ZMP
loxl4
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens LOXL4, lysyl oxidase-like 4 (LOXL4) [Source:UniProtKB/TrEMBL;Acc:
Human Orthologue:
LOXL4
Human Description:
lysyl oxidase-like 4 [Source:HGNC Symbol;Acc:17171]
Mouse Orthologue:
Loxl4
Mouse Description:
lysyl oxidase-like 4 Gene [Source:MGI Symbol;Acc:MGI:1914823]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa1838 | Nonsense | Available for shipment | Available now |
| sa16021 | Essential Splice Site | Available for shipment | Available now |
| sa6327 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa10091 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1838
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044963 | None | None | 836 | None | 17 |
| ENSDART00000134411 | Nonsense | 16 | 280 | 1 | 3 |
| ENSDART00000145635 | None | None | 336 | None | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 40584762)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 40111208 |
| GRCz11 | 13 | 40237098 |
KASP Assay ID:
554-1829.1 (used for ordering genotyping assays)
KASP Sequence:
CCTCCAGAGCCTCATCGGTGTGCAGTCATGATTCGGGTCWGTCCGCTGTG[T/A]ATTCTTTTSTTTGCGCTGCTCTTCATGTGTATGGACGCTCGTCCTGGATC
Long Flanking Sequence:
TACATACAAAACTTACTAACAAAAATACTTACAAACATAAAAATATATTCAGTGTCAAATATATCCAGATTAAGCTGCAGCCATTTCAATAGCATAATAAAAGCTGTTTCATGTGACATGTTGTGGGTCACCTTATGGGTGCTGCCATTTTGAGATCACATGACCATCTGAATACCAGGTTATTTTAATTCATTTATAAATTTTCCTTCGGCTTAGTCCCTTTATTTATTAGGGGTTGCCACAGCTGAATGAACCGCCAACTTATTCAGCATAAGTTTTACACAGCAGATGTCCTTCCAGCTGCAACCCAGTACTGGGAAACATTCATACACACTCATTCACACACATACACTACGACCAAACCACTGAGCCACCGTGTCACCCTGGTTATCTTAATGATCTAGTTTATTTGACTTATTTCTATGATAACATCAGGCTGTATTATTTTGTCCTCCAGAGCCTCATCGGTGTGCAGTCATGATTCGGGTCTGTCCGCTGTG[T/A]ATTCTTTTGTTTGCGCTGCTCTTCATGTGTATGGACGCTCGTCCTGGATCATCAGGGCGCTCAAGACGTGCCCCTGCTGCCAAAGTGCGACTGGCAGGCATTGGCCACCAAGAAAACGAGGGACGTGTCGAAGTCTTGCACAACGGGACATGGGGAACTGTATGTGACGACGAGGTCGACATTAAACTGGCTAATGTGGTTTGCAGAGAACTGGGATTTCAAAGCGGCATCACGTGGGCTCACAGTGCCAGATACGGAGAAGGAGAGGGTGAGTTCATTTCATCATCAAAAGGCATTAATTGTACACTCAAAAAAAGTTTGATCTTTGTTCAAACTACTTAAAATAAGCTAAAACAAGAACTTTTTTTAAAAGTTTTTTGGCACAACTTAATTGTTTTATGTTCAATCCACTTAAATTTGTAAAAACTAACAAGCTAACTTAATTCCTTCAAGTTGATCCAACACAAATCTATAGTGTGGAAAAATAACATTCTGATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16021
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044963 | Essential Splice Site | 201 | 836 | 4 | 17 |
| ENSDART00000134411 | None | None | 280 | None | 3 |
| ENSDART00000145635 | None | None | 336 | None | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 40578902)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 40105348 |
| GRCz11 | 13 | 40231238 |
KASP Assay ID:
554-4772.1 (used for ordering genotyping assays)
KASP Sequence:
TGTGGTCAGATTAATCAGCAYTTCARGTATTTTKTTTAGGGAGAAATGGA[C/T]GTATTTCAACARGAMAAGTACTGAGTGCGGAAGATGAGGATACAAGTACT
Long Flanking Sequence:
AGCATCCAAGAAAGGTCTAGTCCTAAGATGGGCTGAGGATTGCTAGTTTGCCAACAAATACCAAGAAAATGTTTGAATACATTGTTCCTCAAAGCAAAATAGGAGGACATTTGTGCATTTTACTTTTAATGGTGCATAACATATTTAAAAGTTTTAAGGAATCTGGAGGAATTTCAGTGCATAAAAGTTCAGGCTAAATGACCATGACCTCGCAAGCTGAACAACCGCAAGCTGAACAACCATGATCTCCTATGCCTCAGGTGGCACTGCATAAAGAATCATCATTCATCTATAAGCGACATCATTACATGAGCTCAGGATTACTTTAACAAACCAGTTTAAACTGTACTTTGCCAAATGGAATCCCTATGTTAACAGTGTCCAGAAGCACTGTCGACTTCTCTGGGCTCGGAGGCATCCGGTATGAACGATCACAGTGGAAATGTGCGCTGTGGTCAGATTAATCAGCATTTCAGGTATTTTTTTTAGGGAGAAATGGA[C/T]GTATTTCAACAAGACAAGTACTGAGTGCGGAAGATGAGGATACAAGTACTTGACTGGCCTGCCTGCAGTCCTGACCTATTTCCAATAGAGAAAGCGCACAATGCAACAACCCCGTACTGTTGCTCACCTTAAGACACAATTACACCTGAAACACTTCATCACTTGGTGTCTTCAATTCCTAAACATCTTTTAAGTGTTTTGAAAAGGAATGGCAACATTACAAACTGGTAAATAATGTACTGTTCAAACTTTTTGGAAGTGTGTCGCAAGAACCAAAATTGGAATAAGTGTTTATTTAAAAAGTAATTAAATAAATAAACGTCATGAGGAACACATTAAATGGCTGGTGATCCTTGGCCCTTCTTTGCTCCTAAAGGACTAGACCTTTCTGGGATGCTGCTTTTGTATAAATCATAATTAGTTACGGTGGTTCATTCCGCTGTGGCGTCCCCAGATTAATAAAGGGACTAAGCCGACAAGAAAACGAATGAATGAAGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6327
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 |
|---|---|---|---|---|---|
| ENSDART00000044963 | Essential Splice Site | 201 | 836 | 4 | 17 |
| ENSDART00000134411 | None | None | 280 | None | 3 |
| ENSDART00000145635 | None | None | 336 | None | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 40578902)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 40105348 |
| GRCz11 | 13 | 40231238 |
KASP Assay ID:
554-4772.1 (used for ordering genotyping assays)
KASP Sequence:
TGTGGTCAGATTAATCAGCATTTCAGGTATTTTTTTTAGGGAGAAATGGA[C/A]GTATTTCAACARGACAAGTACTGAGTGCGGAAGATGAGGATACAAGTACT
Long Flanking Sequence:
AGCATCCAAGAAAGGTCTAGTCCTAAGATGGGCTGAGGATTGCTAGTTTGCCAACAAATACCAAGAAAATGTTTGAATACATTGTTCCTCAAAGCAAAATAGGAGGACATTTGTGCATTTTACTTTTAATGGTGCATAACATATTTAAAAGTTTTAAGGAATCTGGAGGAATTTCAGTGCATAAAAGTTCAGGCTAAATGACCATGACCTCGCAAGCTGAACAACCGCAAGCTGAACAACCATGATCTCCTATGCCTCAGGTGGCACTGCATAAAGAATCATCATTCATCTATAAGCGACATCATTACATGAGCTCAGGATTACTTTAACAAACCAGTTTAAACTGTACTTTGCCAAATGGAATCCCTATGTTAACAGTGTCCAGAAGCACTGTCGACTTCTCTGGGCTCGGAGGCATCCGGTATGAACGATCACAGTGGAAATGTGCGCTGTGGTCAGATTAATCAGCATTTCAGGTATTTTTTTTAGGGAGAAATGGA[C/A]GTATTTCAACAAGACAAGTACTGAGTGCGGAAGATGAGGATACAAGTACTTGACTGGCCTGCCTGCAGTCCTGACCTATTTCCAATAGAGAAAGCGCACAATGCAACAACCCCGTACTGTTGCTCACCTTAAGACACAATTACACCTGAAACACTTCATCACTTGGTGTCTTCAATTCCTAAACATCTTTTAAGTGTTTTGAAAAGGAATGGCAACATTACAAACTGGTAAATAATGTACTGTTCAAACTTTTTGGAAGTGTGTCGCAAGAACCAAAATTGGAATAAGTGTTTATTTAAAAAGTAATTAAATAAATAAACGTCATGAGGAACACATTAAATGGCTGGTGATCCTTGGCCCTTCTTTGCTCCTAAAGGACTAGACCTTTCTGGGATGCTGCTTTTGTATAAATCATAATTAGTTACGGTGGTTCATTCCGCTGTGGCGTCCCCAGATTAATAAAGGGACTAAGCCGACAAGAAAACGAATGAATGAAGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10091
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 |
|---|---|---|---|---|---|
| ENSDART00000044963 | Essential Splice Site | 692 | 836 | 13 | 17 |
| ENSDART00000134411 | None | None | 280 | None | 3 |
| ENSDART00000145635 | Essential Splice Site | 192 | 336 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 40543087)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 40069533 |
| GRCz11 | 13 | 40195423 |
KASP Assay ID:
2260-6844.1 (used for ordering genotyping assays)
KASP Sequence:
TTCCGGCCAYGGGCTTCAAGRGAGTCCTGGACCTGGCATCAGTGCCACAG[G/A]TGAGGGGCTGTATATATCACATGACAGCATGAATAGCCCATARCAGGAGT
Long Flanking Sequence:
AAATAAATTTTCTTACAGTCTAACAAAATGCTGGGTTGTAATAACCAAATGTTGGGTGTGTCAAATATGAATAAATCCAACCGATGGGTTAAAAAGTTTAATTGGAATTTTATTAAAAATGATTGACCCAACGTTGGGATACAACGACCTGTAATTTTTTAAAGTAAATCAAGAAAATTTTTAGTTATCTCTTATCAGTGTTGTGCCCTTTTATAATGAAATCTCCACTGATTAATGGATCACCCTGCTGTTTTAGCTGCACCTGACCTGGTTTTGGATGCGCAGCTGGTTCAGGAGAGCTCTTATCTGGAAGACCGGCCTCTGCATCTGCTCACCTGTGCCCATGAGGAGAATTGTCTGTCCTCATCTGCCAGCCGCATGCAGTGGCCGTACGGGCATCGCCGTCTGTTGCGCTTCTCCTCCCGGATCATGAATCTGGGTAGAGCCGACTTCCGGCCACGGGCTTCAAGGGAGTCCTGGACCTGGCATCAGTGCCACAG[G/A]TGAGGGGCTGTATATATCACATGACAGCATGAATAGCCCATAGCAGGAGTACTCAAACTTGGTCCTGGAGGACCGTTGTCCTGCAGATTTTAGCTCCAACCTGCCTCAATACTCATGCAAGAATGATTTTAGAAGTCTAGTTAGAGCTTGAGGACCGAGTTTGTGAAGCCCTGGGCTATAGCATGAATACTGTGTTTATCATACTTCATAAAAAAGGTAATTTTTAAAGTTTGTGATGCATTAAAAAGCATGTAAACCATTTCCATTGATCTTTTAAAAAAAAAAGTATTATTATTAATTATTATTATTTTATTATTATTAATTATATTTTTATTTTATTTATATATTTTTATTTTTATACATTATTATTATTATTATTAATTCAATTCAATTCAGCTTTATTTGTATAGCGCTTTTACAATGTAGATTGTGTCAAAGCAGCTTCACATAAATGGTCATAGTAACTGGAACAGTGTGGTTCAGTAACTGGAACAGTGTGG
Associated Phenotype:
Not determined