ZMP
si:dkey-6h5.1
Ensembl ID:
ZFIN ID:
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 16 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22809 | Nonsense | Available for shipment | Available now |
sa11778 | Nonsense | Available for shipment | Available now |
sa22808 | Nonsense | Available for shipment | Available now |
sa18093 | Nonsense | Available for shipment | Available now |
sa22807 | Essential Splice Site | Available for shipment | Available now |
sa22806 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22809
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 |
---|---|---|---|---|---|
ENSDART00000020821 | Nonsense | 423 | 4362 | 8 | 83 |
ENSDART00000148294 | Nonsense | 358 | 1936 | 7 | 35 |
Genomic Location (Zv9):
Chromosome 16 (position 21318145)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 19555020 |
GRCz11 | 16 | 19360839 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTTCAATCTGAATTTGTTTAAAGCTGGTCACCGTGTTCAAACCCCTCT[T/A]GGACAGAGACATCATAAAGGAATCTTTTATTCCCAAGTTCTTTGAAGTGA
Long Flanking Sequence:
ATGATTCCTTGGATTTACTCAATTTTTTTTTTTACGTTAAGTGGTTGTAAACAATTTATTTGTATTGAATTTAAACAAACAAATTAGGTTGAACATTAATAAACTTAATTTGTTTGTTTAAATTCAACACAAATAAATCGTTTGCAACAGTTCTGCATGCAACACTTTTTTCAGTGTACTTTAGAACAGAAGTTAAGTTAAAAAGCACATTTAAAGCTAGATTTGTCTAAATACTGCATTTTGTGTGTTGTTTTGAAGGATTTTGAAAAAGACTTTTCCAGTTTTCAAGAAAAAGTGGCAGATTTTGATCGACAACTGTCCAATATTTTATGCCTGGCCTTTCAAGATTGTTCAGGATTGGAATCAGTTTTCAAAGTAAGCATTTCTGATAGATTTAGTTAGAATTGTTAAGAAAAAAAGAGTATAGCCTAACCTAAACTATGAAATTCACTGTTCAATCTGAATTTGTTTAAAGCTGGTCACCGTGTTCAAACCCCTCT[T/A]GGACAGAGACATCATAAAGGAATCTTTTATTCCCAAGTTCTTTGAAGTGACTGAGCTTTTTGGAAAGGAACTGAACAAATGCAAACACCTGTTTGATGCACATCTTGAACAGGTAAAGTTGCTTTTTGCCAACAGACTGTTGTTCTTTTACACATAAAAATATTATATAAGCTTTATTATTATGCATCAGAAAATCACTTTATTTAATAATATCATTATATCATATCATTATATTTCAGAAAAAGAGGAACAAACTGCATTTGAACAAGAACATGCCTGCAATGACAGGGTCTCTGAAGTGGGCAAAAATGCTAAGAGACAGAATTCAAATCCCTTGGAACAATTTTCGATTTGTTCTAGATATGTAAGTGTTTCAAAGATTTTATGATTTCATTATTTTCTTTTTTATTTTAATGGTGCAGGTCAATTGAAAGTGAATTTGTATTATAGGAAAATGGAAGGAGCAGAAATAGAGTTGGCTTTGCATAATTACCAGGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11778
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 |
---|---|---|---|---|---|
ENSDART00000020821 | Nonsense | 1553 | 4362 | 29 | 83 |
ENSDART00000148294 | Nonsense | 1485 | 1936 | 27 | 35 |
Genomic Location (Zv9):
Chromosome 16 (position 21280088)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 19516963 |
GRCz11 | 16 | 19322782 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGCTAAAGGTGTGAGTTGTTTCTTCTCAGGTTGAGCTCTGGCTGAACTG[T/A]CTGGAGGATGTGATGAAAGAGGGAGTGAGAAGATTCATAGCTGAGGCTGT
Long Flanking Sequence:
CTACACTTATAAATGCATATAATATATATATATATATTATTTTAATAGAATATTTTAATGAAATATTGTATTTTTCATCAAATATGCTAATTAACTGAATTTAAAAAACACTTGTTTTCATTTAACATAATGTTAAAGTTTATAAAAGGTTAATGTATTACATAAACATATAAAGCAATTTAAGAGAGTTCATTGTTTTTCTATAGCACTTAATATATTACTATGCAGATTGTCAAACTGATTTAATTAAACAGAATTAAACTTCAAACTAAACTATACATTAAAATTATTGTATGTAATATTAAATTACATGTTGGTTTCATAAAAAATTAGTTTACAAATTTTAAATGTGTTTAAAAAAAAAAACATGAGGTCTTCACTGACCATATGTATAAAGGTAAATAATAGACCCTGATATGAGGATAATCTAGAAATATTATTGTCAGATTATTGCTAAAGGTGTGAGTTGTTTCTTCTCAGGTTGAGCTCTGGCTGAACTG[T/A]CTGGAGGATGTGATGAAAGAGGGAGTGAGAAGATTCATAGCTGAGGCTGTGGTCATGTATGAGGAGCGCTCACGGGAACACTGGGTCTTGGAGCTGCCGGCTCAGGTGGTCCTGACTGCCTCCCAGATCTGGTGGTCCGCCGACATGAATCTGGCATTTGAACGGCTGGCTGAGGGTTTTGAGACGGCACTCAGAGACTACAACAAGAAACAGGTCAGTCACATACATTATACAAACTGCACAATATTGCTATTATAACTGTCAATGAACTAAATAAATGACACAAAAGAGATTCATTTTTATATTAAAATTATATACTGTATATTGTCTATAAAAATCTGTATTTGATTAAATTTTTCTACCAAGGGGCAGTAAAAACTCATAAGGGGCTTATGAATCTCTCTGAGGATTTTTTTTTTTATCATTTTGATAATATATATATATATATATATATATATATATATATATATATATATATATATAAAAGAGAGAGATCACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22808
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 |
---|---|---|---|---|---|
ENSDART00000020821 | Nonsense | 2030 | 4362 | 39 | 83 |
ENSDART00000148294 | None | None | 1936 | None | 35 |
Genomic Location (Zv9):
Chromosome 16 (position 21257458)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 19494423 |
GRCz11 | 16 | 19300152 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTAATGATCGTGAATAATCCTAAAGAGTATCCCTGCTTTGTCCCAAAA[C/T]AGATCCTAAAAACTCTTCACAAAACTTACTTCAACATGGGAAGGAAGCCT
Long Flanking Sequence:
GTTTATTGTGGGTTTGTTGTTTATATGAAGAAATCAGTGTTACAAGTTAACAGAAATTCTAATAAACAATTATATTTTAAATTTAAATTCTAATAAACAATTATATTTTGAATTTAAATAGTTTTTGTCTTGCGTTTACATTAATTTTACATTTGAATAGCCAAAATTACAAGTTTCAGTATTTTAAATGTGATTAATCGCGATAATTCACTCGTTTCGACTGTAATCAATGTTGTTTCTAAACCATAAACATTAATTTTTGCAATTAGTTACACATTAGAAGAAAACATAATTTTTTATTGACTGATGGAAGGATTAATAAAATATAAAATACCTATGATATATTCATCGTAAATTTTATGTTTGGTTAAATAATAATATTTGGGTGAATTTTCATGCCATTAAACTTCACACAGAATTTGAAGAACACAGTAATTCACAATCAGATGATCCTAATGATCGTGAATAATCCTAAAGAGTATCCCTGCTTTGTCCCAAAA[C/T]AGATCCTAAAAACTCTTCACAAAACTTACTTCAACATGGGAAGGAAGCCTTTCTGGAATGATCTGAACCCCAAATCAATGAGCAATGATGAACTGTTTGGATTCTTTCATCCTGCCACTCGGGAATGGAAAGATGGTACATCAGCATCCAGTGTTTTGTAGAGCTGATCCTGTCCAATTCACAGAACATAACTTACAGTTTAGACAAGAGATCTATTCCCTCTGCAAGACTTTGAGACTGTGAATCTCTTTGTTTGACAGGTTTATTGTCACATTTCATGCGGGATCAAGCCAGTAACTCTCACTCAGGGCCCAAGTGGATTGTTCTGGATGGAGACATTGACCCCATGTGGATTGAGTCTCTTAACACCGTCATGGATGACAACAAGGTACCAGTTTGTGCTAGTCTGTTTTTATGAAGATGTTTGCACTCAGCTGAATAATCTGGAGTGTTACTTTTTGGCATATTTAAACACGGTGCTTAACAATACCTCATACAAT
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.
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 |
---|---|---|---|---|---|
ENSDART00000020821 | Nonsense | 3285 | 4362 | 62 | 83 |
ENSDART00000148294 | None | None | 1936 | None | 35 |
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.
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 |
---|---|---|---|---|---|
ENSDART00000020821 | Essential Splice Site | 3578 | 4362 | None | 83 |
ENSDART00000148294 | None | None | 1936 | None | 35 |
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:
sa22806
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020821 | Nonsense | 4210 | 4362 | 81 | 83 |
ENSDART00000148294 | None | None | 1936 | None | 35 |
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