ZMP
si:dkey-283b15.3
Ensembl ID:
ZFIN ID:
Human Orthologues:
DST, MACF1
Human Descriptions:
dystonin [Source:HGNC Symbol;Acc:1090]
microtubule-actin crosslinking factor 1 [Source:HGNC Symbol;Acc:13664]
microtubule-actin crosslinking factor 1 [Source:HGNC Symbol;Acc:13664]
Mouse Orthologues:
Dst, Macf1
Mouse Descriptions:
dystonin Gene [Source:MGI Symbol;Acc:MGI:104627]
microtubule-actin crosslinking factor 1 Gene [Source:MGI Symbol;Acc:MGI:108559]
microtubule-actin crosslinking factor 1 Gene [Source:MGI Symbol;Acc:MGI:108559]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13927 | Nonsense | Available for shipment | Available now |
sa42652 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45562 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12044 | Nonsense | Available for shipment | Available now |
sa42653 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36031 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42654 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13927
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 |
---|---|---|---|---|---|
ENSDART00000129010 | Nonsense | 583 | 1440 | 11 | 29 |
ENSDART00000147973 | None | None | 241 | None | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 6821562)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 5666093 |
GRCz11 | 16 | 5565719 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAGCKTATGCATCCTGGAGCAGAAGTGGAGTGCCGTCTACGCTAAAATG[C/T]AGGAGCGAAAGGTGATGAGAGATTATTGTGCATGAATAAACGGCRATWAG
Long Flanking Sequence:
ATTCAGTAAGAGTCAAAGAAAAGTCAAGGAATTTAACGTTTGGCTAAAAGTGATTCAAATATAACTATACTATCCTATGATCTCACAGAGTTGCTGTAGAATTGCAGTGAAACTCTGCCTTTCTGGCTGTATTTCAGGTTCAGGACGTGAGCATGGAGATCCAGGATCTTCTGCAGTGGCTGGAGCACACAGACCTCAGGCTGTCCTCCAGTAAGGCGGTATGGGGGATGCCGGATTCTTCAAGCGAGAGACTAAATGCTCACCTGGTGAGGATCAAGGTTTCGGACTCTTGTGTTTGTGAAACGTGCTCCTGGACTGAAGTCTGTGTGTTTGTGCTGCAGGAGCTGTGTAATGAGATGGACTCGAAAATGCACGCCTACACAAACGTTCGCTCCGCCATCCACAGGATGCTGGAGGCCAGTGAAGTGGCCCGCGGCTCCAGCACTGAGCACAGCTTATGCATCCTGGAGCAGAAGTGGAGTGCCGTCTACGCTAAAATG[C/T]AGGAGCGAAAGGTGATGAGAGATTATTGTGCATGAATAAACGGCGATTAGTTGACTTTGCTTTTAAAATGTGAGTAAACCTGTTGCTTTTAAAGCGATTAGTTGACTTTACTAAAGTGAGTAAACCTGTTGCTTTTAAAGCGATTAGTTGACTTTACAGAAGTGAGTAAACCTGTTGCTTTTAAAGCGATTAGTTGACTTTACTGAAGTGAGTAAACCTGTTGCTTTTAAAGCGATTAGTTGACTTTACTAAAGTGAGTAAACCTGTTGCTTTTAAAGCGATTAGTTGACTTTACAGAAGTGAGTAAACCTGTTGCTTTTAAAGCGATTAGTTGACTTTACAGAAGTGAGTAAACCTGTTGCTTTTAAAGCGATTAGTTGACTTTACAGAAGTGAGTAAACCTGTTGCTTTTAAAGCGATTAGTTGACTTTACTAAAGCGAGTAAACCTGTTGCTTTTAAAGCGATTAGTTGACTTTACAGAAGTGAGTAAACCTGTTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42652
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 |
---|---|---|---|---|---|
ENSDART00000129010 | Nonsense | 589 | 1440 | 12 | 29 |
ENSDART00000147973 | None | None | 241 | None | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 6823415)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 5667946 |
GRCz11 | 16 | 5567572 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATACGTTTTTAAAATTATTTATGGATTTATTGATTGTTTTAGGCAAAGT[T/G]AACTGAGGGTCTTGGCCTTGCGAAGGAGTTCAACAGTAACGTCCAGGACC
Long Flanking Sequence:
GGTACACTTTCAAATTTGAGTTTATAAAACAAAAATACAAGAAGCGCCTCTTTTTTTAGGTGTTTATTATAACACAGACAACATATACCGTTATTTTAAATACTTTCAATAGTGTTTTATGAAAATTCAAAGGGTTTTCTTTAAAATGATACCAAACTTTTGCATTTACACGTCAGCATGTGGATTTGGTAAGCTTTTAAATTTGGGTAGGCAAAATCCAGGCGGAAATCCCAAAATAGCAGCAGAGTTTAACTGGTTAAGTGATTAGTTGACTTTACTTAAGAATGTGAATATATTAGTATTAACTTAAAAACATTTTTACTTTTTCAGATTTTCTACACTAGTTTTTTGTTTGTTAGTTTTATTTTATTTTAGTTTAATTTGATATTTATTGGCCAATATTTGATTGTTTTAAAGCTGTCAGCATATCAGCAATAACTGATACCATTAAATACGTTTTTAAAATTATTTATGGATTTATTGATTGTTTTAGGCAAAGT[T/G]AACTGAGGGTCTTGGCCTTGCGAAGGAGTTCAACAGTAACGTCCAGGACCTGCTGACTAAAATGGGCAAGTGTGAGGAAACAATAAACACACTGAGCGCTCCCAGCTTCATCCTGGACACCATCTGTTCACAGCTGCAGGAGCACAGGGTAGGGTGTGTGTGTGTGTGTGTGTGTGTGTGTAAATGCAGTACTGATCCCCTTATACATGGAATATGCAAGGTGTGTAGAGTACCGCAGGTTACAGAAGGCCCCTCCACGTGTATGTGTGTATGTATGTATGTGTGTGTGTGTGTGTGTGTTTGTGTGTGTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGAGAGAATTTGCGACTGTGTGTACATGATTGTGTGCGTGTCAGTGTGTGCGTGGTATTGTTTGTCTAAGAGTGTGTGTGTATTTGTGTATGTGAGTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45562
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 |
---|---|---|---|---|---|
ENSDART00000129010 | Nonsense | 674 | 1440 | 13 | 29 |
ENSDART00000147973 | None | None | 241 | None | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 6824576)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 5669107 |
GRCz11 | 16 | 5568733 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCCACACGTCTGTCTGAGCTCAGCAGGAAAGAGGACTGTGATGTCATA[C/T]AGAACCTGATCATGACCATTCAGGACCGATTCAAAAAACTCCTGCAGCAC
Long Flanking Sequence:
TGCGACTATGTGTACATGATTGTGTGCGTGTCAGTGTGTGCGTGATATTGTTTGTCTATTTGTGTGTGTGTGTATTTGTGTATGTGAGTGCATATGTGTGTATGTTTGTGCACAACTGTGTGTGTTTGTGTCTGTTTATGTGTGTGCATGTGCTGCAGGTATTGTGTGTGATTGTATGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTCTGTGTGTGTGTGTGTGTCTGTATGTGTGTGTTTATGCATATATGTGTATGTGTGGGTGACTGTGTGTTTGTTTATATGCATCTGGGAGTCTGTGTGGGTGTGTGTATGCGTCTGCGACCGTGTGTGTATGTGTGTGTGAGTGATTATCTGGTGTTGTTTGCAGGTGCTGGTCAGTGAGGTTCAGTCTTACGGAGACAGGAAGTCGAGTGTGGAAGCTGCAGCCACACGTCTGTCTGAGCTCAGCAGGAAAGAGGACTGTGATGTCATA[C/T]AGAACCTGATCATGACCATTCAGGACCGATTCAAAAAACTCCTGCAGCACACCACAGAGAGAGGGAAAACTCTGGAGGACGCAAAGAGACTCGCTAAACAGGTACTCGCTTCTCTTCTCATCTGCACAGAAAGCCCTCTGTCCTCAGTCTCCTGGAAAATAAATCAGCTGTTCTGCTTTTGACTTTTGCACAGTTCAGTGAATCGTGGCACTTACTGGTGGACTGGATGACGGAGGTGGAACAGACACTGGACACACATAAAGAGATCGCTGTTTCACAGGAGGAGATCAAACAGCAGCTCACTGAACAGAAGGTTCTACATCCCTAATTCAACTCAATATCTAAACCCAAATATATATATATTTTAAAATGTTATAAATGTTCCTTTTTTAGCATGTGGTGCACAGAAGATTATGTAAAAACTTTAATAATAATAATTAAACCACAAAATATATGTGGTGTTTTAACAAAAAAATAGTAATAGCAATTATTTTTTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12044
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 |
---|---|---|---|---|---|
ENSDART00000129010 | Nonsense | 894 | 1440 | 17 | 29 |
ENSDART00000147973 | None | None | 241 | None | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 6827930)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 5672461 |
GRCz11 | 16 | 5572087 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCGGGATCTGACGCGCAGCAGCACCGCCGATGCTCACTGGCTGCAGGAG[C/T]ARATGGAGGAGCTGGAGAGYCGCTGGGAGGCTGTGTGTAAACTCTCTGTG
Long Flanking Sequence:
GCACCACAAAAGACACTGAGGGGATCTAGACCCCCAATAATCAGTTAATGTAAAATTAGCCATGTATGCTTGGAATACTTTAACAAATACATGTAGACGTGCTTAATCTAATGCACTTTAATGCATAGTGTCATATCACTCAGCTCTTACTGTGATTCCTCTAGGGTCAGAAGATGTCACAACAAAACTCAGGAGCGAAATTGGGTTACTCTGGTTGCTTATATTAGATATTTCACTCATTTCTTCTAGCTAGATAGATAGATAAATGGATGGATGAATGGATGGATGGATGGATGGATGGATGGACGGATGAACGGATGGACCCTCTCCAGCGTTCATGGTAAGGTTATAGGGTATGCTGTAGTCCTGATCTTTTGGCTCTGGGTCTACAGGTGTTCCAGCGGGAGCTTGGGAAGCGGGCCAGTTGTATCCGCACACTGAAGCGCTCGGTGCGGGATCTGACGCGCAGCAGCACCGCCGATGCTCACTGGCTGCAGGAG[C/T]AGATGGAGGAGCTGGAGAGCCGCTGGGAGGCTGTGTGTAAACTCTCTGTGTCTAGACAGGCCCGACTCGAGGCCGCACTGCAGCAGGTACAGCACCAAACATTTTATTTTTACATTTGTGCATTTGGATGATACATTTATCCAGAGCACTGACATCACATTCAAAATACATTAGTGTTGTTTTCATGGATTAAAACTAAGAGAAATTTGGTAACACTCTATTTTGATGGTCCATTTGAGTCTTAGTCAACTGTCTGCTTAATATCTGCTGATCTGCTCCTTCAACAGACATTTAACTGACTATAAGAAATTTGCTAGTACATTTCAACTTAAACTAACCTTAACTCCAAACTAACAGTCTGCTTATAATCAAATGACAATTAGTTGTCATGTAGATGTAATGTCACTTAAATTCAACAAACGGACCATCAAAATAAAGTGTGACCAGAAATTTGTATTAATTATTTCATTAAGTAAATGGGGTAACACAATAATACAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42653
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 |
---|---|---|---|---|---|
ENSDART00000129010 | Nonsense | 1102 | 1440 | 21 | 29 |
ENSDART00000147973 | None | None | 241 | None | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 6833679)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 5678210 |
GRCz11 | 16 | 5577836 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACCGGAGGTTGAAAATGCCACTAAATCCTGTAAACACAAGCTGGTCCCC[A/T]AACAGCAGGTTTCACCCAGTCGCAGACCAGCAGCGAGTGAGTCCAGAATC
Long Flanking Sequence:
GAAACAGTGCCCTCTAGTAGATTTTTTCATCTGAAATGTGCAACAAATTGTATAAAGAAACTATGACAATGAATGAAAACTACATAAATGTATGTTAAAAATAAACTAAATGTGATTAAAATGACAAACACAAACAAAAATTTGTAAACCTTTTACAAAATTTAAACAAAAAACAATTCAATTCCAGCTTATTTGTATAGCGCCTTTCACAATAATTCTTGTTTCAAAGCAGCTTCACATCGTTGCATTACAATCAAATTCTGAAAAGTTAAGGTTATTGGTCATTATAACTTTATTAGTTACTCATAACTTCAACTAATGAACTAGTAACTAATAGCTTTTTAAATGAAACGTAACGGTGATGCCATGCAATAATTTAAGAAGGTTTGAGGTCAGGAAATGCTTCTGTTGGTTTTTTGCAGGATTTTATGGATGAGATGAAAGGCAAGGTACCGGAGGTTGAAAATGCCACTAAATCCTGTAAACACAAGCTGGTCCCC[A/T]AACAGCAGGTTTCACCCAGTCGCAGACCAGCAGCGAGTGAGTCCAGAATCACTGAGATCTGCTGATGTGTTGGCTTGAATTTAACTCTGGATTATATTGCATGTATAGAGAGAAGAGGAGCTGCAAAGCCTCCACCATCTGTCCCTGTTCCTCTGGAGAAACTGGACCCTCAGACCCCCATCATGTGTCGCCTGGTGAAAGACTGGAGGAAACTCTGGCTTCAGGCTCACGGCAGACAGAGCAGACTGGAGGAACATCTGCAGCGGCTCAGAGAGGTGAGAATCCCAACCTGAACCCATACTAGACATCAAAAACTAAACTGGCCGCTGTCGCCGCTGTCAGAGCTTTGAAAAAATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTCTATCTGTCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36031
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 |
---|---|---|---|---|---|
ENSDART00000129010 | Nonsense | 1207 | 1440 | 23 | 29 |
ENSDART00000147973 | Nonsense | 39 | 241 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 6835701)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 5680232 |
GRCz11 | 16 | 5579858 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCACCTCAAATCCCGAATTCTGGATGTTTTCCGAAGCATTGATCGAGAT[C/T]AGGATGGCAGAATCACTCATAAGGAGTTTATTGACAGTGTTCTGGCCTCA
Long Flanking Sequence:
TCAGCAACCAACAGAAAGAAAAATCACAAATGATAACGTAAATATAACTGAAATAAGACATAAAAACAATTAAAAATAGTATTCCAATATACAGAAATGGAGTCAAGTAATCAAGTCTCATTTTTTACAAGTTGCTAGTCATTCAATGATGATCAGTGAAACTCTAAAGTGTAAATTAAAAATATACATACTCTATACATAAAAATTAAAATGATTTGGTAAGAAAATACCAGTTAGACCAGAAGTCTTGGTTCATTTAAGTTACAATGACTGCTTTATGTTTATAATAAGCTCAATTGGGAGGATCGGTTCAGATTATCACTGCACAGTACAATCGATGAAACATGATCTGTATGTTTGTCTAAGACGCTTCTCTTTGGCACCTGCAGTTGGAGGAGTTTGCTAACTTCGACTTCAACATCTGGAGGAAAAGATACATGCAGTGGATCAGTCACCTCAAATCCCGAATTCTGGATGTTTTCCGAAGCATTGATCGAGAT[C/T]AGGATGGCAGAATCACTCATAAGGAGTTTATTGACAGTGTTCTGGCCTCAAGTGAGCTTTTTGAAGTATTCCCATATAGAAACCTGATAAATTGATATATACTAAAATTACATATACAGTATTTCCATGTAAAATATTTCAATATATGCATTGAGACGTTTGTTTTTATATGTGTTACTATTGGTAATATAAACTTTTGCTTGTTGACAGAATTTCCCACCAATGTGCTGGAAATGACTGCGGTTGCCAACATATTTGATGTTAACGGAGACGGATTCATTGACTATTATGAGTTTGTGAGTGCGCTTCACCCCAGCAGAGACCCTTACAGGAGGACAGTAGATATAGACCAGATCAACGAGGAGGTGCGTGCACTTCTACTTTCAGAAACACTCTCGAAATCATCATTATCTTATGCTCAATTATAAATATAAAAAAAAAAAAAACATGAATTAAAGAGGAAATATTATGCAAAAATCACTTTCAAAAGGAGTTTAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42654
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 |
---|---|---|---|---|---|
ENSDART00000129010 | Nonsense | 1250 | 1440 | 24 | 29 |
ENSDART00000147973 | Nonsense | 82 | 241 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 6835991)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 5680522 |
GRCz11 | 16 | 5580148 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGGTTGCCAACATATTTGATGTTAACGGAGACGGATTCATTGACTATTA[T/G]GAGTTTGTGAGTGCGCTTCACCCCAGCAGAGACCCTTACAGGAGGACAGT
Long Flanking Sequence:
GCTCAATTGGGAGGATCGGTTCAGATTATCACTGCACAGTACAATCGATGAAACATGATCTGTATGTTTGTCTAAGACGCTTCTCTTTGGCACCTGCAGTTGGAGGAGTTTGCTAACTTCGACTTCAACATCTGGAGGAAAAGATACATGCAGTGGATCAGTCACCTCAAATCCCGAATTCTGGATGTTTTCCGAAGCATTGATCGAGATCAGGATGGCAGAATCACTCATAAGGAGTTTATTGACAGTGTTCTGGCCTCAAGTGAGCTTTTTGAAGTATTCCCATATAGAAACCTGATAAATTGATATATACTAAAATTACATATACAGTATTTCCATGTAAAATATTTCAATATATGCATTGAGACGTTTGTTTTTATATGTGTTACTATTGGTAATATAAACTTTTGCTTGTTGACAGAATTTCCCACCAATGTGCTGGAAATGACTGCGGTTGCCAACATATTTGATGTTAACGGAGACGGATTCATTGACTATTA[T/G]GAGTTTGTGAGTGCGCTTCACCCCAGCAGAGACCCTTACAGGAGGACAGTAGATATAGACCAGATCAACGAGGAGGTGCGTGCACTTCTACTTTCAGAAACACTCTCGAAATCATCATTATCTTATGCTCAATTATAAATATAAAAAAAAAAAAAACATGAATTAAAGAGGAAATATTATGCAAAAATCACTTTCAAAAGGAGTTTAAAAAGTTGTGTGACTCAATTAATCAAGCTGAAAATTCATCTTTAAAATCACTGGAATAAATTATTAAATTAAATTATAAACTACTTTTGAACAGTTCTTTTATAGTGCAATAACATCTCACAATTTTACAATGTGTTCTGTAATTTAAATGAAATAAATGCAGCCTTGGTGAGCAGGAGAAACTTATTTTAAAATAAAATTATAATGTTTTTTATTATATATATATATATATATATATATATATATATATATATATATATATATATATAATATAAATTATATATATAATTTTT
Associated Phenotype:
Not determined