ZMP
si:dkey-175g6.5
Ensembl ID:
ZFIN ID:
Human Orthologue:
LTN1
Human Description:
listerin E3 ubiquitin protein ligase 1 [Source:HGNC Symbol;Acc:13082]
Mouse Orthologue:
Ltn1
Mouse Description:
listerin E3 ubiquitin protein ligase 1 Gene [Source:MGI Symbol;Acc:MGI:1926163]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21729 | Essential Splice Site | Available for shipment | Available now |
sa21730 | Nonsense | Available for shipment | Available now |
sa41656 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13774 | Nonsense | Available for shipment | Available now |
sa1642 | Essential Splice Site | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa21729
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022170 | Essential Splice Site | 116 | 1751 | 3 | 30 |
ENSDART00000135890 | Essential Splice Site | 116 | 1749 | 3 | 30 |
Genomic Location (Zv9):
Chromosome 10 (position 23361876)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 23133169 |
GRCz11 | 10 | 23102621 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAGGTGTCCTGCCATACTGGCCTCGGATATACTGCCGGATATCGATGG[T/C]AAATATTTAATCATTATAGTTATACATTCGTAAATATGTAATACATCGTT
Long Flanking Sequence:
TTTTCAGCTTAGTCCATTTATTAATCTGGGGTCGCCACAGTGAAACTGAACCAACAACTTTTCCAGTACATGTTTTATGCAGCGGATGTACACACTCATAAACTACGATTTTCTGGGACAATTCAACCTACCCAATTCACCTGTACCGCATGTCTTTGGACTGTGGGGGAAACCGGAGCACCCGGCGGAAACCCACGCGAACGCAGGGAGAACATGCAAACTTTACACAGAAATGCCAACTGACCCAGCCGAGGCTCGAACCAGTGACTTTCTTGCTGTGAGGCGACAGCACTGCCTACTGTGCCACTGCGTCGCCCTACATGCAAATTATTTATCGAATTTTGATTTAACCGACTTAATAACTGAATGTTTTATAAATGTTGGTAAACATGTATTTCAGGCAGTACAAGAGTTTGGAGCAATGTGTCAAGAGCGGCAGACTGATGTTGTAAAAGGTGTCCTGCCATACTGGCCTCGGATATACTGCCGGATATCGATGG[T/C]AAATATTTAATCATTATAGTTATACATTCGTAAATATGTAATACATCGTTATTTTTAGGCTAATTTATTAATTTATTATGTTGAATGTATCATTTTTAACTTTTGTTTACTGTTCGGGATGTTTTCATCCACTCTGGGGTGATTTTTGAGTTGAAATTTGGCCACAACTTTCTCTGTTTCAGCAAATAGAATGATTTTTGGTTACAAATCCTATCTAAAGGGTTAATTGTGCCAACAGTAAAAATGGCAAATCTGACCTCTTTCCAATAAGGAAAACCACCAACAGTCAAGAATATGCATGATTAATTGGTGTCATGGCTTTGCAATCAAAAATAATGCTATAATTAAAGTCAATAGGGCAAAAACAGCCACCAATATATAAAAAGGGTTGTAAATTTGATCAATACACAAAGGTTAATAAAATTGTATTAAATTTGAAAAACTCTTTTTTTTTATGTTTTTTTTTCATCTCACTGTATGTAAAGGCAGCTAGAAGCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21730
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 |
---|---|---|---|---|---|
ENSDART00000022170 | Nonsense | 1023 | 1751 | 17 | 30 |
ENSDART00000135890 | Nonsense | 1023 | 1749 | 17 | 30 |
Genomic Location (Zv9):
Chromosome 10 (position 23376037)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 23147330 |
GRCz11 | 10 | 23116782 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCACCAATACTTTTTTATTGTGTAGTTTCAGAGATTTTTTATGGCCTG[C/T]AGTGGTGTGAAGAAATGGAGTTTTCACCCCTCACAGTGTCTGAATATCAT
Long Flanking Sequence:
TATTATATTATATTATATTATATTATATTATGTATATTTATTATATTTATTATACAAAGCAAATGACAAAGCAAAATTTTACCTAATCCTTAGTTTGACACAACCCTTCAGAAATCATTCAGTGTAGTAATTTTGTGCTTAAGATTAATTTTTTCTGAAATCTTCCTGAATTGAATGATTGGCTTTAATTTAAAATTATAACAATATATATATATATATATATATATATATATATGTATATGTGTATATATATATATATATATATATACACACACACATATATATATATATATATATATATATATATGTATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATATATTTTTTTATTTTATTTTACTTGTATACATTTGTGTCATTGTTGAGCAGCATGGTTTAGATGGACAAATTTATGAGCTGTTAAAACTTTGTTTGCTGATGATTTTTCACCAATACTTTTTTATTGTGTAGTTTCAGAGATTTTTTATGGCCTG[C/T]AGTGGTGTGAAGAAATGGAGTTTTCACCCCTCACAGTGTCTGAATATCATAAATTGCTCCAGTCCTGGAGTTTGGAACAGAAAATTCACAATATCAGCCTGATCAAATCCGCTCTTACAGACACACTTTTTACAAGGTGAAATTATATACCCCCCAGAAATTTACGTTTTAAATACTAATAGCATTGCATATGTATATACCTTTAATTTGTTTTGAATTAGCACTTTTTATATACCCTTGTATCTTTTTTTTAATTACAGATCACAAGAAAATGGATCTCTCTGGTCACTGTGTCTGGCGAAATACTTGCAAATCAATAAAATGGACCCAGGTGACATCAAAGGCTTATATGGAAGTGTTGAAAGGTAATCATCTCCCCAAAACTCCCAATATGTAATTTTTTCCCCCACTAACAAAAAAATAATTTTAAGTTGTACTAATGTTCAGTAGTTTGGGTAAATGGCTTTGTTTTTTTAAAAGAAATTTACTAAATTTATTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41656
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022170 | Nonsense | 1076 | 1751 | 18 | 30 |
ENSDART00000135890 | Nonsense | 1076 | 1749 | 18 | 30 |
Genomic Location (Zv9):
Chromosome 10 (position 23376321)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 23147614 |
GRCz11 | 10 | 23117066 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCTTGTATCTTTTTTTTAATTACAGATCACAAGAAAATGGATCTCTCT[G/A]GTCACTGTGTCTGGCGAAATACTTGCAAATCAATAAAATGGACCCAGGTG
Long Flanking Sequence:
TATATATATATATATATATATATGTATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATATATTTTTTTATTTTATTTTACTTGTATACATTTGTGTCATTGTTGAGCAGCATGGTTTAGATGGACAAATTTATGAGCTGTTAAAACTTTGTTTGCTGATGATTTTTCACCAATACTTTTTTATTGTGTAGTTTCAGAGATTTTTTATGGCCTGCAGTGGTGTGAAGAAATGGAGTTTTCACCCCTCACAGTGTCTGAATATCATAAATTGCTCCAGTCCTGGAGTTTGGAACAGAAAATTCACAATATCAGCCTGATCAAATCCGCTCTTACAGACACACTTTTTACAAGGTGAAATTATATACCCCCCAGAAATTTACGTTTTAAATACTAATAGCATTGCATATGTATATACCTTTAATTTGTTTTGAATTAGCACTTTTTATATACCCTTGTATCTTTTTTTTAATTACAGATCACAAGAAAATGGATCTCTCT[G/A]GTCACTGTGTCTGGCGAAATACTTGCAAATCAATAAAATGGACCCAGGTGACATCAAAGGCTTATATGGAAGTGTTGAAAGGTAATCATCTCCCCAAAACTCCCAATATGTAATTTTTTCCCCCACTAACAAAAAAATAATTTTAAGTTGTACTAATGTTCAGTAGTTTGGGTAAATGGCTTTGTTTTTTTAAAAGAAATTTACTAAATTTATTGAAAAATGTTTTAAATGGAAAATGGCAGGTAATATTATAAAATAATATTACAAACTCAAATAACAGTTTATATATATATATATATATATATATATATATATATTGCTTAAGAAATATTTCACGTTTTAAACACCAGTGCAGCTTTACATATTTTGTGTAAATCCAGCTTTTTTTTAGCTTTCTGTACAATCATATTTGTTTAATGCATCATTGCTAAATAAAAGTGTTTCTTTATTAATATATAAATTATACATAATCCTACTGTATGCAGCCATAAAAGCTGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13774
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 |
---|---|---|---|---|---|
ENSDART00000022170 | Nonsense | 1133 | 1751 | 19 | 30 |
ENSDART00000135890 | Nonsense | 1133 | 1749 | 19 | 30 |
Genomic Location (Zv9):
Chromosome 10 (position 23377850)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 23149143 |
GRCz11 | 10 | 23118595 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTGCTCTGTCCGTTTCTAGCCAGCGAAGACAGAGAATCCCTCATYGCCT[T/A]GTGTGTYGCAGAGCTACTCAACTGGCAGGACCAAGAGCACGACTGCAGTG
Long Flanking Sequence:
TTTTATAGTTATTTTAAAATATTAAAAAATAAATTAGGAAATTACCTCTGGCAACTATATTTACCTTTGACCCACTAGCCTCAATTAAGGTTGGCTTTTGGCCCTTCATAAGGAAATGTTTGGGCGCTCTTGAAATAGAACAACTAAATGTGCTACTTTGTTACTTTTATGGAAATTAATGTTTTTCTTAATTTTTTTCTTCTTCTTTTATTGATAGTATTATTAGATATTAGATTGTAATATATTACATTTAAAATTAACCTTTCCCTACAGTGAACCAGCTCCTGTTCAGACAGCCTTTAACACAGTGTTTTGCTAAACCAGGGAGTAGTTGGTTGTGACATTCCTACTAATTCAGTGGCTTGTTTGTGTGTGTTTGTGTTTGTGTTTGTGTGTGTGTGTGTATGTCAGTTTCTTTCCCCTCTCAGAGCACAGTGTGAATACTCTGCAGGTGCTCTGTCCGTTTCTAGCCAGCGAAGACAGAGAATCCCTCATCGCCT[T/A]GTGTGTCGCAGAGCTACTCAACTGGCAGGACCAAGAGCACGACTGCAGTGATGGTGAGACTCAAAAAACACACACACACACACAACACGCCATGAGTCATATAGGCTGAGTATAATGTGTGTGTGTGTAGGTGTGCTGTGCTGTCTGGCGGTGTTGCTGTGCTGTCTGCAGGCTGATGCTGCTGTGGAGGATGAGATTCTGCTGGCTGTCGTCAGCACGATCGCTGAATGGAGGAACAGTAGAGAGGAGTGGTTCCTCTTCAACAGGTGAGCATGTGTGTGTGTCACTGTAATGAGGAGGACCGTGATGGCAGTCATGTTTATAATGACAGAGCTGTGGTCACTGTGCTTATGTAGGGGACAGGGCTGGACTGGGGCAAAAAATCGGCCCTGGCATTTTGGGCCAGAGCGGCCCACTAAATTCAATCAAAATGCTATCTATCTATACACGTCCAATATTTTTATCAACTCATATTCTATAAAACACAAAAGCCATATTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1642
Status:
F2 line generated
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022170 | Essential Splice Site | 1731 | 1751 | 29 | 30 |
ENSDART00000135890 | Essential Splice Site | 1729 | 1749 | 29 | 30 |
Genomic Location (Zv9):
Chromosome 10 (position 23397038)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 23168331 |
GRCz11 | 10 | 23137783 |
KASP Assay ID:
554-1582.1 (used for ordering genotyping assays)
KASP Sequence:
CAAAGAAAGCTTGCCGTACCTGCAAAAAGAAGTTYCACTCCGCCTGTCTA[G/A]TGAGTGCCACACACACACACACACACACACACACACACACACACACACAC
Long Flanking Sequence:
TCTGTTTTCAATAAAGTTTCAAATGTTTGCTGAATGCTCCTGCAGAATAAGCATAAAACTCCAGTAGAAAACTGCTGCTCCATCTTTCTTACTTGTCGCCAAAGGCAACCGCGTAATAATAACTTAAAACAGTCCAATACAAAACAGCACAAACCATCGCTAATAAATAGGTGGACAAAAATCAACAAATGTCCCCATAAACTAAACATATCAGCTTATGTATTTCAAGCATTTGAATAATAGATAATGAATAAATTGCAATATATTCTTAAAGTATGAAGAACAACTGAAAATGTCCAAACTAATTGAGGCAATGTGCTTGTGTTTGCTAGAATGGTAGTATACTGGAGGGTCTGTCGCTGTGGAAGAACAATGTTGACAAGCGTTTTGAGGGGGTGGAGGACTGTATGATCTGCTTCTCTGTCATTCATGGATCCAATTACTCGCTGCCAAAGAAAGCTTGCCGTACCTGCAAAAAGAAGTTCCACTCCGCCTGTCTA[G/A]TGAGTGCCACACACACACACACACACACACACACACACACACACACACACACACACACAATATCATGCTCTGCCATCGTTCTTATTTTTAGATGAATGTTTGTAAAACAGATCAGTCTTGATGTTTTAGGAACATACATCGGTTAAAGTGAACATGAAACTCATTCTGCTTCTGTAATTCAGAATATTCAGCTGAATTCACACAGTAATCAGACTCAATTGTAATGTTCATACTGATATCAAAGCCCTGTAGAAGGTCACCGGTGCACTTGAAATTGAATCATTTCCCCTATACAGTCTTTCTCCATTTATTGCTTTAATTCTGCAGATGTTTCAGTATCAGCAAAAACACGCAGCCTTGAATGTTCTCAAGCGCTTCTCGTTCCTCACTGACCGCTTGTTTCCATTTCCTTTCATTCCACAGTATAAATGGTTCACGTCTAGCAACAAATCCACGTGTCCTCTTTGCCGAGAGACTTTCTTCTAAACTCTGTCTCCATG
Associated Phenotype:
Not determined