ZMP
zgc:158666
Ensembl ID:
ZFIN ID:
Description:
dynein intermediate chain 1, axonemal [Source:RefSeq peptide;Acc:NP_001074027]
Human Orthologue:
DNAI1
Human Description:
dynein, axonemal, intermediate chain 1 [Source:HGNC Symbol;Acc:2954]
Mouse Orthologue:
Dnaic1
Mouse Description:
dynein, axonemal, intermediate chain 1 Gene [Source:MGI Symbol;Acc:MGI:1916172]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa43615 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa11518 | Essential Splice Site | Available for shipment | Available now |
| sa15293 | Splice Site, Nonsense | Available for shipment | Available now |
| sa17473 | Nonsense | Available for shipment | Available now |
| sa37269 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43615
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000080431 | Essential Splice Site | 14 | 660 | 1 | 18 |
| ENSDART00000142468 | None | None | 150 | None | 7 |
Genomic Location (Zv9):
Chromosome 21 (position 16468566)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 17920345 |
| GRCz11 | 21 | 17956981 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAAAAATGTCAGTTTCTTATAAAGTTGGGACAGTGAAAAGTAAACAGG[T/A]ATGTAAATAGCATTATAACGAACGCAGATTTAATACTATCGTAAAAGAAT
Long Flanking Sequence:
CGTTGATAGGTATAGTTGGGAACTATTCTAAAGAACCGACTCGCTGTTAAATGAATCGGACTTTCCAACACTATCAAGGACACAAAAGCCGCGCCTTCTTACTTCCGTAAATTTTGACACCATAATAACAAACATCGTTATTCAAATTTTATTGTACTTGCTTGCAAATTTGTTTTCACAAAACTTCAAGGTCACCTAAATTGAAACAACGTGAGAAGAAGTTACTTTTTCCAACACAAAACATGGCTTTATATTTATTGTGCAGCGAGGAGGAACGGGAGGGGAGGAGCAGGTGAGGGACTCCAACTACGCGCATGCGCAGTAATGTCTCGCCAGTCCGACGGGTGCAGCTGCCATGGCAACCTCTAAACGCACAAACACTGACACTAGTTTCAGAGAGCGGAGCAGTCTTGTTATTTAAAGAAAGTTGCTTTAACGTTTTTTGAAAAGGAAAAAAATGTCAGTTTCTTATAAAGTTGGGACAGTGAAAAGTAAACAGG[T/A]ATGTAAATAGCATTATAACGAACGCAGATTTAATACTATCGTAAAAGAATAACTTTTATAAGTATCAAACACGTTTTGGCACCTAACGTTAACGTTATAGTTTTAGTAAATTTTGCTTTCTGGTTAACCAATGTTAATTTAACGAATATTGATTTACTTAATGATTGTAATGCATTTATTTTCTCAATTAAGTCACCTAATGTTAACACCCAGCCAAAGGCTCCTGTGGTAAAGGGTGTCAAAACCACTGGAAAGAAGAAGGTAACGTTAGCCTTCAACACGACTATTCATATTCATTCTGAATAAATTCTTTGTCAAATTTTTCAAAAGGCATTTTTTGGTCACGTAGGATGAAGAGGAAGGGATAGACACAGCTGACGGAGAAGAATGGATGCAAGGAAAAACCCTTGTGAAGCCTCCAGACCAGCTGGACTTAACTGAAGAAGTGTGTAAACCTGAATAGAGCCTGTGGTCTGACTCTGCATCTAATAATGTTGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11518
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 |
|---|---|---|---|---|---|
| ENSDART00000080431 | Essential Splice Site | 69 | 660 | 3 | 18 |
| ENSDART00000142468 | Essential Splice Site | 18 | 150 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 21 (position 16469012)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 17920791 |
| GRCz11 | 21 | 17957427 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGGAAAAACCCTTGTGAAGCCTCCAGACCAGCTSGACTTAACTGAAGAA[G/A]TGTGTAAACCTGAATAGAGCCTGTGGTCTGACTCTGCATCTAATAATGTT
Long Flanking Sequence:
AAAGGAAAAAAATGTCAGTTTCTTATAAAGTTGGGACAGTGAAAAGTAAACAGGTATGTAAATAGCATTATAACGAACGCAGATTTAATACTATCGTAAAAGAATAACTTTTATAAGTATCAAACACGTTTTGGCACCTAACGTTAACGTTATAGTTTTAGTAAATTTTGCTTTCTGGTTAACCAATGTTAATTTAACGAATATTGATTTACTTAATGATTGTAATGCATTTATTTTCTCAATTAAGTCACCTAATGTTAACACCCAGCCAAAGGCTCCTGTGGTAAAGGGTGTCAAAACCACTGGAAAGAAGAAGGTAACGTTAGCCTTCAACACGACTATTCATATTCATTCTGAATAAATTCTTTGTCAAATTTTTCAAAAGGCATTTTTTGGTCACGTAGGATGAAGAGGAAGGGATAGACACAGCTGACGGAGAAGAATGGATGCAAGGAAAAACCCTTGTGAAGCCTCCAGACCAGCTGGACTTAACTGAAGAA[G/A]TGTGTAAACCTGAATAGAGCCTGTGGTCTGACTCTGCATCTAATAATGTTGGGATGATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATATCTGTTTCTTGTGTTTAAAAGGAGCTGAAGGAAGAGATTACCAGAGTATTAACAGCAAACAATCCGAATGCCCCTCAGAACGTTGTCAGATACAGTTTCAAAGTAAAAAAATATATATCTCTATAGCTTATAAAGTTAAAGTTATGCTTCTTAAAGAGGATGATTTAAACCACTAAAATGTATTTGTCTTTTCAGGAGGGCTGCTATAAAACTATTGTCTTTGTGGATCAGATGGCTATTCACTTTGAACTAGAAGGGAATCTTGTGCACAAGGAATCAGATGAAGGTCGAAGACTGATGGCTAAACATACTGAAAGGGAAGATTGTGGTGGAGATGAGAGACTAGAAAATGTGCCAATCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15293
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:
Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000080431 | Splice Site, Nonsense | 407 | 660 | 11 | 18 |
| ENSDART00000142468 | None | None | 150 | None | 7 |
Genomic Location (Zv9):
Chromosome 21 (position 16471700)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 17923479 |
| GRCz11 | 21 | 17960115 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATGTATAACAGCATAGCCAGCTCTGGCAAACACACAGGAGCTGTGTGG[C/T]AGGTATGGGTGATGATGTGACCATGGTGTCATTGTTAACTTAAAGCAATA
Long Flanking Sequence:
TATTTATTTTTTTCTTTTTGGCATAAACCTGTCTATGTGAATTTAAAATTTATTGTCAACATTACTAAACTTACCATGTATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAATATATATATATATATATATATATATATATATATATATATATATATAAATGGAATCATTTGTAAGTTAAATGATTCTAAAAATGCGTTTTATCTTACCCCTCTAGATGAATTTACTCAGCAGGAGCGCGGCATGCTTCTCTTTTACACCCTAAAGAATCCCAGTTTCCCTGAATTCATCTTTAACACAGACTCAGGTGTAATGTGTGTGGACATCCATGAACAGCTGTCCTACCTGGTCGCTGTGGGATTATATGATGGCTGTGTGTCCGTGTATGACCTGAGGAAAAAGAGTGACCAACCCATGTATAACAGCATAGCCAGCTCTGGCAAACACACAGGAGCTGTGTGG[C/T]AGGTATGGGTGATGATGTGACCATGGTGTCATTGTTAACTTAAAGCAATAACAGTAAACCTTCATTACAGTTACTGCAATGGAGATGTAATAGCACTCGGACTAAAAAAAAGATGCATACAAATAATTCAGCTTCAAAAATTTTAAGAAATTTGGATATACTTTTGCCAAGTATATTTTGAAATATTTATTGTTCATATACAGTGCTCAGTATGATTGAGAACACCCCATTTTAAAAATATTTGTATCTATTTCTCAGTTATTATTGGCAATGTATTTATGGTGCATTTAAACAAAACGGATTTATTAAATATTTCTTAAATAACATTTTAGCTACCAAACATATTTAGAAATTGAAAGATAATGCAATTAAATTCAAGCAAAATATTGCAAAAAAAAAAAGTTACAACTTACGAAATTTCACCCCAACAAATTTTTTTTTGCTTCTCAAATACATGCTTACTTTTTTTATATTGTTTGTGATATTTTAATTGCTTAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17473
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 |
|---|---|---|---|---|---|
| ENSDART00000080431 | Nonsense | 473 | 660 | 14 | 18 |
| ENSDART00000142468 | None | None | 150 | None | 7 |
Genomic Location (Zv9):
Chromosome 21 (position 16474349)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 17926128 |
| GRCz11 | 21 | 17962764 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTYATAACACTTTCTCTATGGGTCTAGCTGGAACATCTTTGGATTTTCAT[A/T]AACAAAAGGACCACCATTTTCTGGTTGGCACTGAAGCTGGAAAGATTCAC
Long Flanking Sequence:
AGGCGGAAGAAAGTAGTTCCTCATACAAAAGGGTTTTTGACACTCTCCATGTTTGGTTTTGTTTTTATATACACAATTATGCCGTCAAACTGTTGTATAAACGCAACATCACACTCGTAGCAGTGCGATATGGCTGTATATTGGCACTTGTGGGGGCACTAACGCTCGCCTCCCACCAGTGCTGATATACAGCCATATCACACTGCTACTCATGTGATATTGCTCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACATACACACACACACACACACACACACATATACATAAACTCACTCATAACACTTTCTCTATGGGTCTAGCTGGAACATCTTTGGATTTTCAT[A/T]AACAAAAGGACCACCATTTTCTGGTTGGCACTGAAGCTGGAAAGATTCACAAGGTCAGTCATGCACTTTCACAGCCAAGATGATCACTTTACACAAAGGCCAGTCTTAAAATCAATCAACATAAGCCTTGTGAACATCCTGCTGTCTGAAGATCTGCAGTCTTGAGTCATCACATTATTCTTCTGTGTTTGGATCTGGCAGTGATGTTGTTGTGTCTGTGGTACGGGTATCTGTTTATATAATATCCTTGCCATCAAACAGAGAGGAAGTCTTCTTATTAACTGTCTGCACTGCTATCACAGAAGCATAAGGCAGCATCAGCTAATGATATTCCTTCACCCTTTCTTTATTTACCTTTTCATTCCGCCAGCCAGGGGTTTACTAGCATTCAAACCATTCATTTTGACAGACCACTCTTAGTTTTGTTTCTCATCTGTATGCTGTTGTGCTTTACTTTGTTTTGTTCTAAATGACATGTTCATGTAAAATCACAGGCTCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37269
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000080431 | Nonsense | 474 | 660 | 14 | 18 |
| ENSDART00000142468 | None | None | 150 | None | 7 |
Genomic Location (Zv9):
Chromosome 21 (position 16474352)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 17926131 |
| GRCz11 | 21 | 17962767 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAACACTTTCTCTATGGGTCTAGCTGGAACATCTTTGGATTTTCATAAA[C/T]AAAAGGACCACCATTTTCTGGTTGGCACTGAAGCTGGAAAGATTCACAAG
Long Flanking Sequence:
CGGAAGAAAGTAGTTCCTCATACAAAAGGGTTTTTGACACTCTCCATGTTTGGTTTTGTTTTTATATACACAATTATGCCGTCAAACTGTTGTATAAACGCAACATCACACTCGTAGCAGTGCGATATGGCTGTATATTGGCACTTGTGGGGGCACTAACGCTCGCCTCCCACCAGTGCTGATATACAGCCATATCACACTGCTACTCATGTGATATTGCTCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACATACACACACACACACACACACACACATATACATAAACTCACTCATAACACTTTCTCTATGGGTCTAGCTGGAACATCTTTGGATTTTCATAAA[C/T]AAAAGGACCACCATTTTCTGGTTGGCACTGAAGCTGGAAAGATTCACAAGGTCAGTCATGCACTTTCACAGCCAAGATGATCACTTTACACAAAGGCCAGTCTTAAAATCAATCAACATAAGCCTTGTGAACATCCTGCTGTCTGAAGATCTGCAGTCTTGAGTCATCACATTATTCTTCTGTGTTTGGATCTGGCAGTGATGTTGTTGTGTCTGTGGTACGGGTATCTGTTTATATAATATCCTTGCCATCAAACAGAGAGGAAGTCTTCTTATTAACTGTCTGCACTGCTATCACAGAAGCATAAGGCAGCATCAGCTAATGATATTCCTTCACCCTTTCTTTATTTACCTTTTCATTCCGCCAGCCAGGGGTTTACTAGCATTCAAACCATTCATTTTGACAGACCACTCTTAGTTTTGTTTCTCATCTGTATGCTGTTGTGCTTTACTTTGTTTTGTTCTAAATGACATGTTCATGTAAAATCACAGGCTCTCTTT
Associated Phenotype:
Not determined