ZMP
atf2l
Ensembl ID:
ZFIN ID:
Human Orthologue:
ATF2
Human Description:
activating transcription factor 2 [Source:HGNC Symbol;Acc:784]
Mouse Orthologue:
Atf2
Mouse Description:
activating transcription factor 2 Gene [Source:MGI Symbol;Acc:MGI:109349]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41336 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa27322 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41336
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 |
|---|---|---|---|---|---|
| ENSDART00000062292 | Essential Splice Site | 32 | 504 | 1 | 11 |
| ENSDART00000135180 | Essential Splice Site | 16 | 130 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 2340041)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 2348183 |
| GRCz11 | 9 | 2344947 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATGAGTGATGATAAACCGTTCCTCTGCACTGCTCCTGGCTGCGGACAG[G/A]CATGTGATCTCTCTTAAAGCTCTAACACACATTTAAAGCTGCAGGGTCAC
Long Flanking Sequence:
TTTGTGCAACTATGTTAACTTTTGAAAATGTGAAAAAAGGGCATTTTTAAGTTGCTAAAAATTGTCTTTTTTTTGTTGCTATTAGAGCATTTAGCAATACAAAGAAATATAATTATTTAAACTTCTGTTCACCTCTATAAAAATTTACGCAACTATGTTGACTTCTGGGAACAATGGAAATGTAAAAAAATTCTAATAATTAAACTAATAAAAATTATGTCATGTATTTTTTTTAATCGCTATTGGAGTTTTTTAGGATACAATTTAGGAATACAATATAATTATTTTATCTTCTGTTCAACACTATCAAAGTTTTTAACCAACTAAGGTGACTTTTGGGAACACCAGAATTGTGGGAAAAATGTCAATGTTTAAACATTCTTGAATAAAAACTGACTAATTTGTTTGACTTTTCTCCTCATGTTCTCAGGTGGCAGACTGAAGCTGTGAATATGAGTGATGATAAACCGTTCCTCTGCACTGCTCCTGGCTGCGGACAG[G/A]CATGTGATCTCTCTTAAAGCTCTAACACACATTTAAAGCTGCAGGGTCACATTTCTGTTTGGGGCGGTTTGCACCAAGTTTGTTAGTTTTGCAATTTTTAATTGTTTTTTATTTTGAAATATGCTATACATTTCAGTTTGTTTAATTAATGGAGTTTTAATTTTTATTTTGTGATCAGATTGCTATTTTGTTATTCATGTTGAACAGAACACGTCATCATCAGAACAGCGTCAACCAGAGCAAAGTTTAGCATTAAGATGAACTCTTGTTCAAACCTCTTAAAAGTCATAAAATAAAATAATACGTAGTTTTAACAGACACTGAACCCAAAACTACACAAATTCAACTTAAATGAATAAAAGTAGAAATGATAAAGAAATCAGACAAACTTCCTCATATCAAAGATCATGTGTGTAGTTAAACATGTTAGGAAGTGGTTATAAAATATTTAGAAAATTAAGGAATGTGTTTATTTGGCCAGCGCGGTGGCACAGTGGGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27322
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 |
|---|---|---|---|---|---|
| ENSDART00000062292 | Essential Splice Site | 329 | 504 | 8 | 11 |
| ENSDART00000135180 | None | None | 130 | None | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 2359696)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 2380820 |
KASP Assay ID:
2260-1381.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACGCCCAAAATCACTGCAGCAGCCTGCAACATCTACTACTGAAATACCC[G/A]TATGTAGACTGCAGAAATTATTTTCATACCATAGAGCAGGGGTGGGCAAT
Long Flanking Sequence:
CTCTGGAGAAATTCTTATTTCTTTTAGTTGTAACAGTTTCTATTCTCCTGGAGAAAGTATCTTGTTGAACTGCTATAGTGAACTGATGACCTTCACAGCCAATCACAGTCCTTTCTGTTGAACAGTGCTCAATTGTTAGCAGGAAATGGACTTTAGTGCCGATTTCAGTGCTGATTTTAGTGCCAATTGGCACCAAACTCAATACTTTTGACAACACTAGTTGGTAGCATGTTGTCAACATGTTCCTAGTATGAATTAGCATTGTTCTCTTGACGTGTTGATATTTGTGTGAGGGTGTCTAAAACGCTATGTTTTGTGTCTCTGACCTGCAGAAGCTGAAGGCAGCGCTCAGTCAGCAGATCCCTCAGGTAACCAATGGCGACGCAATAGACATCCAAAGCAGCTCCGCCAGTGAAACTCCTCCTCCAGCCCCGCCTCCAGCTGAAGAGCAACGCCCAAAATCACTGCAGCAGCCTGCAACATCTACTACTGAAATACCC[G/A]TATGTAGACTGCAGAAATTATTTTCATACCATAGAGCAGGGGTGGGCAATCTCGGTCCTGGAGGGCCGGTGTCTTGCACAGTTTAGCTCCAACCCTATTCAAACAGACCTCCCTATAGAGTTCAAGTGATCTTGAAGACACTGATTAGTTTGTTCAGGTGTGTTTGACTAGTGTTGGAACAAAACTCTGCAGGGACAGCGGCCCTCGAGGATCAAGTTTGCCCATCCCTGCCATAGAGTGTTGTCATGTTTCTTGATCAAATATCTACAAAGACAAGTAAAAAAAGCTAGTCAAAATTAAGTATTTATTGCTTATGTTATGTTACATTATTATGCTGATGTTATGTGTACATTTATAATCTTATTCTTTGAATTATATATCATAAATGGGAACTATTTTATGATACATGTTTATATATACCCCATTTTACAAGATGTAAAATTAGTCTCTGCTATCCCTAGAGTGAGTTTCAGCTCAAGATACCCCACAAATAATGTTCT
Associated Phenotype:
Not determined