ZMP
ecd
Ensembl ID:
ZFIN ID:
Description:
ecdysoneless [Source:RefSeq peptide;Acc:NP_956185]
Human Orthologue:
ECD
Human Description:
ecdysoneless homolog (Drosophila) [Source:HGNC Symbol;Acc:17029]
Mouse Orthologue:
Ecd
Mouse Description:
ecdysoneless homolog (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1917851]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23044 | Nonsense | Available for shipment | Available now |
| sa36381 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23044
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 |
|---|---|---|---|---|---|
| ENSDART00000033025 | Nonsense | 365 | 630 | 8 | 13 |
| ENSDART00000133650 | Nonsense | 367 | 632 | 8 | 13 |
Genomic Location (Zv9):
Chromosome 17 (position 20026097)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 20176108 |
| GRCz11 | 17 | 20195944 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATCTGCTCGATACAAAGAGCTGATGACATCAGCGGAGAGTTTCTTCAGA[C/T]AGTCAGTGACAAGAACTCACCGGTTAGAGGAGCTTTTACCATTCATTTTA
Long Flanking Sequence:
GCACACTCATTGCAAACACCCATTGTGTAAAGCACTTTAAGTGTCTAGAAAGGTGCTATATAAATGTAAGGAATTATTATTATTATTATTATTTAATGCATCTTTTGTTATGTATAATGTGAATTTGTGCAACTGGTGTACATAGTGCTAACACATTGTACGTTCTATTAATATTTAAGGCCCATGGCTTTGAAATCTTGTGCTCCAAAAATGGAGAGTCTTCATCAGATCAAGAGCCTTCAGTGAGCAGTAACCCATTATGGAGAGGATTTTTAGAGAGCCTCAAAAAGAATGGATACTTTAAGGTAAGAAAGTATTTCTGTGCTCAAAGTATTTAAATCACGCAAATGATGCTGATGCTTTGATGCTGCAAATGATGATGATTGCTTTGCCAGAGAATGTGAAAGATATTAATAAATGTGTTTTTGTTAATCCAGGGGAATCTAGAAGGATCTGCTCGATACAAAGAGCTGATGACATCAGCGGAGAGTTTCTTCAGA[C/T]AGTCAGTGACAAGAACTCACCGGTTAGAGGAGCTTTTACCATTCATTTTATTTTTTCATTCTCATGTTGCTTCAATATTTATTTTTTGAAGTCTGTGTGGAAATCAGCACCAGGCGATAAACAATATCATATTGACATCATAAAGATAAGTTCTGCTTGATATGGATTAATCTGTCAGCTTAATCACACTGCTGAAATAGAAAACATCTACAGCGGTTTGTAAATCAGACTACTGAGTATTTAAAAGTTTGGTTTTGTCAACCACAAACTCAAACACTTGATTCTCATGGTGTTGTCAGTGTTTGCTTTTCAATGTATGTTGATCACAAGCAAAGTCCCTTTAAGGCAAGTCATAACGACCATCTTTGAAATGCCTCTCAGGCATTCTGTTTGAATGGGGAAACATCAAATTCTCCAAAAATGCTTGTCAAGCTTACGATTAAATTTCATATTAGGAATCTGCAATAAAATTATTAACTCTCTCTTTAGTTTCATTTCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36381
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000033025 | Essential Splice Site | 408 | 630 | 9 | 13 |
| ENSDART00000133650 | Essential Splice Site | 410 | 632 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 17 (position 20022007)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 20172018 |
| GRCz11 | 17 | 20191854 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCTAGAAGACTTAAAAAAACAAGAAGCAAATCTGCCACCAGAGGACAG[T/G]ATGTACCACTTCACCTCACATTTTCAAAGAGAATCATTTTCTCATTGGTT
Long Flanking Sequence:
TACAACAGAATTAATGCATTAAATGATAATCTAGTATGTTTAATATTTTATAAAATAATGTATTTAATCATAGCGTAATATTTTATAGTAGAAAAATAGTGTAAGTTACACTTTATAAGCAGTTGAATTCAGTTTAGGCGTTTTTTTATTTATTTATTTTTAAACAGCAGGTGGCACTGTCTGAGAAAACGATAGGTCTGGAAGTGCAGGTCTGAGCGTGCAGTTGGGTCTTCGGGCCTGCAGCTTCATAATGTTGTCCAGTATACACACTATCATAAGGGTCATTGCACTACAGTAAACAACTATTTTTTTAGTATAAAATTACTAAATGATACATTATAATCAATGATATGACTAAATTTTGCCAATACCTGATTTTACTCTTTTTCAAGGCCTGATATTCATAATCCTGGTGGTGAGGTGTTAAAGGTGTTACAAAGCGCCTCCTACAGTCTAGAAGACTTAAAAAAACAAGAAGCAAATCTGCCACCAGAGGACAG[T/G]ATGTACCACTTCACCTCACATTTTCAAAGAGAATCATTTTCTCATTGGTTTGCACATACTGACATCAAATCAGGAGTCTGATCCATCATTTTGAAAGTGAATGCAAGTCATTTGAATACACTTTATTTGTAGGTGATGCGTGGCTGGACATCTCGCCTCAGGAGCTGGAGAGGCTGCTGGCAGAGCGAGGAGGTCGAGGAGGGACTGGTGAAGAGGTGCAGGAGGAGGAATCGGGATACAGTCTGATCGCTGTGACTCAAGGCATGAAGAACTTCATCAATGCCATGTCCTCGCATGAAGGAGCTGAAATACCAAGGTAATGACACTCACTCTGAATGACTAACTATTCATTTTAAAGCACTGTGATTATTGATGTCCCACCCCCTTAATGCGTTTCAGATCCTGCTTGGCTGAGCCTTTTAGGTTTGATCCAGATTCAGTTACTAGTGCCCTTGATAGACTTCTGGGTGAGTTTGATTTTTCAGTGATATTAGAACATG
Associated Phenotype:
Not determined