ZMP
si:dkey-21p9.4
Ensembl ID:
ZFIN ID:
Human Orthologue:
EXD3
Human Description:
exonuclease 3'-5' domain containing 3 [Source:HGNC Symbol;Acc:26023]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10072 | Essential Splice Site | Available for shipment | Available now |
sa9133 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34858 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10072
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092011 | Essential Splice Site | 164 | 861 | 4 | 19 |
ENSDART00000138041 | None | None | 339 | None | 8 |
Genomic Location (Zv9):
Chromosome 10 (position 10912582)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 10988448 |
GRCz11 | 10 | 10946686 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTGTTCAGTGTGAAAATGGAGCTCCAGTCAGATCTGGAYATGGAGAAGG[T/G]KAGTCTCTGTTCATCTGGACTGTTTTATTTCTGTGTGTTTGTGTGCTGTT
Long Flanking Sequence:
TGTCAGTTGCGGAAAAAATTATTGATAAAAGTGTCACGATTAACCGCGGTTTAACTGCAGGCGCAGTGTGATGTGCGTGCATGCGAAGGGGAGTCAGATTTGTCAGAGGAGTTAGATTTTGATATAACTTTCCTTCACCTTCTCTTGCAAGTGAGCTCACGAAGTTTGTGCTATGCACTGGTTGTTACTAACTAAATCTGTTTGTTGTAGCACAGTTATGTTTTGTTAAATAAGTTGCATGTAAAATTTATGTTTCAAAACTGCGCAAATTTTGTCAATCAAATTCAAAAAATCTGGCAACACTGATAAACAGTATCATTGATTTAATGAAACAATGACAGTATTGTGTGTTTTAAATGCATGTTTTAATAAATGTATCCAATAGATTATGTATTGCAGTCCTGGTAAAACCAGCGAATGCTATAAATGTCGTGTTTTGTGTCAGGCGCTGGTGTTCAGTGTGAAAATGGAGCTCCAGTCAGATCTGGACATGGAGAAGG[T/G]GAGTCTCTGTTCATCTGGACTGTTTTATTTCTGTGTGTTTGTGTGCTGTTTTGTTGATGTGTGTTTTATGTTTGTCAGATGTGTGTTCCTCTCATCCTGCTGGACAAGCTGTCTCTGGCTGAGCTCTATGTTCGTCATCATCCAGATCTGCAACAGAGACTCGTATCCCTCCTGGACTCCTGGTGCCGGCCAGACTTCAGCACACAGGCACTCATCAGGTCAACACACACACACTCGGCAGTATTTAATAAATCCATCAGTATTTATTCATCCATCTTTTTTTCAATACATGATTTCCCTTACTAGTTATGGTTTTACTGTGGTCTGTTTAATTTTAATTTAATTTTATTTAATTTTTTATTTTTATTAATTCAAAATAGTGTAAAGGTGATGATGATGATTGTTAATAGTGTGCCCTGTTATAACATTAATAAATATAAAATAATAATTAATTAATAATTGTTACCTTAGTTTTATTAACCAATATACCTCATTAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9133
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 |
---|---|---|---|---|---|
ENSDART00000092011 | Nonsense | 189 | 861 | 5 | 19 |
ENSDART00000138041 | None | None | 339 | None | 8 |
Genomic Location (Zv9):
Chromosome 10 (position 10912431)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 10988297 |
GRCz11 | 10 | 10946535 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGACAAGCTGTCTCTGGCTGAGCTCTAYGTTCGTCATCATCCAGATCTG[C/T]AACAGAGACTCGTATCCCTCCTGGACTCCTGGTGCCGGCCAGACTTCAGC
Long Flanking Sequence:
TGAGCTCACGAAGTTTGTGCTATGCACTGGTTGTTACTAACTAAATCTGTTTGTTGTAGCACAGTTATGTTTTGTTAAATAAGTTGCATGTAAAATTTATGTTTCAAAACTGCGCAAATTTTGTCAATCAAATTCAAAAAATCTGGCAACACTGATAAACAGTATCATTGATTTAATGAAACAATGACAGTATTGTGTGTTTTAAATGCATGTTTTAATAAATGTATCCAATAGATTATGTATTGCAGTCCTGGTAAAACCAGCGAATGCTATAAATGTCGTGTTTTGTGTCAGGCGCTGGTGTTCAGTGTGAAAATGGAGCTCCAGTCAGATCTGGACATGGAGAAGGTGAGTCTCTGTTCATCTGGACTGTTTTATTTCTGTGTGTTTGTGTGCTGTTTTGTTGATGTGTGTTTTATGTTTGTCAGATGTGTGTTCCTCTCATCCTGCTGGACAAGCTGTCTCTGGCTGAGCTCTATGTTCGTCATCATCCAGATCTG[C/T]AACAGAGACTCGTATCCCTCCTGGACTCCTGGTGCCGGCCAGACTTCAGCACACAGGCACTCATCAGGTCAACACACACACACTCGGCAGTATTTAATAAATCCATCAGTATTTATTCATCCATCTTTTTTTCAATACATGATTTCCCTTACTAGTTATGGTTTTACTGTGGTCTGTTTAATTTTAATTTAATTTTATTTAATTTTTTATTTTTATTAATTCAAAATAGTGTAAAGGTGATGATGATGATTGTTAATAGTGTGCCCTGTTATAACATTAATAAATATAAAATAATAATTAATTAATAATTGTTACCTTAGTTTTATTAACCAATATACCTCATTAATTATTAATAAAACAAATGATTGTCTTTGTATTTACCTCTACTACTAATTTATCACTATTAGTAGTGATGTGCAATGAGTGTTTGGATCAGTGATGCTGATAGTGAGCTGTTATGTGTTTCAGTCAGTTTCCTCAGCTGGTTCTCTCCAAACATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34858
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 |
---|---|---|---|---|---|
ENSDART00000092011 | Nonsense | 591 | 861 | 14 | 19 |
ENSDART00000138041 | Nonsense | 210 | 339 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 10 (position 10901318)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 10977184 |
GRCz11 | 10 | 10935422 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTGCCAGAGGATCTTCGCTCTATTCCCACAGCCCAGAAGCCCAAGAGC[C/T]AAGAGGAGAAAAAGCCCAAAGACAAGAAGCAGTTTAAAAGAAGAGAGGTC
Long Flanking Sequence:
CTCCTCATTCATCAGGAGGTGCTGCTGCTAATATCTATTTAAATTCTGATTAAGCAGAAATATTTAGAGATCATTACCTGATGTTGGAACTTGTGTAGATTCTGTCTACTTTTGACCTTTGTCTCTCCAGCTTCAGCGGTGCTGGTTGGGCAACAAAGGGTGCAGGTCTGTGGAAGTGAGTGAGGGACCTGCTGAGAAGGGCCTAAGTCTGCTAGTACAGCAGGTGTTGGGAAAACCACTCAACAAATCCGAGCAACTGTCCAACTGGGAGCGCCGGCCGCTGCGGACCAGCCAACTCCGCTATGCTGGTAACCCACAATTCATGTTCTAGATGGTGGCATGATATGTTTAATCTTTCTCTCATTGTCTTTCTTTTGTGTATCTTAGCTGCAGATGCATACTGTTTGCTAGACATCTACCTCATCCTCTCTCGAGATCCCAAGGCTTTTGGATTGCCAGAGGATCTTCGCTCTATTCCCACAGCCCAGAAGCCCAAGAGC[C/T]AAGAGGAGAAAAAGCCCAAAGACAAGAAGCAGTTTAAAAGAAGAGAGGTCAGTTTATGGGTCTGTGAGCCTCTGACTGTGCTGTTTATGAGCCTGTAGACCAGAAAATGACTCTGTTGTCATAGTTACTGTCATAAATTTCAATATAAAACTAGCTGATGAGAGCATGTGGAGTTTGTGTAATGCAGAAAATAGAGGGAGTATCATATATAAAATGTATGCAATATTTTTTTCTATTCATTTTATAATTTGACATTTAAAGCTGTTACATATTTTACGTATTCATTCGTTAATTTTTCTTCGGCTTAATCCCTGATTTATCAGGGTTCGCCACAGCGGAATAAACGTAATAAAAAATTATGTTTTATGCAGCAAATGCCCTTCCTTAGTATTGGGAAAATACTTTATGTATAATTTATCACAGGGCTATTTATGCTTTCAGATACATACATAATGATTTTAATAATACAATCTTTTGTTTACATTGCACTGAAAGGCACG
Associated Phenotype:
Not determined