ZMP
dnah7l
Ensembl ID:
ZFIN ID:
Human Orthologue:
DNAH6
Human Description:
dynein, axonemal, heavy chain 6 [Source:HGNC Symbol;Acc:2951]
Mouse Orthologue:
Dnahc6
Mouse Description:
dynein, axonemal, heavy chain 6 Gene [Source:MGI Symbol;Acc:MGI:107744]
Alleles
There are 21 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa19487 | Essential Splice Site | Available for shipment | Available now |
| sa14187 | Essential Splice Site | Available for shipment | Available now |
| sa15767 | Essential Splice Site | Available for shipment | Available now |
| sa19488 | Nonsense | Available for shipment | Available now |
| sa19489 | Nonsense | Available for shipment | Available now |
| sa19490 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19487
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000054388 | Essential Splice Site | 50 | 3802 | None | 73 |
| ENSDART00000137429 | None | None | 84 | None | 4 |
| ENSDART00000141317 | Essential Splice Site | 240 | 3966 | None | 75 |
Genomic Location (Zv9):
Chromosome 1 (position 20841815)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 21313911 |
| GRCz11 | 1 | 22006848 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTCTTCAGTACCTAAATCATCAATTAACTTTGACACATATAACCTCAAG[T/A]AAGAAATGCAGTATTTGTACACTACCATTTCAAACTCATTTATTTTATTT
Long Flanking Sequence:
TATGAAACCGTACAACAACCAGAAGCTGACTCCTAAGATGCCCTTTCAATTTGATGAGGTCCAGTCTATTGATTCTTCTACAGAGAGAGGACCCTCCGTATTACAGCTTCCCAAAATTCCACACTACATCAAAGATAGACAGGTTTGACTTTAAACTTCTCTGTTCATAGATGTCTGTTGTAACATTAGTAAAACTGTACATGCTTTTTATGTGATCCTTTTAGGTGCAGTTGACTCAGGGCTCACTCAGGATACCCTCCCCACCTAAAAGAGTAAAAAGCTCCTCCAAAAGTTGCCCAGTTCCATCTCTGAGCTACACTCCCTCTCCACCGCTTTCTGGTTCACTGCTGTTTGACTCAGTGGATGAATTAATACGTGCTAAGATTTGCTCCCCACCCCACATCGTCCAAGCCATCCGGACTAACCCTCACCTGGGATTCTTCTATTTGACGTCTTCAGTACCTAAATCATCAATTAACTTTGACACATATAACCTCAAG[T/A]AAGAAATGCAGTATTTGTACACTACCATTTCAAACTCATTTATTTTATTTGATATTTTATTTCATATTTCATTGATGCATCAAAAAAAAAAAAAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTAAATTGTTGTAAAATTGTTACTTTTTTGTTTTAAATAAACAATGTTCTTTTAAAGTTCATCAAAGATTTTTTTTTAACAACATCAGCATATTTGAAGGATTTATATGGTCATGTCATACTGAAGACTAAAGTAATGTAATAAATTAGTTAATTAAAGTATATTACAATACTGAAATATATGTAAAACATCAAATCAAAACATTTAATTTACAAATACAAAAATCTATTTTTGATTTTAAATATTCATATTAAGTCTTGTTTTTACATATTTCATTAGATCAAGTTTAATATTGAGTGATTTTAATTTGTATTTTGAATGTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14187
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000054388 | Essential Splice Site | 737 | 3802 | 17 | 73 |
| ENSDART00000137429 | None | None | 84 | None | 4 |
| ENSDART00000141317 | Essential Splice Site | 918 | 3966 | 19 | 75 |
Genomic Location (Zv9):
Chromosome 1 (position 20857660)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 21329756 |
| GRCz11 | 1 | 22022693 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGAATTACGGTGTCCTCTAAATGTCACATGGTCAATTATCTCTTTTATAT[A/T]GGATAAGTTKGATGAGCTGGACCCAGAACTGCTGAGCAAGCAGGTGAACA
Long Flanking Sequence:
AGTGGGCAAAAACAGCCACAAACATAATGAAAGAGTAGCCAATTTGCCCAAAGTGTTGAATTTTTTTTTACATTTGCCAAAAGTTTTTCTATAATATTGTGAACATAAGATTTGTTGTCATTTGCTGAAATACTGAAAGTTGTGGCCAAATTAAGACTCAAAATGACCCCAGAGTGGATGAAAACATCCCTAACAGCACACAAGAATTAAAGGTGTATCTAATAAAGTTGCCAGTGCTTGTAAATCTCCTCAGAGGGTCAGCTAGTGCTTAAATTCTTAACCTGAAGGTTGAAGGCTAGTTATTCTGTACTGAGGAGCAGAAATAAAACAGCTAAAGTGTTACTGAGAGACACAGCTAAACTTGTCATAGGTACGTCCTTGAGCAAGGCACTTCACACTAGATAACTTTGGATGAAGTGACTTTGCAAATGGGTATGCTGGAAGCCATTTCGAATTACGGTGTCCTCTAAATGTCACATGGTCAATTATCTCTTTTATAT[A/T]GGATAAGTTTGATGAGCTGGACCCAGAACTGCTGAGCAAGCAGGTGAACAGGTTTGTCAAATATGTCAGCCAGCTGGAGAAGGGACTGCCACCAAACAATGTGGTGCCCTTCCTCAAAGCAAAAGTGGAGAGCATGAGAGAAAAGGTGGGTGAGGTTCACACTAATGAATGCATGTAATTGCCTGAGGTTGACGACAGTATTTTACATTTGCCCATGGAAAAAAAGATGTCTCAAAGCCATAAAACTTGTAGTAGGCCTACTAGGCATAGAGTACTCTTCTAAATGTACAGTGCATACGAAAAGTATTCTTCAGTTTTTCCACATTTGTTTATGTTACAGCCTTACTCCAAAGTGGATTAAATAGATTTATTTCCTCAAAATTCTATACACAATATGTTGCAAATGTATTACAAATAAAAAACCTGGAAATCACATGTATGTAAATATTCATGGCCTTTGCCGTGAAGCTCTAAATTGAGCTCAGGTACATTCTGTTTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15767
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000054388 | Essential Splice Site | 853 | 3802 | 19 | 73 |
| ENSDART00000137429 | None | None | 84 | None | 4 |
| ENSDART00000141317 | Essential Splice Site | 1034 | 3966 | 21 | 75 |
Genomic Location (Zv9):
Chromosome 1 (position 20863650)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 21335746 |
| GRCz11 | 1 | 22028683 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCTGGACAAGCCTCAGGAGAAGCATCTCTGGAGAACATTCTSAGAAAG[G/A]TGATGCCTACATTTATTATTGTCTTTTAACATTATACATACACGTCTYTR
Long Flanking Sequence:
ACACACACACACACACACGCACACACACACACACACACACACACACATTACCCTCTTCCACGGAACGTAAACAAAGCGGGTCGCAGGTTTCAAATCTCCCGGGTTTGCGCGTGCGCGGTAATAACTTCGTTATTACGTCATAGCGAAACACCTAATGACTCGTTATCAAGACGACTCGTTTGAAGCACTATGAGTCGACTCTTTTATAGGTGAATCAACAGTTTTAAACACTGTACATTTACAGATTTAAGCCTTAGCTGGATATTTCACTTCACTTAGAGCTGTGTTACACAATACATGGAAGGGCATTTTCATAATATGGGCTCTTTAACACTCACTGATGTACTAAAAACTCTAGGTTTGAGCCACAACCTAACAGGAAGGCGTAAATCAGCATATAGGAACTACAAATTCATTCTTTAACCGGATGTATCCTGTCAAATTTTCAGGTGTCTGGACAAGCCTCAGGAGAAGCATCTCTGGAGAACATTCTGAGAAAG[G/A]TGATGCCTACATTTATTATTGTCTTTTAACATTATACATACACGTCTCTATGTTGAGCTTCACACATGCACACTGTTGATAGATTGAGGATTCCTGGAAGACGACAGAGTTTATAGTGCTGCCTCATCGGGACACTAAGGATGTGTTTATTCTTGGTGGAACCGATGACATTCAGGTAAATTAAATTTAGATGTAACTCTCATTCTTTCCAGAATTGAATGAAGAACATACAGTTTTTTTTAATATAAGTAATATTTGTATTTTGCCTGTGTGAATTTTGTAGGTGCTTCTTGATGACAGTATAGTCAACGTTGCGACTGTTGCATCATCCCGTTATGCAGGCCCAATCAAGGCCAGAGTTGACAAATGGCAGAGACAGCTTTTGCTGTTCAACCAGACCTTGGTAATCCAAACTAGAGTTATGAACTTCAAAAAAATACATTTTATGTCAAATGTTGGCGTGGGTTTCCCCGGGTGCTCCAGTTTCCCCAACAGTCCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19488
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 |
|---|---|---|---|---|---|
| ENSDART00000054388 | Nonsense | 1870 | 3802 | 38 | 73 |
| ENSDART00000137429 | None | None | 84 | None | 4 |
| ENSDART00000141317 | Nonsense | 2062 | 3966 | 40 | 75 |
Genomic Location (Zv9):
Chromosome 1 (position 20908922)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 21381018 |
| GRCz11 | 1 | 22073955 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCAGCGTAGGTGATTTATGGAGCGTCTATATGAACTTTGATATTAAATG[T/A]TTGGAGCCATGGGAAAGGATCATTCCCGTCTTCAGTTATAACAGTGAGAT
Long Flanking Sequence:
AGATCTTAAAATCGTGAATTACTGCTGAAAACAAGTCAAATCTGCAGAAGCTTTTTAAAAAATAAAATATTGTGCAGAACTTTAAGCATTTTTCTGACTGCCCATGACAAATAAGTTCCATAAACAACTATCACATGACAAAACTAAAAATAACAGATCATCTACAGCAGGTAATTACACATAGTTTTCAGGGCATGTTAATTTTTGTATAGCACAATTTTTTATGAATTCAGTTGTTTGTGAGCATATGTAAACATATGTTATGTGAACTAGCCTAATTATGTTTTTTGGAGATTACAGTAGGTAACACATTTTGTAAATAGGGTAAATTGGGACAGAAATATCGTGGAGTACATAAAATGCCATAAATTAGAAGAAACAAAAACAGATGCTCAATGGCAGCCAAGAAAAAGTCTTAATAGTTAAATAAACTCTGTCTTTTTACAGTTGTCCAGCGTAGGTGATTTATGGAGCGTCTATATGAACTTTGATATTAAATG[T/A]TTGGAGCCATGGGAAAGGATCATTCCCGTCTTCAGTTATAACAGTGAGATACCCTTCTTTGAGATGCTGGTACCCACCACAGACACAGTGAGGTACGGATACCTGATGGAAAAACTGCTGTCTGTCAATCACTCTGTCCTCTTCACTGGCATCACTGGTGTGGGAAAGGTAAGACGGTGTGTGCTTAATATAATGTACAGTAAATGTTTGTGAAGTAGAGTTTAACTTCAATAAGACATTGTTTAAGAGGACAAAATTCTTTTCTAGAATTTCAATTCTTACATTTTACCTCTTAAATGACCTCTTCATTTACTCTCCCTCATGTGGTTGTTAATACAAAAGATTTTGAAGAATGTTGTTGCTGGGACCCATCGGCTTCCATAGTAGGAAAAAAAAGCTATGGAAGTCAATGGGTCCTAGCAACCAGAAAGTTTTAAATCAATATTGTTTGTATTTGATTTGATTTATTTATTTAGAGTAGAACATCATACACTTAAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19489
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 |
|---|---|---|---|---|---|
| ENSDART00000054388 | Nonsense | 2161 | 3802 | 43 | 73 |
| ENSDART00000137429 | None | None | 84 | None | 4 |
| ENSDART00000141317 | Nonsense | 2352 | 3966 | 45 | 75 |
Genomic Location (Zv9):
Chromosome 1 (position 20919700)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 21391796 |
| GRCz11 | 1 | 22084733 |
KASP Assay ID:
2259-0521.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCATATCTTCCGTTTGTTCTGTCATGAGTGTCAACGTGTCTTCCACGAT[C/T]GACTCATAAACAACGAAGACAAAAGCTACTTCAATACCATGATCTCTGAG
Long Flanking Sequence:
ATCTGTTGTACCAAAATCCACCAAAGGCTTTTAATCAGCTTTCTTTGTTTAAGAGCTCTCAAATGACAAATACAAATGCTCTCTCTTAATTTGAAATGCACTTTGGGGGGCTGTTAAAACGTTGGCTTAGGACTCATCCACAGGCCAAATTATAGACTCTCAATAGGAGATACTGTCTATCTAAGCTAAAGCACAACCCCCATCTGATTATGTTTTCATTTTTAGTGAAAGGTCACAGGCAAGTTTATCTTTTACTGATATTGATCTGTAGACACAGTATTGATTGTTTGCCAGCAGTAAGTCTTGCTATAAAGATATATATTAAAGAATCTAATCTGTGTAAACGTTGAACAAAATTTCTTTTCATTATTTGTCTTTGAATGTGTGTGTGTGTGTTTGTTTTCTGTGTAGGTATGCTGCAGTGTGAGCCAACTACGGTTAGAGATCAAACCCATATCTTCCGTTTGTTCTGTCATGAGTGTCAACGTGTCTTCCACGAT[C/T]GACTCATAAACAACGAAGACAAAAGCTACTTCAATACCATGATCTCTGAGATGGCCAGTAAGCACATGACCCTCAAATCCCCTTCAGTGTTAATCTCTCTAGTCCAGACATCTGTTAAGGTGTATATTATAGGGCTTTTCTCTATTAAAATAATTAACACTGGGTCATTCTAAACATAGGATAAATTGAATCCTGGGTTATCTTCACTTTTCACACACTCACTCTTTTTTTCATATCATTTTTTATTATTATTCATTCATTCATTCATTTTCTTGTCGGCTTAGTCCCTTTATTAATCTGGGGTCGCCACAGCGGAATAAACCACTGAACTTATCCAGCAAGTTTTTACGCAGCGGATGCCCTTCCAGCCGCAACCCATCTCTGGGAAACATCCACACATACACACACACACACACTCATACACTACGGACAATTTAGCTTACCCAATTCACCTGAACTGCATGTCTTTGGACTGTGGGGGAAACCGGAGCACCCGGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19490
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000054388 | Essential Splice Site | 2432 | 3802 | 49 | 73 |
| ENSDART00000137429 | None | None | 84 | None | 4 |
| ENSDART00000141317 | Essential Splice Site | 2615 | 3966 | 51 | 75 |
Genomic Location (Zv9):
Chromosome 1 (position 20937366)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 21409462 |
| GRCz11 | 1 | 22102399 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTGTGTTTGTTACATTGCAGTCATTTTCTGTTTCTTGGGTTTATTTTTC[A/T]GTGGCCCCGTGAAGCTCTGCTATCTGTGTCTCAGACCTTCTTCCAGAATG
Long Flanking Sequence:
AGGTCTGTAAAGTCTAAGAAGGGAAGTATTGGTCGTATTAGTATTTTTTTTTATTTTTTTTTGGTACAGTTAGTGTGATATTCAGAGAGGCAATTGCAGATTAGGAGGTGTAGTGGAGACTAAATAGTTGAGTTTTTAGTCGTTAGTCGTTAGTAGTCAGTGCGGCAAGAACAGTCTCAAACATAATAAAAGGGTAGTAAGTTTGTCCAGAGTGAATTGAGTTTTTGAAGGTTTTCAAAGCATTGTGTTAACACAAATGATGTGTTAAAATAAGATTTTTCATCAAAAATGATTGCATTTGCTGAAACACAGAGAAAGTTGTGTACAAATTAAGACTCAAAATCACTCCAGAGTGGATGACAACATCCTCAACAGCACACAAGGGTTAAATAAAAAATACTTTCAGTATTATGCTAATGATAAACAATTGATATGTGCTTTTTACTATGTGTTGTGTTTGTTACATTGCAGTCATTTTCTGTTTCTTGGGTTTATTTTTC[A/T]GTGGCCCCGTGAAGCTCTGCTATCTGTGTCTCAGACCTTCTTCCAGAATGTGGAGTTTGGCAGTGAGGAGATGAAGCAGTGCTTTTCAGAGATGTGTGTGGAGATTCATGTTAGTGTGACTGACATGGCTGAGCGTTTTTACTCAGAACTAAGGAGACACTACTACACCACACCGACCTCCTATTTGGAGCTCATTAACCTGTACCTGGGCATGCTGGGAGAAAAGAGACAACAGCTGCAGGCGGTGAGGATGAGTGATGGATAATGCATTAGTCTCTTATGTTGTTACACCGTTACTTAAAGGGGCTATATGTAGAAATGTTCTTGTATTAGCTGTTATTAATGGACAAAGTGTGAACCGCTTGCAATACAACATTTTATAAACGAGACCTCCTTTTTTTCAGGATAACAAACAAGTTTTTAAGATTTCTGTATTCCCCAAACTATTTAGATAAGACTTGGTTTTGAATGAACTGCCCAGAGATGTTGCAAATGTTGGC
Associated Phenotype:
Not determined