ZMP
zgc:152891
Ensembl ID:
ZFIN ID:
Description:
12-lipoxygenase [Source:RefSeq peptide;Acc:NP_001070178]
Human Orthologues:
ALOX12B, ALOX15B, ALOXE3
Human Descriptions:
arachidonate 12-lipoxygenase, 12R type [Source:HGNC Symbol;Acc:430]
arachidonate 15-lipoxygenase, type B [Source:HGNC Symbol;Acc:434]
arachidonate lipoxygenase 3 [Source:HGNC Symbol;Acc:13743]
arachidonate 15-lipoxygenase, type B [Source:HGNC Symbol;Acc:434]
arachidonate lipoxygenase 3 [Source:HGNC Symbol;Acc:13743]
Mouse Orthologues:
Alox12b, Alox8, Aloxe3
Mouse Descriptions:
arachidonate 12-lipoxygenase, 12R type Gene [Source:MGI Symbol;Acc:MGI:1274782]
arachidonate 8-lipoxygenase Gene [Source:MGI Symbol;Acc:MGI:1098228]
arachidonate lipoxygenase 3 Gene [Source:MGI Symbol;Acc:MGI:1345140]
arachidonate 8-lipoxygenase Gene [Source:MGI Symbol;Acc:MGI:1098228]
arachidonate lipoxygenase 3 Gene [Source:MGI Symbol;Acc:MGI:1345140]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16077 | Nonsense | Available for shipment | Available now |
sa37349 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16077
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 |
---|---|---|---|---|---|
ENSDART00000011572 | Nonsense | 319 | 663 | 8 | 15 |
ENSDART00000123166 | Nonsense | 319 | 663 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 29967472)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 31167723 |
GRCz11 | 21 | 31204418 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGTCTGCTGCATTACAACCAAGATGRAGAACTAAAAYCTATTGCTATA[C/T]AAGTAAGCACAGTWTCAATCAGAACAAAAATTTCATTWGACWGAATTTTA
Long Flanking Sequence:
AGATTTTTGGGTTGATGAACAAATGAACAGGTGTACCTAATAAAGTGGCCTTTGAGTGTAAATATATTAAATACAGATTTAAAAACTTCACAAACAATTTGTCTCACAGAATATGTTCAGGCTCACTGGCAGGAGGACGCATTTTTTGGATATCAGTGCCTCAATGGCTGCAATCCTCTGTGTGTCAGACAGATCCACCATCTGCCACCTAACTTTTCGGTCACTTCAGAAATGCTGAAATCTTTTCTGCCAGAGGGCTCATCGCTGGATCAAGAGATGGAGGTGGGCTTGTGTGGATTTATGTTTTGGATTTATCATTTTGTAACATGCTAGTCAATATTTGTAACTATTTTGCACAGAAAGGACGTGTGTATCTTCTGGATTATGAAGTGCTGGATCAGCTGCCTGCTAACACCGTCAATGGCAAACAGACTTATTTGTCTGCTCCTTTGTGTCTGCTGCATTACAACCAAGATGAAGAACTAAAACCTATTGCTATA[C/T]AAGTAAGCACAGTTTCAATCAGAACAAAAATTTCATTTGACTGAATTTTAATGGCTACGTGAAAAGTGATAATCCTAATATTTCAGCTTCAGCAGGTTCCTGGTCCACAGAATCCTATTTTCTTGCCGTCTGATGCCCCACCAGACTGGTTGTTAGCAAAGATGTGGGTCCGTAATTCAGATTTTCAGATTCATCAGCTACTTTCGCATTTCTTTCGGACTCATCTTTTAGGAGAAGTGTGCTGTACGGCCACGCTCAGGCAGCTGCCAGAGATTCATCCTCTATTTCAGGTAGCTTATTTTTAATGCTGTGTTAAAATGTGTTTTCCACAAACTCAAGGTCAGGAAAACACTAGAATAAAAAGCGCTAGCACTCCAGTTTAAGTACCAATTCCCACTGTTAGAGGTGCAATTGGAAATCTTGAAAAATGCTAACGTTAGCCTGATAGCGCTGAATTACCACCCTGAAAAATGCCTCCTAAAAACATGAATGTGCACTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37349
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 |
---|---|---|---|---|---|
ENSDART00000011572 | Nonsense | 459 | 663 | 11 | 15 |
ENSDART00000123166 | Nonsense | 459 | 663 | 10 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 29965741)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 31165992 |
GRCz11 | 21 | 31202687 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCCAGATGATGTGAAAGAGCGAGGCCTGGATGCTCTGCCGGTCTGTTA[T/G]TATGCTCAAGATGCTCTCAGAGTCTGGGATGCTTTACACAGGTACTTGAT
Long Flanking Sequence:
TAATATGTTCTTTGAACTAACTATACAGAAGATTAAAGATGGTATGGTGTCTTGTACTTATTACCTTGCAGTGTTTGCACGTAGTATTTGTACATCTTGGGTCTGCACTTAATTTTATACGATGACGATAAAGATTTTATTCTATTTTTAAATTCCTAAAGATTATAAACAAATTAATCTTTTTGCTTGTTTGTTTCAGCTCTTAATGCCTCATATCCGCAGCACTCTTCAGATTAACATTCAGGCTAGAGCGACACTTCTAGCTGCAAATGGTGTTTTTGACAAGGTTGGCGAGTTTATTCTTCTCTGTATGCTCCATGAAAGAAAATCATTTACATTTAATTCCATATTCTTTCTCTTTGTTGTCTCTAGTCAGTGGCCTGCGGTCTGGAGGCAATACCACAGCTTTTTACTCGAGCGACCCAGCGTCTCCGCTACAGCTCTCTGTGTGTGCCAGATGATGTGAAAGAGCGAGGCCTGGATGCTCTGCCGGTCTGTTA[T/G]TATGCTCAAGATGCTCTCAGAGTCTGGGATGCTTTACACAGGTACTTGATTCACAATATATGAGTCGGCATCTTAAGGTTTGAAGTGGTCACATGATCTTTGCTGTTTAGGTTTGTTGCAGGCTGGACTCGCTTGTATTACTGCAGCGATGAAGACGTCCAGAGTGACTGTGAGCTGCAGAACTGGATTGGAGAGATCTTCAGGGAGGGTTTCCTCGGCCTCACTCACTTAGGTGCACGGAAAGATCTATCGCACATTTTGTACCCATGTATAGGTGACATTTATTTGTACTGCCTATTTCTTACATACAGCGTCCTGTTAACAATAATACATTTTAGTTTTATAACAGCATTTTAGAACCAAACAACCCAGATTTACACTGGCGTTTCACCTAGCGTTTCTGAAATGCTCTCCATCCAAACTATACAGCTGAAAACCTACATCACGTGACCACACATACTCTCTGGCATGCACTGCACTGTATGCGGAGGTCTGAGCTC
Associated Phenotype:
Not determined