ZMP
DCHS1 (2 of 2)
Ensembl ID:
Description:
dachsous 1 (Drosophila) [Source:HGNC Symbol;Acc:13681]
Human Orthologue:
DCHS1
Human Description:
dachsous 1 (Drosophila) [Source:HGNC Symbol;Acc:13681]
Mouse Orthologue:
Dchs1
Mouse Description:
dachsous 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2685011]
Alleles
There are 10 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa35933 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa9209 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa15468 | Nonsense | Available for shipment | Available now |
| sa35934 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa42580 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa44827 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa22684 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35933
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 |
|---|---|---|---|---|---|
| ENSDART00000102424 | Nonsense | 747 | 3246 | 4 | 21 |
Genomic Location (Zv9):
Chromosome 15 (position 31393861)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 32289513 |
| GRCz11 | 15 | 32147492 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGGGTCAACATCAGTATAGTGGCGGGACTGGTCGCACCCCCTGTATTT[G/T]AGCAAGCTCAGTACTACTTTGTGGTCTCAGAGGATGCCCTGCGTGGAACA
Long Flanking Sequence:
AATCAACCTGCATTCTACCCTGTGAGCTATGCAGTAAGCCTGAGTACACAGAGTGCTCCAGGGACATCCGTCCTGAAGGTGACTGCCCATGACCCCGATGCGGCAGAGAATGGCAGAGTGACCTACCGAACTGTTCCTGAAGGGAGCTCACCTTTCTTCACCCTCAACAAAGACACTGGTGAGAAGATTGTTATGTTTTTTCATCACTTTTATTTTTTGTAGCCTAAATAAAAACAGAAGTCTAATATTTTTCTTACCCCTGTATGAGTTTCTGCATTCAGTAGGTTTGATGTATTCACATACCTTTCAGCCTAATAGAAATATTTATTTTGGTTGTGCATTGCCCAGGAGTGATTTCACTGTCACGCGCTCTACATGGAAAGGCAAACTCAGTCATTACCATGGTGGTCTCAGCCCAAGATGGTGGGGGTCTTACCGCTCCAGTCAATGCCAGGGTCAACATCAGTATAGTGGCGGGACTGGTCGCACCCCCTGTATTT[G/T]AGCAAGCTCAGTACTACTTTGTGGTCTCAGAGGATGCCCTGCGTGGAACACAAGTTGGTGTTGTGCGGGCCAGCACTAAGAATGGTGGGTGAGCTTTTGTCAGAGATTTTTATCTCCTCCACCCCTCACCCCCCTTTGGTCACACATCCTTATTCAACTTGTTTAAACATACAATCCAAACTTCACTGCTTACCCACATTTATCAGTCATACTGGACTTGGTTCAAGGGCTAAAAGACGCCTTTTGTTTTTTTTCACCATGGTGCACCACTTGTACAAATAGGCACAGAACCACTGTACACACCTCATTTACAGTCAACATTAATCATTGATTCTGTTTCACCACTTAGTTTTTAACAATTTGCTTTGGATATTTGATCCACTAAATTCTGGCCTTGTGTTGAAAAAAAACCCTTTGTCTTTGTTTTCACCCCACACTGAACTAACATGTCTCTGGCTATTTGCCTCTTGGTTCTCAGGTGTCTTGAAGGATATCTCCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9209
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 |
|---|---|---|---|---|---|
| ENSDART00000102424 | Nonsense | 960 | 3246 | 5 | 21 |
Genomic Location (Zv9):
Chromosome 15 (position 31394896)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 32290548 |
| GRCz11 | 15 | 32148527 |
KASP Assay ID:
2260-8736.1 (used for ordering genotyping assays)
KASP Sequence:
CACGTACAAGCTGAAAATGGACAAGGCCCTGTGTTTGATAGCCTCACATA[C/A]AGAGTAGAGCTAAAGGAAAGCACCCCRCTTAACACACGCTTTCTACAGGT
Long Flanking Sequence:
ACTGTGGATTCAGAGACTGGGGCTTTGAGAACCAGCTTGCCTCTGGATCATGAGGCCCAGCCAAGCTTGAATCTGGAAGTCCAAGCACACTGTGGAAACCCACCAGCCTTTGGCCAGACTAGGGTACGAATTACGGTGTCTGATGTCAATGACAATGCACCCGTCTTCCTGCCTTCATCCTCTGAATCATTGATTCTACCTGAAGACACACGGATGGGTACAGTGGTTTACAAGGTCCAAGCAGAAGATCGTGATTCTGGACCCAATGGCCTTCTGAGTTTTGACCTGTTCACCAGCAGCGCCCATAGAACCTTCAGTATTGATCGCAACAGCGGACATTTACGCCTAATTGGCAGTTTGTCATATGAGACCATGCCCCGTTATGACCTGCAGGTGATTGCTAAAGACAGTGGAGCACCCCAGCTAAGTTCTACATTTACTCTGGTCATCCACGTACAAGCTGAAAATGGACAAGGCCCTGTGTTTGATAGCCTCACATA[C/A]AGAGTAGAGCTAAAGGAAAGCACCCCACTTAACACACGCTTTCTACAGGTCCGAGCTGTGAACCGAGATGGTGGCATCACCACTGGACTGTCATCTACTTCTGCCTCACTAGCCTACCACCTGCACCCAGATGGTGATGCTGCAGGGTTTGGCATTGTGTCAGACAGTGGCTGGCTGTTCGTGAAAAGTGCCTTGGACAGGGAAGCTAAGGAGATGTACCTGCTCACTGTATTGGCCACATCAGGCAACGGACAGTTGAAGAAGACAGGTAGTGCCACGGTGCGTGTGTCAGTGATGGATGAAAATGACAACACTCCACGGTTTACCCAAGAGAGAGCTTTCCTGGCAGTGCGCGAGAACCTGCCAGCAGGCACTGGTTTTGGCCGAGTGTCTGCCAGCGATCGAGATGCTGGTCTCAACGGTCGGCTGAGCTACCGCCTGCTCCATCTGGATCGCCACTTCCAGATCAACTCCCACACAGGTGAGCGTCAAATATGGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15468
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 |
|---|---|---|---|---|---|
| ENSDART00000102424 | Nonsense | 978 | 3246 | 5 | 21 |
Genomic Location (Zv9):
Chromosome 15 (position 31394948)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 32290600 |
| GRCz11 | 15 | 32148579 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGTAGAGCTAAAGGAAAGCACCCCRCTTAACACACGCTTTCTACAGGTC[C/T]GAGCTGTGAACCGAGATGGTGGCATCACCACTGGMCTGTCATCWAMTTCT
Long Flanking Sequence:
AGGCCCAGCCAAGCTTGAATCTGGAAGTCCAAGCACACTGTGGAAACCCACCAGCCTTTGGCCAGACTAGGGTACGAATTACGGTGTCTGATGTCAATGACAATGCACCCGTCTTCCTGCCTTCATCCTCTGAATCATTGATTCTACCTGAAGACACACGGATGGGTACAGTGGTTTACAAGGTCCAAGCAGAAGATCGTGATTCTGGACCCAATGGCCTTCTGAGTTTTGACCTGTTCACCAGCAGCGCCCATAGAACCTTCAGTATTGATCGCAACAGCGGACATTTACGCCTAATTGGCAGTTTGTCATATGAGACCATGCCCCGTTATGACCTGCAGGTGATTGCTAAAGACAGTGGAGCACCCCAGCTAAGTTCTACATTTACTCTGGTCATCCACGTACAAGCTGAAAATGGACAAGGCCCTGTGTTTGATAGCCTCACATACAGAGTAGAGCTAAAGGAAAGCACCCCACTTAACACACGCTTTCTACAGGTC[C/T]GAGCTGTGAACCGAGATGGTGGCATCACCACTGGACTGTCATCTACTTCTGCCTCACTAGCCTACCACCTGCACCCAGATGGTGATGCTGCAGGGTTTGGCATTGTGTCAGACAGTGGCTGGCTGTTCGTGAAAAGTGCCTTGGACAGGGAAGCTAAGGAGATGTACCTGCTCACTGTATTGGCCACATCAGGCAACGGACAGTTGAAGAAGACAGGTAGTGCCACGGTGCGTGTGTCAGTGATGGATGAAAATGACAACACTCCACGGTTTACCCAAGAGAGAGCTTTCCTGGCAGTGCGCGAGAACCTGCCAGCAGGCACTGGTTTTGGCCGAGTGTCTGCCAGCGATCGAGATGCTGGTCTCAACGGTCGGCTGAGCTACCGCCTGCTCCATCTGGATCGCCACTTCCAGATCAACTCCCACACAGGTGAGCGTCAAATATGGCAGACAGTACGTCAGACAGTCCAACTGTGCAAAATGTTGTCTTTAAATGAGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35934
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 |
|---|---|---|---|---|---|
| ENSDART00000102424 | Nonsense | 1674 | 3246 | 12 | 21 |
Genomic Location (Zv9):
Chromosome 15 (position 31428471)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 32324123 |
| GRCz11 | 15 | 32182102 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATTTCAGTATTCATCCGGTGACAGGAGTCATAACTACCACCAAAGCTT[T/A]GGATAGGGAGGCCCAAGGCGTTTATGCTTTGACAGGTACTGAAGTGCTTA
Long Flanking Sequence:
AATTGAATATCAGCATACTCTTCCTAGAAGTTTCTGTGCATTATATATATAACATAGTTTTCTATCATGTTTTGTATGGTGATGAAATTTCAACTGAATAGTTTCATCTGTTTGAATGTGTTCCCACAATGGGTATAACAACCCATCATGGGTTATTGGAACATGCCATTTGTAAAGCAGTTTAGTGGTCTGTCCTGCAGTACAATTTAAGAATGTTTTTTTTTTTCACCCAGCTGATAATTGATGTGACTTAAAGCTATTTAGAATGTGAAGACATTGTAGAGAAGTTCACTGCTATTTGATAAACTCTTTTTTAAAGATATTTTAAATAAAATCAATAAAAATTGAACGGTGAGGCTGTACAAGCTAGTTAGTAGTGTATATTATATGTCTTTGTTGTTTTTCCATAGGGACCAATGGAATCGTGACATATGGAAGCATTGTGGGAGATGATTTCAGTATTCATCCGGTGACAGGAGTCATAACTACCACCAAAGCTT[T/A]GGATAGGGAGGCCCAAGGCGTTTATGCTTTGACAGGTACTGAAGTGCTTAATTAGAGGAATTTACTCTTGGATATGCTTTTCATTTCTGCCAATGTCATGTCACGGTTGGGCACAATTTTGTTTAGCCAGTTTACAACCTCTCTCATAAACAGTTTATGCCAGAGATGGTGGTTCTCCACCTAATTTCGCCAAAACCACAGTGCGGGTCACTGTGCTGGATGAGAATGACAATAGGCCGGCGTTTGGGAGAGTTTACTACAGTCTGGAGGTGCCGGAGAACCAGGAGCCTGTGACGCTTTTCACCATTAGAGCCACAGATCAAGACTCTGGAGACAGCGGGCTGGTGTACTACAGAATCACAGGTATTAATGGCATGAGCACTATTTATGTTGTCGCATACTAATGCTAATTGTTCACACGTTTTGGTCATGCTCAAAGTCATTTCAGTTCTGCAAATGCTCATTTATTCTTTCCCCATTGTAGTAGTATATCATGCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42580
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 |
|---|---|---|---|---|---|
| ENSDART00000102424 | Essential Splice Site | 2044 | 3246 | 14 | 21 |
Genomic Location (Zv9):
Chromosome 15 (position 31431130)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 32326782 |
| GRCz11 | 15 | 32184761 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCTCGCGCAACACTAGAGATGTGAGCCTGCAGGAAAATGCAGCCAAAG[G/A]TGGGATGATGATCTCTGAATTCAATACAGATATGTTAAAGAGCCCCTATT
Long Flanking Sequence:
AGCGGCAACTCTTGATCGTGAAAAAGTGGCCTCCTACAACTTCCAAGTCTACGCCATGGACTCTTCAGCAACTAATCCTCGTAACTCCTCCGCTGAAGTTGCCGTCCACATTTTAGATGTAAACGACAATGCCCCCTTTTTCATTACAGACCCGCTTATCATCAATGTCTCCATCAGTAGTCTCTCCAACCACAGAGTGCTGGCAACTATGAGAGCAGAAGATAAGGACTTTGGTGCAAATGGGTCTGTGTTCTATCGATTTGCCAATCCTGTCAAAGGCTTCACCATAAACTCCCTGACGGGAGCCATCCAGGCCACAGAGAAGCTCCAAGCACTGACCCAGAGTCAGAGGATCCTCATTGTGGAGGCCATGGATCAGGGCAACCCATCGCAGTCCTCTCTGGGCGTAGTAATTGTGTACATCAGAGAGCAGAGTTACCAGGGCGTCCGCTTCTCGCGCAACACTAGAGATGTGAGCCTGCAGGAAAATGCAGCCAAAG[G/A]TGGGATGATGATCTCTGAATTCAATACAGATATGTTAAAGAGCCCCTATTTTGCACTATAAAAGGTCATTTTTTGGTTTTGGGGGTCTTCAACAACAGACTGTTATGCATGCAAGGTCAAAAAAAACGTTCATTTTCTTATAATATTTATACATTTTTTTAACCTAATTATCCCAACGACTCCCATATGATTTGTTCAGCGATTCATTTTACCTTAACCCCTCCCTTACGGAAGGCTAATCTGCTTTGATTGGTCCGATGACCTAGTCTGTTGTGATTGATCGACTGGGTTCAGAATCGCGAGTTCAGAAACGCATTTAAATCTTTAAAGAAAAAAACATGCAAGCAATATGTGAATATCTCCATAAAGATTTAATCTGACAGATACAGTACAAGACCTGATCAAAAGTGGATTAAATACACACCATTAAACAAATTTTGCAAACTACAGAAAACGAGGCAACCATTTTAATGACACATATTATGATCCGAGAGAAGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44827
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 |
|---|---|---|---|---|---|
| ENSDART00000102424 | Essential Splice Site | 2204 | 3246 | 17 | 21 |
Genomic Location (Zv9):
Chromosome 15 (position 31433750)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 32329402 |
| GRCz11 | 15 | 32187381 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTATATCCACCGCTGCCATCATGGATAGGGAGATCTGGACACAAACCAA[G/A]TACTAAGTTGATCCTTCTGCCATTATAGTAGTTTATGTTTCTAGTGCTGG
Long Flanking Sequence:
CATCCTATCATTCAGGTGCAGTAATCTCTCATGTGTTTGCTCAACAGTTGAGTCTTCATAAAAGTGTAAAGTTGTGGAGTAATAACATCCCTTGGCACTGAATACAGCATATTTTCAGTGCAAGCCAGAAGAGTTTTCTTTGCGTTTCCCACAATGTTTTCATTGTCCATGGTGAGAATATAGGCTCAGCTGTCCCACATATCCACAATCAATTCCCCTTTTTTTAGCTTTTTTTTTTCATAATTCAAGTTCCAAGCCTAACATTGCTTAGAGGTTCACGTTACGCTTAGGCAGCTGTTGCAGATCTCCCTGTGTTTTCATTGACAATTTCACCGGTAATTTCCTCAGGTGTTGGCGAATGACCTGGACCAGGGTCAGAATGGGCAGGTGACCTACTCCATAAGGTCATCCTCCATGAGCGGCCTTTTCAAGATTGACCCTATCACAGGAAGTATATCCACCGCTGCCATCATGGATAGGGAGATCTGGACACAAACCAA[G/A]TACTAAGTTGATCCTTCTGCCATTATAGTAGTTTATGTTTCTAGTGCTGGGAAACAATTAAAACTTTTAATCATGATTAATTGCATGATTTTTCGGCAATTTTTATACACAAAATTCGACAATAAATTCAAAAGTGTTTTGCACACTTTTATTTTAAATGCTCTGGTATATGAATAAAACATTGATGTTTTTTATTAGTATTCCCTTTACTTATTAACAGCTACAACATATGTAAGTCTTAACCTAAACTTTAAGATAATCGAATGAAATATAAAACTAAAACTATTGGCAACTGCCAGGGCATTCAGTGATAATTAAGTAAACATTACATCAGTGGTTCTCAGTTCCTGTCCTTGCACCTCACTGTTCTCAAATAACCAGCTAGATAGATGAGACCTTTATGCATGAATCACTATTATGCATATGTCACTGCTTCCTACTAACCTAATCATGGGAAATATCTACTTCCCTTCAGAATGTTAATTCACGTATTTGCCTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22684
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102424 | Nonsense | 2301 | 3246 | 19 | 21 |
Genomic Location (Zv9):
Chromosome 15 (position 31437318)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 32332970 |
| GRCz11 | 15 | 32190949 |
KASP Assay ID:
2260-8740.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAATACACCGTTATGGAGGAGGGGTGTCCCTTACTACCCCTCTGGACTTT[G/T]AGATTAAAACATGGTACACACTGACAGTCAGCTCTTCAGACTCCAAGCAG
Long Flanking Sequence:
GTCCCACCATTCCTGTTCCACGTGAAGTCCGGGTCCCTGAGAGTAAGTTGACTGCTGTTTGAACTCCATATCACTTCTGTAATCAATGAACAAAATTTCCTATTTTTTCTGGCAGACAAACAATGAGGTACACCGTGCTGAAAGATTGACTCAATTACTAGCTCTTTTTCTCGCCAAAATCCTCAATGGATATTTCCTGTCACTGATGTTGTACAATGTGTCCAATAATGGTGGGCGTTGTCCAGCAAAAGCTAATAGTTCTGAAAGGTGCAACCACAAGTGGAAACGGCTGATTACGTTTTATACAGGGTTATCATGGAGATCGTCTGTTTCTTTCCTTAGATACCTTGATTGGAACCATGATCACTCAGGTCACCGGGAATGATGTGGACTCAGGGCCTGCTCTCTCCTATACCCTTCTTCTGGACTCAGACACTCAAGGGAAGTTTGGAATACACCGTTATGGAGGAGGGGTGTCCCTTACTACCCCTCTGGACTTT[G/T]AGATTAAAACATGGTACACACTGACAGTCAGCTCTTCAGACTCCAAGCAGCAGAGTCATGCAAATCTGACCATACTTGTGGAGGACGTGAACGATAATGCTCCAGTCTTCTCCCAGGACCTGTATGAGGTAGGTTAGGGAAGATCCCAGGTGTAGGATGAGTAGTGATAGTAAAAATTTGTTTGTGGCAGTATTAGATTCCACAAGCTTTAATAATCCCCATCAAAAGGAAACTTCTGTCATCAATTACTCTTTCCTCACTTGATCCAAACCTTTTTGAGTTTCTTTCTTCAGTTGCTCAAAAAAAATATATATTTTGAAGAAAGCTAAAAAGCGTGTTACTACCCTGCTGAAAAATCCAGCCTAAACCAGCCTAGGCTGGTTGGCTGGTTTTAGCTGGTCGACCAGGCTGGTTTTAGAGGGGTTTTGGCCACTTCCAGGCTGGTTTCCAGCCATTTCCAGCCTGGTCTTAGCTGGTCAGGCTGGGAGATGACCAGCTAA
Associated Phenotype:
Not determined