ZMP
zgc:158614
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC791218 [Source:RefSeq peptide;Acc:NP_001074169]
Human Orthologue:
AIFM3
Human Description:
apoptosis-inducing factor, mitochondrion-associated, 3 [Source:HGNC Symbol;Acc:26398]
Mouse Orthologue:
Aifm3
Mouse Description:
apoptosis-inducing factor, mitochondrion-associated 3 Gene [Source:MGI Symbol;Acc:MGI:1919418]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39048 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa18535 | Essential Splice Site | Available for shipment | Available now |
| sa22650 | Splice Site, Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39048
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000125485 | Essential Splice Site | 49 | 456 | 3 | 18 |
| ENSDART00000125955 | Essential Splice Site | 60 | 530 | 2 | 18 |
Genomic Location (Zv9):
Chromosome 15 (position 24771104)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 25504746 |
| GRCz11 | 15 | 25440011 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGCTGTCGGTGGTCTTTGCTCTCATTATGGTGCTCCACTTATCAAAGG[T/C]AGGGTGTAGTCTTATTAATCACACAAGCTGTCACAAGCTGAACAGAAAAA
Long Flanking Sequence:
AGGGACTTTTATTTTACATATTTTATTACAGGATTCTTGTAATTAACTGTAGGCTACTATACTCTAACTGTTAAGCAGATAAGAAACGTTATATTGATTTATTGGTAATTCACAAAAATCATAAAAAAGTCATAGAAAAAAATAAATAATTTAATTTAAAGAAATTAATTACATTTATCCTAAATTTACTCACTTTTTATCAGTTGAACAAATGCAAGTCAATGACAATCAACACTGAGAAATAATAATAATAATAATAATAATAATTTTCCAACTTTATATAAACTTTTAAAGAATGAACAGGCTATTTCTATTTTAAAAGTTCCATCAATATCATTAAAAATATCTCCTTTTTAATCAGCTCAATGTTACATGTGTTCATCTCACAGAATGAAGGAGGTTCTGGTGGATGAGAATAAAATCCTGTTGGTGCGCAATAATGGAGAATTTACTGCTGTCGGTGGTCTTTGCTCTCATTATGGTGCTCCACTTATCAAAGG[T/C]AGGGTGTAGTCTTATTAATCACACAAGCTGTCACAAGCTGAACAGAAAAATAACCCTGCTTACTTAGGACTTTAACGTACAGAGAAAACAGGTTTTTCATTCACCTTTTACCTGTGGGATTATTAATGAGCTATCAGGTTGCTTTGCCTTTTTTCTTTCTCACTTTGCTTTTTTTACAAGTTGGAATTGAGTATGAGTGAATGACATTGTGTATTTAACAATCATAAAAGCAGTGTTATGATTGTAGGTACATTGATTGGAGACCGAGTTCGGTGCCCATTTCATGGAGCGTGTTTCAATACTAAAACTGGAGATATTGAAGAGTTTCCTGGCCTGGATTGTCTGCCTAAATTTAAAGTACGTTTGGTGATCATGGATTAAAAGTTATAGTCGACCCAGAAATTAAAGTTCACTGTTAATAACCCACCCTTTAACCATGTGAGATGTTGGTGATTTTTTTTCTGTCATGCAGGTGTGGATTTAACCAAAGCAAAATAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18535
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 |
|---|---|---|---|---|---|
| ENSDART00000125485 | Essential Splice Site | 266 | 456 | None | 18 |
| ENSDART00000125955 | Essential Splice Site | 340 | 530 | None | 18 |
Genomic Location (Zv9):
Chromosome 15 (position 24776403)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 25510045 |
| GRCz11 | 15 | 25445310 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTCTACACAAGTAATGGTGTGGCTGAAATTCGAGGTGAAAATGGAAAGG[T/C]ACTGCAAGAAGAAACATTATTTTTAAATGATCATAGAKCTGAAGTCAGTG
Long Flanking Sequence:
TGAACGTTGTACTTTTTTTCTTTTAGAGCCAGACCACTGGAGTGTCCTGGTGCTGAGCTAGAAAACGTGAAACTGCTGCAGACCTATGAGGATGCCTCAGAAATCCATCGAATAAGTGCAGGCAAAAAGGCTGTCATTGTTGGAACTTCGTTTATAGGTATACCAGATGAAAAAGATCGTTCTTTCGTGACAGTAATAGCATTACTGTTAATTCTGATTTTATATTGTCTATAAGGAATGGAGGTTGCAGCTTATCTCTCTGACAAGGCTGCCAGTGTCACTGTTATAGGAACCAGTAAGTTTCCTTTCCAGGCATCACTGGGATCAGACATTGGAAAAATGACGATGCAGGTCAGAAAGCATTGGTGTATTTGCCTAGTTTTCAGCTTTCTGTTATTAATTGCAAGATATTTGTCTTCTGTTAAAGATGCTGGAGGAGAAAAATGTGAAGTTCTACACAAGTAATGGTGTGGCTGAAATTCGAGGTGAAAATGGAAAGG[T/C]ACTGCAAGAAGAAACATTATTTTTAAATGATCATAGAGCTGAAGTCAGTGCGTTGTAAACTCACGAACACTATTGTTTAGGTCAAGGAAGTTGTTCTAAAAAATGGTGAAGTCCTTCCAGCGGATATTATAATTGCGGGCATTGGTGTGTACAAAAACAACTTTTTTTATTTCCAGTTTTGTTGTTGTCACTTAAACCAAAACTTTCATCCATTTATTGTTTACAAAGATGTCATTCACAACTCTGATCTCCTTAATATATTGTTTTCAAAGGTGTCATTCCCAACTCTGATTTTCTTAAGGAGACATTGGTGGAAATTGATTCACACAAAGCTGTTGTTGTTGACAAGGTAAAAGCCGTCACATCAAACAGAGTGAACTCAAACGAACTGAACAGTTTTTTTAATGACATCTTTGTTTTTCAGTTCATGAAAACCAACATTCCTGATGTCTTTGCTGCTGGAGATGTGGTGTCTTTTCCACTTACTTTGGTCGGACATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22650
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:
A > T
Consequence:
Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000125485 | Splice Site, Nonsense | 411 | 456 | 16 | 18 |
| ENSDART00000125955 | Splice Site, Nonsense | 485 | 530 | 16 | 18 |
Genomic Location (Zv9):
Chromosome 15 (position 24778085)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 25511727 |
| GRCz11 | 15 | 25446992 |
KASP Assay ID:
2260-8536.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTTTTCAAAGGAAGTACGGAGGAAAGAAAATTCTTGGCATTTTATATT[A/T]AGTAAGCTAATAGTTCAACAAGAAATCACTTGACTTTTCATATGTGCACC
Long Flanking Sequence:
TTTCAGTTCTTTGCTAAATTTTACGATTGTGTTTTACTCCCTGACCCAATGATAGCAGTTTTTTGTTGATCAGAATTTCTAGAGACTCTCAACTAAAGTGTACTGTTACCTGTTCAGTATGACATGATCACTAAAAAAGTTATACTTTGTTTCTGGAGGAAAAATGTTAGACCTCTTTTTTTTCTGATTGGCTTATTGTACTTGCCTCCACTTTACATTTGGAAAGAATTAGTAATATTTGAATTTGGATATTTGTAAGTTTTTTCTCTCTCTTTTTACATCCAATGCTGTGCCTTTTTGTAGGTCATATATGTCTTGTATGTTGCCACTTTCCCTTGTTTTTATGCTTTATTTTACATTTTGCACAGATTATTGTTTCATGCAAAAACTATAATAAAAAATATACACATTTTTTTTACCTTTTAGGCTATGGAGAAGGATACACTGAGATTGTTTTCAAAGGAAGTACGGAGGAAAGAAAATTCTTGGCATTTTATATT[A/T]AGTAAGCTAATAGTTCAACAAGAAATCACTTGACTTTTCATATGTGCACCCTAGGGTCCCTTTTTAGTGCGCATGTTGTGAGCAAATTTAGTCACCAGAATAGTATGTGCATAAGATTACACACCACCTACATTTTGCACATGGGTTTGAATTGTTTTTGCACTACTTAATCTGTCCAAAAGGTGTCAACACTGAATCAGGCTGCAGTTTAAAGGGATAGGTCACCCATAAATAAATATTCAGTCATCATTACTCATCTGCCACTAGTTCTTTTGTCAAATACAAAGATATTCTGAAGAATGTTAGAAAAAAACAGCCATTAATTTCCATAATATTTTTAGTTCCTTCTGTGGATGTCAATGGCTGCTTTTTATATGCAACATTCTTTAGAATATCTTCTTTTATGTTTAACTGAAGAAAGTTTCATCATATACAATTGAAGAGTATGCAAATATTTAGATGATTTAAGTACAATACAATTTGTAAAGTAATATTTTTAT
Associated Phenotype:
Not determined