ZMP
dock5
Ensembl ID:
ZFIN ID:
Description:
dedicator of cytokinesis protein 5 [Source:RefSeq peptide;Acc:NP_001103482]
Human Orthologue:
DOCK5
Human Description:
dedicator of cytokinesis 5 [Source:HGNC Symbol;Acc:23476]
Mouse Orthologue:
Dock5
Mouse Description:
dedicator of cytokinesis 5 Gene [Source:MGI Symbol;Acc:MGI:2652871]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa44680 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa21189 | Essential Splice Site | Available for shipment | Available now |
| sa1688 | Essential Splice Site | Available for shipment | Available now |
| sa34291 | Essential Splice Site | Available for shipment | Available now |
| sa41113 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa12362 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa44680
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 |
|---|---|---|---|---|---|
| ENSDART00000015126 | Nonsense | 64 | 1854 | 4 | 50 |
| ENSDART00000135834 | Nonsense | 77 | 1867 | 5 | 51 |
Genomic Location (Zv9):
Chromosome 8 (position 7356784)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 6743587 |
| GRCz11 | 8 | 6787135 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAATCATTTTGATTTGAATTTCTGAATTATGTTTTTTATTTGCAGAAAA[C/T]AAGAGACCGTCGTGCCTACAGAATTGCCTTTAGTTCAGGAGCTCGGAACC
Long Flanking Sequence:
TCCGGTTTCCTCCACAGTTCGAAGACATGCACTATAGGTGGACTGAATAAACTAAATTGGCCGTGGTGTATGAGTGTGTCTGGGTGTTTCCCAGTACCGGGTTGCAGCTGATAGGGCATCCGCTGTGTAAAATATATGCTGGTTAAGTTGGCGGTTCATTCCTCTGTGGTGACCTCTGATGACTAAAGGGACACTTAAACATTTAGTGTTTTTAGAGCTATTTTTGCCAGTGCTATAATGATACTTAAAAGATATTAAAATTCATAAAGGTTACATAACCATATCTCCACAGATTGAAATTTATTATTCATTATACTGAATTGAAATGCCCAACAATTAATTTCCCTCCATCCAAAATCAAACCCTGTTAAAAATTTAGCATTAATTAAGTTGTTTTATAATACATCATGAATATCACTGTGTGGCTCTCTCAGGGTTAAAGAACCATGAAAAATCATTTTGATTTGAATTTCTGAATTATGTTTTTTATTTGCAGAAAA[C/T]AAGAGACCGTCGTGCCTACAGAATTGCCTTTAGTTCAGGAGCTCGGAACCACACTTCGAGAATGGACACAAATATGGCACAAACTTTATGTGGTACGTAAACTCACTTGTCTTTGCTTTGCATCTAATTTATGGATTCATTTGTTTGTGGTTTTTATATACTTGTTTATTTTCTCCTCAGTTTTATTTTCAAATTTTTGTAAAACAAATTGTACAAACATTAACAGACATTTTTTTTACTTAATCAAAAGCAAACAAAGAAAAAAAGCTAAATATCAGAGAGATGAAAACATAATAATAATAATAATAATAATAATAATAATAATAATATTTATAATAATAGTAATAATAATAATAATATTAATGGTAATAATAATAGCAATATTAATAATAATATTCATATTATTAATATCATTAATAAAGAAAATAATAATAAATAATAATAATAATAATAATAATAATAATAATAGTAATATTATTAATACAAATAATAATAATATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21189
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 |
|---|---|---|---|---|---|
| ENSDART00000015126 | Essential Splice Site | 189 | 1854 | 6 | 50 |
| ENSDART00000135834 | Essential Splice Site | 202 | 1867 | 7 | 51 |
Genomic Location (Zv9):
Chromosome 8 (position 7349931)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 6736734 |
| GRCz11 | 8 | 6780282 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCACGAGTCGGCATCTCACAGCATTGACGAGAGGATACAGGAGGAGAAG[G/A]TAAAGCACTTGATTTCGCTGTGTGCATTAGCGAATTTGTTGATTTGCAAC
Long Flanking Sequence:
CAACTGACCCAGCTGGGACTCGAACCAGAGACCTTCTTGCTGTGAGGTGACTGTGCTAACCACTGAGCCACTATGTCACCTCGTCAATCCTTTATCCATCACTTCCGAACTCCAAACATTTACTTGTTTTAGAGATGTACATCCAATACTTTTTTGTTTGTTTGTGCTTTTCTCATGGTTTAAATTATCATGTTTTTTGTTCAACCTGCTGTATCTGCTTCATCTTTGTTGAAACGCATAACAATTAAAGTGTATAAAAGCATGTATAAACCTTTAGATTTACTGAGGTGCTACTTGTAACCGTATATAATTGATAACAAGTGATGCTGTTTTGTTATAAAATCTGACTTTGCCTTTTACACAGAATTCTGGGTCTCGATTTAGTGGTGCGCGATGAAGCTGGAAACACTTTAGACCCTGAAAGCAGCAGCACAGTCAGTCTGTTCAGGGCTCACGAGTCGGCATCTCACAGCATTGACGAGAGGATACAGGAGGAGAAG[G/A]TAAAGCACTTGATTTCGCTGTGTGCATTAGCGAATTTGTTGATTTGCAACAATGATAATGTAATGATAGCTGGCTTGGTATTTAGCTGCCAAATAATTTATAAGTGAGGCTTAAAATGTATGTGCTTTTAGTTTTAGTTTAGGTTAGTACAAGATTAGAAACTGTTGAATATTTAAAAAAAAAATTTTTTATGTACATCAGAAATTTCCACATGAAGGTTGCCAGATTGGCTTTGAGTAAATCCAATAGATGTCTGGTAACTGGATAGTACATGGTTTGAAATGTTTGGAATGATTAAATAGTTGTATATTACGCTGTTCTGATATGAAACAAATCAATAGTCTGAATATCTTTTATAAAACCCCATTAAGTCTGAGATCTCATTCACAAGGGTGACCTGGCCAAGAGGTCTGCAGCTTATGAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAAAACAATATAAAAATACAGATTGGTTATATAGCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1688
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 |
|---|---|---|---|---|---|
| ENSDART00000015126 | Essential Splice Site | 190 | 1854 | 7 | 50 |
| ENSDART00000135834 | Essential Splice Site | 203 | 1867 | 8 | 51 |
Genomic Location (Zv9):
Chromosome 8 (position 7347254)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 6734057 |
| GRCz11 | 8 | 6777605 |
KASP Assay ID:
554-1634.1 (used for ordering genotyping assays)
KASP Sequence:
ATGAGGGCTTTTGCTTTTTATCCTGTTTTATTTATTTGTTTCTTTTTGTT[A/T]GATGCGCCTGCAGAACCTGGAGAAGCGGAGACAGAGCCTTTTTAGTGGCG
Long Flanking Sequence:
AAGCTATGAGACTACTTTTATGTGCACATAAAACAAAATAATGACTTTATTCAACAGTTTCTAACCTTGTAATGAACAAATGAGATAAGGATAAACTTAGCCTCACCTATGAATTATTTGGTGGCTAAATAACTAGCCAGCTTTCATGTCTTTCTGTGCTCTTGAGATAAAATTGAAGTAATTTCTAAACATTCCCATGCAGCTGAAAGCCGTGTTCATATTTTTATAATACAGCATCCATTTTTAATCAGTATTCATTGAGTTGAACATCTATTATTTATAGAATTTAATATTTTTTATATTTAATATTTAAATATTATATATATTTTTGCTTAAGCTTAAAAAAAACTTTGTACAATAAAAATGAGTACAATTTTCTTTTAAAATTAATTTCTTATAATTTTTAATGTTAATGTTAATGATGTCTTTTCCAGCGCAGGTAACATTTAAATGAGGGCTTTTGCTTTTTATCCTGTTTTATTTATTTGTTTCTTTTTGTT[A/T]GATGCGCCTGCAGAACCTGGAGAAGCGGAGACAGAGCCTTTTTAGTGGCGTTCACACGTACAGCCTTTTAATGAATCTTAGAAACTTTGTGTGCAACATCGGCGAGGACGCAGAGCTTTTCATGTCATTATATGATCCTGACAAGTCTGAGTTTATTAGGTGAGTGACTTTCTTTTGAGATTTACACTATAGGTTATTATTCTTAGAAATGTAGAATGAGGAATGTGGAGAATCAATTTTACGTACTGTAATGATGTCAATTTTTAAATAGGTATTATTTAATAATATAATTTTAGCCTATTCAACACAGCTAGTGTGATCATGTCAATTTCAGTCACCACTTTCAGTCGTAATTGCACAAAAAAACTGAATTATGTTTTATTTTATTTCATTTATATTGCTTTGTGAGAATCCTTTTGTTAAAGCAACAGAAAGAAGATTTCCCCCCCCCAAAAGATATACAGTGGAAGTCAGAATTTATTTGCCCCCTTTGAATTTTT
Associated Phenotype:
Normal
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa34291
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000015126 | Essential Splice Site | 190 | 1854 | 7 | 50 |
| ENSDART00000135834 | Essential Splice Site | 203 | 1867 | 8 | 51 |
Genomic Location (Zv9):
Chromosome 8 (position 7347253)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 6734056 |
| GRCz11 | 8 | 6777604 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGGGCTTTTGCTTTTTATCCTGTTTTATTTATTTGTTTCTTTTTGTTA[G/T]ATGCGCCTGCAGAACCTGGAGAAGCGGAGACAGAGCCTTTTTAGTGGCGT
Long Flanking Sequence:
AGCTATGAGACTACTTTTATGTGCACATAAAACAAAATAATGACTTTATTCAACAGTTTCTAACCTTGTAATGAACAAATGAGATAAGGATAAACTTAGCCTCACCTATGAATTATTTGGTGGCTAAATAACTAGCCAGCTTTCATGTCTTTCTGTGCTCTTGAGATAAAATTGAAGTAATTTCTAAACATTCCCATGCAGCTGAAAGCCGTGTTCATATTTTTATAATACAGCATCCATTTTTAATCAGTATTCATTGAGTTGAACATCTATTATTTATAGAATTTAATATTTTTTATATTTAATATTTAAATATTATATATATTTTTGCTTAAGCTTAAAAAAAACTTTGTACAATAAAAATGAGTACAATTTTCTTTTAAAATTAATTTCTTATAATTTTTAATGTTAATGTTAATGATGTCTTTTCCAGCGCAGGTAACATTTAAATGAGGGCTTTTGCTTTTTATCCTGTTTTATTTATTTGTTTCTTTTTGTTA[G/T]ATGCGCCTGCAGAACCTGGAGAAGCGGAGACAGAGCCTTTTTAGTGGCGTTCACACGTACAGCCTTTTAATGAATCTTAGAAACTTTGTGTGCAACATCGGCGAGGACGCAGAGCTTTTCATGTCATTATATGATCCTGACAAGTCTGAGTTTATTAGGTGAGTGACTTTCTTTTGAGATTTACACTATAGGTTATTATTCTTAGAAATGTAGAATGAGGAATGTGGAGAATCAATTTTACGTACTGTAATGATGTCAATTTTTAAATAGGTATTATTTAATAATATAATTTTAGCCTATTCAACACAGCTAGTGTGATCATGTCAATTTCAGTCACCACTTTCAGTCGTAATTGCACAAAAAAACTGAATTATGTTTTATTTTATTTCATTTATATTGCTTTGTGAGAATCCTTTTGTTAAAGCAACAGAAAGAAGATTTCCCCCCCCCAAAAGATATACAGTGGAAGTCAGAATTTATTTGCCCCCTTTGAATTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41113
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000015126 | Nonsense | 805 | 1854 | 23 | 50 |
| ENSDART00000135834 | Nonsense | 818 | 1867 | 24 | 51 |
Genomic Location (Zv9):
Chromosome 8 (position 7304365)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 6691168 |
| GRCz11 | 8 | 6734716 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATTAAATTCAATATATATATATTTTTTACAGGGAGCAATCTTGAAATA[T/G]CTTCCCACCATCATCAATGATTTGCAGAAGGTCTTTGATGCTGTGGAGCT
Long Flanking Sequence:
TCACTGATAGCCCCCCTAAAGCATTGATTGTCCCACCCTAAATGACTGATGTCCCCACCCTATACCACTAATAGTCCCACCCTATAGGACTGATAGCCCCGCCCTAAAACACTAATTGTTCTGCCGTAAAGGACTGATAGCCCCACCCTAAAGCACTGATAATCCCGCACTAAAGGACTGACAGCCCCACCATAAAGCACTAATAGTCCATTCCTATAGGGCTGACAGCCCCGCCCTAAAGCCCTTCAACAGACAAACAAACAAAAGATTACATTTTATTTGAAAAGACAATTTCTAAAGCATCCCCATCATTCTCCCACTTTTCTCAGATGGGATGGCTGGCCAATTTAAAGGATACCATGGGCCAACTTTGCCCTGCGTGTCCTAGTTTGTGCATCGCTGCTCTAAAGGCTGGATTAATGATGTTGAAAATTATATATATAATAATATGTATTAAATTCAATATATATATATTTTTTACAGGGAGCAATCTTGAAATA[T/G]CTTCCCACCATCATCAATGATTTGCAGAAGGTCTTTGATGCTGTGGAGCTCAGGTAAAGTGAATGACGTCTTTCACACTGGTGTGAAAACATCTGCTGCATCTTTGCCGCACCGCCGGTTTATAGATTTCATTAGAGAGAGGATCATTTAAAGGAGTATTCCTGTTTCTAAAGATATCCTAGTTCTTTACACAGCATTTGTGGCAAATTGATAAGCAAAAATCAACTTTTAAGAGAAAAATCATGGTTATGTAAGCGACTTATAATCTGAAATAATTTGCACCAGTGCTTCCGATGGTGGAAAAACATAAATATAAAGCTTGTATTTTTGTTAAAGCGCTCGCAAGAACTATTCAGGAAAAAACTGTTTATTTTTTAAGCTTTCATCAGTGACTTGAAGAAGGTCTTTGATGCATTCAAAGTCAGATAAAGGAAAGGACTTGTTTCGCATGGGTGTGAAGCACCAGTTTATATAATGTTGTTTACCATCGTGAGAAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12362
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 |
|---|---|---|---|---|---|
| ENSDART00000015126 | Nonsense | 1433 | 1854 | 40 | 50 |
| ENSDART00000135834 | Nonsense | 1446 | 1867 | 41 | 51 |
| ENSDART00000015126 | Nonsense | 1433 | 1854 | 40 | 50 |
| ENSDART00000135834 | Nonsense | 1446 | 1867 | 41 | 51 |
Genomic Location (Zv9):
Chromosome 8 (position 7259368)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 6646171 |
| GRCz11 | 8 | 6689719 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCCAGTCCTAAACTTACCTTCCCATTTCAAGGACAAGGGACTACCTGAA[C/T]AAATCCTCAAGTATAACTTTTTATTCACATCTTTCACGATTGAGATCTCT
Long Flanking Sequence:
ATAAGGGTTGCAACTGAAATCTGCAGGAAGGTAGATCTCCAGGAACAGGGTTGAGCACCCCTGCTCTAGAGGCTTTTGCCTTTCATATAAGCCACTTCTGATATCAAATGATCAACTAGAAGTCAAGCTATTACTTGTTGTTACTAAAACTTGGATATTCGACAAGACTTTTTTTTTTTAGGTAGGATTGAACAAGCATGCATAAAATTGATTTAAAAAACTAATAATTAATTTAATTTAATCACGTCATTATAGACACTAAAAGTTGCCTTACAAAATACATGTTACGTTTGTAAAAAAACAAGTAACACTAAAGACAGTAATAATGTAATAAATGGACAGAGCAGCACATCCTTCAGTCCAAGTTCAGCAACATACTGACAGCAATACAAAAGTAAAATATGTCTCCCCTTAATGGATTCTCTGCAGATATTCAGTGTTTTACGGTGAAGCCAGTCCTAAACTTACCTTCCCATTTCAAGGACAAGGGACTACCTGAA[C/T]AAATCCTCAAGTATAACTTTTTATTCACATCTTTCACGATTGAGATCTCTCATAAATAATGCTCTGACAGATCACGATTTCCTCCTGTTGTCTTCTCAGTTACTACAGGACAAATGAGGTGGACAAGTTTCAGTACTCCAGACCGTTCAGGAAAGGAGAGAAAGATCCCGACAATGAGTTTGCCGTGAGTTATTATTTATTTTCTTGCCGTTATCGCACGCAAACATTGGCAAATATTGAAGCTCAGAGGACGACCGATAAAGAAAGATAAGGATAATTAGGTTGCCTGAAAAGATGAATTCTGATGAAAATAGGCTGATGTGTTTCTTTCTATGTTGTTGACATTACACATACTTTAAAAATGATGAAGTTGAAGCTGTCAATCAAGCATCTGTTTAGTGTTGAAACCCCACAAGTGAATGGAGGATGAGTTTCAACATGATTGATGACCTGTAAGCAAGGAAATGAATGCAGGGATCATACATAATGAAATAAATACA
Associated Phenotype:
Not determined