ZMP
DOCK6
Ensembl ID:
Description:
dedicator of cytokinesis 6 [Source:HGNC Symbol;Acc:19189]
Human Orthologue:
DOCK6
Human Description:
dedicator of cytokinesis 6 [Source:HGNC Symbol;Acc:19189]
Mouse Orthologue:
Dock6
Mouse Description:
dedicator of cytokinesis 6 Gene [Source:MGI Symbol;Acc:MGI:1914789]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1010 | Nonsense | Available for shipment | Available now |
sa40178 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6922 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa26161 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12512 | Nonsense | Available for shipment | Available now |
sa33330 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa899 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1010
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082944 | Nonsense | 271 | 2114 | 8 | 50 |
Genomic Location (Zv9):
Chromosome 3 (position 56154393)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 55048119 |
GRCz11 | 3 | 55302721 |
KASP Assay ID:
554-0914.1 (used for ordering genotyping assays)
KASP Sequence:
TAAGCTGCCTGCAGTCTGTTCTGACCTGTTGCGGTTGTATTTCCAGATTC[G/T]AGATTGAAATCGAGCCAATATTTGGATCACTGGCTCTGTATGATGTTAGA
Long Flanking Sequence:
CCGCCTGAAATTTGTCAAAAGGCATCTGAAGGACTCTCAGACCATAAGAAACTAAATTCTCTGGTCTGATGAGATTAAAATTTAACTCTCTGGAGTGAATGCCAGGCATTACGTTTGGAAAAAACCAGGCACCACTCAACACCAGGCTAATACAATCCCTACTGTGAAGCATGTTCTATTAAACATCTCTGGATGCTCTCCATTTTGCAATAAGGCTGTAACGTAAAAAAAATGTGAAAAAACTGAAGCTCTATAAAAACTTTTCGCATGCACTGTAATGGACACATAAAATAACATATTTTATATTTTTAGTCTCAACATCAGGTATTTTTAAAAAACAATTCTGGAACTACAAATGTTCTACCGGTGCCCTTTGTTTTTCACTTAGTAACTGCATTCATTGATTTTTAATGAAACACACCTTCTGATTACACATCCATCCTCAACACTTAAGCTGCCTGCAGTCTGTTCTGACCTGTTGCGGTTGTATTTCCAGATTC[G/T]AGATTGAAATCGAGCCAATATTTGGATCACTGGCTCTGTATGATGTTAGAGAAAAGAAAAAGGTATGACTGTTTTCTTAACCTTTTGGTATAATTCCTGAAAAGCTTGTGGGTTCAAACTCTATACTGTAAAAAATCGTATGTGCTATTTCCTTTAAAAAAAATAATGGTAACAATATTGTACAAATTTTTTAAAGGAGTTTTCAAGACTTGATTTTTTAATAAGAAAAACTAGTTGGAAAATAAAATAAAAATTTAAAAGAAAATAACTCAATTTTTTGGAGTGATGGATTTTAAAGTTTTTAGTGGAATGTGCGTTTAAAATTCAAGCAAATAAATCACAATTTACTCATATTTAATAATTAAAATTACTCATTCATATCATTTAAAATATAGAATGTTTTAATCAAACAAATATACAATGCATTTTTGGCCAAACATCTTTTTATTGCATGTTCAACTGATAAAAATATACATACAATTTGTTGTAAAAGATCAAAA
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:
sa40178
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 |
---|---|---|---|---|---|
ENSDART00000082944 | Nonsense | 422 | 2114 | 12 | 50 |
Genomic Location (Zv9):
Chromosome 3 (position 56146183)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 55039909 |
GRCz11 | 3 | 55294511 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATAAAACGGTTCTCTAGCTGAAACATCATTCTGTCATTCCCTTCAGAG[C/T]GAAAGGGGACGTGGAATGAGAGGAAGAAGAAGGGATTTGAAAGGATGAGT
Long Flanking Sequence:
TTGGCTCCAAATTAAATGTTTATTATTTATTTGTATATCAAATTGTTTGTACTTTTGATTATAGGTTTTTGCTTATTTTGGCTTCAGATTGTGGGAAGTGTTTCAGGTGGAGTGTGCTGCTTGTTTGATTGTTTGTTTGTCTTGTCAAATGTATTTACGTTGTGATGTGTTGTACTCTGTTTGATTTATGAACTTTTTAGGGACCCCCTCGAAAATGAGATGATTAATTTCATGGGGCTATCCCATTCAATAAATTAAATTCAATTCCTGCAACAATTTAATAAACATAGCTGATATAAATAACTTTCTTGTTAGTCAAAATATTGTTTGTTTTATTTCACCTACCAATATTTTTCACCAAAGCTTTTTTATCATCATAAGTGGTGTTTCATTGCTAAATGAATCTTTTCAACAAATTCAGAAAAATGATTCAGTACCCACTCCATAAATTCATAAAACGGTTCTCTAGCTGAAACATCATTCTGTCATTCCCTTCAGAG[C/T]GAAAGGGGACGTGGAATGAGAGGAAGAAGAAGGGATTTGAAAGGATGAGTGTAGGAGAGGACATGTGCAACTTCACGAACTTCCGTCCGGCCACTCTCACAGTCACCAACTTTTTTAAACAGGTCTGTTCTCAGATTGTGTGTGTGTGTGTGCGCGCATCTCTGGTGTTAGCGGGATGTGTTGTTTAATGCTGTGTGTTTGTGCGGTGCTGCAGGAAGGGGACAGACTGAGTGATGAAGACTTATATAAGTTTCTGGCAGACATGAGGAGGCCGTCATCAGTGCTGCGTCGACTCAGGCCTGTGACAGGTATCTGTCCACACTTATTCTTACATCATCTCTTTTATTATTTAGCCGCTTTCTCACTGTGTGTGTGTGTGTGCGTGCTTGCGTCTGTGTGTGCGCGTGCGTGTGGCGTGTGTGTGTGTGTGTGTGTGTGTGTGGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6922
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 |
---|---|---|---|---|---|
ENSDART00000082944 | Nonsense | 564 | 2114 | 15 | 50 |
Genomic Location (Zv9):
Chromosome 3 (position 56136548)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 55030274 |
GRCz11 | 3 | 55284876 |
KASP Assay ID:
554-4685.1 (used for ordering genotyping assays)
KASP Sequence:
TTAGGAACTTGCTGTACGTTTACCCTCAGTCCGTGAACTTCAGCAGCCGG[C/T]AGGGTTCGGTGAGGAACATTGCTGTGAAGGTGCAGTTCATGGCAGGAGAG
Long Flanking Sequence:
AGCACTCTTGAAAGTCACTCAGTATGACCTCAGTATTGTTAAAAAAATGTTGCTTCTAAAGATAGCGTTGCTATGTCTTTTTTTTTTGTTGCTGAAATGGGGACACTTTCATTACCCAGTGCAAATTTGGTTGCAAAACTGGCCAAACAGAAATGCCTTTCTCTCGAAGCCCCTTTAGTGTCTGCATACACTCTATTGCCCTCAAAAATGAAGTACATGCCTGAGTGCGCAACACTTTGTTGAGTGAAGAAAGTTGTATTTATCCAGAAAAGTGAAAGAAGTGAAGAAAAACTAAAATTACTATCAATTTCATTGTCTTTGCTAAAAAGAACTCAATGTAATATTTTGGAACCTGTAAATGTGCATAATATACAGGGCTCTCCTAAATCATTGCTGTTCTAATGGAGATGAGATCTTTGTTTCACCTTCATTTCATTCTCCCTCTCCTGCTTAGGAACTTGCTGTACGTTTACCCTCAGTCCGTGAACTTCAGCAGCCGG[C/T]AGGGTTCGGTGAGGAACATTGCTGTGAAGGTGCAGTTCATGGCAGGAGAGGATCCCAGTCAGGCCATGCCGGTGAGTCACAGATTACACTGTCACAGCACATATTCTAAGCTTCTCAGACAAAAGAAAAGCACTTGGGATTATGCAAGCGCATTTGATATGATGATCTAATCACTTAGACAAACTAATTGTGAACAATAAAGCCCTCCAGATGTGTGCCAAGAGTATGACAGCTCCTCCCTAAAACACATTGATCCAAAAACAAACTGCTTACATTAGTCACTCGAACCACACTCCGTCGCCAGATGTATTAAACGGAACAATACATCGTTTTATGGTGTACATTGTCTCTAGAAATTTCTTAATATGGTTTTGTCAGAATTTATTTAGCTATTTTGATCATTTTAAATAATAAACAAAACATTAAAATTTAGATGAACACTGCATAATTTTTTTAAAAGGGCTCACTTTTTTAAGTCTCAAATCAGTGTTTCTCAACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26161
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082944 | Nonsense | 940 | 2114 | 23 | 50 |
Genomic Location (Zv9):
Chromosome 3 (position 56118208)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 55011934 |
GRCz11 | 3 | 55266536 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCCAGGGGGCTCGAGGGCCGTGCTCCGCCGGAACCCCAACTCGAGCTG[T/A]GAGCTCAAGCAGGTGCCGATCAATCCCTATAACCTAATGTCCCGCTCTAC
Long Flanking Sequence:
AAAACTAACCGACTGAAACTTGCATCTAAACATTTTTATTTTTATTTTACATGACCTTTAAGCCAAAGTGTTATTAAATGCTGAAAAATTCCTTTTTGACTTGATTTAGGAAGTAACTGGATGAACTGATTAAATAGTAAGCTGCAGTTCTGCTTTTGATGTTGTTTGTTGGAGTGATGGGTAAGCCTGTGCGGTGTTTCCTGCACCAGCTGTTGATCACTCTGCTTATGTCTGTACTTTGTTTTTACTGTGGTACAGCCTCTTTCCTGGCTTCCCGCTTCTTCCCACCCTCTTCTCAATTAATTCTTGTTCCTGCGCTTTGTCTCCTCCCTGCGACGCCTGTGTGTGGCTGTTGTGCCCTCCCCCGTGTTGCCCTGTGCTGTTTGTTTTGTGTCGTCGATGGATGAGCAGGGAATAGACCGCTCTCATTCCTGGGTAAACTCTGCTTACGCTCCAGGGGGCTCGAGGGCCGTGCTCCGCCGGAACCCCAACTCGAGCTG[T/A]GAGCTCAAGCAGGTGCCGATCAATCCCTATAACCTAATGTCCCGCTCTACTGCCTCAAACCATACACCCTACTGTGTACCATCCTGCATCACCCCTTCAGCATAACATCATTCATTACAATCTCTTTTATTTGATGCGTGTTTTTATTTGATGTTCTTATTAATACTATTTATTCTCTAAAAATATACAACCTGTCAAAACCTGATACTGTCAAAACCTAAACCCTAACATTTTTTTATGATTACTTTCATACATTTAAAGGAATACCTCACAAAATAAAATCTGTCGTCATTTACTTTATGCTATCATTTACTCTGTCCTATACCCTAACCCTTTACTTTTTCTGAACATTTATGAGTCTCTTTTTCTGTTGAACACACACAAGATATATTAAGAAATGTTGTACCTGTACCATTGACTTCCATAGTATTTGGTTTTTCTGCTACAATCTCAGAAAAAATGGTACAATGTTGTACAAAAGTAGGTACAAACCCTTGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12512
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082944 | Nonsense | 1322 | 2114 | 32 | 50 |
Genomic Location (Zv9):
Chromosome 3 (position 56101351)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 54995077 |
GRCz11 | 3 | 55249679 |
KASP Assay ID:
2259-4178.1 (used for ordering genotyping assays)
KASP Sequence:
GGTGTCCTCTCAGCGGAGTGCAGCAGGACGCTGCTGGTGTGTTTTCTGTG[G/A]GTCTGGAAGAACGCTGATGCAGGRCTGCTGGAGCGATGGGTTTCAGACCT
Long Flanking Sequence:
AAATCATGGAAAAGTCATGGAATTTTAGTAGTAAAAATGTGTATGAACCCTGTAAATAGTAATTGTGATAAACAGTTCATGGTCTTCTGGAATTTTCCCTCATGTTCATGGCTGCAGTTTCTCAATTTCACCATTAGAGAAGCTCTTCATACACACATATACTCATGTTCATTCTGAGTGCCACAGTCCTGATCTCTTCCACTAGAAGTGCAGTTTTACTGCACTCTCTCCTACGAACAGTGTTTCCTGGTCATTAGTGAGTATTAATGACTCGCACAAAGCTGAGGAAATAAAAAACATGTGTGTTTAAGTGTTTATTATCCGCTCGGGTGTGTAAGGACATCCTCTGTGCGTGCCGGATGTGGTGTCCGATGGGGCCCGGCTCTGTTGTGTTTGGTCTGTGTTTAAATGTGGGTTTATTTGTGTCTCCATCAGGCTGGCCGCCAGTGTGGTGTCCTCTCAGCGGAGTGCAGCAGGACGCTGCTGGTGTGTTTTCTGTG[G/A]GTCTGGAAGAACGCTGATGCAGGGCTGCTGGAGCGATGGGTTTCAGACCTGTCTGTGCCACAGATCAACCGTCTGCTGGATCTGCTCCACCTCTGTCTGTCCTGTTTCGAATACAAGGTACATTAACACATGTTCCCTGTTGATCAGGATGGATTTGATAAAGATTTAAATGCATTTTTTTAATTAGAATTAGGGAAATAATGACATTTCCATAATGCATTATTTGTAGGATTTTTTTTGTCCTACGATATATTGCTCCAAAATATATTGCGATAAACTATATTATTGTCATTTTAAGACCATTTTATGCCACTCATTATATAATGCCATCACAATGCAAGTGCACTCTTTCAGAAAACACATAATTTTTTATGCCTAAGAATATTTCATTTAATTATAGTGATTTTAAAAATTTAAAAATAAGGCATTGGAATCAGAATGTAAATGCACATCCTAAATAAACAATAATACATGTTAAAGAGGTGCAAGGTAAAAAAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33330
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082944 | Nonsense | 1360 | 2114 | 32 | 50 |
Genomic Location (Zv9):
Chromosome 3 (position 56101237)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 54994963 |
GRCz11 | 3 | 55249565 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCAACCGTCTGCTGGATCTGCTCCACCTCTGTCTGTCCTGTTTCGAATA[C/A]AAGGTACATTAACACATGTTCCCTGTTGATCAGGATGGATTTGATAAAGA
Long Flanking Sequence:
CAGTTTCTCAATTTCACCATTAGAGAAGCTCTTCATACACACATATACTCATGTTCATTCTGAGTGCCACAGTCCTGATCTCTTCCACTAGAAGTGCAGTTTTACTGCACTCTCTCCTACGAACAGTGTTTCCTGGTCATTAGTGAGTATTAATGACTCGCACAAAGCTGAGGAAATAAAAAACATGTGTGTTTAAGTGTTTATTATCCGCTCGGGTGTGTAAGGACATCCTCTGTGCGTGCCGGATGTGGTGTCCGATGGGGCCCGGCTCTGTTGTGTTTGGTCTGTGTTTAAATGTGGGTTTATTTGTGTCTCCATCAGGCTGGCCGCCAGTGTGGTGTCCTCTCAGCGGAGTGCAGCAGGACGCTGCTGGTGTGTTTTCTGTGGGTCTGGAAGAACGCTGATGCAGGGCTGCTGGAGCGATGGGTTTCAGACCTGTCTGTGCCACAGATCAACCGTCTGCTGGATCTGCTCCACCTCTGTCTGTCCTGTTTCGAATA[C/A]AAGGTACATTAACACATGTTCCCTGTTGATCAGGATGGATTTGATAAAGATTTAAATGCATTTTTTTAATTAGAATTAGGGAAATAATGACATTTCCATAATGCATTATTTGTAGGATTTTTTTTGTCCTACGATATATTGCTCCAAAATATATTGCGATAAACTATATTATTGTCATTTTAAGACCATTTTATGCCACTCATTATATAATGCCATCACAATGCAAGTGCACTCTTTCAGAAAACACATAATTTTTTATGCCTAAGAATATTTCATTTAATTATAGTGATTTTAAAAATTTAAAAATAAGGCATTGGAATCAGAATGTAAATGCACATCCTAAATAAACAATAATACATGTTAAAGAGGTGCAAGGTAAAAAAGTGACTGAGGCTGTGAAATCTGCTGCCAGATCTATTTTCAGTTGTCAGACACCCACAGAAAAATATACTAATATGTCTCATAGTCAATACTATAGTGATTTTTTTAACCATACTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa899
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 |
---|---|---|---|---|---|
ENSDART00000082944 | Essential Splice Site | 1403 | 2114 | 33 | 50 |
Genomic Location (Zv9):
Chromosome 3 (position 56096347)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 54990073 |
GRCz11 | 3 | 55244675 |
KASP Assay ID:
554-0806.1 (used for ordering genotyping assays)
KASP Sequence:
CATACTGGGCACTATTGGAGCAAGACAAGAGATGGTCCGCCGCTGCAGAG[G/A]TACAAACACACACTTTCTTGCTTTATATGCAAGAAAAACGTGAAAAGGYA
Long Flanking Sequence:
AGTTTACCAAGCATGAACTTTCTAATGCAGCGAAATGCAAAACTTAGTGCACAATCTTGCGTTTTCGGTCTAATGCATATGAATGGAAGTCTATAGGGAGAAAAGTGCGGTGTGATCTCAGCTTAAGTCTGTAATTTTATCCATAAGGATCTTGAAAAGGTATTAAGTCTGACTGAAACCTGCAGAAACCCTGTAAATGTGAACCACAAGGGGAAAATAAACTGAAAATAAATGAAATCATTCAAGTTTCTTGAAACTATTTTTGTGTAATGTATCTTATGTTACCCTTTCATTAAGAGGTTTTTATTTGTATAGCTCAGATGTGTGTGTTTCCCAAAGTTCACACATCTTGATTTATTGTGCCTCCTGTCAGGGAAAGAAAGCTCTGGAGAGAATCAACAGCCTGACCTTTAAGAAGTCTCAGGACATGAAGGCCCGTCTTGAGGAGGCCATACTGGGCACTATTGGAGCAAGACAAGAGATGGTCCGCCGCTGCAGAG[G/A]TACAAACACACACTTTCTTGCTTTATATGCAAGAAAAACGTGAAAAGGCACGACAAAACAAACTAAACTCACCATTCACCACTGTACCCCAGAGCGCAGTCCATATGGAGGACAGGAAAATGTGCGCTGGAGGAAGAACGTCACTCACTGGAGGCAGAATGCAGACAGAGTGGACAAGTATGTCTTTTCCTCCGTGTCTCTTGATTTCTGGGTGTCTTTATATTGTTGACACTTTCACTGGACGCGTAGAAGCTGCTGTTCCTGCTTAGACGCATATTCACAGGGTGCACGTACTGTGCGTGTGTGTGTCTTTCTCTCTCAATTCAATTAAATAATTGTTTATTGGTATGACAACTCTTACAAATGTATTGCCAAAGCATCTGTAGAGTTTAAATTACAAAAGAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAATTACAAAAGAATATATAAATATATAATATATATT
Associated Phenotype:
Not determined