGACGCTATCTCAATTCAAGCTGCTAAAGCTTCATGTGCCATTGCCAGTAATGTAAGTTTTTTAACCTTATTATAATCCTGCAAATAATTACTGGGTACTGTGAAAGTGATTAATGTTTTAATGAACTTATCGCAGTACAAGTA[C/A]AAAGCTGGGTATCGTAAGCAAGTCGGTCACCACATTGGAGCTCGCAGTGTCCAGGATGATCCTCTGCTCATGCTGGCTTTGAACTCAGCTAAAATTGCTAGTGATGCTCTCTACAAGAAAGACTTCAACAAGTCCAAGACCAAGTTCCACCTCCCAGTTGACATGTTGTCATTTGAGTTGGCTAAGAAATGCCAGGTCCAGGTCAACGATGCCCACTACAGAACCTACCTGCACAACTGGACCTGCCTGCCTGACTCCAATGATGTTGTCCAGGCTAGACAAGTCTACGACATCCAGAGTAATGTAGGTCAAAATTACTGCAGTTTTATACATGAATAAATATATTGAAGCGTCATCATAACAATATTTCTAAGCATGTTTTCACATGTGTGCCCTTAGGCGGTATACAAGGCTGATCTGAAATGGCTTCAAGGCCTCGGATGGGTTCCCATTGGTTCTGTTGATGTTGAGAAAGTAAAAAAAGCTGGAGAAATCCTGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15997
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
ENSDART00000032130 None None 334 None 8
ENSDART00000061293 Nonsense 2285 6235 46 134
ENSDART00000101711 None None 610 None 17
ENSDART00000142020 None None 175 None 6
ENSDART00000142585 None None 564 None 15
ENSDART00000143888 Nonsense 2290 6177 49 135
ENSDART00000146486 None None 388 None 11

The following transcripts of ENSDARG00000032630 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 23889582)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 23045368
GRCz11 9 22856237
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCATGCTGGCCTTGAACTCAGCTAAGATTGCTAGTGATGCTCTGTACAAG[A/T]AAGACTTCAAMAAGTCTAAGACCAAGTTCCACCTCCCGGTGGACCTTCTG
Long Flanking Sequence:
CTCACTTGATTATCTGAATATTTTTATTATTTTATTTTATTATATTAATTTATATTTTTTTAAAAATTGACTGTTTATATATAATTAGCTGAAAATTTAGATTTTATATGAGGATAAAAACAAATAATACATTGTGTTTTGATATTCCAGTTTGTTTATATATTTTGTATCATTTGTACATCAGAAACAATATAAACTCGCCTATGAACTGGCCAAGAAGAAGGGTTATGATATGCGCAATGATGCCATTTCAATCCTTGCTGCCAAAGCCTCCAGAGACATTGCAAGTGATGTAAGTACAACAAAAAGATATGGCTATACTTTATATGACACACTATAAGTTGTTACGCTGATCATATTTTCTTTCCTTAAAGTACAAGTACAAGACTGGTTATCGTAAGCAAGTTGGTCACCACATTGGAGCTCGCAGCATCCAGGATGATCCTCTCCTCATGCTGGCCTTGAACTCAGCTAAGATTGCTAGTGATGCTCTGTACAAG[A/T]AAGACTTCAACAAGTCTAAGACCAAGTTCCACCTCCCGGTGGACCTTCTGTCTCTTGAACTGGCAAAGAAATGTCAGATCCAGGTCAATGATGCTAATTACAGGACTTACCTCCACAACTGGACCTGCTTGCCTGATTCCAATGACGTCGTCCAGGCCAGACAAATCTATGACCTCCAGAGTGATGTATGTAATATCCAGCTTCGGTTGAGCAATATTAATACATACATCAAATTGACTTTCCATTTTTATTTTAGTTGGTTGCCAGTATGTAAAGTTGACAATTCAAGAAAAAGAGGAACTGCATGGATCCGATTGTCTCCTTCATGTTGATAAAAAGATAAAGAGCTGCATGAATGTTTTCTTTAAACATAATGTCTGCTTTTAGGCGGTGTACAAAGCTGATCTAAAATGGCTTCAAGGTCTTGGATGGGTTCCTATTGGTTCAATTGATGTTGAGAAAGTGAAAAAGGCTGGCGAAATCCTAAGTGAAGCGAAGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16506
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
ENSDART00000032130 None None 334 None 8
ENSDART00000061293 Nonsense 2349 6235 47 134
ENSDART00000101711 None None 610 None 17
ENSDART00000142020 None None 175 None 6
ENSDART00000142585 None None 564 None 15
ENSDART00000143888 Nonsense 2354 6177 50 135
ENSDART00000146486 None None 388 None 11

The following transcripts of ENSDARG00000032630 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 23889186)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 23044972
GRCz11 9 22855841
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTGCNTGAATGTTTTCTTTAAACATAATKTCTGCTTTTAGGCGGTGTA[C/A]AAAGCTGRTCTAAAATGGCTTCRAGGTCTTGGATGGGTTCCTATTGGTTC
Long Flanking Sequence:
GTAAGCAAGTTGGTCACCACATTGGAGCTCGCAGCATCCAGGATGATCCTCTCCTCATGCTGGCCTTGAACTCAGCTAAGATTGCTAGTGATGCTCTGTACAAGAAAGACTTCAACAAGTCTAAGACCAAGTTCCACCTCCCGGTGGACCTTCTGTCTCTTGAACTGGCAAAGAAATGTCAGATCCAGGTCAATGATGCTAATTACAGGACTTACCTCCACAACTGGACCTGCTTGCCTGATTCCAATGACGTCGTCCAGGCCAGACAAATCTATGACCTCCAGAGTGATGTATGTAATATCCAGCTTCGGTTGAGCAATATTAATACATACATCAAATTGACTTTCCATTTTTATTTTAGTTGGTTGCCAGTATGTAAAGTTGACAATTCAAGAAAAAGAGGAACTGCATGGATCCGATTGTCTCCTTCATGTTGATAAAAAGATAAAGAGCTGCATGAATGTTTTCTTTAAACATAATGTCTGCTTTTAGGCGGTGTA[C/A]AAAGCTGATCTAAAATGGCTTCAAGGTCTTGGATGGGTTCCTATTGGTTCAATTGATGTTGAGAAAGTGAAAAAGGCTGGCGAAATCCTAAGTGAAGCGAAGTACCGTCAGCACCCAAGCAACTTCAAGTTCACTTTGACAACTCAAGACATGCCAATGGTCTTAGCTAAAGCCAACAATGATGTTATGAACAAGGTAAATGCAGGACTGATATAACACATGATATGCACTTTTCGAATTCAGTTAATTTATTTGGTATGTGAGAGAGTTAATTTGTGGAAGTAAAATTATTTTAGCAATTTTCTTTGTTTCTTTGACAGCAACAATATGCTAGTGCCTGGAACAAAGACAAGACAAAGATCCATGTTATGCCAGATGCAATGGACATTGTACTAGCAAAACAAAACAGGGTCAACTACAGTTTGGTAAGTATAAGGGTGCTTTCGCACCTGCCTTATTTAGTTTGGTTGAATCATACTAGAGTTCGTTTTCCCTCTTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21476
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
ENSDART00000032130 None None 334 None 8
ENSDART00000061293 Essential Splice Site 3421 6235 64 134
ENSDART00000101711 None None 610 None 17
ENSDART00000142020 None None 175 None 6
ENSDART00000142585 None None 564 None 15
ENSDART00000143888 Essential Splice Site 3426 6177 67 135
ENSDART00000146486 None None 388 None 11

The following transcripts of ENSDARG00000032630 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 23883195)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 23038981
GRCz11 9 22849850
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACCCCTGAGATCATCCTTGGAAAACAGAATAAACTCAACACAAGCATT[G/A]TAAGTGCAGCAGCACTGCTTTGTAGTAACCAATAAATCTTGAATAAATGT
Long Flanking Sequence:
TTTGTTAATAATAATCAATACCACTAGAACTTTTAGTTTTCTAATTTTCTTTCGTGTTTCTTGCAATAAGGCTGTGTACAAGGCTGATATGGAATGGATCAGAGGTACTGGATGGGTACCAATAGGCTCAGTGGACGTAGAAAAAGCTAAAAAGGCTGGTGAGATTCTAAATGAAAGAAAGTACAGACAGCATCCAAGCAAGTTTAAGTTTACATGCAAGACAGATGGCATTCCTTATGCTCTTGCCCAAGCCAATGCCAAGACTATGGATAAGGTAGATATTTTTTATAAACTGTGTAAAAGCCTGCTATTTGAAATCACTGTTGATGGCTGGAATTTCGTAGACCACAGATGAATGTGTCTAAAGTTTTGTATTCCTTTTTATGTCATTACAGAATGCATATGTTGAAGCCTGGAACAAGGAAAAAATCAATATTCATGTCATGCCAGACACCCCTGAGATCATCCTTGGAAAACAGAATAAACTCAACACAAGCATT[G/A]TAAGTGCAGCAGCACTGCTTTGTAGTAACCAATAAATCTTGAATAAATGTACACAATTTTATGTTTCAAATCCTGATAAAACTGTATGTTTTTTTCATGTTACTGCAGAAATATTACCGTCAAGACTACGAGGAAAGTCTTAAGAAGGGCTACTTCCTGCCCAAAGATGCAGTCTCTGTGAAATCTGCCAAGGCCTCCAGAGACATCATTAGTGATGTAAGTGCAGATGTGGAACTTTTTCTAATACATTAAACACACAGCATTCAATTATTGTGCTCAATTTCTTACATGTATTATTACTTTGCAGTACAAGTACAAAGCCGGATACAGGAAGCAGCAAGGACACCACATTGGAGCCCTCAGCATCAAGGATGATCCCTTGATCATGCTGGCCTTAAACTCAGGCAAAATTGCAAGTGATCTTCTGTACAAGAAAGACTTCAACAAATCCAAGACCAAGTATAACCTCCCAGCAGACCTGCTGTCTCTTGAGTTGGCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34626
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
ENSDART00000032130 None None 334 None 8
ENSDART00000061293 Nonsense 4021 6235 75 134
ENSDART00000101711 None None 610 None 17
ENSDART00000142020 None None 175 None 6
ENSDART00000142585 None None 564 None 15
ENSDART00000143888 Nonsense 4026 6177 78 135
ENSDART00000146486 None None 388 None 11

The following transcripts of ENSDARG00000032630 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 23879450)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 23035236
GRCz11 9 22846105
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACATGCAAAGAAGTGCCAGATCCAAGTCAATGACGATAAATACAGAACT[C/T]GACTGCACCAGTGGACATGCTTGCCTGATCAGAATGATGTCATTCAGGCC
Long Flanking Sequence:
TAGAAAATCCAAAACCCTATCTGTAATAACGGCTCAAATTTAAGAACTAACTAAAATGTTATTTTATCATTACCTATAGCATTTTTACACCAAAAACTGGAACAAATCCAAAGCCACATCATACTTCATGCCCGGAGATGCAGTCCCGATTAAACAATGCATCCATAACAGTAAAGTACAGAGTGATGTAAGTAAATAAATAAAAGTAAACCTAATTCCAGCTCACCTTAATGTTATCAACACAAATAAAATGGACTTTTTTTCAGTACAAGTACAAGACTGGTTATCGTAAGCAAGTTGGTCATCACATTGGAGCCCTCAGCGTCCAGGATGATCCTCTGCTCATGCTGGCCTTGAATTCAGCTAAGATTGCTAGCGATGCTCTCTACAAGAAAGACTTCAACAAGTCCAAGACCAAGTTTAATCTCCCAGTAGACATGGTGGCCTTTGAACATGCAAAGAAGTGCCAGATCCAAGTCAATGACGATAAATACAGAACT[C/T]GACTGCACCAGTGGACATGCTTGCCTGATCAGAATGATGTCATTCAGGCCCGTAAAGTGTATGACTTGTGCAGTGATGTAAGTTTTATTTGCTTCATAATACATTTGATTTTATAAAAAATATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAACGTTCTACCTCCAGAACATCTACAAAGCAGATATGGAATGGTTGCGTGGTTGTGGATGGGTTGCTGCTGATTCTGTGGAGCATGTCAAAGTCCGAAAAGCCCAAGAGATTATCAATGATGTAAGTTTCAACAGTGGTTTTTTTTTTTTTTTTTGTCAAATTTGCACTTATAGCATGAACAATGTCTTACAACAGTTTATGTTTCTTTTGTCCCTGCACAGAGACATTACAAAAAAGATGCAAAGGACAACTTTAGCAAATATACTCATATTGTGGATCGCCCAGAGATTGTCCTTGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11973
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
ENSDART00000032130 None None 334 None 8
ENSDART00000061293 Nonsense 4476 6235 87 134
ENSDART00000101711 None None 610 None 17
ENSDART00000142020 None None 175 None 6
ENSDART00000142585 None None 564 None 15
ENSDART00000143888 Nonsense 4445 6177 89 135
ENSDART00000146486 None None 388 None 11

The following transcripts of ENSDARG00000032630 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 23876861)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 23032647
GRCz11 9 22843516
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAAACCTTGTCGTAATSTTTTRTCTCTTAGCGCCTGTACAAAGAAAACTA[T/A]GAGAAGACCAAAGCAAAAATCAATGTACCTCCCGACATGCTTGACATCGT
Long Flanking Sequence:
GCTTAAAGTTCCTGGTTTATTTTGCCGTCACAGTTTTTAAGATATTTTTTATGAACATTCAGAAAGCATACTCTGCTGCCTGGAACAAGATCAAGGCCAAGAGCTACTCAATCCCTCACGATTCCCATGCCTTAGCCCATGCTAAACAACAGAAGGTCATCCTGAGCAACGTGAGTCACTTTTCTAATACCTACTCCAGTCCTTCCAAAGAAAAAAAATACTGAATCTGAGTGGAATCTGATTGTTCTTGACATACTAGAGTTCTCCTTTGGCTTCTGTAGGTTAAATACAAGGAAGATTATGAGAAGTTCAAGACCCTGTATAGCCTGCCTAAGTGTCTTGAGGACGACCCCCAAACTGCAAGATGTGTGAAGTCTGGAAAGCTTGTCCTGGATGTGAGTAAAGTATCAGCTAAGCTGTGAGTTTATTACTTACTGAATGTCAAACTTTTAAACCTTGTCGTAATCTTTTGTCTCTTAGCGCCTGTACAAAGAAAACTA[T/A]GAGAAGACCAAAGCAAAAATCAATGTACCTCCCGACATGCTTGACATCGTATCTGCACGCAATACTCAGAAGACTGTCAGTGGTGTTGACTACCGAAAATACCTACACCAATGGATCTGCCTGCCTGACATGCAGGTGTACGTACATGCCCGCAAAGTCAATGAGCAACTGAGCGACGTAAGTGACATGAAAGTTATAGCAAAGTCAAGTCAGAGTGCTAACTGGAATGTGGTCTCTTTGTTGCTGTAACCCTCACATTGCATCTAATTTCAGATTTTCTACAAAGATGACCTCAACTGGCTGAAGGGAGCTGGCTGCTATGCTTGGGACACTCCTGAGATTCTTCGTGTCAAGCAAGCGATGAAACTGCAGAGTGACGTAGGTGTAGTTTCATGTCATTTTCTGTAAGTTTATTCTTCCTCTATCTTCTCACATGCTGTCTTCACCCTGGTGATTTTCTTTTTCAGAACTTGTACAGAGCTAAAGGAATCGAGCACTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11545
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
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Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000032130 None None 334 None 8
ENSDART00000061293 Essential Splice Site 4535 6235 87 134
ENSDART00000101711 None None 610 None 17
ENSDART00000142020 None None 175 None 6
ENSDART00000142585 None None 564 None 15
ENSDART00000143888 Essential Splice Site 4504 6177 89 135
ENSDART00000146486 None None 388 None 11

The following transcripts of ENSDARG00000032630 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 23876683)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 23032469
GRCz11 9 22843338
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATGCAGGTGTACGTACATGCCCGYAAAGKCAATGAGCAACTGAGCGAC[G/T]TAAGTGACATRAAAGTTATAGCRAAGTCAAGTCAGAGTGCTAACTGGAAT
Long Flanking Sequence:
CTTTTCTAATACCTACTCCAGTCCTTCCAAAGAAAAAAAATACTGAATCTGAGTGGAATCTGATTGTTCTTGACATACTAGAGTTCTCCTTTGGCTTCTGTAGGTTAAATACAAGGAAGATTATGAGAAGTTCAAGACCCTGTATAGCCTGCCTAAGTGTCTTGAGGACGACCCCCAAACTGCAAGATGTGTGAAGTCTGGAAAGCTTGTCCTGGATGTGAGTAAAGTATCAGCTAAGCTGTGAGTTTATTACTTACTGAATGTCAAACTTTTAAACCTTGTCGTAATCTTTTGTCTCTTAGCGCCTGTACAAAGAAAACTATGAGAAGACCAAAGCAAAAATCAATGTACCTCCCGACATGCTTGACATCGTATCTGCACGCAATACTCAGAAGACTGTCAGTGGTGTTGACTACCGAAAATACCTACACCAATGGATCTGCCTGCCTGACATGCAGGTGTACGTACATGCCCGCAAAGTCAATGAGCAACTGAGCGAC[G/T]TAAGTGACATGAAAGTTATAGCAAAGTCAAGTCAGAGTGCTAACTGGAATGTGGTCTCTTTGTTGCTGTAACCCTCACATTGCATCTAATTTCAGATTTTCTACAAAGATGACCTCAACTGGCTGAAGGGAGCTGGCTGCTATGCTTGGGACACTCCTGAGATTCTTCGTGTCAAGCAAGCGATGAAACTGCAGAGTGACGTAGGTGTAGTTTCATGTCATTTTCTGTAAGTTTATTCTTCCTCTATCTTCTCACATGCTGTCTTCACCCTGGTGATTTTCTTTTTCAGAACTTGTACAGAGCTAAAGGAATCGAGCACTTTAAGCAGTACACTGTTGTGATGGACACGCCAGTCTATGAAACATGCAAACAGAGCGCTAAGAACTTGAGTGAGGTAACACCTCAAAAACATCCATCAGCTAACACTATAATTCCTTTACTTAATTTTGGTTGAAGCTGGATTTTCTGACTCCTATACGTTTTATCTGCAGCTCAACTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21475
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000032130 None None 334 None 8
ENSDART00000061293 Essential Splice Site 5097 6235 104 134
ENSDART00000101711 None None 610 None 17
ENSDART00000142020 None None 175 None 6
ENSDART00000142585 None None 564 None 15
ENSDART00000143888 Essential Splice Site 5066 6177 106 135
ENSDART00000146486 None None 388 None 11

The following transcripts of ENSDARG00000032630 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 23871807)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 23027593
GRCz11 9 22838462
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACTGCTCTCGAGGCAGTTGTCTTTAACTCCAATTTTGAAATTCTGAGC[A/C]GAGGTCCTACCGTGCCAGCTATGAGAAGTCTAAGGATAAGTACACCATAG
Long Flanking Sequence:
TATTTGCTGCTGTTTAATTGTGTTTTTGACAGAGACTCTACAAAGCATCATTTGAGAAAAACAGAGCCAACTTCAAGTACACATGTGACACACCATTCTTTGAGGCTGCCAAGAACGCTTCACTTCTGATCAATGACGTAAGTCAATAGTAGTATAACTTTATATCTTAATACTCTGGTATAATACATAAATAAAATTAGAGAAATCCAGAAGCAAGTAAATCATTACAGATATGCAATAAAATATGAAAACTGTCCTTGCATAACCTGAATTTCTTCCACTGCTTTAATAATGGATACAAATTGAAAGGTAAACCATTATCTAATCTCTTTCTGATGACGGTCTCATTTATATTTTAGGAATTGTTTTATCCATGTCTTTACCATGTCTAAGATTTCAATGTATTTACCCACCATGCCTTATTTTCTCCTCCTAAATAAGTGTTTGTTTTCACTGCTCTCGAGGCAGTTGTCTTTAACTCCAATTTTGAAATTCTGAGC[A/C]GAGGTCCTACCGTGCCAGCTATGAGAAGTCTAAGGATAAGTACACCATAGTTGTAGATGACCCTAGAAACGTCTTGGCTAAGGAGAACAGCAAGATGAGTCAGGTAAAGCTACCAGCTGCAGCTGCCTCTACGGGTCCGTCGCCTGCCACAGGGGCCTGAGCATGAGGTCATCTTCAGTCCACTGGATGACTATGTCGCATGGCTACAACGTCACTTGATTGTGTCACTTTCTCTCCACTGATTTAGGTTTCCCTTTAAGTGACATTCAAAAAAATAATTTTTTGAGTGTGCACCGCTACTTCCAAATCTCTGTGCTCCAGATAATGCTTTGTCTGAAAGTGCGGTAGTTTGAGTGATATTCACAGTTGCTCAGTTAAATTTTGGTAATGAAAGTCAAACATTCTCCCACAGATTTTTTTATTATTTTCACCATATTGACAAACAGAAACATGATTGGTTTTCAAGCGACTACTGTATGAGCTTAAAATAGGGTTACTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18354
Status:
Available for shipment
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Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000032130 None None 334 None 8
ENSDART00000061293 Essential Splice Site 5586 6235 117 134
ENSDART00000101711 Essential Splice Site 156 610 5 17
ENSDART00000142020 None None 175 None 6
ENSDART00000142585 Essential Splice Site 47 564 2 15
ENSDART00000143888 Essential Splice Site 5555 6177 119 135
ENSDART00000146486 Essential Splice Site 174 388 5 11

The following transcripts of ENSDARG00000032630 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 23863867)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 23019653
GRCz11 9 22830522
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAGCAAGATATATCAGACTCTGAAGGATGCTAATACACTTGCAAGCGAG[G/T]TGCTTTTAAGACTAAAACATTTTTTNNNNNNNNNNGTCTATTTATAAATATTACCMATCA
Long Flanking Sequence:
CACCTAAATGACAGTTTTATCATTAGTTAATATAATTTCATCTTTATTTTGTTCCATATATTTGGAGTCCAGTGGTTTGGTGATGTTTTCACACACTTCAGCTTTAATTCAACAAATTGTAAACTGTATGTTGTTGTGGTGTGTTTGAATGCTCTGAACTTTGTTTTGATCCTCCTTTTTGGGACTAGTACAATCTGAATATCATCTGATTCATACTGTATTAGGCCCTGTTGTAAGACTCTTTCCAGTGTACTTTTCTATTCTCTGGTTATTGCATGAAGGAAAATGATAGATGTTTCTGTGCTTTTTGCAAGTATTTTGGCTCATACGACTTTGATAATATATCACTAACAGCAGCTAACAATGTCAATATCCTCTCTCAAAAGGTAAAGTACAAGGAGAAGTTTGACAAGGAAATGAAAGGAAAGAGACCACAGTATGACTTGAAGAACAGCAAGATATATCAGACTCTGAAGGATGCTAATACACTTGCAAGCGAG[G/T]TGCTTTTAAGACTAAAACATTTTTTGTCTATTTATAAATATTACCCATCACAAATAATGACAAATGTTGTGTTTTTTTTTATATATATTATGTAGGTGAAATACAAAGGTGACCTGAAGAAGATTCACAAGCCTGTTACAGACATGGCAGAATCTCTGTCCATGCAACACAACCTGAGCACTAGCAAGCTGGCCAGTGATGTAAGATTATTTTAAGCAGCTTTATTTTCTTTCATCAACACAACATTTCCTTTAATCACTTCCTTTCACATCAACATCTTACACACTATAACAGTGTAACATCACATTTTCACATAACAAGATCTATCCATCATCCTTTAAAGAAAGCTACCATCTTTAAACTATTTACTCATTCTAGGCTATCATGTGGTAGTGACCCTCATCTTCCGATTCTAAAAGTACTACTACTAGCATTAGATTTTAACTACCATCATTTTTGCTCTTGTTTGACCCTGGTACTATTCTTCTTCTTCTTTAATA
Associated Phenotype:
Not determined