Busch Lab

ZMP

si:dkey-233k19.3

Ensembl ID:
ENSDARG00000094282
ZFIN ID:
ZDB-GENE-100922-177
Human Orthologue:
DNAH11
Human Description:
dynein, axonemal, heavy chain 11 [Source:HGNC Symbol;Acc:2942]
Mouse Orthologue:
Dnahc11
Mouse Description:
dynein, axonemal, heavy chain 11 Gene [Source:MGI Symbol;Acc:MGI:1100864]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa39095 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa18093 Nonsense Available for shipment Available now
sa22807 Essential Splice Site Available for shipment Available now
sa42698 Nonsense Mutation detected in F1 DNA Not yet available
sa6421 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa22806 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa39095
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
ENSDART00000138744 Essential Splice Site 42 1547 None 29

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 16 (position 21211802)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 19448557
GRCz11 16 19254196
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGAAAACTGCTGGAGGTTCTTTATGAATCGAGTGCGACATCAGCTCAAGG[T/A]CTTTCTGCAGTTTTTTTTTTTTTTTTTTGTATGCACAGCAGTTATTTGTA
Long Flanking Sequence:
TTGATTTTAATTATGCTTATTTACAGCTTACGGGATTTTAAACAACCACTACTGTATCTTGAATACATTTTTTCCTATTAAGCAGTATCAAAATCTCTTTAAGGCTAGTCATTTCACTCAAGGATGATTTGCTCAGCAATGGATAATTTGCTCTTGTACTCGAAGGCGGGCTTTATTTGCCCTATAGACCATTACACTTTTCCCCATTTAAAAACGATACAAGTGAGATGTCTTGTCTTGTGTATTCTATGGTCTTTGGTAGTATCTAAATGTTACCTACTCAGTATTAAGTGGTAAATGCTTGCATGCAATTGACGTGCTTCCAGTAAAATAACTGTGTTGTTGTGTGAACCCAGGTGAGATTCCTGATCTCTTGAGTGAAGAGGAGGTGGAAGGTGTCAGGAAAGCAGTGAAGAGTGAAGTGCGGGATCTAGGTCTGCTGGACAACAACGAAAACTGCTGGAGGTTCTTTATGAATCGAGTGCGACATCAGCTCAAGG[T/A]CTTTCTGCAGTTTTTTTTTTTTTTTTTTGTATGCACAGCAGTTATTTGTATTGTCTATCTGGTTTAACAGAGTGTGTTTGTGTATTGTATGTGTTTGTAGGTCGTGCTATGCATGTCTCCAGTTGGTAATGCTCTGCGCCTGCGTGTCCGGCGTTTCCCGGCTCTGCTGAGCTGCACCACTCTGGACTGGTTCCAGGAATGGCCCCAGGAGGCTCTTCAGTCTGTCAGCTTAAAGTACCTGCAGGAAATCCCAAGTATTGAGGTAAACCTCACTGTCATTCAGTCAGCGAAATTAGTTTCATTGGGTTTCCACATCATTCACCTCATCATTTTTGGCTACTGCTCTTGCGTAACTACTGGAAGTCCTAAAGGCCATCAAATATAGATGACAAAGCGTTTTCACTCAGAGATGAAAAGAAGCTTGAAATAACTTTGCAACGGGATGCTTTATCAAACATGACTAGTGAATAGTGCCATGAAATAACAAAATAGAAACAGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18093
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000138744 Nonsense 504 1547 10 29

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 16 (position 21178016)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 19414771
GRCz11 16 19220410
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACAGCCATATCGCCAKCAGCTCCTTCAYGACAWGCTGATTCCTTTYCTC[A/T]GAGAACTCCGGGTATGATTTCYGCTTCACATTATTCTCAGTTGTCATTTT
Long Flanking Sequence:
CGGCGCAAGGCAGATTTCCCATCCTTAAATTAGCAAAAACGCGTCCTGACACGCCCTGAAAGCATTTGCGCCCTGCGTTTTGCGCTCTGCGCATGGACCGTCAAAATAGAGCCCTATATTGTAATGCTTTCAAAAGTAACTTTCCTCAACATTGCCTAAACCCAACTACTACTTTTACATTAGCAATACATTAGGAGTTTACTGAGCTTTTAGGTAAAGGTAGTAGTAGTGAAAATTTGAACCTTAACTTAAAGTGTGACAAGATGTCTTTGTCTTGTGTTACATAATATGTTTTTGCTTGCTTAAGTTAGATTTACCCAGTAATTCGTTGATTATAGGCAGAAAATGTGCGCTGGTCGGAGGGTCAGCTGGAGCTGGAGGGTCAGCTGAAGACTGTGTGTGGTGATGTGCTCATAGCAGCTGCTTTTGTCTCCTACGCTGGATATTTCACACAGCCATATCGCCATCAGCTCCTTCACGACATGCTGATTCCTTTCCTC[A/T]GAGAACTCCGGGTATGATTTCTGCTTCACATTATTCTCAGTTGTCATTTTTTGGGGACATGCAGTATAGTGGTTAAATAGGTATTGGAAGTAGTTATTTCATATTATTACATTTTAGTTGTATTGTTATTATTATTATTTTGTGAAAATGTGGTTTTGCTTGGTAAAAGAATACCTATAAAAAGTATAAGTCCACTGAATGGATGCAATGTTCTCAAAAAAATAAAAATAAGTTCTTTAGATCTTTACTTTTCTAACAAAGACATTAGTAAATCAAGAAATATTTATACTAGAAAAGAACTAATCATTTAAGAGTAATGTAATCCTTATAGAGGTAAACTAATTGTCCACACTTTTTGTTTTTGTATTATTTCTAGTCTAAGTAGATTAGGTAACAATTTATTTTGATGACCCATTTGAGTGTTAGTACACTGTCTGCTTAATATCTGTTTATACTGCTCCTTAAAAGGACATTTTACTGACTATAAGAAACTTTGCAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22807
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000138744 Essential Splice Site 797 1547 None 29

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 16 (position 21167833)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 19404588
GRCz11 16 19210227
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTAAAGAACTTCACAATGTTAATCCCATGTACCAGTACTCCCTCAAGG[T/C]AACACACTACACATCTGCCTTATTTACAGTAGTTCAGATAAATAGCTCTA
Long Flanking Sequence:
GCTGAAGAGACTTGAGGATGAGCTGTTAAGCAAACTGTCTGCGGCAGAGGGAAACTTCCTGAGAGATACAGCCCTAGTGGAGCAGCTGGAACACACCAAGAACACTGCCAGACACATCCAGAACAAGGTACCATTTTTACTGTCCAGTTACCTCATTTTGGTTTTTGCCAGTTCAGGTGTCACTTTTGCATTGTTTGAGGAGAAGTCTGAAAGAAGTATGATGGTTGTAAAGTAAAAGACTGAAATTTGAAAAGACAATCAGTCTTCGTTCCTATAGCCTGTTATATTAAATACTACTGTATAATTAAAACTTGTACCATATGTAATTGTATATTTCAACAGTGTACTGTTTACACAGGCTGTTGCAGCTCGAGAGAATGAGATAAAGACCAACGAGGCACGAGATCTCTACAGGCCAGCAGCTGAGAGAGCCGCACTGCTCTACTTCATTATTAAAGAACTTCACAATGTTAATCCCATGTACCAGTACTCCCTCAAGG[T/C]AACACACTACACATCTGCCTTATTTACAGTAGTTCAGATAAATAGCTCTAGAATTTGTTTTGCCATTTTGTACGGTTGATTTGTGCATTTATGAATGACAAATCACAATCGAGTGTGAACCAAAAACAGAAAAAATAAGTTTACTGAGACCTGGGCCATGGTATTATGAAGCAGCTGAGCAATGTTCATGGTACATAAAACCCAGAACTGGTGCTTACTAAACTGAAACTTAACTGGCGAGCTTGCTAATCTGGCTTTATGGTACAGGCCCCTGCTACTCGGTGTGCTTTCAGATAAACACTGGAGCAGTTAATTTGGGGTTAGAACATAATCTAAACTTGAACAGACCAAAATGCAAAAAAATATATACTTTTTTTTTTTTTTTTGACTAAGTCAGCAACCATAGTCAACTGTGCTGTGTATTATTATAGAATGAAGGCAAGAATTTGTTTACAGGCCTTAAGCAACAGCTCTATTGTAAGCACAGCTTGTGGACAAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42698
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000138744 Nonsense 1166 1547 22 29

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 16 (position 21160409)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 19397164
GRCz11 16 19202803
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATACCCATTCAACAATGGAGATCTGAATATTTCAGCTAATGTTCTGTA[C/A]AACTACCTGGAGGCCAGTACCAAAGTAAGATATCACTATTCATTACCCTG
Long Flanking Sequence:
TCCATTCATGTTTTGTTTAAATTCATCATTTTGTTGTTGTTCTTAACAGTGAAAACTGCTTATAATTGGGAGTGAATGCACTTAAAACATTTTATGAAAATAGACTTATCACTTGCTCGCCCTGAAGTTATTCCAAACTGGAATGACTTTTGTTCTTCTTCTGAATGAAGAAGAAGTAAATGTTTTAAACTTGCACTGGGTTAAGAACAACTTGAGGATAAGTAAATAAAGACAGAATTTTTATTTCATTTTTTTATTTCTATTATTTATATCAGTAAGAACGTTATGAATTATTCTTAGTTTGTTCTTCATCTTGTCTTTTGTGTTTTGCAGGATACTCTGGAAATGTGTTCTCGAGAGCAGGAGTTTAAAGGACTCATGTTCTCGCTGTGTTACTTCCATGCCTGTGTGAGTGAGAGGCGGAAGTTTGGACCTCAGGGTTGGAACCACAAATACCCATTCAACAATGGAGATCTGAATATTTCAGCTAATGTTCTGTA[C/A]AACTACCTGGAGGCCAGTACCAAAGTAAGATATCACTATTCATTACCCTGATAAAATAATAATAATAATAATAATAATAACTGTCATTATTATTATTATTATTATTATTTACAACTTATAAACATGACATGATAAAATAATTAGATATATTTTTTGAAAGTCAGCATATGATAATGATATCTGAAGGATTATGTCACATTAAAGACTATATTTATGGTGCTGAAAAATGAGCTATGTCATCACAGGGATATTGTGATAAGTTTGGATATCTACTTGTTAAGCCTGGGAGTATGAAGTACTTTTTCCAGCTTCAAGCCTTCACAAACTGTGAAAATAGCTTATGTTATGACCACGGTTTAGTCATATCACACACAATGGCACAATATGTAAGTTTGTGCTTACTGTAGATTATCCTGAATGCATTGAAGAACTTTAATTCATCAGTGCTTTAATTCATTTAAATATTGCTCATTTTAACTATTTTAATTGTATGCTATTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6421
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
ENSDART00000138744 Essential Splice Site 1395 1547 None 29

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 16 (position 21143431)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 19380186
GRCz11 16 19185825
KASP Assay ID:
554-4894.1 (used for ordering genotyping assays)
KASP Sequence:
AGAGTTGGAGCAGGCTGACCTTTCCTTCAACTAAAACCCTGCCTCARTGG[T/A]ATAATCACCTACATAGATCTTTCTGATACAGACAAACACTAAACCATTTG
Long Flanking Sequence:
AATTTCTGAGAAAAAACTAGTCAATTACAGTAGGTTGAGTATTTGTAATTTGTTATTTTACACCACTGTACATTACACGTTTTATTTAAATTGTATCTTTTTATAGCACATGTATAATGTTATAAGCAATATACAGCATACATATATAATAAAACGTAATTAGTAAGTAATTACAAATTATTTTTTCATGAATACCACATTGACATCTCAAACATTCCTAAAACATTCCTAATGCATTTCAAGGAATATTGTTTTATTAATGTATGTCTATTGTTTGTGCATGAAAACTTAAAAAAAAAAAAAATTCTGCTCACCATGTTATACATGCACATATAGCTTAATAAGTGTCAACTGAATATATGTTCTCTGACGTGGTATTACAGGGTGAACTGAGTCTTTCTTCAGACATGGAGCTCCTCCAAACAGCTTTGTTCTATGATGTTGTTCCTGAGAGTTGGAGCAGGCTGACCTTTCCTTCAACTAAAACCCTGCCTCAGTGG[T/A]ATAATCACCTACATAGATCTTTCTGATACAGACAAACACTAAACCATTTGAATAATAAGAGCTGCATGATCTGATCCTGCAGGTTTAGTGATGTTCTGGCTCAGTGTCGAGAGCTGGACACATGGACTCACGACTTTGTGTTTCCCGCCGTGGTTTGGATCTCTGGACTTTTTAGCCCTCAGTCATTTCTTACAGGTGAGATGAGAAAAAAATATAAACAAAAATTCACAAATCCAAAATAGAGACTTGTGCTGAAATAGTTTTGCTTTGCAGCAATTATGCAGAGTATAGCTCGCAAAAACAAGTGGCCTTTAAATAAGATGAGCCTGTCTGTGGATGTCACTAAGAAAAGCAAGGATGATTATGGGCATCCACCTCGAGAGGGAGCCTACATACATGGACTCTACATAGAGGGTGAGTATAAACTCGAGTTTATGTATGTAGCTGGAGTATGTATCGAAATAAAATGTATAATTCAGGTATCCTGCAATGTTATTAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22806
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000138744 Nonsense 1407 1547 27 29

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 16 (position 21143306)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 19380061
GRCz11 16 19185700
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTGCAGGTTTAGTGATGTTCTGGCTCAGTGTCGAGAGCTGGACACATG[G/A]ACTCACGACTTTGTGTTTCCCGCCGTGGTTTGGATCTCTGGACTTTTTAG
Long Flanking Sequence:
GCAATATACAGCATACATATATAATAAAACGTAATTAGTAAGTAATTACAAATTATTTTTTCATGAATACCACATTGACATCTCAAACATTCCTAAAACATTCCTAATGCATTTCAAGGAATATTGTTTTATTAATGTATGTCTATTGTTTGTGCATGAAAACTTAAAAAAAAAAAAAATTCTGCTCACCATGTTATACATGCACATATAGCTTAATAAGTGTCAACTGAATATATGTTCTCTGACGTGGTATTACAGGGTGAACTGAGTCTTTCTTCAGACATGGAGCTCCTCCAAACAGCTTTGTTCTATGATGTTGTTCCTGAGAGTTGGAGCAGGCTGACCTTTCCTTCAACTAAAACCCTGCCTCAGTGGTATAATCACCTACATAGATCTTTCTGATACAGACAAACACTAAACCATTTGAATAATAAGAGCTGCATGATCTGATCCTGCAGGTTTAGTGATGTTCTGGCTCAGTGTCGAGAGCTGGACACATG[G/A]ACTCACGACTTTGTGTTTCCCGCCGTGGTTTGGATCTCTGGACTTTTTAGCCCTCAGTCATTTCTTACAGGTGAGATGAGAAAAAAATATAAACAAAAATTCACAAATCCAAAATAGAGACTTGTGCTGAAATAGTTTTGCTTTGCAGCAATTATGCAGAGTATAGCTCGCAAAAACAAGTGGCCTTTAAATAAGATGAGCCTGTCTGTGGATGTCACTAAGAAAAGCAAGGATGATTATGGGCATCCACCTCGAGAGGGAGCCTACATACATGGACTCTACATAGAGGGTGAGTATAAACTCGAGTTTATGTATGTAGCTGGAGTATGTATCGAAATAAAATGTATAATTCAGGTATCCTGCAATGTTATTAAAGGGGTGGCCTTAATCAATTTCAAAGACTATTTTAGGCTTTTGTGGTACACTGAAATTTTTTTTTGTAAATTAGCAGTTTTTCAGAAAAAGGGTCTTCTCATAGGATAAGAAAACTCAGCTATGAG
Associated Phenotype:
Not determined