ZMP
si:dkey-194n13.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate arachidonate 5-lipoxygenase (ALOX5) [Source:UniProtKB/TrEMBL;Acc
Human Orthologue:
ALOX5
Human Description:
arachidonate 5-lipoxygenase [Source:HGNC Symbol;Acc:435]
Mouse Orthologue:
Alox5
Mouse Description:
arachidonate 5-lipoxygenase Gene [Source:MGI Symbol;Acc:MGI:87999]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22263 | Nonsense | Available for shipment | Available now |
sa12277 | Essential Splice Site | Available for shipment | Available now |
sa1464 | Nonsense | Available for shipment | Available now |
sa17538 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22263
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079884 | Nonsense | 53 | 674 | 2 | 14 |
The following transcripts of ENSDARG00000057273 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 18216870)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 18036905 |
GRCz11 | 13 | 18167897 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAAAATTGAATTTTAAAAGCATTTGGCATTTTGTGATTCAAGGTGGACT[C/A]ATATGACATCAGCGTAGGAGAGGATCTTGGTGAAATTCAGCTGGTTAAAA
Long Flanking Sequence:
CACTCGAGCAAACTTACAAAATAAAATTCACAATTAAGACATATTATTATATAATTAAGACATATATCATGATATACATTTTTGCCATATCGTCCAGCCCTAGTCCTTACCAAGCCAGCCGATGTTTCAGTGCAGAGTTTACATGTTCTCCCTGTGCTCACCGTCCAAAAACATACAACTTAAGTTAATGAACTAATCCAAATCGGCACCATAGACATGCTCCTAAGTAGTTATCTCTTAAGAGCAATCACTATCTGTTCATTAGCTACTACAGCTGGGGAGTTCTTGAGATTTACCTGAGCTCAAACTCCCCTCTCGCCTTGCAAACGGGAGCGAGCCCCGGGCTCAGGGATCTTATGAGCTTGGGGCTCTCTCCTGGGACAGCATGCCAAACAAGCTTTATAATCAATCATCAGCTAAGTTCCGCATTTTGTTCTCAAACCTTATTGTGTAAAATTGAATTTTAAAAGCATTTGGCATTTTGTGATTCAAGGTGGACT[C/A]ATATGACATCAGCGTAGGAGAGGATCTTGGTGAAATTCAGCTGGTTAAAATTGAAAAGAAGAAATACTGGATGCACGACGACTGGTACTGTAAATACATCACGGTGAAGACACCCTATGGAGATTATGTGGAGTTCCCCTGCTTCCGCTGGTTGGTTGATGACAAAGAGGTGATCCTCAGAGATGGCAGGGGTACGTTCCCATTGGACATATCACTTCCTGTAATACAGCATTCAATTTTAGTATAACATTTGGATGCTTGTTGTGTTTCAGCTCGATTGCCACAGCACGACAAGACCGGAGTGGCGAAACAGCACAGGCGCAAAGAACTGGAACAGAGACAGAAGACATACAGGTTTGATGCAACTTTTAAAATAAGGTCAACCACTGCAGCAGTTGCGGACATCAAGAAAAGGGATTTCCTCATACGTGCACTTGTGGTCGTCGATTATTTCATCATATAAAACATTAATTTCCCTTTTCTTTTCGATAATCTTATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12277
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079884 | Essential Splice Site | 117 | 674 | 3 | 14 |
The following transcripts of ENSDARG00000057273 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 18216598)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 18036633 |
GRCz11 | 13 | 18167625 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TARTACAGCATTCAATTTTAGTATAACATTTGGATGCTTGTTGKGTTTCA[G/A]CTCGATTGCCACAGCACGACAAGACCGGAGTGGCGAAACAGCACAGGCGC
Long Flanking Sequence:
AGCTGGGGAGTTCTTGAGATTTACCTGAGCTCAAACTCCCCTCTCGCCTTGCAAACGGGAGCGAGCCCCGGGCTCAGGGATCTTATGAGCTTGGGGCTCTCTCCTGGGACAGCATGCCAAACAAGCTTTATAATCAATCATCAGCTAAGTTCCGCATTTTGTTCTCAAACCTTATTGTGTAAAATTGAATTTTAAAAGCATTTGGCATTTTGTGATTCAAGGTGGACTCATATGACATCAGCGTAGGAGAGGATCTTGGTGAAATTCAGCTGGTTAAAATTGAAAAGAAGAAATACTGGATGCACGACGACTGGTACTGTAAATACATCACGGTGAAGACACCCTATGGAGATTATGTGGAGTTCCCCTGCTTCCGCTGGTTGGTTGATGACAAAGAGGTGATCCTCAGAGATGGCAGGGGTACGTTCCCATTGGACATATCACTTCCTGTAATACAGCATTCAATTTTAGTATAACATTTGGATGCTTGTTGTGTTTCA[G/A]CTCGATTGCCACAGCACGACAAGACCGGAGTGGCGAAACAGCACAGGCGCAAAGAACTGGAACAGAGACAGAAGACATACAGGTTTGATGCAACTTTTAAAATAAGGTCAACCACTGCAGCAGTTGCGGACATCAAGAAAAGGGATTTCCTCATACGTGCACTTGTGGTCGTCGATTATTTCATCATATAAAACATTAATTTCCCTTTTCTTTTCGATAATCTTATAAACATTACTGCTGAAGATAGATGCAAAAACTTCCACATTTTCTTTTATCATGCTCAGGTTCAGCAATTTCACATTCACATGCAAAAACCTCTAAGTGCCGTCTGTAATTATCTCCTAAAATATGCATTTTCTTAGCATCCTGTTCATTTTCAGTTGTTGCAGTGTTTGTAAGTAAAGTTTCATGTAAGGCAATGAAAATAACCTATTATTTGCCATGAAAAGTAGAATTGAATAACCTACACATAGGAACCTAAGAAAAAAATCTGAAGAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1464
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079884 | Nonsense | 201 | 674 | 5 | 14 |
The following transcripts of ENSDARG00000057273 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 18196746)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 18016781 |
GRCz11 | 13 | 18147773 |
KASP Assay ID:
554-1389.1 (used for ordering genotyping assays)
KASP Sequence:
TAGGATCGAGAATCTGTATGTGAACCAGTTCATGCACATGTTCCAGTCCT[C/A]ATGGGGAGATTTCGCAGACTTTGAGCGGATATTTGTGAGAATTAAGAACA
Long Flanking Sequence:
TTTTTTTTTACAACAATATACACATACAGCATGTGTTTCCTTCATTATAAGGCTTATATAAGACTTTACACTTTTTGCGGCTCCAAACATATTTGTTTTTTGTTTTTTTTGGTCCAATATGGCTCTTTCAACATTTTGGGTTGCCGACCCCTGATCTAGCGCCTAATTCTCTGACCACTAACAGTTACTTTGTATAACTTCCTGTGTGTACTGCATCTTGTTCAATAGCTGAATGTCTCCTCAATTGTAAGTCGCATTGCACAAAGGCATCTGCCAAATGACTAAATGTAAAATGCAATGTTCTAATGTTCTAATTAGTGACATACCGTAAGAATTTACTCGCTCACCACTTCACTGTAATGTACCAGATATCTTCATTTATTTGTTATGCAACATAATATGTCAATATGTCACAACTTCTGTTTGCTTATTTTGCTATACTTTATTCCTTAGGATCGAGAATCTGTATGTGAACCAGTTCATGCACATGTTCCAGTCCT[C/A]ATGGGGAGATTTCGCAGACTTTGAGCGGATATTTGTGAGAATTAAGAACACAATATCAGGTTGGAACTGCCAGCATACACCTGTAGCAGATCTTTATGAGTATTTTAGTTAAGAATTGAGCATACACAATTATCCATGGGCGTAGGGTGGATAGAGGGGACGCGCCCGACCAATATCCACCTACCATTGCAATGTCCCCACCAATAATTTAATCCACTTTTAAAAAAAAGTTGCGCTATCAATATTAACCTAGACAAGCAGAGAGAATTAAATGCATAGACTGTAAAATATTAAATCACATTCTCTCATTGAGTCCTCTCGCCACCAAAACGCATATGGACATCTTGATTGGCTGTGCCTTTACTTGCTGTCATGTAAGAGGCTGTGGCTGCATTCAGATACAAGCAGCACATTTAACTTTTCTCAGTCAGAATTTGGTCATTTGAATAATTAGAACAATTCAATAATAATAATAATAGTATTAATAATAATAATAATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17538
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079884 | Essential Splice Site | 328 | 674 | 8 | 14 |
The following transcripts of ENSDARG00000057273 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 18191124)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 18011159 |
GRCz11 | 13 | 18142151 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATAAAATTATTACTGATGAGTTCTGAAAATGATCRTGATTTCTTTTACRT[A/G]GCTGCATCAGWAACCAGGAGAGGACAATCCCATCTTCCTTCCCAGTGACG
Long Flanking Sequence:
TTTATTCAAGGATTTGCTGCCTTTATGAAACTCCAGTAATTACAGCCTATAAACGCACTACATGGCAAATATTTTGAAATGTAGTAAGTCCGTGCAGGGAAAAAAGGAAGGAAGTCATGGAGGGAAGTCATATTGATTTTAATAAAAGGGTGTGAAAAGATTACGACAAACACGGAAGCCTCCCACATGCACAATACAAACTCACACGCACTATTACAGTCATTAAATTCTGTTATTATTCACTCTCCCTTCACTTGTTTGAAACCTATTCGACTTTCTTTTTTCTGCTGAGCACAAAAAGAAGATATTTTGAAGAATGCACCCATTGACTTCCATTTTTCAAAATATCTTATTCTGCTTTCAAACTACATCAGGGAGAATAAATGATTATGGTAAATTTCATTTTTGAGTGAACTTTCCCTTTAAGAACAATGCCACCTATGATTGTCAATAAAATTATTACTGATGAGTTCTGAAAATGATCATGATTTCTTTTACAT[A/G]GCTGCATCAGAAACCAGGAGAGGACAATCCCATCTTCCTTCCCAGTGACGATGAGTATGACTGGTTGCTGGCCAAAATCTGGGTGAGATCTTCAGACTTTCACGTCCATCAGACAGTCACTCATCTCCTCAGGACGCATCTGATTTCTGAGGTCTTTGGCATAGCCATGTTCAGACAGCTGCCTGCAGTTCATCCTGTTTTTAAGGTAATGTATTTCTATATTGTTTCTATTCTACACTTGCTGGCCACTTTATTAGGTACAACTGTTTAAATGCTTGTTAATGCAAATATTTAATAAGCCAATCATATGGGAGCAACTCAATACATTTATCCGTGTGGAGACATGATCATGGTGATCTACTGAAGTTTAAACTGGTGGAGAAAAATATATATTTTAAAAGATAGTTCACCCCAAAAAAATAACATTTACACACTATTTATTCAACTTCAAATGGTTTCTTTATTCTGTCGAACACAAAAAAAGATATTTCTGTCACAGT
Associated Phenotype:
Not determined