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 |
|---|---|---|---|
| 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 |
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