ZMP
apaf1
Ensembl ID:
ZFIN ID:
Description:
Apoptotic protease-activating factor 1 [Source:UniProtKB/Swiss-Prot;Acc:Q9I9H8]
Human Orthologue:
APAF1
Human Description:
apoptotic peptidase activating factor 1 [Source:HGNC Symbol;Acc:576]
Mouse Orthologue:
Apaf1
Mouse Description:
apoptotic peptidase activating factor 1 Gene [Source:MGI Symbol;Acc:MGI:1306796]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16025 | Nonsense | Available for shipment | Available now |
sa14399 | Essential Splice Site | Available for shipment | Available now |
sa10293 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16025
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 |
---|---|---|---|---|---|
ENSDART00000019165 | Nonsense | 129 | 1261 | 4 | 27 |
ENSDART00000113507 | Nonsense | 129 | 464 | 4 | 11 |
ENSDART00000127261 | Nonsense | 130 | 1264 | 4 | 27 |
The following transcripts of ENSDARG00000021239 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 16914489)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 17857329 |
GRCz11 | 4 | 17846305 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGATTCTGAGTGTAGGAGGTGTTCCTCAGAGACCTGTGGTGTTCGTGAGT[C/T]GACCTCCACTGCTCAATCTGATCCGGGAGATGCTGTACCRGCTGCGGGAC
Long Flanking Sequence:
TCTAAGCTGAACTGAAGCAGTTTTAATTCACTAGAACTTCTATATTAAGCTGCTTTGAGACAATCTGCATTGTAAAAGCGCTGTAGAAATCAAGATGAATTGAATTAATTTTTGCAAAGCACTAATAAAAAGTGAATATGTGTGAAATTTTCCCATTTTTGTTTCTCCAGGCCACTAGAAAAGAGCAGGCCGTGGCTCTGCTTGAGACCCTGTTGAGGAAAGACAATCGTGCCTACATTTCCTTCTACAACGCCCTGATCAGGGAGAGTTATGGAGATCTGGCCAGTCTCCTTCACAGTGATTTGCCTCTGCTCAGCCCTGAGGGAGAGAAGAGCTTCGCTGATGGAGTCTCTCCCTCTGGTAAAAGCTCAGTTGTGTTTGAACTTGTTTTTTCAAGTGGCTTTATGTGTGAGGTACTAGAGGTTTTCTTTGCTTTGGTTTCAGTCCAGGCGATTCTGAGTGTAGGAGGTGTTCCTCAGAGACCTGTGGTGTTCGTGAGT[C/T]GACCTCCACTGCTCAATCTGATCCGGGAGATGCTGTACCGGCTGCGGGACACACCGGGCTGGGTAACTGTATTTGGCATGGCTGGCTCAGGGAAGTCTGTGATGGCTGCCGAGGTTGTTCGAGATCGTTCACTCATTAAGGGTAATGATGTGTTGTTTATTTACATTTATCCAAACGTTTAGTACATTTTTTTTTTTTTTAAATAAAGATTTTATTCTATTTGTAATTTGTTTTCGGATTTATTTTAATTGAGGTTTTATTGTGTTCATTTTAGTTTGCGTCATGTATTTATATTATTTTATTTTATATTTGGTTGAAATGTTATTTGTTTTATTGTTAAACTAAGGTTTTATTTCAAAGTGTTTTTATTAGTAATTTTTAGTTTGTTTTTTTTCATTTGTTTATTATAGTCTTTTGTATTTTTAATTTTATTTAATGGTTTTTATTTGTAGCTTTAAGTTTAAGAATTATCTCTGTTTTTGTATTTATATTTTACTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14399
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019165 | Essential Splice Site | 176 | 1261 | 5 | 27 |
ENSDART00000113507 | Essential Splice Site | 176 | 464 | 5 | 11 |
ENSDART00000127261 | Essential Splice Site | 177 | 1264 | 5 | 27 |
The following transcripts of ENSDARG00000021239 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 16915194)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 17858034 |
GRCz11 | 4 | 17847010 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAATGCACAGAGTACAGTGTACGTGAATGTATTTTTGTCTCTRTTCTCC[A/T]GAGTGTTTTCCTGATGGTGTTCACTGGCTGTCTGTGGGTCAGTGTGAGCG
Long Flanking Sequence:
AAAGATTTTATTCTATTTGTAATTTGTTTTCGGATTTATTTTAATTGAGGTTTTATTGTGTTCATTTTAGTTTGCGTCATGTATTTATATTATTTTATTTTATATTTGGTTGAAATGTTATTTGTTTTATTGTTAAACTAAGGTTTTATTTCAAAGTGTTTTTATTAGTAATTTTTAGTTTGTTTTTTTTCATTTGTTTATTATAGTCTTTTGTATTTTTAATTTTATTTAATGGTTTTTATTTGTAGCTTTAAGTTTAAGAATTATCTCTGTTTTTGTATTTATATTTTACTTATTTTAATTTTGTTGTAGTTACGATTTTTTTGGCTTTGTCTGAATTTGCTTTTATAAAAAAACATTGCATTTAAAAAAAAAAAAAAAAGTTTGAGCAAACATTTTTTAATTTTTTTAAGTTTATTTAATTTTATTCTTTAAGACCAAAGGACTAAAAAAATGCACAGAGTACAGTGTACGTGAATGTATTTTTGTCTCTGTTCTCC[A/T]GAGTGTTTTCCTGATGGTGTTCACTGGCTGTCTGTGGGTCAGTGTGAGCGGGCAGACCTGTTGGTTAGGATGCAGTCTCTGTGCTTTCGTTTGGAGCAGTGTCAAAGTTCAGACACCAGTCAGCGGCCACCCAGCACTGTGGAGGAGGCCAAAGAGCGCCTGCGCTTCCTAATGCTCCGCAGATTCCCCAGGTCAGTTCGCTTGGAAGAACATAGTACATCATGGAATAGTGTTTCCTGGTCCAAGCCTTTATTAATTTAAATAAAAAAAAATTAACTATTAATTAAAAGTAGCTGCTACTGGGTCATAACCGCACATTAAAGTGGATCTTACAAAATCATGGTCTACCTACCGTCTGTGGACTTGCTACACCTCAGAGCTTCATATTTTAACTATTCATCAAAGGTGAATCACTACAGTACCTGAGATTAGGTGTGGATGAAAACATACTTTAAGATCATGACGTTCAATAGTAATACAGAATACTCTGAGCTAAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10293
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019165 | Nonsense | 886 | 1261 | 19 | 27 |
ENSDART00000113507 | None | None | 464 | None | 11 |
ENSDART00000127261 | Nonsense | 887 | 1264 | 19 | 27 |
The following transcripts of ENSDARG00000021239 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 16923329)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 17866169 |
GRCz11 | 4 | 17855145 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACTTCGAAAGCAGTAAGAAGAAAGCCGAATGCAGTGGTCATCTGAGCTG[G/A]GTTCACTGTGTGCAGTTTTCACCCGACGGCTCACTCCTGCTGTCCTCCTC
Long Flanking Sequence:
GCGTATTTAAAAACCTATTGCTGTATGCCAATAACTGTTCTAAGGTTTTTGAACATAACCAGTGTTTTATTTTAGATTTTATATATATTTTTTAGATTGAATTAATTTAAATAATTTTATTTTATTCATAAATCATGTATAATTTTTTCTAACGCTGTTACACAGTCCCTCTGGGATTTTGGAAGTCCTGTCCTTCTAAGATTAAAAAAATATTTATATGTAGTTTTGTTCTATTTTACAAACTTTTAGTGCTTTCACAGCAAAATACAATAATTGAAGCTAATAAAGCCATAGGTTTTGAAGAAAGTGATCATAAAATCAGTGATTGATTTTATTGTAGGGAAGCCATGTTTTTGTGTTTTTTGTTTTTTTTGTTAACTCTGGTTGAAGTAATTCTGGCTGGCATAAGTGTGGTGAAGTGCTAAGAAGTGTTGTTTATTTCAGCTGTGGAACTTCGAAAGCAGTAAGAAGAAAGCCGAATGCAGTGGTCATCTGAGCTG[G/A]GTTCACTGTGTGCAGTTTTCACCCGACGGCTCACTCCTGCTGTCCTCCTCTGATGATCAGACTATCAGGGTGAGTTGCTTTTACTCCCGTCTTCCCTGCGTTGTGTCAGTTGCATTACAGCGATCTTTTGAACAGCACTGACCTGTGATCATGAAGTGTTGAATGTTATCCAGTTGTGGGAGACGGACCGGGTTCACACTTCTTCTGCTGTGGCTCTGAAGAGGGACACTGATGTGCTGTTCTCTCACAGTGATGCTACGATCATCGCACCCGATAGCAGTAACAGATTACAGGTACTGGACACAAGGGACCAGTGCAATTAGTTGATGTACTGCCATTTTTACTAGGATTTTTTTGCTCATTTGATCTGTTTATTTTTGTTAAGAAATATTAAAATCGGTTCCTTTTTTTTATTTTTTATTTTTTAATGGTTCAATTATTTTACTGCCGTTCTCACATTTTAAAAGCGAGCATTTTAAATTTAACATTAATTCATATCA
Associated Phenotype:
Not determined