ZMP
ENSDARG00000086298
Ensembl 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 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa30419 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa38205 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa30419
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000124466 | Essential Splice Site | 143 | 479 | 3 | 11 |
Genomic Location (Zv9):
Chromosome Zv9_NA667 (position 9246)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 10434830 |
| GRCz11 | KZ116000.1 | 9246 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCGATATTCTTCATCAGACTAGAGGAGCCCTACAAACTCATTGACAAG[G/T]TACTTTTGTGTTTTTATTTCTGAGTGTGTTTTCAACTCATTGCCAAAGTG
Long Flanking Sequence:
TGTTAAAGTGTAAAAAGTTTAACAGTAAGTTAAAAAACAATTGGTAACTTAATCAGATGTTCCCTTTCCAATGATATTCAAGTATTTTGCGCAATTTTATATTAATAATAGATTCAGTTTACTGTAAACTGTACATTTGTTGTGCTGTAAATCATTCTAGTTGAAGGAAAATGAATGGAAAGTGTTTGAAATGTACCTTCAAATCTGGAATGAGGCACGCATGTATGAATAAAATGACATACTAGTATATAAATAATGTAAAAATATCAGATAAATAAATATATAAACATAAAAGTAGCAAACCCAAAGTTAGATTTCGTGGTCGTTTTTGTTGTACAAGAGACAAGCAGAAAAAAATCTTATTGTTGTGACCTTTTGAACATGATACTGATCATCTGTTGTTGGATTCTTAGATTAAACAGCATGAATTCAGAGAGCAGTTCCGCTCTGAACCGATATTCTTCATCAGACTAGAGGAGCCCTACAAACTCATTGACAAG[G/T]TACTTTTGTGTTTTTATTTCTGAGTGTGTTTTCAACTCATTGCCAAAGTGGGGTTTCAAGTAAGTTAAATGGTTTTGTCTTTGCTTTAGCTCAGACAGTGCTTACTCAAAAAATTATTTACGAGTGTTGCATTTTATATGCTTAAATTAGCATAATGTCCATGTTGGTTTTTGTTTGTAGACTAACCGTGCCGTGGCTCATTTAGAGAGTGAGATGGCTAAGCTTCAACAAACAGCCAATCTGTTTGAGGTCAGTTTTCCTGACTACAAACAACTTCGTCAGTGTCGGTCAGACATCATCCTGGTTAAAGCAGTCTGGGATATGGTTATGTTTGTCAAGGTATAATCTTTATCACACACAATATTTACAGTACAAAGTACTCCAATAACACATTTACAATGAAACATCTGTGGTGTCCTTTCTAAAAAATTTCCCTAATATTATTCTCTTTTCGGCTTCCTCTTGGGAATAATGGGTAATGTAGTCTAGCATCTCAGACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38205
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 |
|---|---|---|---|---|---|
| ENSDART00000124466 | Essential Splice Site | 143 | 479 | 3 | 11 |
Genomic Location (Zv9):
Chromosome Zv9_NA667 (position 9245)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 10434829 |
| GRCz11 | KZ116000.1 | 9245 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCGATATTCTTCATCAGACTAGAGGAGCCCTACAAACTCATTGACAAGG[T/C]ACTTTTGTGTTTTTATTTCTGAGTGTGTTTTCAACTCATTGCCAAAGTGG
Long Flanking Sequence:
GTTAAAGTGTAAAAAGTTTAACAGTAAGTTAAAAAACAATTGGTAACTTAATCAGATGTTCCCTTTCCAATGATATTCAAGTATTTTGCGCAATTTTATATTAATAATAGATTCAGTTTACTGTAAACTGTACATTTGTTGTGCTGTAAATCATTCTAGTTGAAGGAAAATGAATGGAAAGTGTTTGAAATGTACCTTCAAATCTGGAATGAGGCACGCATGTATGAATAAAATGACATACTAGTATATAAATAATGTAAAAATATCAGATAAATAAATATATAAACATAAAAGTAGCAAACCCAAAGTTAGATTTCGTGGTCGTTTTTGTTGTACAAGAGACAAGCAGAAAAAAATCTTATTGTTGTGACCTTTTGAACATGATACTGATCATCTGTTGTTGGATTCTTAGATTAAACAGCATGAATTCAGAGAGCAGTTCCGCTCTGAACCGATATTCTTCATCAGACTAGAGGAGCCCTACAAACTCATTGACAAGG[T/C]ACTTTTGTGTTTTTATTTCTGAGTGTGTTTTCAACTCATTGCCAAAGTGGGGTTTCAAGTAAGTTAAATGGTTTTGTCTTTGCTTTAGCTCAGACAGTGCTTACTCAAAAAATTATTTACGAGTGTTGCATTTTATATGCTTAAATTAGCATAATGTCCATGTTGGTTTTTGTTTGTAGACTAACCGTGCCGTGGCTCATTTAGAGAGTGAGATGGCTAAGCTTCAACAAACAGCCAATCTGTTTGAGGTCAGTTTTCCTGACTACAAACAACTTCGTCAGTGTCGGTCAGACATCATCCTGGTTAAAGCAGTCTGGGATATGGTTATGTTTGTCAAGGTATAATCTTTATCACACACAATATTTACAGTACAAAGTACTCCAATAACACATTTACAATGAAACATCTGTGGTGTCCTTTCTAAAAAATTTCCCTAATATTATTCTCTTTTCGGCTTCCTCTTGGGAATAATGGGTAATGTAGTCTAGCATCTCAGACTG
Associated Phenotype:
Not determined