ZMP
si:dkey-24p1.6
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q1LY87]
Human Orthologue:
SEL1L3
Human Description:
sel-1 suppressor of lin-12-like 3 (C. elegans) [Source:HGNC Symbol;Acc:29108]
Mouse Orthologue:
Sel1l3
Mouse Description:
sel-1 suppressor of lin-12-like 3 (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:1916941]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42606 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22710 | Nonsense | Available for shipment | Available now |
sa22711 | Essential Splice Site | Available for shipment | Available now |
sa30685 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24994 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa28520 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42606
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 |
---|---|---|---|---|---|
ENSDART00000099375 | Essential Splice Site | 16 | 1028 | 1 | 23 |
ENSDART00000129941 | None | None | 448 | None | 13 |
ENSDART00000142403 | Essential Splice Site | 16 | 279 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 15 (position 36998022)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 38398026 |
GRCz11 | 15 | 38299611 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATGAGGGATCTAAAGAGTTTATACTTGTGCTCATATGTCATTGTTTGT[G/T]TAAGTATATCCTACACATATCAGTTACCATGCTTAATGTTGTTTACATCC
Long Flanking Sequence:
GAACTAAATCCCACATTATATACAACACTAAACAATGATAAACATATTTATGTATGCCAGTTACCCCATAGCTGTTTTAAACACTGGTTTTCCATCGTTTAAAAATATATATATCTACACCAATCAACGACAGGCAATCTAAACTGCACTTGAGAGTAGGCTTAATTATTCATGAGGATCCTAGATTTGCATTGGAGGGTGGTACTGTTCGTTGTGTTTACTTAAACTCTTACACCTGTAGCCGAACAGGATGTTATTCCGGGCCTCTCAGGTACCTGCTTCGGCATTTAATCACATGAAATCCGGCGCTTCGACGGTTGTTGATGCGGATATGGCGCAAACAGACAAATAACGCAACAAAACAGCGTGTCTGTGCATCACGATGACCACAGCAGAAATCTTCATTTTATAGTTGTTTCGTTTAATCCAAATCTTAATTTTATAGACGAAAAATGAGGGATCTAAAGAGTTTATACTTGTGCTCATATGTCATTGTTTGT[G/T]TAAGTATATCCTACACATATCAGTTACCATGCTTAATGTTGTTTACATCCATGACTTATGTGTATTTGTTTGCAACAGATGTTTTTAACTGGCTGTTTGAGTCGCTCCAGCTCAGGTAACGTGGCTTTTCTCGACGCACCAGATTCGCCAGTCTCCAAGTGTCCTTTACGCGTTCAGTTCAGCTGTTTTCAGCCGTCAGTGGTGCACGTTCAGGTTCTGGTCACTTTTGATACTGGATCCACCTCAGTTGTTTTTCACAAACACTGGAACTGCGAGCCGGGACGACCCAGAACCCGAGTGGTATTCGTGGGGTTTCCTGACTGGATTGTGTACCGTCCTGACCGGGTAATCCGCGGTTCTGATTGGGCGCTCAGCTGTTTGTTGCGCGGTTGGATCGGCCCAGATGAAACCTCCGGGCCGGACAGGTTTTTTGGAGCCAGTGTGTCGATTCCTCTCAACATTCAGTCACCACTGAGTCGACCCTTAAAACAACACCAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22710
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099375 | Nonsense | 384 | 1028 | 8 | 23 |
ENSDART00000129941 | None | None | 448 | None | 13 |
ENSDART00000142403 | None | None | 279 | None | 5 |
Genomic Location (Zv9):
Chromosome 15 (position 37008297)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 38408301 |
GRCz11 | 15 | 38309886 |
KASP Assay ID:
2260-8887.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTGAGATTCACCTTCCTCATGTATTATCAAAAGTCAATATAACCGGCT[G/A]GTTCCAGTCTTGTCAGAACTTCAGATCAGAACTTGAGCTCTTTTCCTCTC
Long Flanking Sequence:
TAATTTATTTTAATTTATTTAGTATTTATTTAGATATTTTTATTATTATTATTATTATTATTATTATTATTATTAGTATTATTATTATTATTATTGTTATTGATTTATTTTATTTTTATCTATTTATGTTTAGAGAAATTGGTCAAATCTAGTGGTGAAAGAGATTGAAAAAGCTTATTGAAACACCACAGTATTTTATGGCTTCAAATTGGTCAACATCATCAAAATATTTTTCTTCTAAATATGCCTGACAAGACATTAATAATATAACACTGAAGGACATTTTATTTAGTAAATGTGTGTATCTGTGTAAATAGTAAACATGTATGATAGTACTTTATTTGCCTCAGAACTAAACCAATAAAAATGCTGGATTGCACGTTTTGATTCTTATACAAAAATCTATTTTACTCCATTGTACTAAGCATAATAATATCATACACATTCCCAGGCTGAGATTCACCTTCCTCATGTATTATCAAAAGTCAATATAACCGGCT[G/A]GTTCCAGTCTTGTCAGAACTTCAGATCAGAACTTGAGCTCTTTTCCTCTCTCACTGGAAGGAGACCTTCAGGTAAATATCACAAGTGTCCACTAGCTGGCGCTATGGATCATTATATGTATTTAATTGTGTATAGTTACAGTATGTTTTGTGTGTTGAAATGCAGACTGCTGTTTAGACCCATACACTGAGCTGCTACTGAATCACAGCACAGTGAACTCAACAGAGCAGCTCATGCTCTTCCAATCATCAGCTGATCCTTATAGAAGAGCAGTTGTACAGATGACTAAACAACTCGCACAGAAATCTGGTAAGATTGAAAAGATTAAACAGTTAAGTGTGTGATATATACAGTACACCACCATGCAAAAGTAATAAATAGTAATAATGCTATTATTTAGCAAGGTTGCATTAAATTAATCAAAAGTGATATTTAAGTATAACGCTTGTAAACGCTTACATAATTTTTTAAGATTAAGTTTTTCTTTCTTTCTTTCTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22711
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099375 | Essential Splice Site | 670 | 1028 | 14 | 23 |
ENSDART00000129941 | Essential Splice Site | 90 | 448 | 4 | 13 |
ENSDART00000142403 | None | None | 279 | None | 5 |
Genomic Location (Zv9):
Chromosome 15 (position 37015139)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 38415143 |
GRCz11 | 15 | 38316728 |
KASP Assay ID:
2260-8888.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCTTGGAGGACAGTAAGCTTACTAAATATCACACTTGCTTCTGTTAAC[A/T]GGGTCAAGGAGTTCAGAAAGATGTTCGCAAAGCTGTTACGTTCCTTAAGA
Long Flanking Sequence:
TGAAGACTGATGTGAATACAACGATGATGACAATTAAATTGCTATCACATAAATTAAATTAATTTAATTTATTATTATTATTTGTTTATTTAATTTATTCTTTATTTTTATTTATTTAATTTATTATTATTATTATTATTATTATTATTATTAACTTTTTTCCTTTATTTATTTTCTTATTCATTAGCAAGCAATGGGTCGTATGCTATTCTGGGGTCAGCAAGGATTGTCCCCTGACATTCAGACAGCAGTGAAGCATTATGAGAGAGGAGCCATCAAACTCAATGACCCTGTTTCCATGTATGACTACGCCATTGTGCTCCTGACAGTCAGTATACTTCATATATACCCTGTTTGTATCTGATCTTGTGTTTAAAAAGGAAACAATATGTAATATGACCAGCAGAGGGCAGTCTTTCAAAGCATTTTGAGTTAATATTACTGAAGAGGAAGCTTGGAGGACAGTAAGCTTACTAAATATCACACTTGCTTCTGTTAAC[A/T]GGGTCAAGGAGTTCAGAAAGATGTTCGCAAAGCTGTTACGTTCCTTAAGAAAGCTATAGAACAGGTAAATACATCAAATCCAATGTTGGGGGTCTACATGAAAGTGATTAGGGGTCTGTAAATAATTTATTTAAATTTAATGAAAATTACTAAAAATCTAAATAAACTAATCAAATTTAATAAAGCATTATTGATAATATTAAAATGTATAAAATAAACAGTTGGAAAATGATTCATGAGGTATTATAGTTAGACCAATGATGTAAAACCATGTATTTAAAAACTAGAAGAAACATTTATACATTTTAAATAAACTTAAACATGTCATCATAACAATGTTAAAATTATTAATTAAATTAATATAATTATTAATTATTAATAAAATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTAATCAATATTTATTCATTATAAATGTATAAATAACTGTTGTTATGTCCTATCTAGTGGCCACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30685
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099375 | Nonsense | 784 | 1028 | 16 | 23 |
ENSDART00000129941 | Nonsense | 204 | 448 | 6 | 13 |
ENSDART00000142403 | None | None | 279 | None | 5 |
Genomic Location (Zv9):
Chromosome 15 (position 37021534)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 38421538 |
GRCz11 | 15 | 38323123 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATTGAATTGGCTGATATCTGGATTCATGGACTCCCTGGTCAAGTTGCT[C/T]GACGTCCATCAGACGCTGTTCTGTATGTATCTCAAAATACTTGTTCATCA
Long Flanking Sequence:
ACAAATAAAAACTAAACTAAAACTAAGCAATTTCAAAATATAGAAACTAAGAAAAACTAAATTTACCTCAAAAATCTAAATAAAACGAACTGAATTTGAAAACAAAGTCAAAACGAAATAGAAACTAAAACTTATAAGGAATCTATTACTCTTATAACCTTGGTTGTAAGTAGGATTAAGTTGTTGTTTTTGCAGAATAGGTTCCTTCGGTCAGTCAGACTTAACTCTGTGATAACAGCCACCTCGATGTACTCTATTTCTCCCTAGATCTTTACATTTTCTTACTTTTTTAAAACTTTTTTTTATTGTTTTAAAACTTATTGGAATGCTCTCATTATTTCTCTTTTGTAAGTATTATACGTATGGACTTATCTAATGTGGACTCTTTTCATCAGTTCAAAGGGTATAAGTATTTTCTGAAGTCAGCTCAGAGAGGACTTTTATCTGGTGGCATTGAATTGGCTGATATCTGGATTCATGGACTCCCTGGTCAAGTTGCT[C/T]GACGTCCATCAGACGCTGTTCTGTATGTATCTCAAAATACTTGTTCATCATAATATAACACTGTTATTGTTAGTCTACACGCAATATATCAGTGTGCACTTGTTCAGTCAGTATGAACTAGCAAGATCCCGATTCTGCCCACAATCCCATACATCAGTGGTTCCCATAGTGGGGGTCGCATGACAATGAGAGGGAGTCGCTTAGTGATTTCCAAAAATCGAATAAACTAATAAACTTTTGAAATGACCATTGTTAATCCACAACCTACAGAAGATAAAACTAGTTGCATTAAAATACATGCAAATATATATATTTTTCCATTCAATTGGTGTGTTTACGTTAGATTAACAACACTGCAATAGTGTCATTTGCAGCAGATGGATTTTATGTCACCAGCCTAAACTTTGACACCTTTATGGCAATCAGGTACATTTAAAATAAACACAGGCCACAACTGTACATGGAAGATGATCTCTGAGAGGCAGTCTCTAAAATTAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24994
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099375 | Essential Splice Site | 819 | 1028 | 17 | 23 |
ENSDART00000129941 | Essential Splice Site | 239 | 448 | 7 | 13 |
ENSDART00000142403 | None | None | 279 | None | 5 |
Genomic Location (Zv9):
Chromosome 15 (position 37023942)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 38423946 |
GRCz11 | 15 | 38325531 |
KASP Assay ID:
554-7694.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGAAGAGTCTTACGGAAAGGACTGAATGCTTATTTCAGAGGAAACTGG[T/C]AAACCTTTGTTTAAGCTGTACATGCAGTCTACTGTACTTGTATGTTTAAA
Long Flanking Sequence:
TTAAAGGAGTGGTCCTCAAACTGTGGTATGTGTACCACTAGTGGTACGCAGGCTTCCTTCTAGTGGTATGTGGAGGAATGAAATATGTCATGTACATGCAACTCACATTTCAAAATTTATCAAAAATGATGTATATAATTTGACACATTATAAAACATTGGGTCAAAAATGTAACTAAAAAACGCAAACCAACTGTTTTCCCATACTTGACTCAAAATTGATTGAAAGCAACTAATTTTATGAAGTGAATGATATCAGTGTTTCTCTGCATCTGCTGAAGGATGTTGATGATACATTGTACAAGTTTAATCTGGTAAATGAGATTCACTCTTATTTCACCACTGGACTGTTTTTAAGTCAACATTTTACTATTGTAATTATAGGAAAGGTGTGTATTTTTTTCTTTTACTTGTAGGTGGGTTAAATGGGCGTCTGAACAGAATGGGCATCTGGGAAGAGTCTTACGGAAAGGACTGAATGCTTATTTCAGAGGAAACTGG[T/C]AAACCTTTGTTTAAGCTGTACATGCAGTCTACTGTACTTGTATGTTTAAAATATTAGCTTACACCGTCAAAAAACAAAACAAAAACTATATTTCAGATTTTACAATTTATACTGAATTTGACTAATATTTTCTGATTGTTTTACCTGTATAACCACATTCAGAAGAGGACAATTGATAAAAAAACAAATTAAATGCTTTTATTCTAATTATTAAATTTTTTTATTATTATTATTATTATTATTATTATTAGATTTTAAGAACATTGCTATTACATTGGTTTATTTTTATATGAAATAATAATAATTGTGTGTGTGTTTTTTAATTGGTTGTTGATGATGATTATTATTATTATTTATTATTATTATTGTTATACCATTGCTGTGATATTTGTATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATTTTATATAAAGTTTTTTAAAGTGTATTTTTTATTTTAATTGGTTGTTTATTATTATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28520
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099375 | Essential Splice Site | 878 | 1028 | 20 | 23 |
ENSDART00000129941 | Essential Splice Site | 298 | 448 | 10 | 13 |
ENSDART00000142403 | None | None | 279 | None | 5 |
Genomic Location (Zv9):
Chromosome 15 (position 37026442)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 38426446 |
GRCz11 | 15 | 38328031 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCTCCTGGAGCTCAGTCCTCCCTGTCTGCATGTGTTTGTTTCTCTCTC[A/C]GCTTTGATCCGGACAGGAGATCTGATCTATGGAGAAAACCAGCATTCTGA
Long Flanking Sequence:
TACAGTAATGTATAAACAGATCTGGAGTCTTCTCTGTTAGTATAGCTCATTAACCATGTGGCTGATGAGTAGTAGGCACAGAATGCCCCTTTTGGCCCATACCTACCAGCTGATAACCACTGATAACGCCCATTCAATGGAGTGATTACATTCGAAGTGGGTGATTATCATCAATATTTTACTTCTACAACACTATTACTACTAGTACTATTATTACTACTACTACTGCTAATAATAATAATAATGGTAACAATAACAGTTATAAAGTAGCAGAAGTATTTTATATATTTAGTATTTTTAATGTTGTACTTTAGTAATACAAAAGTTTATTATACAAAATAATTTAATGATCACTATCCTAGATCTAAAGATCTTGTGAAGCGTTTGTGTATGTTCGTGCGTGCAGTTGCGCATTCTTGTGTCTGGTGTCCAGTTGCTGTGTTTTTCTTCTGCCTCCTGGAGCTCAGTCCTCCCTGTCTGCATGTGTTTGTTTCTCTCTC[A/C]GCTTTGATCCGGACAGGAGATCTGATCTATGGAGAAAACCAGCATTCTGAAGCAGCACAGATGTACAAGCGAGCAGCTCTCAGGAATGAACCACAGGTACGGCTCACCTGCGCCATGCAAATCTGAAGTTCACTTGAAAAATAAACTGCTTCATTGGCATTGATCATCACATAATACACCTGGAACATCCATGGAGATATTTCATCCACAAAAAGCCTCTTGATTGAGAAAAAAGATCTTTAGAATGTAAAAACAGAAATAAATTAACAAAATAAAAATAAAAACGTACTGTATTTTTTATTATTCTTAGTTTTTTTTCATGCCATTCCCTCATATGTGATTTTCTGACTCCTCAGGGCTGGTATAATCTGGGTCTGCTCGTCCAGAATGGAGCGTCTCTGCCCTTTAGTGTCCTTTCTGAGCTTCATTTACTGCACCTTCACCTAAGAGACAGACAGAAGCTTCTTTGCGCCCTCTTCCAGAGGTAAAACAACACCATT
Associated Phenotype:
Not determined