ZMP
dock7
Ensembl ID:
ZFIN ID:
Description:
Dock7 protein [Source:UniProtKB/TrEMBL;Acc:Q4QRD5]
Human Orthologue:
DOCK7
Human Description:
dedicator of cytokinesis 7 [Source:HGNC Symbol;Acc:19190]
Mouse Orthologue:
Dock7
Mouse Description:
dedicator of cytokinesis 7 Gene [Source:MGI Symbol;Acc:MGI:1914549]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40719 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40720 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20727 | Nonsense | Available for shipment | Available now |
sa16309 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa40719
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 |
---|---|---|---|---|---|
ENSDART00000042134 | Nonsense | 177 | 2129 | 6 | 49 |
ENSDART00000065149 | None | None | 319 | None | 8 |
ENSDART00000124551 | Nonsense | 177 | 295 | 6 | 9 |
The following transcripts of ENSDARG00000078675 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 32028694)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 32349610 |
GRCz11 | 6 | 32336524 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCCCTGAATAAAATCAGTGATTGCTGTATGTTACAGGATGATTTGAAA[C/T]GAAGGTCCATGTCAATTGATGACACGCCACGGGGCAGCTGGGCCTGCAGT
Long Flanking Sequence:
TATTGCTCTGAATTAAATAATATTAATATTAAACTAAAACAGCCTTTTTAAAACCAGATATTCATTCGTTTGTTAATGCAAGGTTTGAAAGATTTTGTTTAGGCTTTGAAACGTGCCTGAATATTTTTTGTTGCAAATGCTTGTGTGGATATTTGAACAAAAACATTTGATCAGTTTATTTATCAGGTTGCATGCTAATTATCAAACCAATAAAAATGGGTGTATTCTGGATGCACAGGTACCACAAGTTGGGCACAGCATTTAACCCTAACACTTTGGATAAGCAGAAGGAGAGGCAGAGAGGTTTGCCAAAGCAGGTCTTTGAGTCTGATGAGTTGCCAGATCAAAGCAGTTATCAGGACGATCAGGTAAACATTCCTTTACTACTATTATGCTTTTGTTGTTGTTGTTGTTGCTAAGCTCAGTAGAATAATTGCACTGTGTTCTTATGCTCCCTGAATAAAATCAGTGATTGCTGTATGTTACAGGATGATTTGAAA[C/T]GAAGGTCCATGTCAATTGATGACACGCCACGGGGCAGCTGGGCCTGCAGTATATTCGACTTAAAGAACTCTCAGCCTGATGCTCTGCTGCCTCACCTTCTGGATCGAGTTCCAAATGAGGAGATCGACCGCCACAATGAAGACCTGCGCAAGTCAAACCGCCACCGTGAGCTCTTCGCTCTGCATCCTGCTCTTGATGAGGTTGAGTATTAATTTATTTTTTGTTTTATTAGCTCTCACTAATCTAAAAACACGAAAAGATAAATCAGTTAAGTTTATACAATGATCGTTATTAATTTTTTTCCCCATTAATGTAGGAAGAACCCATCGAGCGCCACTGTGTGCCTGATGTTCCAAAAGAACATTTTGGTCAAAGGCTTCTAGTCAAGTGTTTGTCTTTGAAGTAAGTGAGAAACTGCTTTTGTAGACTGATTTGTAATTCTTATCACCACAGTTTTGCTGACATTTTTCTCATTCAAGGTTTGAAATAGAAATTGAGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40720
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042134 | Nonsense | 549 | 2129 | 14 | 49 |
ENSDART00000065149 | Nonsense | 155 | 319 | 4 | 8 |
ENSDART00000124551 | None | None | 295 | None | 9 |
The following transcripts of ENSDARG00000078675 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 32032257)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 32353173 |
GRCz11 | 6 | 32340087 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCCGACAGTCGAGTGCGGCCAACAAAAGAGATCCTGGAGTTCCCTGCC[A/T]GAGACGTTTATGTGCCCAACACCACTTACAGGTACAAAGACCCTTTCAGT
Long Flanking Sequence:
TGACGGTCACCAACTTCTTTAAACAGGTCACACTGTTATTCTAAAAAACATCCCAGTATTGATTTTATTCATAGGAAGTTTACAGTCCTTCAGTTTGCAGTCATTACATTGCTAAAGCAATTAAAATAATGCTTTTGAGTTTTTAATAATTAAAGATGTTTTGTTTTTCCGTCATTTATTAGGAAGGAGATCGACTAAGTGATGAAGATCTCTACAAGTTCCTAGCCGACATGCGGCGTCCGTCCTCTGTACTGCGTAGACTGAGGCCCATTACAGGTATAGTTACTATGACGTCTTTAATCAATGGATTTTGACTCTATTGACCCTTTATGTGAAGGCTTGCATAACTTGTTTACTCTATGCCTGTAGCTCAGCTGAAGATCGACATCTCTCCAGCCCCCGAGAACCCGCACTATTGCCTGACTCCTGACCTGCTTCAAGTCAAGCCTTACCCCGACAGTCGAGTGCGGCCAACAAAAGAGATCCTGGAGTTCCCTGCC[A/T]GAGACGTTTATGTGCCCAACACCACTTACAGGTACAAAGACCCTTTCAGTGTATAGATCAGACTCCCAACTCTTTCACGTCATCCACAATCCTATTTAAAGTCCTCCGGTAGCCCTGCTGTATTTTCAAATGGTAAAGTAACTCAAAAACAAAAAAAAACACAATTTGGAATTTTGGAATGTTCAAATTACATACTTTTTATGCAATTATTTTTATTAACTGCACAATATCGTAAAAATCCAACATTGCATTATTTTTTTATTTTGTGATGTATATTGCGATATAAATACAATTTTACCAGGTGACTAGGGCCAGACAGAATCTGCGGACATTTTTTTTTGCATTTTTTTGCATTTCTGCGCAGAATATTGTAAAAAATCTGCAGATTTATGTGGAATGATTTTGGGTGTATCATAACTAAAAACTTATTATGATACATTTATTAATGATACATTAGAAACTTTTATTTAATGTTTAATAAATAATAGTCTACCAATGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20727
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 |
---|---|---|---|---|---|
ENSDART00000042134 | Nonsense | 1059 | 2129 | 26 | 49 |
ENSDART00000065149 | None | None | 319 | None | 8 |
ENSDART00000124551 | None | None | 295 | None | 9 |
The following transcripts of ENSDARG00000078675 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 32061180)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 32382096 |
GRCz11 | 6 | 32369010 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATCACTGCACTGGTTAGCACTATTGCTGGTGACATCGTCTCACGTTTT[C/T]AGAAGGTGAGAACATTGCAACTGCATGAATTCCTTGAGCTGTTTTTGTTA
Long Flanking Sequence:
TATTTCAAAATGTTAAAGTTTTAATTGTATTGTCAATCAAAATAAATGCAACCTTGATGAGCGGAATAGCCATCTTTTTAAAGCATTAGTCTTGCTGATCCCAAACCTTTGACCGGTAGTGTACTAAACTATGTGCAAAGTATTTGACGCTGTCTGTGTGTCTGATGTTTTCTTCCTATCCTCAGCTCTTTCATGAGGAGCTCGCCCTGCAGTGGGTTGTCAGCAGTGGCAGTGTGAGGGAGGGAGCCCTGCAACAGGCCTGGTTCTTCTTTGAGCTAATGGTAAGATGTTTCTTCTATGAACGATTAAACAATTTGAATCATTTGTTTTGAGATTGTTTATATAACAAGATGTTTGCATTTTAGGTTAAGAGCATCATCCACCACTTATACTTTACTGACCGTTTGGAGTCTCCCAGGAAAAACCGTTTCCCTGAACGCTTCATGGATGACATCACTGCACTGGTTAGCACTATTGCTGGTGACATCGTCTCACGTTTT[C/T]AGAAGGTGAGAACATTGCAACTGCATGAATTCCTTGAGCTGTTTTTGTTAACTGATTTTAAAATGCTTTTTAAATTTAGTTTATACTTCTGCGTCAAGTGATCGGTGTGACCCATGGCGCATGCACGGAGCATACGTGTGCGCTTGATGAAATATAAATTAGCCTTAACGTAATAATATCATTTCCCAGAGATGGGTTGCGGCTGGGAGGGCATCTGCTGCGTATAAACTTGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGTGACCCCGGATTAATAAAGGGACTGAGTCGAAAATAAAATAAATGAATAATAATATCATTGTTGCTTTAGAAATGTCACATGTACAACAGTATTGTGTTTTTGTTTTATGTCAAAAATCAAAAATTATTTAGCCACTTTGGAAAATCTTTACCATATCTGCTCATCTCTGGTAGCATCTTTCAAGTAGCATCTTAAAACATTAGCATAGGTTATGTTTAATAGGATTGTATAGGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16309
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 |
---|---|---|---|---|---|
ENSDART00000042134 | Nonsense | 1811 | 2129 | 42 | 49 |
ENSDART00000065149 | None | None | 319 | None | 8 |
ENSDART00000124551 | None | None | 295 | None | 9 |
The following transcripts of ENSDARG00000078675 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 32081299)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 32402215 |
GRCz11 | 6 | 32389129 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTATTCACGAGGCCAACAGGGATGCTAAGAAGCTTGCCACTATTCATGGT[A/T]AACTTCAGGAAGCCTTTGGCAAAATCGTRCACCAGGTAAATGCTTATGYT
Long Flanking Sequence:
CTTTTTTCTTTCATTTATAATTATAATTATTTATTTATTTATTTTACATTTAAATCAAGATAAGACATAAAATAATCTCATACTTATGCAAATCGCTTCAGAATTGAATAAATATTTCTAACCTGGCTCAGAGGAAGATTGTTAAATGTTCATACAAAACATTGTAAAACCTATAACGCTGTCATATTTCATTTATCATGTTTTGTAAGTGTGACATGCTATTGCAAAACAGGCACCATTTAGGAAACTAGCCTTCCACAGTTATTCAAATATTTACAGTACATCTTAAAATACTTTTGTAATACATTTTGAGTGAAATAAAACATCTGGTCTGCCATCAAATAACTGTATTACATCAGATATTTTGTAGGGCATCAGCCACTCTTATCATCATTTCTCTCCAGGCTGGCATGTACGAAGCGGTCAATGAAGTCTACAAAGTGCTCATCCCTATTCACGAGGCCAACAGGGATGCTAAGAAGCTTGCCACTATTCATGGT[A/T]AACTTCAGGAAGCCTTTGGCAAAATCGTGCACCAGGTAAATGCTTATGTTCAACAAAATCATGCTTAAAATAGATGCTCGGTTTAGCTGAGTGTAAGACAACAAGCGTAAGCAGTGTAAGACAACTGGACTTTGTATGATTGCCCTAGTACTGTAGTACAAAGCAACAATCAGCCAGTTGTCTACATTGGCAACATTTTTGTTGTGTATACAAACAGACGTGAGTTCTGTGTGACACGTGAAAGAGACTTTGAGTTTACATGACTGCGTGACTCTGTTTATCTCTTCATCTGTGAGAGTTCATGGGCAATATCAGTGGAATTCACACCAAGAATGATAACTCTTATTAGCAGCTTTGAGATTTAAAACCACAAGCTGATTTAGCTTGGAATAATTCTAATTTGCTGTCAAAATTTTTTATTGTTCATAAGCGGAGAAAAAAAAAACACTCTAAATATGATTTCAACTATTTTTTGTGATTATTTTTGTGGCTGTTCTGAA
Associated Phenotype:
Not determined