ZMP
dock11
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate dedicator of cytokinesis 9 (DOCK9) [Source:UniProtKB/TrEMBL;Acc:
Human Orthologue:
DOCK11
Human Description:
dedicator of cytokinesis 11 [Source:HGNC Symbol;Acc:23483]
Mouse Orthologue:
Dock11
Mouse Description:
dedicator of cytokinesis 11 Gene [Source:MGI Symbol;Acc:MGI:1923224]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa26923 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13474 | Essential Splice Site | Available for shipment | Available now |
sa45273 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7593 | Missense | Mutation detected in F1 DNA | Not yet available |
sa14188 | Essential Splice Site | Available for shipment | Available now |
sa13398 | Nonsense | Available for shipment | Available now |
sa38601 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa26923
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 |
---|---|---|---|---|---|
ENSDART00000090406 | Essential Splice Site | 291 | 2075 | 9 | 57 |
ENSDART00000137575 | None | None | 982 | None | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 20512255)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 19048886 |
GRCz11 | 7 | 19301153 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAATGGAGGACCGGAGGAATGGCTCAGAAACGTCTGAAGGGTCTCTGGG[T/A]AAATAATGCACACACACACACTGAAAACATGAGCACACATGATCATGTAT
Long Flanking Sequence:
AATTCATACAAAGATGAGAAGAACTACAAAGAATCAAAAGGCTCAATCTATCTGGATTCCTGTATAGATGTAGTTCCGGTACACACTTTTTTGCATTCTTATACGGTTGTTGCAGTCCCGCTTATCTTGTAAATATCTGGCTTAATGCATTTCTCAGGAAGTTCTACAACATCATTAAAGCAGGCCTTAGGCTGGGGTGTAATATCAGTTACACAACCAGAGGAGTGTTTCTTACTGAACACCCATTATTATTACAACCACAAACCACTCTTAAAGTCGCCATGTTAAATTCCTCCATCGGCTGACACAGTACTTTTCCTGCAGTGCCCTAAAATGCGGCGCAATGGCTTCGAGCTGAAGATGCAGGAGCGCTACAGTCACTATCTGGCGGCCGACAGCGAGGCTGAGATGGAGGACTGGGTGAACACGATAAAACAGGCCTTACTCAGCACAATGGAGGACCGGAGGAATGGCTCAGAAACGTCTGAAGGGTCTCTGGG[T/A]AAATAATGCACACACACACACTGAAAACATGAGCACACATGATCATGTATCGCATGTTGTGTTTGACCATGGTATAACAATATATACTGGTTCGGAAATGACATTAGTGTGGATGAATAAGGACAGAACATTAACTCTTAAAATGCATTTGTGTCCGTTTTGACCTGGAAGCTAGTGTATGTGTTTAAATGAGTCTGTATGGATGTTTCCCGGTGATGGATTGCAACTGGAAGTGCATCCTCTGCATCAAACATGCTGGATAAGTTGGTGGTTTATTCCGCTGTGGCGACCCGATTAATAAAGCGGCCAAACCGAAAAGAAAATGAATGAATGAACACAAATAAAGATGTTTTGAAGAAACAATAAAACAGGTACCCATTGACTTGTATAGAAGAGGAGAAATAAATGCACTATGGAAGTCAATGGTAAATGGGTAACTTTTTAAAACTATCTTCTTTTGTGTTCAACAACAACAAAAAAAGAACCTCAAACAGGTTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13474
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090406 | Essential Splice Site | 345 | 2075 | 11 | 57 |
ENSDART00000137575 | None | None | 982 | None | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 20503306)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 19039937 |
GRCz11 | 7 | 19292204 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGGAATGAGGGCCGACAGAAGATCTTCTCCCTCGATCCTGAGGTGCAGG[T/C]TAGTCAATTTYTCCCAATTATCACCTTCTGCATTACAAAGCGGAAAGCAK
Long Flanking Sequence:
TTAAATGAAAACAAAGAAGAGGCCTGTCTAATGAGATATATTTAATATAACCACTTTCTATTTAATCAAAATGACATTAAATCATAGCGGTGCCAATACCCTAGTGGTTAGTGTGTTGAATCATGGCACCAAGGTGCTCACGACCGGAATTCGATTCCCAGCTCAAGATCCTTTGCTGATCCTTCCCCTATCTCTGCTCCCCATACTTTCCTGTCTATAAATCTCCACTGTCCTATCACAATAAAGGAAAAAACTCTTAAAAAAGGTAAACCTTATATCTCATCCTTTATTTTCTCAAGAAGGACACAAATAGAAAGGGAATAGAAAAGACTGTCAAAACTCTTGTTAATGAGGTCTCTATACACTGTGCTCAACTCCGTGCATCACTTCATTTTTTTTGTCCTGTTCTCTTCAGTATGCTAGAGAAACTGACCAGCTGAGTAAAATGAGCAGGAATGAGGGCCGACAGAAGATCTTCTCCCTCGATCCTGAGGTGCAGG[T/C]TAGTCAATTTCTCCCAATTATCACCTTCTGCATTACAAAGCGGAAAGCAGTCGGTAGCGCGCCGACAAATGGTGCACGTCAGGGCGTCCTGAGTTCAAATCCTGGCTCGAGGACATTTCCCTACCTCTACCCCCCCCCTCTCTATCTCTCTCTCTCTCTCTCTCTCCAACTTTGCTTCCTGTCTCAATACTGCAAAAAGCCCAAAAATAAATCTTAAAATAAAAAAAAAAATAGAAAGCGGAATGCAAAATGAGTTAATGAAATGTCCCTCTTTCCCTTTAGAGATTGGATTTCTCAGGCATCGAGCCTGACGTGAAGCCATTTGAAGAACGATTTGGCCGAAGAATCATGGTCAGTTGTCACAACTTGACCTTTAATCTGCAAGGATGCGTCAGTGAGAAGAATGACGGTGTCTTGACCAATGTGAGTAAACACATTTAAACACAAGGAATGGCAATATTTATTTCTAAAGCTACTGTAATGGTGATCACAGTCAAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45273
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 |
---|---|---|---|---|---|
ENSDART00000090406 | Nonsense | 651 | 2075 | 18 | 57 |
ENSDART00000137575 | None | None | 982 | None | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 20489144)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 19025775 |
GRCz11 | 7 | 19278042 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGAGGCTCGATTCAACCACCCGTTCACCATCTACAACAACCACCTCTA[C/A]ATCTATCCTCAGCAGCTCAAATATGACAGTCAGAAGGCCTTCGACAAAGT
Long Flanking Sequence:
GTCTTAAATTTAACTTGGCAGAAACCCTGTGCAAGATATTTTTCAAGATACTAGTATTCAGCTTAAAATGCAATTTAAAGGCTTAACTAGGTTGATTAGGCAAAATAAGGTAAATAAGCAAATTTACTGCTTAAAAGGGCCAATAATAGTGACCTTAAAAAAAATTGAAAAATTAAAAAACACTTTTATTCTAGCAGAAATAAAAAATAAATAAGACTTTTTCCTGAAGAAAAAATATTATAGGAAATACTGTGAAAAATCCCTTGATCTGTTCAAGATCATTTGGAAAATATTTGAAAAAGAAAAAAAATCACCGGAGGGCGAATAATTTTGACTTCAACTGTATACATCGTCATCTTCACAGACTCTGTCACATCGTCTTACATTCCCGTAAAGCCATTTGCGGATCAGTGTGACAGCGTGTCGGTGGAAGTGGAGGAATTTGTCCCGGAAGAGGCTCGATTCAACCACCCGTTCACCATCTACAACAACCACCTCTA[C/A]ATCTATCCTCAGCAGCTCAAATATGACAGTCAGAAGGCCTTCGACAAAGTAAGTTTCCTTTTACGTCTAACAGAACAAGGTTATTAAAGATTGAAGAAAATGTTCTCTTGTGAGGGCTGAAATAATTAAACATTAGCTTGCTTGCAGATACATTAAGGTGCAGTAGGTGATCTGCCAAAATGCTAGCCGGTTAGTGTAATATCTTTGAAACAGTCCCACCCCTGCCGTCCAAAACCAGCGGACAACCCACTAGACCATGTCATTTTCCACTTAGAAAACTTTATAGTACTTTATAAAACTACAATTTCAAACGAAAAACTGTATTACATCTAGATTACATTTTATGTTTTACATTCAAGACATTTAAAATTTTACATCTTTTCCAGCTTTAATAAAGGAAAAGTACAGCAGTTCTGTTGAAGCATTTAGTATATGAATTATTTTTATAATGTTTGTGTTTTCTCTTAGGCTCGAAACATTGCAGTGTGTGTTCAATTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7593
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090406 | Missense | 1155 | 2075 | 32 | 57 |
ENSDART00000137575 | Missense | 82 | 982 | 2 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 20462498)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 18999129 |
GRCz11 | 7 | 19251396 |
KASP Assay ID:
554-4019.1 (used for ordering genotyping assays)
KASP Sequence:
CTGCCCAGAGATYAGACAGYTGGCTGTGGCTGTGCTKAAAAATCTCAWGA[T/A]CAAACACGCCATGGATGACCGGTACAATGCCTTTAAGGTAAGGTATGGCA
Long Flanking Sequence:
CAAGGCTTTTCTATCACTCTTTGCTTTCTGTTTCTGCCGCTGTCAGATGTCTGGAATGCAGTGAAGTCTGCTTTCACAACATTTCAGTTTAGTCAGCCATCAAATCCTAGACATGCTGTTTTCATTCGAATGCTTTTCACTATCACAAATATCTCAAGGACTGTTTCTACTGTATGTTAAGCATCATTTGCATATATGCATCTTTAATACTATTGCGTCTTCAGGATGCATGGAAAAAAATGTTGCTTGTTTCTTTCTACTGAAAGGCCATACAGATTAAAAAGTGCATCATAATGAATGTGAAATCAAATATAGTGAGTAAAAAGCAATCTCTGACCTGAAAAAACATGTTTTAGATCAGAGTCTGGAGTACAGCTTGACTGAAGATTACTGCAAGAATCATTTTCTGGTGGGTTTGCTTCTGCGCGAGGTGGCTGATGGACTTCAGGCCTGCCCAGAGATTAGACAGCTGGCTGTGGCTGTGCTTAAAAATCTCATGA[T/A]CAAACACGCCATGGATGACCGGTACAATGCCTTTAAGGTAAGGTATGGCATATTAAAAACTTGTGATGCTCATGATTTGGTTGGTATTACAATCTTAGGGTCACTGTTTCATTGGTCCCTACCAATATCAACAGCAAACCTATGCTTTTTTTGTTTGAAAGCAGAGGGTTGGTTCATTATTTTGATATATAATATGGTCATATATTAGCAAAAAAATTCTGAGGACTGTCAAATTTAGATGAAACTCGTAAAAAATGCTGTCAGTGGCTGGCAACTTTTTAAAAAAATGCTGGTAGTGAAAGAATGAACTGCTCCTTCAGACAAAAAAACAGCGGTATGGCAGCATTTTTAGCTTTCAAACGCACGTTGTAAATGGTACTGATGCATACTAAACACATATTTAAGATGTTATGCTGAAAAACAATTCAACTCGCTTCATTGACTTTCTATTGTGGGAGGGAGACTCTCTGTCATTTCAGACTTATAACTTGAGACAAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14188
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 |
---|---|---|---|---|---|
ENSDART00000090406 | Essential Splice Site | 1658 | 2075 | 47 | 57 |
ENSDART00000137575 | Essential Splice Site | 576 | 982 | 15 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 20422404)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 18959035 |
GRCz11 | 7 | 19211302 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTAATGTTCATGTTGCCGCTTTAATGGCAGAGTATTTGCACAGGAAAA[G/A]TAAGTTTGCAAAGATTCTTTACAGTCAACAGTAGTTTCATGCTCACTTGT
Long Flanking Sequence:
ATTATTTACTTGGTCATGAATTATTTAACAGTTTGGCAGTCGCGTGTATTCATATGCTCTTCTGATATCTTTAGGTTTGCAGCAATGTTTGCTTCTTCATATAAATACATTCCCCCCATTATGACCAAAAACAGGAATTGAACTGGAGGAAAGGTCACATCTTGGCCAGTGCTCTCAAGTGTTCCTATTTTAGTCACATGCAGGAAATATACCCATGTATGGGAAAGATCATGCAAGGACATTGCCTTCTAAAACATAAAAATGGCATGCAAACATATTTTTACCAGTTTTGTACTAAATCCACTTGAATATTAAACAAGTTACACACAAAAAAGGCAGTTATTATTATCAGTAGACTCTAGTAAAAATCAGTCAATGCCTGAGATTTGTGTTCTTGATCCTGTAAGCCTCTTATGTTTTTCTTTTTCTTCTATTTCCGCAGGCTGCCATGTGTAATGTTCATGTTGCCGCTTTAATGGCAGAGTATTTGCACAGGAAAA[G/A]TAAGTTTGCAAAGATTCTTTACAGTCAACAGTAGTTTCATGCTCACTTGTTTGGGTCAAATAAATTCTTCCTTAAACATCGATTTTTACACTGATTGCTAATCTAAAATCACAATGAATGTCTGAAGTCGGATTAAAATGCTGTAATTAATTTTAAAAAATTGTCAAAAACAGCAACAACCAGGGTTGGGCATGTTAGTTAAACTCAACTACCAGTCCATGGATCGGTTGGTACCGGGCCACACAAGAAATCATGAATTATTTCAGCTTTATTTATGATCCGAGTGCGAATAATCTTTTATTTTGAAAAAACTTTTATTTTGATAAATGACCATATTCTCTCAGTTACATTTCGGTCACTTGAGTGCCCAAATTCCACCTACAAGCAGCAAAATGAGTAAAAAACAGACGTCTTTAGAAAGTTTCTTTGCCAAGCAGAAAAGGCCCTGTTAAGGACCTGCAAACTGCCAAGAAATCCATTCGCAACCCATTTGTCAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13398
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090406 | Nonsense | 1728 | 2075 | 49 | 57 |
ENSDART00000137575 | Nonsense | 646 | 982 | 17 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 20418478)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 18955109 |
GRCz11 | 7 | 19207376 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGAGKTTTGAGCTCATAACACACATCGCCAGACTCATCAYTCCGGTWTA[T/G]GAAAAGCGACACGAGTTTGAGGTAAGAGAGAATGAAGGGGTRGYGCAATC
Long Flanking Sequence:
AGACGTCAAAGCTCCTGCTCCTGCCTATAGATGTAATTTACAGATCAAAACTGTTGACTTGATGTGGATACCAATTTAGTTATCAGTATAGTTATTGTTTTTGTTTCAAACAACTGGCTAATATAGTGCCATGCTTTTATATCTACAGTATAGTTAAACAATGTATCTCAATGTTTCAGAGCTATTCCCCAGTGGACTGGCAGCTTTTAAGAGAACCACTCAGAACATTGATGAGGAAGGAGCCATGAAAGAAGACATCGGCATGCAAGATGTGTACTACACTGAGGTAAAACACACTAGCTTTCTTTATCAATGCTAAAAAAAAAAAAACGTTTTATCAGCAGTGATTATTGAAGCCTCTCAGAAATGTTGGTTTAAAAGTGGCATTTTGCATGACAGGACGTCCTGGTGGAGCAATTGGAGGTGTGTGTGGAGAGTCTGTGGAAAGCTGAGAGGTTTGAGCTCATAACACACATCGCCAGACTCATCATTCCGGTTTA[T/G]GAAAAGCGACACGAGTTTGAGGTAAGAGAGAATGAAGGGGTGGCGCAATCATGCTGTGCTGCTTCAAATAAATGTGCTAATATCCTGGAAGTTCCACTTGCCCAATTCTTTGATTTCTTTCTCAATGCTGTGACTCTGAGACTCTGCGGCCCCTGTGGCAGACATCAGACAGAAGCTCATTACTTAGGCCTGGATTAACAATGACCAGACAAGAAGCGAGTCGGTTTGTTTGTATGAACAATGAGGGATTTTTCTCAGCCATTATAAACCGAGCTTTCATCTGTTTCACTTTTACTCTCAGTTAAATGTGGAGAAGGTATAAAGAAGTATGAAAAAACATGTTGAATGAAAATAACGAGCAATATCTAAAAAGCAAAAAGTCTGATACTGTTATTTGGACATCAGGGTGGTAGGGTTTTGTGGTTTTATAGAACATACAGTAACTAAACTTTTTCAGTGTACTATTTATTTCCTGCTCTGAAAGCCCTTAGATGAATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38601
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 |
---|---|---|---|---|---|
ENSDART00000090406 | Nonsense | 1740 | 2075 | 50 | 57 |
ENSDART00000137575 | Nonsense | 658 | 982 | 18 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 20412336)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 18948967 |
GRCz11 | 7 | 19201234 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACATCTCACACACTCTTTCTGTCTCGGTCCTGTAGAAACTGAGGCGAT[T/A]GTACGACACACTGCAGCGAGCTTATGCAAAGATATTGGAGGTGATGCAGT
Long Flanking Sequence:
TTACAACATACCTTGTAAAGATTATGTGAATTAAACAGCACAACCCAATAAAAATAATGCTAACCAAAAGGAAAAGACTTGGCTCTCTATAGAATATTATTTATCTTATTTTATTTGAAGTGTTTTGCATTAATGAGGAAAACGCTTCGATATGGATGTGACATCTATCTATAACCAGATGTGAAATTGCCACTTGTGTGACTTTTGTAAGTCAATTAAATTAGTTTAAAAACCTTGACAGACATTTGAGTATTTTTACAGCTCTGTAAAATAAAAGCCTACTTAAACAACTTAGAAAGTTTTTTTTTTTTTTTTTTTTAAGCAAAAGCAATTGCTATTTTGACTTAAATGTACAACTTCTGCTTTTTGTAAAATGTCAGAGATGTTGTTTTTTTAGGAAATGATGTCGTAAATAATGTTTTTTAAAAAAGGATTGTGGTATAGCAGCTCCAACATCTCACACACTCTTTCTGTCTCGGTCCTGTAGAAACTGAGGCGAT[T/A]GTACGACACACTGCAGCGAGCTTATGCAAAGATATTGGAGGTGATGCAGTCGGGTCGACGGCTGCTCGGAACGTATTTTAGAGTCGCCTTTTTCGGACAGGTGAGTTGAAGCAATAAACAAACCACCTACAGTACAGTACAGTACAGTACTCAACCTATTGTATGTTAATGCTTGCATCATTTTGGCTTGCGCTCTGCTACCACTTCACAAAATCACTTCTCTCTGTGTGTAGACATTGTGCATTTCATAAACAGCTGATATTTTAATGCGTCTAGACATTGTTCATAAATCAATGGCTCAATTATGGGTTATCAGCACATTTTAACTAAAATGTACGCTTTTTCTTTTACGATTACCAATGTTGCATTTATGTGATCAAAAATATAGTGGAAAATGTGGAACATTAAAGTTTGAAATTGCTGTTTTTTTGCACTGTATTTGACAGCACATAATATTTTACTAGTTATATTGCAAGATAATAGTGTTCAGCCTAAAAGGC
Associated Phenotype:
Not determined