ZMP
wu:fi27d05
Ensembl ID:
ZFIN ID:
Human Orthologue:
DTX3
Human Description:
deltex homolog 3 (Drosophila) [Source:HGNC Symbol;Acc:24457]
Mouse Orthologue:
Dtx3
Mouse Description:
deltex 3 homolog (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2135752]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16636 | Nonsense | Available for shipment | Available now |
sa5835 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6187 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16636
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112597 | Nonsense | 32 | 1006 | 3 | 18 |
Genomic Location (Zv9):
Chromosome 11 (position 1552279)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 1560419 |
GRCz11 | 11 | 1587007 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCACTTTTAMTATCACAAACTGAGTTGYATTCTTGCTCTTCCAGATTTA[T/A]CAAAATGTGATCCAAACACAACCGACCAGCRTTAAAAATTCTCCTATTCA
Long Flanking Sequence:
AAAGTCCTAACTAGGCTAATTAGGTTAAATATACAAGTTAGCGTAATTAGGAAAAGCAATGAACTACAGTGGTTTGTTCTGTAGCCAGTCGAATACAATAATAATGAATTAATTGTAATAATTTATTTATTTAGCTAATAAGATTGACCTTAGCAGTCTATAAAATGTATAAAATATTTAGTTCAGTTTAGCTAGAATAAAAAAGACAGCAGAAGAAAAATATAGTAGCACTGTGAAAAACGAGCTTGCTCTGTAAAACAGCACTTTTAAAATACTTTAACTTAATTCAGCAGGGTCCATCTTCACATGCTGCACGCGATACATGGCTAAAACATCTGACACCTGATGATCCGGTGAGCACCAGACACATATTCAACTGATATATACAGTTCATGCCTGGAAACAATCCATGTCATGTATAAGAGGGAACTTTATTGAAATTAAATTATGTGCACTTTTACTATCACAAACTGAGTTGCATTCTTGCTCTTCCAGATTTA[T/A]CAAAATGTGATCCAAACACAACCGACCAGCATTAAAAATTCTCCTATTCAGGTAAATTTTTTAAATGTTTCTAGAGTAAAATAGTTATGAGAAATAATAACCTTGATTAATAAATAAATAATATATAGTTGAAGGCAATATAATTAGCTCTTTGTGAAATTTTAATTCTTTTTTATATATTTATCAAGTTAAGTTTAATGTAAATCAAAGGCGGCAACACCAATGCTCCAAAAATACAAATTTATTAAATTAAAAAGGCTGACACAGAGCGTGTAACGTTTCGAGCCGCCGGGTGTTCATCAGACAATGTTTATCACAATCAAGTGCTTCTTTTTATACACTTCCGGATCACATGATCTCCTCTCGCATATATGCCAACATATACATACATGCATATGTATACATACACAGTTGTTCACATATACATATACATACACATGAATACGTATACACATTCACATATAGTCTATAGCTTTGATATTATAAATCAAATTACAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5835
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 |
---|---|---|---|---|---|
ENSDART00000112597 | Nonsense | 893 | 1006 | 16 | 18 |
Genomic Location (Zv9):
Chromosome 11 (position 1570050)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 1578190 |
GRCz11 | 11 | 1604778 |
KASP Assay ID:
554-3788.1 (used for ordering genotyping assays)
KASP Sequence:
CCAAAAGGAACAATGCAGGTCAACAAAAGCAGTTTGAGTCTCCCYGGATA[T/A]CCACACTGYGGCTCTATTGAAATCCTCTACAACATACCCAGCGGTACTCA
Long Flanking Sequence:
ACACTCACTGGACTGCCAGAACACCTCGGTCCTGCTATTGCTGAAACTGAGAAGATCCTTCAGAGGAAAGTGTTTGATGACAAGATGAAGAAACTGATTGGTTACTCAGAGGACATTCCTTATGCTAGAAGAATCAAACTCAATCAGATCCCTGATTATGGAGCAGGAGCGGCAGGAGGAGCAGATCTGGATGAGCGAGTGAACTTTAGAGAGCAAATTAAAAGAGAAAGCAGTTTCAGTGAAGATTCAAAAGGAAATTCTGGACATGACAGTAAAGATGCTGCTGCTGAAGAGGACAAGTGTGTTATCTGCATGGACAGCTTCACTGATAAGGAAAAACTGAAGTGTGGTCATGAGTTCTGTCGGGACTGTTTAAAGCAGTCAGTGGAGAGTATGGGATCCATCTGTCCTGTGTGTAAAGAAGTGTTTGGGAAACTGGAGGGAAACCAACCAAAAGGAACAATGCAGGTCAACAAAAGCAGTTTGAGTCTCCCCGGATA[T/A]CCACACTGCGGCTCTATTGAAATCCTCTACAACATACCCAGCGGTACTCAAACGGTAAGAGTTTGTAACACCTAATTAAAACTATCTAATTAATGATAAATCACAGTATAAAATAATCAAAGCACTTTATTTGTGATTTCCTTGTAGCTCTTTTAAAAAAATAAAAAAGTTGTAAGTTTAGAGTGTGTGGGTGTTTCCCAGCACTGGGGTTGAGCCAGTGCACAGTAAACATATGCCAGAGATGTGATAAAGAAGAAAATAACCTATAGAAAATGAAGTGAGTCCTAATATTGTGGTACAGTAATGCATAATTTTAAAATGTATTTTTTAGAATAAGCATCCAAACCCAGGGAAGCCTTATTATGGGACAACTCGTCGTGCTTACTTACCAGACAACCATGAAGGAAAAGAAGTGCTTGCACTGCTGCAGAGAGCTTTTGACCAGAAGCTGATCTTTACAGTCGGGACCTCAACAACCTCCGGTTTGGAAAATACAGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6187
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112597 | Essential Splice Site | 984 | 1006 | 17 | 18 |
Genomic Location (Zv9):
Chromosome 11 (position 1570601)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 1578741 |
GRCz11 | 11 | 1605329 |
KASP Assay ID:
554-4451.1 (used for ordering genotyping assays)
KASP Sequence:
CCTGGAATGATATCCATCATAARACMAGTCMATWTGGTGGAGCTCAAAGG[T/A]ATGAGTTCATCTCTAAAATCTGMTTGCATRCTTAACCAGAAATCAAGTGA
Long Flanking Sequence:
AACGGTAAGAGTTTGTAACACCTAATTAAAACTATCTAATTAATGATAAATCACAGTATAAAATAATCAAAGCACTTTATTTGTGATTTCCTTGTAGCTCTTTTAAAAAAATAAAAAAGTTGTAAGTTTAGAGTGTGTGGGTGTTTCCCAGCACTGGGGTTGAGCCAGTGCACAGTAAACATATGCCAGAGATGTGATAAAGAAGAAAATAACCTATAGAAAATGAAGTGAGTCCTAATATTGTGGTACAGTAATGCATAATTTTAAAATGTATTTTTTAGAATAAGCATCCAAACCCAGGGAAGCCTTATTATGGGACAACTCGTCGTGCTTACTTACCAGACAACCATGAAGGAAAAGAAGTGCTTGCACTGCTGCAGAGAGCTTTTGACCAGAAGCTGATCTTTACAGTCGGGACCTCAACAACCTCCGGTTTGGAAAATACAGTTACCTGGAATGATATCCATCATAAGACCAGTCAATTTGGTGGAGCTCAAAGG[T/A]ATGAGTTCATCTCTAAAATCTGCTTGCATGCTTAACCAGAAATCAAGTGAACTTAAACTTGTATTCCTCATTTTTTATTTGCACAGTTATGGTTATCCAGACCCAGACTATCTGAAGAGAGTGAAAGATGAGTTAAAGGCCAAAGGCATTGAATAAACAATGTGGTAAAAATGCAACACCCCTGCACTGGAGCTCCATGTTTACACCATTGATATATAGCATCAAATCACAAGTAGTTTCTTTCCTGGCAATGTAACTGTGTTCATTATACATGTAAGGTGTTTGGTATTGTATTAATACAACTACATCTAAAGAGCACACTACATTCATTGGAAAAAAAAGGCCTGATTTGAGACACCACAAACTTTGGAAAACGTCAATCTAAAGCTTCAAGAGACAACAGAGAAGTATTAAACCGTTTGCATCTGTTGATTGTAAAATTGTGACTTCATTGTGAATTACATTACCTAGGTCAGGGGTGGCCAACCCTGTTCCTGGAG
Associated Phenotype:
Not determined