ZMP
dnah1
Ensembl ID:
ZFIN ID:
Human Orthologue:
DNAH1
Human Description:
dynein, axonemal, heavy chain 1 [Source:HGNC Symbol;Acc:2940]
Mouse Orthologue:
Dnahc1
Mouse Description:
dynein, axonemal, heavy chain 1 Gene [Source:MGI Symbol;Acc:MGI:107721]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31843 | Nonsense | Available for shipment | Available now |
sa35130 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41883 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31843
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 |
---|---|---|---|---|---|
ENSDART00000077928 | Nonsense | 282 | 2635 | 7 | 49 |
Genomic Location (Zv9):
Chromosome 11 (position 35528466)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 34420682 |
GRCz11 | 11 | 34682675 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGCTCTGAAAGGCCAGCCCTCAGTTAGCGGAGGAGAATATGAGGCTGTA[C/T]AGACCTATGTGCTTAATCCAAAGTCCATCACCATGGGGCAGCTTTACGGA
Long Flanking Sequence:
TTTATCTTTGCCATGATGACAGTAAATAATATTTTACTAGATATTTTTTAAGATGTTAGTACTCTGCTTAAAGTGACAATTAAAGGCTTAACCAGGTTAATTAGGCAAGTTAGGGTAATGAGGCAAGTCATTGCATAACAATGGTTTGTTCTGTAGACAATCAGAAAAAATATTGCTTAAAGGGGCTACTAGTATTGACCTTAAAATAGTTTTTAACAAATTCAAAACTGCTTTTATTCTAGCCAAAAATAAAACAAATAAGACTTTATCCAGAAGAAAAAATATTATAGGAAATACTGTGAAAAGTTCCTTGCTCTCTTAAACATACTTTGGGAAATATTTAAAAAAGAAACAAAAAACTCACAGGAAGGCTAATAGTTTTGAATTCAACTATAAATATATGCACTCTCACATACTTTTAGTGTTATGAAGTGCTGGCAGCAGCCATGACGGCTCTGAAAGGCCAGCCCTCAGTTAGCGGAGGAGAATATGAGGCTGTA[C/T]AGACCTATGTGCTTAATCCAAAGTCCATCACCATGGGGCAGCTTTACGGAGAATTCGACCAGCTTACTCACGAATGGTGAGTGTGCTGTGCACTGGATTTTTGTGTTTTCTCGTACCGTACAGGTTGTTAAAGTCCACATAAACCAGATGCTGCGACCGTTTTTTTTTTTTTTTTCGTATTGTGACAGTTCCTAGAGAAACAGAATATTAAATTTAAAAAAAAATACCTCGAGCCGATTGGATTTGGTAAAGTTGGCATTTCATTCCGAAAGATCTGGAAAAAGGTTTGGGGAGAGTTATTACAACCTAACAGACTCCTCCTCCTCACCATTTCTGTTTGTTATCAAAACTGACAGCTGGAGGGGTGTGGTTAAGTATGTTAGCCACGCCCAATACCCCAGACAGATGCAATCTGACAATTTAACTGAAAACAAACAGGAAGTGCATTTTCAGATTTTAATTTTAGATTACATGGACAAACTTTTTTTTTCTTAATGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35130
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077928 | Nonsense | 342 | 2635 | 8 | 49 |
Genomic Location (Zv9):
Chromosome 11 (position 35527766)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 34419982 |
GRCz11 | 11 | 34681975 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAAAAGAAGTGGTACATGTTTGACGGGCCTGTAGATGCCGTGTGGATC[G/T]AGAACATGAACACAGTTCTGGATGACAACAAGAAACTGTGTCTGAGTTCC
Long Flanking Sequence:
ACAGAATATTAAATTTAAAAAAAAATACCTCGAGCCGATTGGATTTGGTAAAGTTGGCATTTCATTCCGAAAGATCTGGAAAAAGGTTTGGGGAGAGTTATTACAACCTAACAGACTCCTCCTCCTCACCATTTCTGTTTGTTATCAAAACTGACAGCTGGAGGGGTGTGGTTAAGTATGTTAGCCACGCCCAATACCCCAGACAGATGCAATCTGACAATTTAACTGAAAACAAACAGGAAGTGCATTTTCAGATTTTAATTTTAGATTACATGGACAAACTTTTTTTTTCTTAATGACATGCACAGATGTTAAAACTAGCCATGAGCTAACAAAATCATATGTTAGTTTTGGTTTAATTTGTACTTTAGATGTAACTCACACTATTTTATTACAGGACAGATGGTATACTGTCTTGTCTCATTCGGGATGGAGCTTCATCCATGGAGCAGGAAAAGAAGTGGTACATGTTTGACGGGCCTGTAGATGCCGTGTGGATC[G/T]AGAACATGAACACAGTTCTGGATGACAACAAGAAACTGTGTCTGAGTTCCGGAGAGATCATCAAACTCTCTGATGTATGAGAGTTTCTAGATAATTGTCTGTATGTGTTGTATCGCCTCATAATTTTTAGTTTGCTTCTTTGACATTTTGACAGGCGATGACAATGATGTTTGAGGTGCAGGATTTGGCGGTGGCCTCTCCTGCCACAGTTTCTCGCTGTGGCATGGTGTATCTGGAGCCGAGCATTCTGGGTTTGACTCCATTCACAGAGTGTTGGCTCCGAACAATCCCTGACATGTTTCGGCCCTACGCGGATCAAATCAACTCGCTCTTTACAAGGTTCTTGCAGGTGACTGGTCTTAGAGTGTTTTTGTTAAATTCGTTAAGTAAAATTAAACTAAAAGACAACAGAATGTGGGGTGGCACAGTGGGTAGCGATTTCGCCTCACAGCAAGAACGTCGCTGGTTCGAACTTTGGCTGGGTCAGTTGGCATTTCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41883
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077928 | Essential Splice Site | 660 | 2635 | 14 | 49 |
Genomic Location (Zv9):
Chromosome 11 (position 35524815)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 34417031 |
GRCz11 | 11 | 34679024 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTCCGCCAACCAGACACAAGACTATATTGACAGCAAACTGGATAGGAG[G/A]TTTTTGTTTCTCTAATCAGTCTTTTAATTCTCTGTATATATTATTTTGAA
Long Flanking Sequence:
GGGACATCAGAGACTTGTTTTAATTTTTTTTTTCAAAGGGACCTCCTTTAATGTGTGATGATTATGCAAAAGTAAAAGTCATTTTTTGAAGTGCATTAATTAGATTTTTCATATACTTCAGGTACAGTGGGTCAGCTGGATGAAATATGCCCAGGAAGTGGTCATCACCCCTGAAACAAGATACTCAGACATCATTGTGCCCACAGTCGACACCGTTCGCATGTCTTTCCTGATAGACATGCTACTTTCCAATAAGAACCCTGTAGGTCATTCAACATAGAGTCAACATAATGCCTTTCATATGTGTTGCTAAGCTCGCTCCCTTCTCTAATTTGTCAGGTCTTATGCATTGGGCCCACCGGCACAGGAAAGACCCTGACCATATCAGACAAGCTTCTGAAAAATATGCCTGCTGAATACATAACTCACTTCCTGATGTTCTCAGCTCGTACCTCCGCCAACCAGACACAAGACTATATTGACAGCAAACTGGATAGGAG[G/A]TTTTTGTTTCTCTAATCAGTCTTTTAATTCTCTGTATATATTATTTTGAACATCAAATTTAGAATTTGCATGTGTTACAGGCGTAAAGGTGTGTTTGGGCCTCCTCTGGGAAAATATTTCATCTTCTTTATCGATGATCTGAACATGCCCATGCTAGAGACATATGGAGCTCAGCCTCCAATTGAACTCCTGCGCCAGTGGATGGATCACGGAGGCTGGTATGACAGGAAACAGATAGGTGTGTTTAACAAGAATGAAGCATTTTTAAACTCAAACTACTGGTCAAATGTTTTTGGGTTCAGTCAAAATTTTGGCTGATACCGATAACCGATACACAGTATAAGCCATTAAATACAAATATTGGTTTGTATTTTTCAGAAAATGGCTAAAAAAAATGCAAACAAATACAGTGGACATTTGAATTTATTTAAAAAATGTAACAGTTTTTTTGCTACTGGCTCATATATATTTTTTTATTTATGTATTTATTGCATTTCATA
Associated Phenotype:
Not determined