Busch Lab

ZMP

myo9b

Ensembl ID:
ENSDARG00000077410
ZFIN ID:
ZDB-GENE-030131-938
Human Orthologue:
MYO9B
Human Description:
myosin IXB [Source:HGNC Symbol;Acc:7609]
Mouse Orthologue:
Myo9b
Mouse Description:
myosin IXb Gene [Source:MGI Symbol;Acc:MGI:106624]

Alleles

There are 10 alleles of this gene:

Allele Name Consequence Status Availability
sa19821 Nonsense Available for shipment Available now
sa8631 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa45111 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa39887 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa32969 Essential Splice Site Available for shipment Available now
sa31289 Nonsense Available for shipment Available now
sa16154 Essential Splice Site Available for shipment Available now
sa15461 Essential Splice Site Available for shipment Available now
sa17368 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa19821
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088040 Nonsense 334 2227 4 56
ENSDART00000131590 None None 678 None 16
ENSDART00000144807 Nonsense 334 998 5 22

The following transcripts of ENSDARG00000077410 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 37448755)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 37745465
GRCz11 2 37727922
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTACTCAACGCAAATTCCTTGTCTGCTTGTTATCTGACCTACAGGAATTA[T/A]CATGTTTTTTATTACCTTTTGATTGGCGCCTCAGAGGAGGAGAGAGATGA
Long Flanking Sequence:
TGAGTTACTAAACCACCCACGAAGGTGCGCACCTTACTTTGTCCAGCAAGTTGGAGAGCAAGCTTTTTTCACTATGCTGATTGAATATGTTTTTAAAGACATGTCTGAAGTACCGTTATGTTTTCTCAATCAGGAAGTGATGTTTTTGTTAGACTGAAGTTGCTAGGCAGCAGAGACAGATTAAGACAGACCTCTTATATTTTCTGGTCCCATTCTCTAAAATAATTATCGGAAAGTCTAGCTATTGCTGGCATTGATCTGAAATTCCTAATACAGCTTTTGTTCAATGTTTCAGGGCTGTTGTTGAGAAGTATTTACTAGAGAAATGCCGCCTAGTGTCCAGAGGAAAAACTGAAAGGTAATAAATTGGAAACCATTTTATATATATCAATTTTATCCATATCCCTTTTACGTTTGAACTCCTTAGTGTCACAAGTGGAATTAAATGTATTACTCAACGCAAATTCCTTGTCTGCTTGTTATCTGACCTACAGGAATTA[T/A]CATGTTTTTTATTACCTTTTGATTGGCGCCTCAGAGGAGGAGAGAGATGAGTTTAAGCTTCTGCAGCCTAATGACTACCACTACCTCAAAGAGGTAAGGATTATCTTAGTTTTTCTTGTCTTTGCTGAACAAATTTTTTTGTCATCATTTACTTATCGTCCACTTGTTTCAAACTTGTTAGACTTTCCTGTTTCTGTTAAAGATAAATGCAAGTATTTTAAAGATTGTGAGAAACTAGTAACCATTGACATGTCTATTTTGTTTAAGTCAATTGTTGGACTTTCTTCAAAAAATCTTCTTTTCAAGAGAAGAAAGAATCTAATAGTCTTCTAATGTTCTTACTGTATGTCTTATTGGATTATTTGCTTTTTTTGTTATTGTTAAAATATCACAGCTAAGCTTTTCCATTAATTATCTGTTTTTCAACTTAACCTCACAGGAAATGCCAATTTCAGAGGATCAAGCTGAAATGACACATGAATTCCGGAGACTTCATCAGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8631
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088040 Essential Splice Site 417 2227 None 56
ENSDART00000131590 None None 678 None 16
ENSDART00000144807 Essential Splice Site 399 998 None 22

The following transcripts of ENSDARG00000077410 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 37448213)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 37744923
GRCz11 2 37727380
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCAWCAGGCCATGGAGATGGTCGGTTTTCTGCCTCCAACCAAAAAGCAG[T/C]AAGTTTATTTTTTGNATTTAGATTTTTCTCTTTAGTCTGCATCCTAAACCA
Long Flanking Sequence:
GAGAGATGAGTTTAAGCTTCTGCAGCCTAATGACTACCACTACCTCAAAGAGGTAAGGATTATCTTAGTTTTTCTTGTCTTTGCTGAACAAATTTTTTTGTCATCATTTACTTATCGTCCACTTGTTTCAAACTTGTTAGACTTTCCTGTTTCTGTTAAAGATAAATGCAAGTATTTTAAAGATTGTGAGAAACTAGTAACCATTGACATGTCTATTTTGTTTAAGTCAATTGTTGGACTTTCTTCAAAAAATCTTCTTTTCAAGAGAAGAAAGAATCTAATAGTCTTCTAATGTTCTTACTGTATGTCTTATTGGATTATTTGCTTTTTTTGTTATTGTTAAAATATCACAGCTAAGCTTTTCCATTAATTATCTGTTTTTCAACTTAACCTCACAGGAAATGCCAATTTCAGAGGATCAAGCTGAAATGACACATGAATTCCGGAGACTTCATCAGGCCATGGAGATGGTCGGTTTTCTGCCTCCAACCAAAAAGCAG[T/C]AAGTTTATTTTTTGATTTAGATTTTTCTCTTTAGTCTGCATCCTAAACCATTACTTTTTAGAAGTCTTTACATATTATGTAAAACTATGTCTTTAACGTTTAATTACAAACAAACAACCTTAAAATAAAATTTCCTGAAGGTTTTTTTTTCTCCATTAATACCATATTCCCAAAAGAACCTTTGAAAGGACAGTTCTTGTAGAAAATACACTACCGGTCAAAAGTTGGGATAATTTATTTTTTCATGTTTTTTTTTCTCTTTTAAATTATTCTATTCATCAAGGTGGCATTTAATAAATGTAAAAAAAAAATCAATTGTTTAATATTTATTAAAAGTTTAAATAACTGATTTCTTTTTGTTAGTGGTTTAAATGATTAAATTAATGATTAAAATTAAATGATTAAAATTAAATGATTTCTGTTATAATGTTTAAAGGTTCTTTGTGCATCCATCAGTGCATATATAGAGAACCTTTATTTTAAGATTGCATTGATTTTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45111
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088040 Essential Splice Site 458 2227 6 56
ENSDART00000131590 None None 678 None 16
ENSDART00000144807 Essential Splice Site 440 998 7 22

The following transcripts of ENSDARG00000077410 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 37447039)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 37743749
GRCz11 2 37726206
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAAGTTGGACCTGATCATGTCCTTTCAGCTCTGTCTGACCTTCTAAAG[G/A]TACCACAAGCTACTTTAATGTTTAATATAAATTCACAATAGTAAGCCAAA
Long Flanking Sequence:
AGGGGTGAAGTCACTGAAAAATTACCAGCTGTATGCATGACTAACAAATAAAGAATTCTGGTCTGGGACAAGTCTGTGCTTGTCATTTAGGGGGGAAATGCATCAAGAAATGCTCTGTGCTATTTTGGTCATGAAATGCAGTGTGATGATTATGAGCTGCCTTCCAAAAAAATTTTGGAATTAAATGTAACTGTTATATAATACTGGTAACAAACAGCTTATTACTTAGAATTGTAATTAGTCAAAATATTGACTTATTCCATTGTTCAAAATGCATGATTTGCATTGTTGTAGTAATATGCTTTTTATACATGAATTTTATGAGGCACTTTGCAAAGAAAAAGTGTTTGTAATGTGTTTTTCTGTTCTTTTTCAGGATATTCTCTGTGCTCTCTGCCATTCTGTACCTGGGAAATGTGACGTACAAGCCAAAAGATGTTGGCGAAGGGCTTAAAGTTGGACCTGATCATGTCCTTTCAGCTCTGTCTGACCTTCTAAAG[G/A]TACCACAAGCTACTTTAATGTTTAATATAAATTCACAATAGTAAGCCAAATTTGTCTCTTTGGTTCCACTTTTTCCATTAAACATGGGACACCACAATACTAGCTTTAAATAACGTAAACTATAAAATCACCTCACCCAATAGTTTGGAAATATGGTAGAGTGACATATTAATGAATCAGGTCACTGCCACAATGTATTATTGTCTTTATCATATATTTAAACTCTTAAACTTAAATATGTGGTGACATGTATTCAATGGATGCTGTACAACCGTATAAGAATTATTTAGAAATTATCTTTCCAATCGAAATCAATGTGTGCATCTAGATGGCTTTGTTTTTAGTCCATTCGTTGTAGTTTAAGGTTTATTTTGGTCGCTTCTTTTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGGGCAATTCCAGACAAATGTCAACCTTGCCATAAAAAATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39887
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088040 Essential Splice Site 488 2227 7 56
ENSDART00000131590 None None 678 None 16
ENSDART00000144807 Essential Splice Site 470 998 8 22

The following transcripts of ENSDARG00000077410 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 37445102)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 37741812
GRCz11 2 37724269
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAATGACTGCTAATGACAAGCTGATTCTGCCTTACAGCCTCAATGAGG[T/A]AAATTATAATATAACCGATAATATAATAGTGATGCATGTGATGACATTTT
Long Flanking Sequence:
CATATAAAACAGCTACTTATTAAAGAAATGAAGCATAATATTTTTGTAGTTATACTAGTAAACAAATAACTGTTTTTTTTTTAAGTTTTTTTTTTATGGAAGGCAGTGCATTTTTACTCTGTGTCCACGTTTTCTGTAGACAGCACAAAGTCTGACATTCCTGGAGGGAAATACAAAAATTAAAGTTTACTATGAGATTTGGATATTGCATGAGACTAACAAGAAACTATCACATCAGTTGAATATTGCTGTTTGTTTGTTGCTTTGATCTGTTAAAGTGATTAAATGTAATGTAAAAATTGAGCTGTTATATAAAGCATTACACATTGACAGACTCGTGTTTTCAAATGTTTAAATGTCGTCTTTATTACCATAAAATATGTCTTACATCATTGCTTTTCAATTCCAGGTTAAAGTTGAGCTGCTTGTTGAAGCACTGACTACAAGGAAAGCAATGACTGCTAATGACAAGCTGATTCTGCCTTACAGCCTCAATGAGG[T/A]AAATTATAATATAACCGATAATATAATAGTGATGCATGTGATGACATTTTCTGCTATGTACTGATCATTCATTAATTCAGTCATGTGTTAAGTACAAATCTATAAATAACTCTGTCTTTAGGCTATTACTGCCAGAGACTCTATGGCCAAGTCTTTGTACAGTGCCCTGTTTGATTGGATCGTCCTGCGAATCAATCATGCTCTACTCAACAAGAGAGATTTGGAGGACTCTGTACCGGTACATAAATACACTATATATTAGGCTTATGATGGTATCAGTTTTATATCTAAACTTTTTTGGGATTAAATGTTGAAGCTTGTATCACGGTAAGTGGTATTAAAAAACTGAGCTGAGCTGCAAAAGAGGTTGCTTTTAACTGATATAATCAGGGCTTGACATTAACTTTTTTGATTACCAGCCACTGTGGCTAGTAGTTTTCCAACATTAATGGCCATCACTTTTTCCTCTAACCAATTTTGTTGTTGGTAAAATATATTTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32969
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088040 Essential Splice Site 489 2227 8 56
ENSDART00000131590 None None 678 None 16
ENSDART00000144807 Essential Splice Site 471 998 9 22

The following transcripts of ENSDARG00000077410 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 37444982)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 37741692
GRCz11 2 37724149
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTAATTCAGTCATGTGTTAAGTACAAATCTATAAATAACTCTGTCTTT[A/T]GGCTATTACTGCCAGAGACTCTATGGCCAAGTCTTTGTACAGTGCCCTGT
Long Flanking Sequence:
GTGTCCACGTTTTCTGTAGACAGCACAAAGTCTGACATTCCTGGAGGGAAATACAAAAATTAAAGTTTACTATGAGATTTGGATATTGCATGAGACTAACAAGAAACTATCACATCAGTTGAATATTGCTGTTTGTTTGTTGCTTTGATCTGTTAAAGTGATTAAATGTAATGTAAAAATTGAGCTGTTATATAAAGCATTACACATTGACAGACTCGTGTTTTCAAATGTTTAAATGTCGTCTTTATTACCATAAAATATGTCTTACATCATTGCTTTTCAATTCCAGGTTAAAGTTGAGCTGCTTGTTGAAGCACTGACTACAAGGAAAGCAATGACTGCTAATGACAAGCTGATTCTGCCTTACAGCCTCAATGAGGTAAATTATAATATAACCGATAATATAATAGTGATGCATGTGATGACATTTTCTGCTATGTACTGATCATTCATTAATTCAGTCATGTGTTAAGTACAAATCTATAAATAACTCTGTCTTT[A/T]GGCTATTACTGCCAGAGACTCTATGGCCAAGTCTTTGTACAGTGCCCTGTTTGATTGGATCGTCCTGCGAATCAATCATGCTCTACTCAACAAGAGAGATTTGGAGGACTCTGTACCGGTACATAAATACACTATATATTAGGCTTATGATGGTATCAGTTTTATATCTAAACTTTTTTGGGATTAAATGTTGAAGCTTGTATCACGGTAAGTGGTATTAAAAAACTGAGCTGAGCTGCAAAAGAGGTTGCTTTTAACTGATATAATCAGGGCTTGACATTAACTTTTTTGATTACCAGCCACTGTGGCTAGTAGTTTTCCAACATTAATGGCCATCACTTTTTCCTCTAACCAATTTTGTTGTTGGTAAAATATATTTCATACATTCATAAATTTAACTTTGTCTTGCTAAAATACTATTAGATGTTATGACTCCTTATTCATTTCACTTTTTGTGTGTTATGTATGACCTTGTTCTATGAGCAAATGGATTGTGGTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31289
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088040 Nonsense 887 2227 20 56
ENSDART00000131590 None None 678 None 16
ENSDART00000144807 Nonsense 830 998 18 22

The following transcripts of ENSDARG00000077410 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 37430860)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 37727570
GRCz11 2 37710027
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTATGTCTTGGTCTGTTCAGGCATCCCTAAGCAAGTTGTTGGAAACCT[T/A]GAGGAAAGCAGAACCTTTCTTTGTTCGCTGTATCAGATCAAATGGGGATA
Long Flanking Sequence:
GACTCAAAATCACCTCCAAGTGGATGAAAACATCCCTAACCTCACAAAAAGGGTTAATTGGTTATATTCAAAAATGCGAGTAATAACACTAAGCTTTACTGTCCTCTACAGAATCTCATCGACTCACACTCTCTGAAGTTCATCATGGCCCTGACACAGCACAACCGCGTGACCAGATCCCTGCTCCATCTGCACACCAAGAAGAAACCACCTAGCATCAGCGCTCAATTCCAGGTTCAATATTATCATCTTAGCGTGGAAAAAAAAATGCATGGAGTAATCTCCAGCATCTGAGGTTTCAGGGATCAGTTTGCTCCGGCTCTGTGAAAGCCTGTTTTGTGGTAGTTGTAAATGAGATAAAAGGCTCAGACCCCCTAAGCTGTGGGGAGGTTTTGATATGATTTGCAGGGGTTTAATGGATGCTGATGGACAAATCAATGAGTCACATGCTTTTATGTCTTGGTCTGTTCAGGCATCCCTAAGCAAGTTGTTGGAAACCT[T/A]GAGGAAAGCAGAACCTTTCTTTGTTCGCTGTATCAGATCAAATGGGGATAAGGTATGGCGGAGAGCTTTCGTTTGAAGATTTGTAACAAATCTGTGGAATCTGTTTATGTTTTGGGTGATAAATGTTGATGCATACATGTTGGTGGATGTGTTTACAGAGGGAAATGCACTTTGATGATGCTCTAGTTCTTCAGCAACTGAGATACACCGGCATGTTACAAACCGTTCGGATTAGAAGGTCTGGATATGGAGCCAAATTCACCTTTAGGGTAATGTACTGAAATACTTTTTAAAATGTGTAACATTTCATTAGGGCTAATAATTGAATGGAATAAAGTAATAATTTTTTTTCAAATATTTGTAAATGATTAATGTAATGACTAATGATGCCTGAGTTTGAGGAGTAATTTAATAAAAAAGAGCAGAGATTAATAAGTAGTTTTTCTTAGGATATGCATATTGATTTTTGTTTTATGTCTAGTCATAAAGGTACTTATCTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16154
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088040 Essential Splice Site 904 2227 20 56
ENSDART00000131590 None None 678 None 16
ENSDART00000144807 Essential Splice Site 847 998 18 22

The following transcripts of ENSDARG00000077410 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 37430807)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 37727517
GRCz11 2 37709974
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAAAGCAGAACCTTTCTTTGTTCGCTGTATCAGATCAAATGGGGATAAG[G/A]TATGGCGGAGAGCTKTYGTTTGAAGATTTGTRAYAAATCTGTGGAATCTG
Long Flanking Sequence:
TTAATTGGTTATATTCAAAAATGCGAGTAATAACACTAAGCTTTACTGTCCTCTACAGAATCTCATCGACTCACACTCTCTGAAGTTCATCATGGCCCTGACACAGCACAACCGCGTGACCAGATCCCTGCTCCATCTGCACACCAAGAAGAAACCACCTAGCATCAGCGCTCAATTCCAGGTTCAATATTATCATCTTAGCGTGGAAAAAAAAATGCATGGAGTAATCTCCAGCATCTGAGGTTTCAGGGATCAGTTTGCTCCGGCTCTGTGAAAGCCTGTTTTGTGGTAGTTGTAAATGAGATAAAAGGCTCAGACCCCCTAAGCTGTGGGGAGGTTTTGATATGATTTGCAGGGGTTTAATGGATGCTGATGGACAAATCAATGAGTCACATGCTTTTATGTCTTGGTCTGTTCAGGCATCCCTAAGCAAGTTGTTGGAAACCTTGAGGAAAGCAGAACCTTTCTTTGTTCGCTGTATCAGATCAAATGGGGATAAG[G/A]TATGGCGGAGAGCTTTCGTTTGAAGATTTGTAACAAATCTGTGGAATCTGTTTATGTTTTGGGTGATAAATGTTGATGCATACATGTTGGTGGATGTGTTTACAGAGGGAAATGCACTTTGATGATGCTCTAGTTCTTCAGCAACTGAGATACACCGGCATGTTACAAACCGTTCGGATTAGAAGGTCTGGATATGGAGCCAAATTCACCTTTAGGGTAATGTACTGAAATACTTTTTAAAATGTGTAACATTTCATTAGGGCTAATAATTGAATGGAATAAAGTAATAATTTTTTTTCAAATATTTGTAAATGATTAATGTAATGACTAATGATGCCTGAGTTTGAGGAGTAATTTAATAAAAAAGAGCAGAGATTAATAAGTAGTTTTTCTTAGGATATGCATATTGATTTTTGTTTTATGTCTAGTCATAAAGGTACTTATCTATAAAGTAATATTACTACTTTCATCTTTAATATGACTCAGTAAATGTTAATATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15461
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088040 Essential Splice Site 941 2227 21 56
ENSDART00000131590 None None 678 None 16
ENSDART00000144807 Essential Splice Site 884 998 19 22

The following transcripts of ENSDARG00000077410 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 37430589)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 37727299
GRCz11 2 37709756
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACCGTTCGGATTAGAAGGTCTGGATATGGAGCCAAATTCACCTTTAGGG[T/A]AATGTACTGAAATACTTTTTAAAATGTGTWACRTTTCATTARGGCTAATA
Long Flanking Sequence:
ATGGAGTAATCTCCAGCATCTGAGGTTTCAGGGATCAGTTTGCTCCGGCTCTGTGAAAGCCTGTTTTGTGGTAGTTGTAAATGAGATAAAAGGCTCAGACCCCCTAAGCTGTGGGGAGGTTTTGATATGATTTGCAGGGGTTTAATGGATGCTGATGGACAAATCAATGAGTCACATGCTTTTATGTCTTGGTCTGTTCAGGCATCCCTAAGCAAGTTGTTGGAAACCTTGAGGAAAGCAGAACCTTTCTTTGTTCGCTGTATCAGATCAAATGGGGATAAGGTATGGCGGAGAGCTTTCGTTTGAAGATTTGTAACAAATCTGTGGAATCTGTTTATGTTTTGGGTGATAAATGTTGATGCATACATGTTGGTGGATGTGTTTACAGAGGGAAATGCACTTTGATGATGCTCTAGTTCTTCAGCAACTGAGATACACCGGCATGTTACAAACCGTTCGGATTAGAAGGTCTGGATATGGAGCCAAATTCACCTTTAGGG[T/A]AATGTACTGAAATACTTTTTAAAATGTGTAACATTTCATTAGGGCTAATAATTGAATGGAATAAAGTAATAATTTTTTTTCAAATATTTGTAAATGATTAATGTAATGACTAATGATGCCTGAGTTTGAGGAGTAATTTAATAAAAAAGAGCAGAGATTAATAAGTAGTTTTTCTTAGGATATGCATATTGATTTTTGTTTTATGTCTAGTCATAAAGGTACTTATCTATAAAGTAATATTACTACTTTCATCTTTAATATGACTCAGTAAATGTTAATATTTTTAAAGATTATTGCTTTAAAACATGAAACAAATGTTTGTACTGTTCTAGATACTGTTGGAAGAGACATTCTGTACTGTAATGTTAGTGTTAGGGATTCATTTGTGTATGTATATGTGTGTCTGGGGGAGTGTCTGTCTGTCTATCTATCTTTTTTCAAACAGTTTTTATCTATCCGTCTGTCTATCCCTCTATCCGTCTATCTGTCTATCCGTCTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17368
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088040 Nonsense 1077 2227 25 56
ENSDART00000131590 None None 678 None 16
ENSDART00000144807 None None 998 None 22

The following transcripts of ENSDARG00000077410 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 37426499)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 37723209
GRCz11 2 37705666
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATKTAACACTTTTACAGTATTTATAATTTATTTGTGACCMTCTTCACMCT[C/T]AAATGTATTGCAAATWYGTTTGGGAAGCTAAATAAATGATAATMGAGCCA
Long Flanking Sequence:
AAAAGTGATCTTTCTAATGTGCTAATTTGCCATTCTATTATGATTAGCTATAATTAGTGCTAAATCACAAATAATAGTTGTGAAATAAAAAAAATCTGCTTTGTGTTTTTAAGTAAACTGACAATATTATTGCAAATTAGATTTTTTAAAAACTTTTTTTAATTAGTTGAAATGTCACATTAAGATCATTTATTTGAAATAAACATTACATTATACGTATATTTTAAATGCATTTACTGTCACTTTTTATCAATCTAATGTATCTGATGAAAAAAAATATTAAAAACAAAGTTGTTTTCAATATGCTTCTTACAAAAAAGTCATATTAGTATACTTTATGATAATGCCATGGATTTCACAAAATATATAGCAGCACAACTGTATTCGATATTGAGATTCAAGTGGAAAAAAATATTTGTACTTTGTCCTGCACTTTATACTGCATATATTATGTAACACTTTTACAGTATTTATAATTTATTTGTGACCATCTTCACACT[C/T]AAATGTATTGCAAATATGTTTGGGAAGCTAAATAAATGATAATCGAGCCATTTTTTCCTCCTCTCATTCCACAGCGATCATGGCGTTATGTGCGTGAGACGTACAGATGCAGAGCTGCTATTGTGATTCAGATTGCATGGCGAAAGTCCAGGCAGAGAGCAGAGCAAGAAAAACTCAAAGCACAGGCGTATGTCAAGGTTATCTTTGGTTTGTTTTTGTTCAGGTTTTGTTCAAAAGTCTTAGTAATTTGTTTGTCCTTTTTAGATTTCAGAGAGATCTGAACAAGATTGAGGAGAAGAAGCCCAGCCAGCCCAAACCACTGCCTTCACTGCCTAATGAATCCCGCACAGCTGAATCAAAGAAAACTGATGAACCGAGACCACAGTTAAACACAGACACCAAACCTAAAATCCCAACACAACCTACTCCGGGAATCACAAAGCAACTTAGCGTTAAAGAGGACCGACTGGGTCGGAGTAATCGAGGAATGGTTGGCAATA
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa25863
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088040 None None 2227 None 56
ENSDART00000131590 Essential Splice Site 552 678 15 16
ENSDART00000144807 None None 998 None 22

The following transcripts of ENSDARG00000077410 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 37408924)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 37705634
GRCz11 2 37688091
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTGAAACACTGAATTAGTTGGTACTGATGTTAAGAATGTTGTGATTTA[G/T]GAATATTTTGGCCTACACACTGCCTGAGTTTGACCGGGACAGCTCTGATG
Long Flanking Sequence:
CTGCTTTTTTCTAACATTCTTCAGTATATCTTCATTCATGCTCAACAGAAGAAAGAAACTTGGGTTTGGAATAGATCATTTTTGGGTGAACTGTCCCTTTAAGCTGCAGTTCACTAATCAGCCACAGGTGGTGCTAGTATTTTTATTTCATTCTAATCTAGTTTAGCTTGTTTAGAAGTAAAGCTTGCAAAATGCATCTCGTAACTCTGATTTTACACTTTCCAGCAGATATTTGAACCGCCGAAATCAGATTCAAATGCTTCGTCGAAGGACAGAGCTGGGCTTGAAATTGAAAAGAACCTACTTAAGCGGATCAAGTCTATCAAGAATGAGAAGTGAGTTACACGTTTAACTTTTTTTTGTTTCCTTAATTGCTTTTCCTGCAGAACAAAAAAACTAGTGAAATCCTTTAATTTTACATTTTGATTTCATTTGTTCCTCTGTAATGTTCTCTGAAACACTGAATTAGTTGGTACTGATGTTAAGAATGTTGTGATTTA[G/T]GAATATTTTGGCCTACACACTGCCTGAGTTTGACCGGGACAGCTCTGATGCTGAGAACATGGACTCTGAATCATTAGTCAGCTCTGAAAGTCTACTAGAAGATCATTTTTCGAGTTTGGGCTTGGAAGGTCAGTACTGAGGTACAGAGCATTTTGAATACAATATCCTTGGATGCCCTGCATGCTCGGTGATAGAGAGGGCTTGGATTTGCTGCAACTGCGGTGAGCTGTTTATTGTGCTTGAGTTGTGTTTTTTAACCTGCTGTGTCTATAACCATGGGTTTGCTCTGCTGCTCTTACATTACATATAAAAAAATGTTTGCATATTTATTTTTATTACATATTGTTTAAATGTATTTCAGTGCTTCCTACAGGTTTGAAATATACTTGTGGCGGCAGCCAGATTGAAACGCACCTTTTACCCACAGCACATAAATGGTCAACTATAGACGTTAACACTTCAATATGTTCCCTCTGCTGCCGTGTTTGCTGTAGCCACTT
Associated Phenotype:
Not determined