ZMP
si:dkey-81j8.6
Ensembl ID:
ZFIN ID:
Human Orthologue:
SLK
Human Description:
STE20-like kinase [Source:HGNC Symbol;Acc:11088]
Mouse Orthologue:
Slk
Mouse Description:
STE20-like kinase (yeast) Gene [Source:MGI Symbol;Acc:MGI:103241]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41641 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa21714 | Nonsense | Available for shipment | Available now |
| sa21715 | Nonsense | Available for shipment | Available now |
| sa31778 | Nonsense | Available for shipment | Available now |
| sa18421 | Splice Site, Nonsense | Available for shipment | Available now |
| sa34886 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41641
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000127235 | Nonsense | 101 | 1293 | 2 | 17 |
| ENSDART00000140141 | Nonsense | 101 | 693 | 2 | 15 |
Genomic Location (Zv9):
Chromosome 10 (position 20693086)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 20654500 |
| GRCz11 | 10 | 20611881 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGCCTGTCGACATCCGAACATCCTCTCCCTGCTGGACGCCATCTTCTTT[G/T]AGGGCTGGCTCTGGGTGAGAAATCTGTTTCCTTGTGTTTGTTTTGCAGGA
Long Flanking Sequence:
ACTTTGAGAATGGAAACATTAAAAATATAGTATGAAAAACATGCACGCTGTTGTTTATTTATAGGTTTCCAAGGTGACAGAAAATGGGGGTTTCGGGCTATGCTGCGGTTTGACAACTTCCTGTTAAACCAAAATGTGAAAGATTAAAGATGGCTTCCTGTTAGAATATTCACATAATCAACCTACTCATCTTCATACCTCTCTTAAAATGAACAGCACTTTGCAATTTAGCAGTTTCTGTGCTGTGCACATCTTTGCACTGTGGCCTTTCCAGCATAAACATTGTTGATTGTTTTCTTGCACTTCAAAGTGTCAAAGGCAAGTATTACAGTATGTAGTATTGATCTCAGGCCCAGAATCAGACTACAGGAGTGCTGGGAGCTGTTAAAGTGATTGAAGTGCGCAGTGAGGAGCAGCTGGACGACTACATCACTGAGATAGACATCTTAGCGGCCTGTCGACATCCGAACATCCTCTCCCTGCTGGACGCCATCTTCTTT[G/T]AGGGCTGGCTCTGGGTGAGAAATCTGTTTCCTTGTGTTTGTTTTGCAGGATAGTTCAACCAAAACTGAAAACTCTGTCATCGTTTACTCACTCTTTACTTGTTACAAATCCATTTGAGTTTCTTTGTTTTGTTGAGCACAAAATAAACAATAAAAAAAATGTCAACCATTGACGTTCATTTTTGTTTTTCTTGCTATTGATGTAAGTGGTTACCGGTTTCTAACATTCTTCAAAATATCTTATTTTTGTGTTCACAAATGTGTATGTTTTATAAATGCTACATACAATATTGAATACATAATATCGAGTGCTTCCTCTGTGCAGATCCTGCTGGAGTACTGTCCCGGGGGAGCTCTGGATGATATCATGCTGGGTGAGTGTTGATCAGATATTGTTTACAGTAGTATATGCATGACATCATCGTCATCATCATCTTATAGACCATTTCAATGCGATGATGTCATTGGCCCATGAACATTTCCTGCTTGTTATCAAACTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21714
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 |
|---|---|---|---|---|---|
| ENSDART00000127235 | Nonsense | 299 | 1293 | 7 | 17 |
| ENSDART00000140141 | Nonsense | 299 | 693 | 7 | 15 |
Genomic Location (Zv9):
Chromosome 10 (position 20696133)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 20657547 |
| GRCz11 | 10 | 20614928 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACCCAGCAGCTCATGGCTCACCCCTTCTCTTATGCTGGACGAGATGGA[C/T]GAGCCCTAAAAGAGCTCATCGCTGAGGCCAAAGCAGAGGTCACTGAGGTC
Long Flanking Sequence:
ATAAAACCCCTCAGCACTCTCTTTGCAGGTCCTTAGTTTAACAAACCCCTAATCAAATGTTAGAACGTTTAAAAAGTTACATCAGTAGTGGATCAGCATATTCTGTCTTTCAAGGATGGCACCTGAGGTGATCATGTGCGAAACATCGAAGGACAATCCCTACACCTCTAAAGCTGACATCTGGTCAATGGGAATCACTTTAATCGAGGCGGCAGAGATGGAGCCCCCTCATCACTCACTCAACCCAATGAGGGTCCTGTTGAAGATCACCAAATCTCCTCCACCAACACTCTCCAATCCTCGCCAGTGGTGGGTTTTCACTTCCTCATCCCATTTCTAGACCTGCTGTGGTTTACGTTTAAAGGTTTATCTCGATTTCTAAAACCAGGTCGTCACATTTCCAAGACTTCCTTCGAAGGAGCTTGCAGAAGAACCCAGAGGCTCGATGGGGAACCCAGCAGCTCATGGCTCACCCCTTCTCTTATGCTGGACGAGATGGA[C/T]GAGCCCTAAAAGAGCTCATCGCTGAGGCCAAAGCAGAGGTCACTGAGGTCGTAGAAAATGAGGTATTAACATGCAATTAATAACTGATGATTACGTTTGCATTTAATCATCTGGCTACAGAGGCTTTTTTCTAAAGTGATTCACAAATAAGGATAATAAAATTAATCAAAGCAGTCAGAACAGAAATATGTGCAAAAAATTCAATTCCCAGCTAAAGTAGTCTATAACACACACGTATATATGTAGAAACAGAGTAGACAGTAGAATAGAGAATAGATAAAAAGTGTTTCTATAAGAAAGTCAGAGTTTTTCAAAGGAAAAAATTAAAAACATAAAGAATGTTTTATTAAATATTATTAATTTATTATTCCTTAAAAAGGGTCATTCATTCTGCTATGGTAACCCCTGATAATGAAAAATGAGTGAGTATTAATTAGGTATTAATAGAAATAATGTATTCAATAATTAAAATTATTCCTTGCACAGAATACATTAAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21715
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 |
|---|---|---|---|---|---|
| ENSDART00000127235 | Nonsense | 342 | 1293 | 8 | 17 |
| ENSDART00000140141 | None | None | 693 | None | 15 |
Genomic Location (Zv9):
Chromosome 10 (position 20698400)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 20659814 |
| GRCz11 | 10 | 20617195 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCCTCCGTGGAAGACACAATCACCACAGAATCCGAGAAAACACTGCCA[C/T]GACCAGAACAAGCAATAGAAGAACAGGGACCACAAGAACCTGAGACCCCA
Long Flanking Sequence:
TTTCACTTTCAGGGCTATGCTTAGGTTTGTTCTTTCCATTCCCTTTAAAGTGAAATAACTGAACATAAACTTTAGAGCCAGAAAAAAATGCTAATTTTAGAAGAACATTTTAGAAAGCACTTTTGCATATGAATGCTTCACATGTTGTTGGTTATGTTAAACATTATGTGAGGTCTAGCAGTAAAACATAAATGTCAAAGTCAATTGTTGAAGGGCCGCAGCTCTGCACAATTTTGCTCCAACCCTAATCAAACACAGCAGATCCAAATCATTGAGGTGTTCAAAAGAATCTCTAACACCTTGATTAGTTGTATTAGCCGTGTTTGATTAGTTTTGGAGCAAAACTGTGCAGAGCTGCGGCCCTTCAGGAATTGACTTTGACACCTCTGCAGTATAAGATTAATGCATCTTTTTCTGCATCTTTACTTTCACAGTCTTTGTTCAATATCCAATCCTCCGTGGAAGACACAATCACCACAGAATCCGAGAAAACACTGCCA[C/T]GACCAGAACAAGCAATAGAAGAACAGGGACCACAAGAACCTGAGACCCCAAAGAAGACCTCGGTTCTGGACACTGTTCCTCAATCCCCCATCAACTCAGAGCTAAATCCTGAGGTCAAAGTGACCCGCAGGGCTTCACAGGCCACTAATCAGGTCAAAACTCAAAAGAGGGCAAGACGCCTCTCTGTTCCAGGAAATCTCCTTTCGTTTCTGTCTGGCGGCTCCCGTCGCTGCAAATCTGGATTCTGGGGTGACAATTCACCAGTTCAGGTAACTAAAAACTCAGAAGATTCAAGTGCAGCTGAAACTGTGGGAACATGCCCTTCAGATGGTACTGAAAGTGAAAACACTGCCAAACCAAAAGAGGAAACACCTGACGTAGTCGATGCTCCAAGTAACAAAGTTGCTGACATCAAAGATGAGGTTGATACAGAAGAAACTGACAAGAACTTAAATCTCTCCAGTGCACCAGCACAAACAACAGTTTCTTCTGAAAGTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31778
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 |
|---|---|---|---|---|---|
| ENSDART00000127235 | Nonsense | 922 | 1293 | 9 | 17 |
| ENSDART00000140141 | Nonsense | 361 | 693 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 10 (position 20700231)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 20661645 |
| GRCz11 | 10 | 20619026 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTCCAAAGTGGTTAGCGAGGGAGACAGCAAAGAAAAACTAATGCGCTA[C/A]AACAGGTAACAAGTCTTTATGCTTTACACCAGGGGTGTCCAAACTCGGTC
Long Flanking Sequence:
TGAAGAAGAGTTTCCAGAAATCTCTAATACAACACCTGACAGTACAGAAGAGGACTCAAAGGATGCTGTTGAGGATACAACAGTTGTTTCTGAATCAAAGCTGAAAAAGCAGGTAATGTTTGTAGTTCAGGATGACAAAAACAAAGAGAAGCTTGCAAATGGCTTGAATGATTCAGACTCAGTTCTACCACATGAATCGAATGGATCCACACATAAAGAATCTAATGAGGACATGATACCACCTCTTTCTCCCACCAGTCCTCCGATGTCTCCTGGGTTTGAAGGGGTGAGTCTGAAACTAGCAATGTGCTTAAGACATTAGCAAACAGTCAATTTCAACATTGTTCTAACTTTTATTAATTTTGGGGTATTTAGGAATTGCATCCCAGCAGGATGACCGTTAAAAAGACCCGCAAATTTATGGTGGATGGTCGTGAAGTCAGTGTCACCACTTCCAAAGTGGTTAGCGAGGGAGACAGCAAAGAAAAACTAATGCGCTA[C/A]AACAGGTAACAAGTCTTTATGCTTTACACCAGGGGTGTCCAAACTCGGTCCTGGAGGGCCTGTGTCTGGGAGAATTTAGCTCTAACCCTAATCAAACACACCTGAACCAGCTAATCAAGCTCTTATTAGAGATACTAAAAGCTTCCTGGCAGGCCTATTGAAGCAAGTTCGATATAAACTCTCCAGGACCAAGTTTGGACACCCCTGCTTTACACTATTTAAAATAAAGGTTGACACCAATAGTTGCATGAAGAACGTTTTAACTCCCATGGAGACTTTCCATTCCACAAGAATAAAGAAGCTCTGTAAATTAACAGAATGTTCTTCAAAAAGAAAAACTTGACCCCTGAAATGTTCTTTAGAGAATCAAAAATGTTTCTTTGCCATCATTGTGAATTTTTTTAGCTTGGAACATTTATTTTTTAAAGTAACTTTATGGTGTACGTGGAAAGTGTCACATTCTAAATATGTTTGGGTGTTTATAGACGGCAGGAGCTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18421
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:
Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000127235 | Splice Site, Nonsense | 924 | 1293 | 9 | 17 |
| ENSDART00000140141 | Splice Site, Nonsense | 363 | 693 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 10 (position 20700235)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 20661649 |
| GRCz11 | 10 | 20619030 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAAAGTGGTTAGCGAGGGAGACAGCAAAGAAAAACTAATGCGCTAYAAC[A/T]GGTAACAAGTCTTTATGCTTTACACCARGGGTGTCCAAACTYGGTCCTGG
Long Flanking Sequence:
GAAGAGTTTCCAGAAATCTCTAATACAACACCTGACAGTACAGAAGAGGACTCAAAGGATGCTGTTGAGGATACAACAGTTGTTTCTGAATCAAAGCTGAAAAAGCAGGTAATGTTTGTAGTTCAGGATGACAAAAACAAAGAGAAGCTTGCAAATGGCTTGAATGATTCAGACTCAGTTCTACCACATGAATCGAATGGATCCACACATAAAGAATCTAATGAGGACATGATACCACCTCTTTCTCCCACCAGTCCTCCGATGTCTCCTGGGTTTGAAGGGGTGAGTCTGAAACTAGCAATGTGCTTAAGACATTAGCAAACAGTCAATTTCAACATTGTTCTAACTTTTATTAATTTTGGGGTATTTAGGAATTGCATCCCAGCAGGATGACCGTTAAAAAGACCCGCAAATTTATGGTGGATGGTCGTGAAGTCAGTGTCACCACTTCCAAAGTGGTTAGCGAGGGAGACAGCAAAGAAAAACTAATGCGCTACAAC[A/T]GGTAACAAGTCTTTATGCTTTACACCAGGGGTGTCCAAACTCGGTCCTGGAGGGCCTGTGTCTGGGAGAATTTAGCTCTAACCCTAATCAAACACACCTGAACCAGCTAATCAAGCTCTTATTAGAGATACTAAAAGCTTCCTGGCAGGCCTATTGAAGCAAGTTCGATATAAACTCTCCAGGACCAAGTTTGGACACCCCTGCTTTACACTATTTAAAATAAAGGTTGACACCAATAGTTGCATGAAGAACGTTTTAACTCCCATGGAGACTTTCCATTCCACAAGAATAAAGAAGCTCTGTAAATTAACAGAATGTTCTTCAAAAAGAAAAACTTGACCCCTGAAATGTTCTTTAGAGAATCAAAAATGTTTCTTTGCCATCATTGTGAATTTTTTTAGCTTGGAACATTTATTTTTTAAAGTAACTTTATGGTGTACGTGGAAAGTGTCACATTCTAAATATGTTTGGGTGTTTATAGACGGCAGGAGCTGCATGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34886
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 |
|---|---|---|---|---|---|
| ENSDART00000127235 | Nonsense | 1168 | 1293 | 14 | 17 |
| ENSDART00000140141 | Nonsense | 607 | 693 | 13 | 15 |
Genomic Location (Zv9):
Chromosome 10 (position 20706582)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 20667996 |
| GRCz11 | 10 | 20625377 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTGAAAATGGAGCTGAGAAAGCAAGGTCTGAGCGGCCCTGAGCAGAGA[C/T]AACATCTCACACAGGTTTGGATGCAGAAACCTCAGTGTCAGAATAATGTG
Long Flanking Sequence:
CCTGACCCAAGTGTACACTATACTTTCATGCATTATGAACAGTAAAACTAAATAAACAGTGGCTTTAAAACATACTTACAGGTGGTAAATGATTCCAAACATGCATTTTCCTCTTCCTTAAGCTCGAGAAGCTGTGATCTGGGAGTTAGAACAGCGCCATCTACAGGAAAAGTATCATCTATTTAAACAGCAGGTGAAAGAGCAATATTCCCTACAAAGACAGCAGCTGACCAAGAGACATAACAAGGTAACATCCAAAACAATCTGTTTGTTTTTTATCCTCTATGTTTATTTGTATCTTAGTGACACCTTTGTTTCTCTTCTGGCAGGATAAAGAGAGAGCGTCCCGCTTCCAGCAGTCTCTCCTGGAGGAGCAGAAGTCACTGCAGGCCCAGGAGAGAGCGTCGTTCCTGAAGACCCAAAAAGCTGAAGCAAAATCCCGTCTGAATCAGTTGAAAATGGAGCTGAGAAAGCAAGGTCTGAGCGGCCCTGAGCAGAGA[C/T]AACATCTCACACAGGTTTGGATGCAGAAACCTCAGTGTCAGAATAATGTGTGGTTAATTAATAACACTTTGATTAAAATGGAACTGTTCCTCTCTGGGTTTATATTTAGCTTTTGTCTGAAGAAGAGGCCAGACAGAAGCAAGAGAAACAGAGTCTTCAAGAAAGTCACGAGAGCCAATTGAAAGCAGTGCAGGAACAATGTGATGCCAGTACAGCTGAACTACAGCAGCTTCAGGTACGTCAGCAACAGCTTGTTTAGAGCCTAAAGAAAAAATCAGACTGAATAAGGTTTTAAAAAGTATATGTATAATAGTTCAATATATTTTGAAAAGTGATGGGAATAATGGCGCTATAAATAAACGGTATTACTAATGGTAGTACTTTTTTTTCAATAACGAGTAGGGTTGGGTATCTTTAGGGTTATTTCGATACCGGTGCTAAAGTGATACTTTTAAAACGGTACGAGTGCCAAAACAGTGCCTGAACCTAAACTTTTGAGC
Associated Phenotype:
Not determined