ZMP
zgc:158869
Ensembl ID:
ZFIN ID:
Description:
dachshund homolog 1 [Source:RefSeq peptide;Acc:NP_001074142]
Human Orthologue:
DACH1
Human Description:
dachshund homolog 1 (Drosophila) [Source:HGNC Symbol;Acc:2663]
Mouse Orthologue:
Dach1
Mouse Description:
dachshund 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1277991]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9313 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44705 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15020 | Nonsense | Available for shipment | Available now |
sa7192 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9313
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 |
---|---|---|---|---|---|
ENSDART00000101070 | Nonsense | 29 | 611 | 1 | 11 |
The following transcripts of ENSDARG00000069440 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 31924133)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 31080079 |
GRCz11 | 9 | 30890825 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGGTCCATCCGTGTCCGATCTCAACTTCTTCGTCAGCATCATCAGCAT[C/A]ATCATCATCATGCTCCGCGACCGCAGCATCATCATCCTCGCCCTCGGCCA
Long Flanking Sequence:
AAAGAGTTTGAGAGCGCATTCCTGGATGAAGCGCACGCCGTTTTCTCATCCGAGCTCGCAAAGCCTGTGTAAGTAAACGCTGGAAATGTTCCGGCGTCCGCTGTTCCACTAGGGTCGCATTAGATTGTGCATGTCTCCGTTTCAAAGCGCTGATAGTGGCTCCTCCCTCTCTGTACCTTGTGACAACAACAACTCATCCACAGAGCACAGGCACACTTTTCTGCTCATTTTCTTCCTGTCATTCTCTCCCAATCTTTCTCAGAGTCCTAATTTCAGCACGGCACCTCTCCACGTCCATTGGCGCGTCGGCGGAGCGCACTCGGGTGGATTTCTTCTTCTTTGCGCTACTTTTGCAGACTGGCTCTCTTTCCCATCTGAACTTACTTGATAGGCGGACAGGCAGACAGAACACACCATGGCCGTACCGGCTGCTCTGATTCCCCCATCGGCTCTGGTCCATCCGTGTCCGATCTCAACTTCTTCGTCAGCATCATCAGCAT[C/A]ATCATCATCATGCTCCGCGACCGCAGCATCATCATCCTCGCCCTCGGCCACTTCTGCGTCTCCTTCTCAGTCAGCGACCCAGAATCTGTTCCGCGCGGATCTGATCAGCACCAACTGCACCAGTAGCATCCCACTGGCCGGCAAGCCCGTGTACTCGACCCCGTCTCCAGTTGAAAACACTCCGCAAAATAATGAGTGTCGGATGGTGGAGCTGAGGGGCGCAAAGGTGGCCTCGTTCACAGTGGACGGACAGGAGCTCATCTGCCTGCCCCAGGCATTTGACTTGTTTCTCAAACACCTGGTCGGGGGTCTGCACACCGTCTACACCAAACTCAAGCGGCTGGAGATCACGCCGGTGGTGTGTAACGTGGAGCAGGTCCGCATCCTGCGCGGGCTGGGGGCCATCCAGCCCGGGGTCAACCGCTGCAAACTCATCTCCAGAAAAGACTTCGAGACCCTCTACAACGACTGCACCAATGCCAGGTTAGAACAAACTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44705
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000101070 | Essential Splice Site | 190 | 611 | 1 | 11 |
The following transcripts of ENSDARG00000069440 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 31924617)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 31080563 |
GRCz11 | 9 | 30891309 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTCCAGAAAAGACTTCGAGACCCTCTACAACGACTGCACCAATGCCAG[G/A]TTAGAACAAACTCTTTTACCTTTCCACAACAGGCAATCGATAGCTAAGTT
Long Flanking Sequence:
TCAGCATCATCAGCATCATCATCATCATGCTCCGCGACCGCAGCATCATCATCCTCGCCCTCGGCCACTTCTGCGTCTCCTTCTCAGTCAGCGACCCAGAATCTGTTCCGCGCGGATCTGATCAGCACCAACTGCACCAGTAGCATCCCACTGGCCGGCAAGCCCGTGTACTCGACCCCGTCTCCAGTTGAAAACACTCCGCAAAATAATGAGTGTCGGATGGTGGAGCTGAGGGGCGCAAAGGTGGCCTCGTTCACAGTGGACGGACAGGAGCTCATCTGCCTGCCCCAGGCATTTGACTTGTTTCTCAAACACCTGGTCGGGGGTCTGCACACCGTCTACACCAAACTCAAGCGGCTGGAGATCACGCCGGTGGTGTGTAACGTGGAGCAGGTCCGCATCCTGCGCGGGCTGGGGGCCATCCAGCCCGGGGTCAACCGCTGCAAACTCATCTCCAGAAAAGACTTCGAGACCCTCTACAACGACTGCACCAATGCCAG[G/A]TTAGAACAAACTCTTTTACCTTTCCACAACAGGCAATCGATAGCTAAGTTGGATGAGAAATTTCGTTAGAAATGAATTCTAAACTTATGTACTTCATGCTAATTGTTTGAGTCTTATACGTGAAGGAAATACTTTCAAAATTGTCTTTGCACTTAAAAAAAAAAAAAAAAGAATAGGCTACAATTATAGGTCAAAAAAATTATTAGTACAAGTAAAGCTTTTTAAACTTTGCATGTGTTAACTTTACTCCCAAAGTTACTTCAGTAACTTTAAAGAACCTCATTTGAAATGTTTTGATAAGTGCACACATTATTAAAGAAAGGCGTATTTTTTATTATTTTAAACAATAATATAAATATTTGCATCAAATTTTTTAATATTATAAAATTACATTTCGCAAAGGTATAAAGTTAAATATATCTATTAATAAATAATACCACTTTTACTGAATTGTTGTAGTGCATGCAAAATGCAGTGCTCTTTTTTTTTCTTCAACTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15020
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 |
---|---|---|---|---|---|
ENSDART00000101070 | Nonsense | 366 | 611 | 5 | 11 |
The following transcripts of ENSDARG00000069440 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 32049054)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 31205000 |
GRCz11 | 9 | 31015746 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGCCCCCTCTCTGGAAGAYGGCAGGAGGCCGGGGAGCCGTCCCTYGTCC[C/T]AGCGCAGCAGCAGCGTCYCYAGCTCTCCAGCACAYACCGAGAGCTCCTCC
Long Flanking Sequence:
GAGTCAGATGAACCACCTCAGCACCATCGCCAATATGGCCGCCGCAGCACAGGGACAGAGTGCCCCATCCCGAATGGTGACATCAGTGATTAAGGTAACCCACGGCGCCGTTCTCTCATTGTGTCGTGCACATCTCTCTCTCTCATCAGCCATTGGGGGAAGGTGGGTGGTGCGCGATCCGTGCTTTTGGTACGGCATTGCAGGGGGTAGTGTTTCAGACAATAGCCTGTGAAAGAATGAAAGCAAAGATGCAGAGAATGGGTGAAGGGAGGGAGGAGGGGTTATATCCAAAAATGCAAAAAAACATATAAAAAGACGAGGCAGCAGCATGGATGCTTCTCTGTCCATGAAGGTGTGTTGGCTGAAAAGAGTGTGTCATGTAATGGCCGCCCCGGCTGTGTTTGTTTTTCCTGTTGGCTGTGCAGGAACGGGTCCCCGACAGTCCCTCCCCTGCCCCCTCTCTGGAAGACGGCAGGAGGCCGGGGAGCCGTCCCTCGTCC[C/T]AGCGCAGCAGCAGCGTCTCCAGCTCTCCAGCACACACCGAGAGCTCCTCCGACAGAATGCGTATGTTCACCTCATAAATCTCTCTCTCCCACTCTCTTTGTCTCTCCATTTCTCTCCCCTGTCACACACGCACTGCTAAATACTGCACTAAACATGCCCCTTGTTAAGCCCGGAGCACACGTGCATCCCTTTATGCTTTCTGTTGTCTCCAACAGATGGGGGGGTGGGGGGGGATATTAGCAATCTTTAAATTTTGCTCCGGCAAGTGTTGTGCAAAAACAGACCTCCAATGTTTTCATCATTAGCTGTGCCATAAAATCAAAACAATGTTCTTAATCACTGGAAGAGCGTGGATGTTTTTCGTCATCTCTGAAATATGCTGCCAATGTTTTATGAAGTTATTCTTTACGAGTAACTGTTTATTTTGATTAGAAACGTGTTTTGAGTTCTGAAAGTTATATTGTATGCGTTTAGATTCCCTCAGTTACCGGATCACAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7192
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 |
---|---|---|---|---|---|
ENSDART00000101070 | Nonsense | 564 | 611 | 9 | 11 |
The following transcripts of ENSDARG00000069440 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 32085787)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 31241733 |
GRCz11 | 9 | 31052479 |
KASP Assay ID:
554-4503.1 (used for ordering genotyping assays)
KASP Sequence:
CGCTGGAATATGAGTCGAAGCGACGAGAGCAGGCGGAGCAGACCCTGAAA[C/T]AGACATCACCTACAGAAAGTCTCAGATCACTYAATGGTGAGACATTTTAC
Long Flanking Sequence:
TACATAATGAATCAAATTGAGCTTATTAAGCCAGTTTCACAGAAGGATCCTTATAAATGTGCCCACAGCCCTCCAGCATTCTTCTGTTTAATATTCAGCTCGCCTCTTTCCGTTCCTTTTTTACAGAAAGTTTCCCTTAACCCCGTCTCATTGGCATTTTAACCTAGGTTAATCCAGGTTATCGCTGGCTCAATTATTTCACTAATGACACAGTCAATTTCTCATTGAACAAGAACAGTTTTTCTTTTTTCAGCTGCAACTTTTCTATGAATTTTCCCCTCGCCGAGGGAGTTTGAAAATTAGCTCTCCTTCCTTTGGTCCTCAATATTAGATGTGCCGCCGCATATGACTGGGGTCCTTGACTGCTGCTTTTTCTGTATTCTTTGCGCACAGCGATCATTCAGAAAAGGTTGAAGAAAGAGAAGAAAGCCAAGAGGAAATTGCAGGAGGCGCTGGAATATGAGTCGAAGCGACGAGAGCAGGCGGAGCAGACCCTGAAA[C/T]AGACATCACCTACAGAAAGTCTCAGATCACTCAATGGTGAGACATTTTACTTAAATAGTGTGCATAACTGCAATGTAGAGCCGGTTTGTTAGTTGCCTGATGAGTGTAATCTGATGAAATATGCTTCTGTATGTGGGAGATAATATACTGTATAGGAAGGCAGTCATTTTTACTAAATTAATGCTTTACGTTAATGCAAGACTTGCAACTATTACACAACAAAAAAAACATAATTTATAAAAAATTATTTATCATTAAATATAAAGAACTTCATAAATACTTTCTGCAGAAATAAGCTCAAATAAAATTTGAGAACATTCAATTATGAGCAATACATGCCAATTATGACCAACTCAATACAAGCAATACAATGTATTTTTAAATATTAAGATCCCAGATATGATTCAAAGATTTCTGTTAAAGCTTGTTAGCATTGGTTAACTAGTTAACATGTCTTAACAGATATTTTACAGTCTTGGCCAACTCTTATTTCAAAATGA
Associated Phenotype:
Not determined