ZMP
agps
Ensembl ID:
ZFIN ID:
Description:
alkyldihydroxyacetonephosphate synthase, peroxisomal [Source:RefSeq peptide;Acc:NP_956407]
Human Orthologue:
AGPS
Human Description:
alkylglycerone phosphate synthase [Source:HGNC Symbol;Acc:327]
Mouse Orthologue:
Agps
Mouse Description:
alkylglycerone phosphate synthase Gene [Source:MGI Symbol;Acc:MGI:2443065]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21415 | Nonsense | Available for shipment | Available now |
| sa13105 | Nonsense | Available for shipment | Available now |
| sa38719 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa34543 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa14227 | Nonsense | Available for shipment | Available now |
| sa41334 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa34542 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21415
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 |
|---|---|---|---|---|---|
| ENSDART00000062850 | Nonsense | 30 | 629 | 1 | 20 |
| ENSDART00000143130 | None | None | 230 | None | 8 |
Genomic Location (Zv9):
Chromosome 9 (position 1629144)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 1637649 |
| GRCz11 | 9 | 1639797 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCACAGGCTGAGGATCATCGCCGGACACTTGCAGAAGCGCACAGAAGAT[C/T]AACACACCAGTCTCTCCGCGCAAAACTGCAGAGCCGAGTCTCCCGGATCC
Long Flanking Sequence:
AGATAGATGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATGAACCTATGACATACAGATAGATCGGAGAATCTATCGGATATGAAAATACAGTACAGTACAGGCAGCTCGACGAAGACAATAATAACAGGGAAACAAAGTATTAGCCCGTTTGCAAACATTGCTCTAATGTCATACTTGAGATGTAAATATATTTTCAGATTTGTGCCAGATTTTGTAGTCTTTCCTCCTCTTCCCTCTTCCAGCCAGTGAGCAGAGAGATGTATCAGAGCGGGCGGGTCTGGAGCTGGAGGCGGGGTGCGCTGCGGTGCATGCCGGGACGCGGTTGCTCATCTCCGCCTTCAGCCTCCATCAGCCGCCGCTGACCTCTGACAGCAAACACGGAAGCAGCATGGCGTCCAACGGCAGCAGCAGCAGCAGCAGATCACAGCACAGGCTGAGGATCATCGCCGGACACTTGCAGAAGCGCACAGAAGAT[C/T]AACACACCAGTCTCTCCGCGCAAAACTGCAGAGCCGAGTCTCCCGGATCCAGCCCGAGCCGCCAGACACCGGTGCCCAGGAGGAGGTGCGTGTGTGCGGGGCTCAGTCCCCGGTGCCGCTCGCCTTAAAAACATGCATTATACACACAAACAAACAGCGCGTTTTATTGGAGTAAAGCGGTTACACTGTATCTCTGTGTGTGAGAGAGTGTGTATGTGTGAGTGTGTGTGTGTTTGAGGTCCAAACAAAGTGTTCATTCATCCTGGAGGAGGGCGCGGTGTCTGTGCACTGATGGACACTCATTTCTGGACATATTTCACAATTCCGATATATCGCGATAATAAACACACAATATCGTGAAAGTCCATAAGTTGTTGTTTATATAGAGTAAATAACTTGAAAACTCTGATAATATAGGCTATGCTGATATATTTCAATGCTATCGCATGCCAGTTCCTCACTTTTTTATTTAGTGGCTAATTTTACGATTAGCTAATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13105
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 |
|---|---|---|---|---|---|
| ENSDART00000062850 | Nonsense | 156 | 629 | 4 | 20 |
| ENSDART00000143130 | None | None | 230 | None | 8 |
Genomic Location (Zv9):
Chromosome 9 (position 1616314)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 1625000 |
| GRCz11 | 9 | 1627153 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAAAGCTGCAGGTCTGCTGGCGTCTCATGATGCGGAGGATCGGGTTTTC[C/T]GAGCTCATGGTAAAACACACACACACACACACACACACACACACACACTT
Long Flanking Sequence:
CACAATGCAAATGTTTAAAAAAAATAGAAGCATTGAATTGCTTAATGACATGATTTTATTCATATAGTATGTACACAGTTTTAAGCCATAAAATCAGCATTTAGTGTGTGTGTGTATGTGTGTGTGTGTTGTCTTTAGGTATCGGTTGAGTGGGTTGATTCTGCCGAGTCTGAAGGACTGGTTTGAAGGGACGTTTGGAGCCAGTTTACAGCATAAATCTCCTGCTACTGTGAGTGTAATGGTGTATGTGTGTGTGTGTGTGTGTGTGTATTTGCATGAGTGAGGTTTCTGTGTGTGTTAGTCTGAAATGGCGGGGATGTGTTTGTCTTATGGTGTGTGTCTGTTTGTTTGATTTGGTCTGTATTTGTAATGTGTATGTGTGTGTGCAGTCGTCTCTGAATGTGAGCGCAGTGTCGCCTCCAAACCTGAATGAAGCATTCTCTGAGGATCTGAAAGCTGCAGGTCTGCTGGCGTCTCATGATGCGGAGGATCGGGTTTTC[C/T]GAGCTCATGGTAAAACACACACACACACACACACACACACACACACACTTACAGTTTCTGTTTCACGCACAGGCTTTTATTCAATTTTGCTTTCATTGTATAAAAGTTTACCAAACTTTCAAGCATGCACAGGGGAATTTTACTATGATTTACCTCATTTTTACAGGTCATGTGATCATTTTAGTTTTGATTTTATTGTTTTAGCTAAAAATTATTTAGTTCAAAGTGTTTAATATGATTTAATAGTAGAATTAAATAAATAATGAAATAGTAAAATAAATAAATAATTAAATAATAAAATAAATAAATAATTAAATAGTAAAATAAATAATTAAATAATTAAATAGTAAAAAAATACATGAATATATAAATAGTAAAAATACATAAATAAATAATAAAATAAATACATAAAAATTAAATTGTAAAATAAATTTATAAATAATTAAATAGTTAAATAAATAAATAATTAATTAAATAGTAAAATATATACATAAATAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38719
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000062850 | Essential Splice Site | 158 | 629 | 4 | 20 |
| ENSDART00000143130 | None | None | 230 | None | 8 |
Genomic Location (Zv9):
Chromosome 9 (position 1616304)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 1624990 |
| GRCz11 | 9 | 1627143 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTCTGCTGGCGTCTCATGATGCGGAGGATCGGGTTTTCCGAGCTCATG[G/T]TAAAACACACACACACACACACACACACACACACACACTTACAGTTTCTG
Long Flanking Sequence:
ATGTTTAAAAAAAATAGAAGCATTGAATTGCTTAATGACATGATTTTATTCATATAGTATGTACACAGTTTTAAGCCATAAAATCAGCATTTAGTGTGTGTGTGTATGTGTGTGTGTGTTGTCTTTAGGTATCGGTTGAGTGGGTTGATTCTGCCGAGTCTGAAGGACTGGTTTGAAGGGACGTTTGGAGCCAGTTTACAGCATAAATCTCCTGCTACTGTGAGTGTAATGGTGTATGTGTGTGTGTGTGTGTGTGTGTATTTGCATGAGTGAGGTTTCTGTGTGTGTTAGTCTGAAATGGCGGGGATGTGTTTGTCTTATGGTGTGTGTCTGTTTGTTTGATTTGGTCTGTATTTGTAATGTGTATGTGTGTGTGCAGTCGTCTCTGAATGTGAGCGCAGTGTCGCCTCCAAACCTGAATGAAGCATTCTCTGAGGATCTGAAAGCTGCAGGTCTGCTGGCGTCTCATGATGCGGAGGATCGGGTTTTCCGAGCTCATG[G/T]TAAAACACACACACACACACACACACACACACACACACTTACAGTTTCTGTTTCACGCACAGGCTTTTATTCAATTTTGCTTTCATTGTATAAAAGTTTACCAAACTTTCAAGCATGCACAGGGGAATTTTACTATGATTTACCTCATTTTTACAGGTCATGTGATCATTTTAGTTTTGATTTTATTGTTTTAGCTAAAAATTATTTAGTTCAAAGTGTTTAATATGATTTAATAGTAGAATTAAATAAATAATGAAATAGTAAAATAAATAAATAATTAAATAATAAAATAAATAAATAATTAAATAGTAAAATAAATAATTAAATAATTAAATAGTAAAAAAATACATGAATATATAAATAGTAAAAATACATAAATAAATAATAAAATAAATACATAAAAATTAAATTGTAAAATAAATTTATAAATAATTAAATAGTTAAATAAATAAATAATTAATTAAATAGTAAAATATATACATAAATAATTAAATAGCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34543
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000062850 | Essential Splice Site | 208 | 629 | 6 | 20 |
| ENSDART00000143130 | None | None | 230 | None | 8 |
Genomic Location (Zv9):
Chromosome 9 (position 1612183)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 1620869 |
| GRCz11 | 9 | 1623027 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGTGGATCTTGCCTGCAAACACAACGTCTGCTTGATTCCCTACGGAGG[C/A]AAGTAAAGCATCAGCAAATGATGCAATCATCAGCTTTAGATGTAATTGAC
Long Flanking Sequence:
ATTGTTGAATTCATTTAGCTGATTCTTTGTTCTGGAAAAAAGCTTTATTGTTTTTAATGAAATGCTAATGGTCTAATTAATTTCCATTCATTATGCTAAGCTAAGCTAAAAGTGACCTCACCAGAACAAGAAATTAGCAAAATGGATTTAAAAATGGTTTCAAAATATGTGGGGAAAAAAATGTTGATTTCATAAGAGGGTATATTACAAGTGTGTAGTATGATAGTTACTTTATTTGGAACAATATTCCATCACTTTTGCTGTCGTGACTTGATTTTTGATTTAGCTTTAGTGAACATAGAAATTTCTTTCAAAAACATTAAAGAAAATCTTTGGTATATGAGTTGTGCTGTTGTGATAGATCTACAAGGGCTATAAATAAGCGTGTTGTAACCAGTATTGTTTTTATTTTATTATTATTATTCAGGCTGTCACAGTGATGTGGAGAAGATTGTGGATCTTGCCTGCAAACACAACGTCTGCTTGATTCCCTACGGAGG[C/A]AAGTAAAGCATCAGCAAATGATGCAATCATCAGCTTTAGATGTAATTGACAATCAAAACAGCATCACACATCGTCTTAAAGCAGTCTGCTGCCTGTTCACAGTTTGAATGAACAAACGGCATAATTTCCCTACATTTTACACAAAATAATTAGCATTTTTAACATGAATGAATGAGTGAAACAAAAACATAGGCTATATTAATTTATTGTTAAAGAAATAAACTGCTTTAAGACCTGGTCTCCCAAAAATATTGATCACAACTTTTTTTGCACCTTGATGATGATCATAAATGCATACATTTGTTATATTATTTTTGAAATGTTTAATATTGGAGACTGAAGCAATGATGCTGATAATAAATTACATTTAATAATCTGTTTTATCATTTTATTTTGCAATAATATACAGCAAATTGCACCAGGAAAGTTGTTATCACTTATTATTAACCTTAAATATCGTATCTATCAATGAAATTTTCCTGCCGTGAAACTAGCCTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14227
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 |
|---|---|---|---|---|---|
| ENSDART00000062850 | Nonsense | 396 | 629 | 12 | 20 |
| ENSDART00000143130 | None | None | 230 | None | 8 |
Genomic Location (Zv9):
Chromosome 9 (position 1598918)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 1607604 |
| GRCz11 | 9 | 1609892 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTGTTTCAGAGATGTGCTCCAGCATCTATTCGGCTAATGGACAACGAG[C/T]AGTTTCAGTTCGGTGAGTTWAWTGTTATCTTCAGATCTRCAAAAGATCTC
Long Flanking Sequence:
GTCTCTTCAAACTCGTATGCTAACTGTGTGTGTTTCTCCTCAGGAACTCTGGGAGTGGTGACTGAGGTCACGATGAAGATCCGACCCATTCCTGAGTACCAGAAGTACGGCTCGGTGGTGTTCCCCAACTTCCAGCAGGGTGTGGCGTGTCTGAGAGAGGTGGCCCGACAGGTCAGCACTACACACACACACACACACTAGTGATATTCAAATTAAGTAACTGACTCTGCTGTTCAGGTTCCGCTCTGCTCCTCTATCTGTTCATCTCAACTCGCTCTTGCTTTAAAAATAAAGTAAAACAGGCTTAAATTTGCCGTACTGTAGGCAATAATAAATTGTAGCTGAGCAATAACAGTGTTGTAGATTTGTTTAGACGTGCAGGAGATCATCATAACAAATGTCTGTGTATTAACCTGTTTCTGTCTGAGCAAGTTGATTTGATTATTATTCTTTTGTTTCAGAGATGTGCTCCAGCATCTATTCGGCTAATGGACAACGAG[C/T]AGTTTCAGTTCGGTGAGTTTAATGTTATCTTCAGATCTACAAAAGATCTCAGTAAGGTTAAAATAGTTTTGCAAAGTTTATATTTTAATTTTTAAAATCTGCTGCACATTTCTGTTTCGTTTTTAGGTTGTTTCATTACGTTTTTTTCAGTTTAGTTTTTATTTTGTGAACAGATCTGCATGTCGTGTTTATATTTCGATTTTAGTTTTGATAATTCTAGTTTAATAAAAAGCACATGTAGTGTCGAGCAGAGCAAAGTTTTGTGTTTGCACATCAAGTCTCGTGCAAAGCGCTTATATAAAAAAATGATCGTTTGAAGAAACACTGAATATAAAACCATGCAAAGCAACTTAAACGAATGAAAGTAGAAATGATGAAGAATTCAGACAGTTTTTATTTTAACGATCGTGTTGTTGAAGGTGTTCAGCGTGTAGTTTGCATTTATTGGGGCAAATAAAGAAAAGTTAAAAGCGTATATAGCAAAGATGTGCCTTTATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41334
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000062850 | Nonsense | 476 | 629 | 15 | 20 |
| ENSDART00000143130 | Nonsense | 77 | 230 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 9 (position 1590557)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 1599610 |
| GRCz11 | 9 | 1601898 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTGTGTAGGGGTCTGGCAGCAGGAGAGGACAACGGTCAGAGGGGCTA[C/A]ATGCTGACGTTTGTGATCGCCTATCTGCGGGTGTGTCACACCACCAACAC
Long Flanking Sequence:
TGTCTGTGTGACTTGAGTGTGTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGTGTGTGTATGAGTGTGTGAGTGTGTGTGAGAATGCTTGGGTTTTGTGTGCATTTGTGTGTCTGTGTGAATGTTTGTGTGTGTGTCTGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGGTTGTCTGGGAGTGTGTGGGAATGGGGTTATGTATGTTTGTGTGTGTGGGATCTGTGTATCTGTCTTTCTCTTACACACACACACACACACACACACACTCAGACACACACAAACATTCACACCGACACACAAATGCACACAAAACCCAAGCATTCTCACACACACTCAACACACAAACAAAAACACAAATACATGCAAACACACACACACACACACACACACGTTAGGCTTGTGACTTTTCTAGAGAGTTTGTTGTGTGTGTGTGTAGGGGTCTGGCAGCAGGAGAGGACAACGGTCAGAGGGGCTA[C/A]ATGCTGACGTTTGTGATCGCCTATCTGCGGGTGTGTCACACCACCAACACTCCTTCATTTACACCTAATAGATTTTAAAAAGCCACTTTGAAATAAATCATTGTTTATATCTCACCTTAAATGTGTGTTTAATGTTTTAATACACACTAATATGTTATATAGCACACACACATATATATATATATATATATATATATATATATATATACATACATACATACAGTTGAAGTCAGAATTATTCACCCCCTTGTTTATTTTTTCCCCAATTTCTGTTTAGCAGTGAGCAGATATATTTCAACACACTTCTAATCATAATAGTTTTAATAACTCTTCTCTAATCACTCATTTATTTTCTCTTTCTTATGATGACAGTAAATAATATTAGACTAGATATTCTTCAAGACACTTCTATACAGCTTAAAGTGACATTTGAAGGCTTCACTAGGTTAATTAGGTTAACTAGGCAGGTTAGGGTAATTAGGCAAGTCATTGTATAATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34542
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000062850 | Essential Splice Site | 507 | 629 | 17 | 20 |
| ENSDART00000143130 | Essential Splice Site | 108 | 230 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 9 (position 1587873)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 1596926 |
| GRCz11 | 9 | 1599214 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTGCACTTTATTTAGTATTCATCTTTTTTATTTATTCTCTCTCGTTCA[G/T]GGTGTTGGATTTGTGTCGAAATGTAAAGGAGAGGATAATAAGAGAGTGTA
Long Flanking Sequence:
AAAATGATGCTTAAAAATTATTTATTAAAAAACTATAAGTCTGATAAACCTTAAAGATATAGCAACAAAATCTAACGCATCTAAATACAGCTTTTGGCCAAATTTGGGGCTTGTATAATTTTTTTATATGCTCGGATTAAAAAAATTTAATATGTAACATTTTTTTATTAAAAAAATGATAAGTCTTACAGGCATGAGGAGATATAGCAACAATCTTGAATGTAGAAAGCACATTTTGACCACATTTGGGCCTTGTGGCATTAACGGCCTAGGAGGAGATACGTTTGTTTTCAAGGACAGAGTAGTATAACAGTATGTTTTCTTTCTCAAGCCAACATAATGATTCAAAATAAAGTGTCATTTAAGCATTGTACTTCATTACACACTGATCATTACATTATTTTACAGTAATAGTCAGAAGTGAGTTTATGTCATTATTTGTCCAGTATTGTCTGCACTTTATTTAGTATTCATCTTTTTTATTTATTCTCTCTCGTTCA[G/T]GGTGTTGGATTTGTGTCGAAATGTAAAGGAGAGGATAATAAGAGAGTGTAAAGAGAGAGGAGTGCAGTTCCCACCGCTGTCCACATGCAGGTACACACACACACACACACAGACTTCTCAGCCATTCATTTCCTGTCTTCCAGCTGTGCAGGACATGATTGATGGGAAGGTTTAACCTCTGCAGGGGCAGATAACACACACTTAAACTTTCTCCAGCTCAAAGTCAAGGAAAGAGCAGGACGGAAAGTGTGCCCATGTCTCTGTTACTGCCCTTCTGGCTTCATAAAACCACACAACGCAGCCACTTATCTGATGTATCAGTATGACATTAAGACCATGTCCACAGTCAGAATTATTGGCCCCCCTCTGTATTCTCCTCCAATTTCGGTTTAATGGAGAGAAGGTTGTTTTTAAGCCGTCTCTAAGCATATTAGTTTTAGGGTGCTTTCACACAATTGCCTGGACCGTACCCAAGTTAGATCGGTCATTCTGCTTTTACT
Associated Phenotype:
Not determined