ZMP
si:ch211-167h3.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
DYM
Human Description:
dymeclin [Source:HGNC Symbol;Acc:21317]
Mouse Orthologue:
Dym
Mouse Description:
dymeclin Gene [Source:MGI Symbol;Acc:MGI:1918480]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23843 | Nonsense | Available for shipment | Available now |
sa45724 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10263 | Nonsense | Available for shipment | Available now |
sa11233 | Essential Splice Site | Available for shipment | Available now |
sa11707 | Essential Splice Site | Available for shipment | Available now |
sa23842 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23843
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 |
---|---|---|---|---|---|
ENSDART00000062418 | Nonsense | 96 | 623 | 3 | 15 |
ENSDART00000139194 | Nonsense | 96 | 525 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 3851809)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 3449065 |
GRCz11 | 21 | 3600486 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGAGTTTTTCTCAGCAGAACCAAAGAGCTGAAGATTTCCACAGAATGC[C/T]AAGAGTAAGTCAGAAACCTCTACATTGAGGTGTGCTTATTTCTATGGCTT
Long Flanking Sequence:
CTGTCTCTGTGTGTGTGTGTGTTTGCAGTGCTGATGCTAAACTCCTGGAGGAGGCTGTCGTCCCGCTGGCCAAGACTCTGAGTATGTGTGTGTTTCTATGAGTGATTTACTGCCGTTTCATTATAGTCCAGACACGCACTGATTTCAGAGCCTCTATCTTGTGAAATAAAGCTCTGTAATTGCAGGCGCATGAAGCCACAGCATTCAGACTGATACCGATCACATGTCAGCTTTGCTTTTATCACGGACTGTGTATAATTTATAGAGTTTATTGATCCATTTTTTTTTAACAACTAAATCACAGGGATCTTAAATGTGTTGAGTTGATCTGGTTTAGTAGCACGTACAGTTACATGAACAGCCTTAAGTTGGTATGGGAATGATGTTTTGTGTTTTTGATCATCTTCATAGTTGAGAATAACCCCAGGTCCGGGAACTTCGGGGCGTTGGTGAGAGTTTTTCTCAGCAGAACCAAAGAGCTGAAGATTTCCACAGAATGC[C/T]AAGAGTAAGTCAGAAACCTCTACATTGAGGTGTGCTTATTTCTATGGCTTTTAATGTGTTTTTTGTGTCATCTGTTATTGAACTATGAACACTGTAAAAATATTTGTTAGTGAACAGATTCTGTATTTAAAATTATTTTTACTGTTTTTTCTGTATTGTCAATAACATTATATATATATACTCGCCTGTCACTTTATTAGGTACACCTTACTAGTACTGGGTTCGACCCACTTTTGCCTTCAGAACTGCTTTAATCCTTCGTTTCATAGATTCAACAAGGTGCTGGAAATATTCCTCTAGAGATTTTGCTCCATATTGACATGATATGGCATTGATTTGTCGACTGCACATCTATGATGTGAATCTCCCGTTCCACTACATCCCAAAGGTGCTCTATTGAATTGAGATCTGGTGACTGTGGAGGCCATTTGAGTACAATGAACTCATTGTCATGTTCAGGTAAACCAGTCTGAGATGATTAACGCTTTATGACACAGCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45724
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062418 | Nonsense | 126 | 623 | 4 | 15 |
ENSDART00000139194 | Nonsense | 126 | 525 | 5 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 3848752)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 3446008 |
GRCz11 | 21 | 3597429 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTGGTGCGCTGTTTGCTGAAGGTCTTCATCAGGGAGATGAGTGAAGAA[G/T]AGCTGCATCTACAGTTCTCCTACCAGGAGAGGGCGCCGGGAACATATGGT
Long Flanking Sequence:
CTTTGAGGGTCGGGCTTAAGGGGAAGGCCATATAATAATAATAATAATTTTTACATAAAATAATATTGTAAATATTGTAAAAAAGCTGAAATCGCAAAATACAGTTTTATACTGGGCGACCCAGTGGTTAGCACTGTCACCTCAGAGTAAGAAGGTCACTGGTTCAAGTCCCGGCTGGGTCAGTTGGCATTTCTGTGTGAAGTTTGCATGTTCTCCCCGTGTTAGCATGGGTTTCCTCCGGGTGCTCCAACACAATCCAAACACATGCACTATAGGTGAATTAAATGAACTAAATTGGCTGTAGTGCATGAGAGTGTATGGGGGTTTCCCAGTACTGGTTTGCCGCTGACAGGGTGAAGCTGCAGTTCACAGTCAGTAATCATCTTTCTCCCTCTCTTTCTGTTTCTCTCTGTAGTCAGTTGTTCATCTGGCAGGCCCATAATGCTCTGTTCCTGGTGCGCTGTTTGCTGAAGGTCTTCATCAGGGAGATGAGTGAAGAA[G/T]AGCTGCATCTACAGTTCTCCTACCAGGAGAGGGCGCCGGGAACATATGGTATGACACACTCATTCAACGCTTACACTGGATTCATGTCCACTTTTTGAGCTCGGTTATGTGGCCCTCATATATAGAGCAAGATTTTTGGTAACACTTTAGTTTAAGCAGCAATTCTCTCTATTAATTATTGGCTTATTATAAGGATATTGGCTGTTTATTAGTACCTCTAAAGCACATATTCTGCATGATTTTATTCTACATTCCTAATTATACCCAATACTTTAACCCAACCTTAATAACTATTAACAAGCAGCAAGTTAGGAGTTGATTGAGCTAAAAGTCATAGATAATGGTTCGTTAATACACAGAATTGTACTTTAAAATAAAATAAAGCGTGACCAGATTTATACCTTGTTAGCAAATTGTAAACAGAACAGATTTAATTGTTGTTTTTTATAATAGAAAATAAGATAATCAACATATTTTAGATGATAAACATATCATCTCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10263
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062418 | Nonsense | 424 | 623 | 11 | 15 |
ENSDART00000139194 | Nonsense | 426 | 525 | 12 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 3784826)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 3382082 |
GRCz11 | 21 | 3533503 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATTGATTCCTATGTATTATTAATTCTCTCTCAGCTGTTGAARAACATCT[C/A]GTGGTACACCGAACGTGTCCTAACAGAGATCTCCCTAGGAAGTCTGCTAA
Long Flanking Sequence:
TAGTATATACTCTCATTCAGTTATTAGAACAGTAGCATTACACTGAGATCAAATTTGAGAAGCGGTGAACCGATAATGCTGCACATGCGTGATTCAGTGAACCAAACCCAAACGTGTTTGACATGATCTCAACTAAAACATGAAGAGAGGGCGGGACATAACGTAGCTCCTCCCCTTTTTGAAAATAACATTCATTCATGCAAACTCCTTACAGAAACGCCAACTGAGCCAAGGCTCGAACCAGCGACACACCGACCTTCTTGCTGTGAGGTGATAGCACAACCTACTGCGCCACTGCTTCCCCGAAAATAACATTGCCAATAACATTTTGTTTTATTACTATTTATTAATATGTTTTTATTATTCTTTTGTTTAGCTTTGCCAGTGAGAGTGGTTGAGCTCAAGCACATCAAATCTGTTGTTTTAAAGCTGTGTGATGATAAGCTAATGTATTGATTCCTATGTATTATTAATTCTCTCTCAGCTGTTGAAGAACATCT[C/A]GTGGTACACCGAACGTGTCCTAACAGAGATCTCCCTAGGAAGTCTGCTAATCCTGGTCGTCATCCGAACCATCCAATTCAACATGACCCGCACAAGGGTGAGTCCAGAACCACAGAGACAAATACAGTTTGAAACATCCACAACTTTGGCCATGTACATTTATTACTCTACATCTTATATACAGTTGAAGTCAGAATTATTTGCCCTCCTGTGAACTTGTTTTCTTTTTCAAATATTTCCCAAATGATGTTTAACAGAGCAAGGAAATTTTCACAGTATTTCCTGTAATATTTTTTCTTCTGGAGAAAGGCTTATTCGTTTTGTTTCGGCTAGAATAAAAGCATTTATTTCAAACCATTTTAAGGTCAATATTATTAGCCCCCTTAAGCAATATTTTGTTTTCAGTTGTCTACAGAACAAACCACTGTTATACAATAACTTGCCTAATTACCTTAATTAACCTAGTTAAGCCTTTAAATGTGACTTTAAGCTAAATATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11233
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 |
---|---|---|---|---|---|
ENSDART00000062418 | Essential Splice Site | 456 | 623 | 11 | 15 |
ENSDART00000139194 | Essential Splice Site | 458 | 525 | 12 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 3784728)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 3381984 |
GRCz11 | 21 | 3533405 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAATCCTGGTCGTCATCCGAACCATCCAATTYAACATGACCCGCACAAGG[G/A]YGAGTCCAGAACCACAGWGAYAAATACAGTTTGAAACATCCACAACTTTG
Long Flanking Sequence:
GAACCAAACCCAAACGTGTTTGACATGATCTCAACTAAAACATGAAGAGAGGGCGGGACATAACGTAGCTCCTCCCCTTTTTGAAAATAACATTCATTCATGCAAACTCCTTACAGAAACGCCAACTGAGCCAAGGCTCGAACCAGCGACACACCGACCTTCTTGCTGTGAGGTGATAGCACAACCTACTGCGCCACTGCTTCCCCGAAAATAACATTGCCAATAACATTTTGTTTTATTACTATTTATTAATATGTTTTTATTATTCTTTTGTTTAGCTTTGCCAGTGAGAGTGGTTGAGCTCAAGCACATCAAATCTGTTGTTTTAAAGCTGTGTGATGATAAGCTAATGTATTGATTCCTATGTATTATTAATTCTCTCTCAGCTGTTGAAGAACATCTCGTGGTACACCGAACGTGTCCTAACAGAGATCTCCCTAGGAAGTCTGCTAATCCTGGTCGTCATCCGAACCATCCAATTCAACATGACCCGCACAAGG[G/A]TGAGTCCAGAACCACAGAGACAAATACAGTTTGAAACATCCACAACTTTGGCCATGTACATTTATTACTCTACATCTTATATACAGTTGAAGTCAGAATTATTTGCCCTCCTGTGAACTTGTTTTCTTTTTCAAATATTTCCCAAATGATGTTTAACAGAGCAAGGAAATTTTCACAGTATTTCCTGTAATATTTTTTCTTCTGGAGAAAGGCTTATTCGTTTTGTTTCGGCTAGAATAAAAGCATTTATTTCAAACCATTTTAAGGTCAATATTATTAGCCCCCTTAAGCAATATTTTGTTTTCAGTTGTCTACAGAACAAACCACTGTTATACAATAACTTGCCTAATTACCTTAATTAACCTAGTTAAGCCTTTAAATGTGACTTTAAGCTAAATATTATGCAACAATACAGTTAGCTCAAGGTTCAATACATACCTCGGTTTTTTAACTCTGATTTCGGTTCGGTTCTTATGGCTTGACACGTGTTTTTTGTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11707
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 |
---|---|---|---|---|---|
ENSDART00000062418 | Essential Splice Site | 456 | 623 | 11 | 15 |
ENSDART00000139194 | Essential Splice Site | 458 | 525 | 12 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 3784727)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 3381983 |
GRCz11 | 21 | 3533404 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATCCTGGTCGTCATCCGAACCATCCAATTYAACATGACCCGCACAAGGR[T/C]GAGTCCAGAACCACAGWGAYAAATACAGTTTGAAACATCCACAACTTTGG
Long Flanking Sequence:
AACCAAACCCAAACGTGTTTGACATGATCTCAACTAAAACATGAAGAGAGGGCGGGACATAACGTAGCTCCTCCCCTTTTTGAAAATAACATTCATTCATGCAAACTCCTTACAGAAACGCCAACTGAGCCAAGGCTCGAACCAGCGACACACCGACCTTCTTGCTGTGAGGTGATAGCACAACCTACTGCGCCACTGCTTCCCCGAAAATAACATTGCCAATAACATTTTGTTTTATTACTATTTATTAATATGTTTTTATTATTCTTTTGTTTAGCTTTGCCAGTGAGAGTGGTTGAGCTCAAGCACATCAAATCTGTTGTTTTAAAGCTGTGTGATGATAAGCTAATGTATTGATTCCTATGTATTATTAATTCTCTCTCAGCTGTTGAAGAACATCTCGTGGTACACCGAACGTGTCCTAACAGAGATCTCCCTAGGAAGTCTGCTAATCCTGGTCGTCATCCGAACCATCCAATTCAACATGACCCGCACAAGGG[T/C]GAGTCCAGAACCACAGAGACAAATACAGTTTGAAACATCCACAACTTTGGCCATGTACATTTATTACTCTACATCTTATATACAGTTGAAGTCAGAATTATTTGCCCTCCTGTGAACTTGTTTTCTTTTTCAAATATTTCCCAAATGATGTTTAACAGAGCAAGGAAATTTTCACAGTATTTCCTGTAATATTTTTTCTTCTGGAGAAAGGCTTATTCGTTTTGTTTCGGCTAGAATAAAAGCATTTATTTCAAACCATTTTAAGGTCAATATTATTAGCCCCCTTAAGCAATATTTTGTTTTCAGTTGTCTACAGAACAAACCACTGTTATACAATAACTTGCCTAATTACCTTAATTAACCTAGTTAAGCCTTTAAATGTGACTTTAAGCTAAATATTATGCAACAATACAGTTAGCTCAAGGTTCAATACATACCTCGGTTTTTTAACTCTGATTTCGGTTCGGTTCTTATGGCTTGACACGTGTTTTTTGTTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23842
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 |
---|---|---|---|---|---|
ENSDART00000062418 | Essential Splice Site | 523 | 623 | None | 15 |
ENSDART00000139194 | None | 525 | 525 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 3760355)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 3357611 |
GRCz11 | 21 | 3509032 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTACGAGGGCCTCTTGGAGACGAGGACAGGACCGTCCTGCCAGACTATG[T/C]AAGTCCATCCTTCAGTTGTATGAAAGCGTTTTGGCTTTCCTGTAAAATAT
Long Flanking Sequence:
GGCCAGTGAGTGTGGTTCATGTTAGTAAATACATTAACTAATGAAACCTTTTTGTAAAGTGTGGCTGACTTATATCTGAAAACAAAACAATATGTGCTGCACATCCAGAAAATGCTTCTTGGTTTTATAATTTTTAGATATTTGGATTAGAAACAAGACGAAATAATCAAGTTAAAGCATTTTTTGCAATGTAAACGACCTCTAAATGATAATGAAATGAGCATCTGAAAATGTCCATCTCATAATCTGATACAAACTGCTGTTGGTTTGATTTTTTTTGTTCGTTCTAGGAAAGACACATTATTTATTTAGGAAGGATAAATAAGTTGCATCGAATGCTTTCAAGAAACAATTTCAGTTCTGACTCTTTCCTCCTTTCTGTTTTTCTCTCAGTTTGTTTGCTCTGCTGTCAAAGAAGCACAATAAGGTTTTGGAGCAGGCGACGCAGTCTTTACGAGGGCCTCTTGGAGACGAGGACAGGACCGTCCTGCCAGACTATG[T/C]AAGTCCATCCTTCAGTTGTATGAAAGCGTTTTGGCTTTCCTGTAAAATATAATGATGACGGAAGAAGTTGTGATGGGACCTAAATGCTTTCTTAGGTTATTAAAGGTGTTAGGTTATTAAAGGTGTCACTTCTTGTTTAGGCTGCATTAATGCAGTGTAGCTGCACAATTGATCATTAAAAGATCAGGATCTCAATTCACACCCACACAACAGTTATTAAAGACCATGATGTGCATGTTTATTAATCATTCCAAGCGCTGCATTCAAATCTGCGTTTGACCAAGAAAGATTCAGTCTTTAGTGTTCAGCCAGTGTCTTTTTAGAGTTAAAGGGCCACTAATCCCCCCTGTTTCAGCAGGGTGTTTTCACACCTCTTGTTTGGAAAAAGTGGGCGTGTCCCGTTCCGTTTAGGGGGGAGTGTCGGAGGAGAGAAAGAGGGAAGGTGCATTAAAATTTGCACAAAAATGGGAGTTTTGGTTTGGCCACACACCGATTTTCAC
Associated Phenotype:
Not determined