ZMP
zgc:110605
Ensembl ID:
ZFIN ID:
Description:
etoposide induced 2.4 [Source:RefSeq peptide;Acc:NP_001017898]
Human Orthologue:
EI24
Human Description:
etoposide induced 2.4 mRNA [Source:HGNC Symbol;Acc:13276]
Mouse Orthologue:
Ei24
Mouse Description:
etoposide induced 2.4 mRNA Gene [Source:MGI Symbol;Acc:MGI:108090]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34968 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa18995 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa9477 | Nonsense | Available for shipment | Available now |
| sa21796 | Nonsense | Available for shipment | Available now |
| sa31796 | Essential Splice Site | Available for shipment | Available now |
| sa21795 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34968
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 |
|---|---|---|---|---|---|
| ENSDART00000075943 | Nonsense | 26 | 326 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 10 (position 40618186)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 39278135 |
| GRCz11 | 10 | 39199622 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGAACCATCTCCAAACTCGATGCTCGGATTCAGCAGAAGCGAGAGGAG[C/T]AGAGGAGGCGCAGGTCGTCTGGAGCTCTGGCGATGAGACGAGCTCAAAGC
Long Flanking Sequence:
NNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTAAATACATATATATATATATATTATATACCTCATATAATTGTTAGTGTGTATATATACACAAAAGTGAATTCTATTTACATAGAAAGCCTTCGTAAGTTTTAATAATGTCTTCTTTAATATATAAAATTTTTAAGTATTTAGATCACAAGACCAGTCATAAGTGTCAGTTATTGATTTAATATATTATGTTATTATGAGATATATATTTCTGAGAAGCTGAATAATTAGGCTTTTCATTGATTGATGGTTTGTTATGATCCTTTATTCTTATTTCATTTATGGAAATGGGACTCAGTCTTGAGCAGCAGTCTTTCTGTTTTTCCAGGGTATCAAGGACTCGATCCTGGGCATTGGAACCATCTCCAAACTCGATGCTCGGATTCAGCAGAAGCGAGAGGAG[C/T]AGAGGAGGCGCAGGTCGTCTGGAGCTCTGGCGATGAGACGAGCTCAAAGCGAAGAACGAAAACAAGACAGGTGGAACAATAACTGTATTAGCATTCACACTAGCATACTATATCATTCTGATTATTATAAGCACGCAATGCGCTTTAGTCATCTGCTGCTTTAAAGTTCAGTCTGCAGAAACACTTTGGTTGACATTCTCCCTTTGTACGTGTCATCAAAGGGGGAAAGCCCCGCCCATTAGTGACCATCTCTCCCTCATTAGCATAGTATGTTGGTCTTGTTTTTGAATCTGCCACAATGNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAAACAAGACAGGTGGAACAATAACTGTATTAGCATTCACACTAGCATACTATATCATTCTGATTATTATAAGCACGCAATGCGCTTTAGTCATCTGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18995
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 |
|---|---|---|---|---|---|
| ENSDART00000075943 | Nonsense | 45 | 326 | 1 | 9 |
| ENSDART00000075943 | Nonsense | 45 | 326 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 10 (position 40618129)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 39278192 |
| GRCz11 | 10 | 39199679 |
KASP Assay ID:
2260-3596.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCGCAGGTCGTCTGGAGCTCTGGCGATGAGACGAGCTCAAAGCGAAGAA[C/T]GAAAACAAGACAGGTGGAACAATAACTGTATTAGCATTCACACTAGCATA
Long Flanking Sequence:
NNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTAAATACATATATATATATATATTATATACCTCATATAATTGTTAGTGTGTATATATACACAAAAGTGAATTCTATTTACATAGAAAGCCTTCGTAAGTTTTAATAATGTCTTCTTTAATATATAAAATTTTTAAGTATTTAGATCACAAGACCAGTCATAAGTGTCAGTTATTGATTTAATATATTATGTTATTATGAGATATATATTTCTGAGAAGCTGAATAATTAGGCTTTTCATTGATTGATGGTTTGTTATGATCCTTTATTCTTATTTCATTTATGGAAATGGGACTCAGTCTTGAGCAGCAGTCTTTCTGTTTTTCCAGGGTATCAAGGACTCGATCCTGGGCATTGGAACCATCTCCAAACTCGATGCTCGGATTCAGCAGAAGCGAGAGGAGCAGAGGAGGCGCAGGTCGTCTGGAGCTCTGGCGATGAGACGAGCTCAAAGCGAAGAA[C/T]GAAAACAAGACAGGTGGAACAATAACTGTATTAGCATTCACACTAGCATACTATATCATTCTGATTATTATAAGCACGCAATGCGCTTTAGTCATCTGCTGCTTTAAAGTTCAGTCTGCAGAAACACTTTGGTTGACATTCTCCCTTTGTACGTGTCATCAAAGGGGGAAAGCCCCGCCCATTAGTGACCATCTCTCCCTCATTAGCATAGTATGTTGGTCTTGTTTTTGAATCTGCCACAATGNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAAACAAGACAGGTGGAACAATAACTGTATTAGCATTCACACTAGCATACTATATCATTCTGATTATTATAAGCACGCAATGCGCTTTAGTCATCTGCTGCTTTAAAGTTCAGTCTGCAGAAACACTTTGGTTGACATTCTCCCTTTGTACGTGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9477
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 |
|---|---|---|---|---|---|
| ENSDART00000075943 | Nonsense | 45 | 326 | 1 | 9 |
| ENSDART00000075943 | Nonsense | 45 | 326 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 10 (position 40618129)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 39278192 |
| GRCz11 | 10 | 39199679 |
KASP Assay ID:
2260-3596.1 (used for ordering genotyping assays)
KASP Sequence:
GGCGCAGRTCRTCTGGAGCTCTGGCGATGAGACGAGCTCAAAGCGAAGAA[C/T]GAAAACAAGACAGGTGGAACAATAACTGTATTAGCATTCACACTAGCATA
Long Flanking Sequence:
NNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTAAATACATATATATATATATATTATATACCTCATATAATTGTTAGTGTGTATATATACACAAAAGTGAATTCTATTTACATAGAAAGCCTTCGTAAGTTTTAATAATGTCTTCTTTAATATATAAAATTTTTAAGTATTTAGATCACAAGACCAGTCATAAGTGTCAGTTATTGATTTAATATATTATGTTATTATGAGATATATATTTCTGAGAAGCTGAATAATTAGGCTTTTCATTGATTGATGGTTTGTTATGATCCTTTATTCTTATTTCATTTATGGAAATGGGACTCAGTCTTGAGCAGCAGTCTTTCTGTTTTTCCAGGGTATCAAGGACTCGATCCTGGGCATTGGAACCATCTCCAAACTCGATGCTCGGATTCAGCAGAAGCGAGAGGAGCAGAGGAGGCGCAGGTCGTCTGGAGCTCTGGCGATGAGACGAGCTCAAAGCGAAGAA[C/T]GAAAACAAGACAGGTGGAACAATAACTGTATTAGCATTCACACTAGCATACTATATCATTCTGATTATTATAAGCACGCAATGCGCTTTAGTCATCTGCTGCTTTAAAGTTCAGTCTGCAGAAACACTTTGGTTGACATTCTCCCTTTGTACGTGTCATCAAAGGGGGAAAGCCCCGCCCATTAGTGACCATCTCTCCCTCATTAGCATAGTATGTTGGTCTTGTTTTTGAATCTGCCACAATGNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAAACAAGACAGGTGGAACAATAACTGTATTAGCATTCACACTAGCATACTATATCATTCTGATTATTATAAGCACGCAATGCGCTTTAGTCATCTGCTGCTTTAAAGTTCAGTCTGCAGAAACACTTTGGTTGACATTCTCCCTTTGTACGTGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21796
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000075943 | Nonsense | 76 | 326 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 10 (position 40617071)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 39278908 |
| GRCz11 | 10 | 39200395 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTAAAATCCTATTTGTTTGATCTCACAGCTAAGCCTGTTCCTGTTTTA[T/G]CGAGTGTTTATCCCGCTGCTGCAGTCTCTCACTGCTAGAATTATAGGTAA
Long Flanking Sequence:
TTGGTCTTGTTTTTGAATCTGCCACAATGCTGACACACAGGCATTTGTAGCTCCGCCCTCTTTTGAAAAGAGCACAATCTCATTTGAATTTAAAGTCACAGTCACCAAAACAGCACAATTAGGATCAAAGTGGCCTAAAAGCGGCCTTTTCAAAGAGTTTTAAAACATTATTTTTGTGGTATTTTGAGCTGAAACTACACATACACACTCTAGAGACATCATAGACTTGTTTTACATCTTGTAAAATGGTGCATAATAGGTCCCCTTTAATACTTGTGACATTACAGCCTTGATCATTACTTTGTTTTGTTTTTCTTAACAGTGAACCCAAACTAGTAAGTCGAATTTTCCAGTGCTGTGCCTGGAATGGAGGTGTATTTTGGGTATGTTTCTCTGTTTCTCATTGGTCAGCAAAATGTTTGTCTGTTTGTCTGTTTGTGTTCAAGGTTATATTAAAATCCTATTTGTTTGATCTCACAGCTAAGCCTGTTCCTGTTTTA[T/G]CGAGTGTTTATCCCGCTGCTGCAGTCTCTCACTGCTAGAATTATAGGTAAGTGTCACATTAAAGACAGTCCATATGCTCTAGATACAGTTGAAGTCAAAATGCTTCGCCCTCCTGTGTATTTTTTCTTTTTCAAATATCTCCCAAGTTATGATTAACAGAGCAAGGAGTTTTTCATTGTAATTTCTATAATATTTTTTCTCCTGGAGAAAGTCTTATTTGTTTTATTTCGGCTAGAACAAAAGCAGTTTTTAATATTTAAAAGCCATTTTAAGGTCCATATTATTTGCCCCATTAAGGAATATTTTTTTCGGATTGTCTACAAACCATCTTTATACAATGATTTGCCTGATTACCTGCCTTATTAACCTAGTTAAGCCTTTAAATGCCACTTTAAGTTGAATACTAGTATCTTGAAAAATATCTAGTCAATTATTATTCACTTTCATCATGGCAAAGATAAAATAAATCAGTTATTAGAAATGAGTTATTAAAACTATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31796
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000075943 | Essential Splice Site | 92 | 326 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 10 (position 40617023)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 39278956 |
| GRCz11 | 10 | 39200443 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCGAGTGTTTATCCCGCTGCTGCAGTCTCTCACTGCTAGAATTATAGG[T/A]AAGTGTCACATTAAAGACAGTCCATATGCTCTAGATACAGTTGAAGTCAA
Long Flanking Sequence:
AGCTCCGCCCTCTTTTGAAAAGAGCACAATCTCATTTGAATTTAAAGTCACAGTCACCAAAACAGCACAATTAGGATCAAAGTGGCCTAAAAGCGGCCTTTTCAAAGAGTTTTAAAACATTATTTTTGTGGTATTTTGAGCTGAAACTACACATACACACTCTAGAGACATCATAGACTTGTTTTACATCTTGTAAAATGGTGCATAATAGGTCCCCTTTAATACTTGTGACATTACAGCCTTGATCATTACTTTGTTTTGTTTTTCTTAACAGTGAACCCAAACTAGTAAGTCGAATTTTCCAGTGCTGTGCCTGGAATGGAGGTGTATTTTGGGTATGTTTCTCTGTTTCTCATTGGTCAGCAAAATGTTTGTCTGTTTGTCTGTTTGTGTTCAAGGTTATATTAAAATCCTATTTGTTTGATCTCACAGCTAAGCCTGTTCCTGTTTTATCGAGTGTTTATCCCGCTGCTGCAGTCTCTCACTGCTAGAATTATAGG[T/A]AAGTGTCACATTAAAGACAGTCCATATGCTCTAGATACAGTTGAAGTCAAAATGCTTCGCCCTCCTGTGTATTTTTTCTTTTTCAAATATCTCCCAAGTTATGATTAACAGAGCAAGGAGTTTTTCATTGTAATTTCTATAATATTTTTTCTCCTGGAGAAAGTCTTATTTGTTTTATTTCGGCTAGAACAAAAGCAGTTTTTAATATTTAAAAGCCATTTTAAGGTCCATATTATTTGCCCCATTAAGGAATATTTTTTTCGGATTGTCTACAAACCATCTTTATACAATGATTTGCCTGATTACCTGCCTTATTAACCTAGTTAAGCCTTTAAATGCCACTTTAAGTTGAATACTAGTATCTTGAAAAATATCTAGTCAATTATTATTCACTTTCATCATGGCAAAGATAAAATAAATCAGTTATTAGAAATGAGTTATTAAAACTATTATGTTCAGAAATGCCGAGGCAGTGGCGCAGTAGGTAGTGCTGTCGCCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21795
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000075943 | Essential Splice Site | 211 | 326 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 10 (position 40612195)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 39283784 |
| GRCz11 | 10 | 39205271 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTGCTCTACTCGCTTTACTGCTTCGAATATCGCTGGTTTAATCACGG[T/C]AAGTGTGTGGTCAGTCAGGGAGGCATAAAATAAGATTGTTTAAAGCTAAC
Long Flanking Sequence:
CAGGACACCGGCCCTCCAGGAACAAGTTTGGTGACCCCTGCATACAAATACACACACTATGAAATGTATGGAAATTACGATTTTTCAGCAGTTGTAACAAATGATTCATTTCATTATTATAAGTACAGATCAGTTAAGGCCTCCTGATATAAAATGATATGTAAATGTTGGTTTGGTGCTGTTTTGTTGTGCAGGACATTGCTGATCTGGCGTTTGAAGTGTCTGGACGTAAAGCTCAACCTTTTCCCAGCGTCAGTAAGATCATCGCAGACATGCTCTTCAATCTTCTGCTCCAGGCTCTCTTCCTGATTCAGGTGCAAATCTTTACATCTCTATCGTGTATCTCCTTTTTTTTAAACATGCTATTAATGCAAGCCATTTTTTTAGGGATGGATTGTGAGTCTCTTTCCCATCGATGCTATTGGTCAGCTGGTCAGTCTCCTGCACATGTCTCTGCTCTACTCGCTTTACTGCTTCGAATATCGCTGGTTTAATCACGG[T/C]AAGTGTGTGGTCAGTCAGGGAGGCATAAAATAAGATTGTTTAAAGCTAACATTTGATCTCTTGACTGAAGGAATTGAAATGCACCAAAGGCTGTCAAACATCGAGAGGAACTGGCCGTATTATTTTGGCTTCGGTTTGCCCATGGCTCTACTGACCGCTCTGCCCTCTTCATACATCATAAGGTACAATTTCAGACTCTTCTGATCAAGTTATGCTCTGATCAGACACATGTCGATATTTAGTAACTCGATATGTTGTCATAATGAACATGAACAATGTTTATATCATCGGCACTTGATGAATTGTTTATTATTACGATTTTTGGAGTGCTTTTTGAGATTATAATGATTGTATTTCAGCAGTTGTTCATCACAGATGCTTGACTGAATCATCTGTGATTTATTTTCAAACATTCACACTTTCACTTTAATCTAGCCTACAAAGATGAACAGGACGCTTTTCATTTGCGTTTATCTTCAGTGTTTTTTCAAGACGTTTTT
Associated Phenotype:
Not determined