ZMP
slka
Ensembl ID:
ZFIN ID:
Description:
STE20-like serine/threonine-protein kinase [Source:RefSeq peptide;Acc:NP_001139073]
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 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6301 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa5860 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6301
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 |
---|---|---|---|---|---|
ENSDART00000087786 | Nonsense | 857 | 1206 | 12 | 19 |
ENSDART00000136177 | None | None | 121 | None | 3 |
ENSDART00000142745 | Nonsense | 852 | 1201 | 11 | 18 |
The following transcripts of ENSDARG00000061525 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 25026736)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 24672396 |
GRCz11 | 13 | 24802846 |
KASP Assay ID:
554-5448.1 (used for ordering genotyping assays)
KASP Sequence:
AAAAAGAGGAGCAAAGGGCTCAACAGCAGCTCAGCAATAAACTGCAGCAG[C/T]AGAAAGAGCAACTCTTCAGACGCTTTGAGCAGGAAATGTCGGTCAGCAGC
Long Flanking Sequence:
ATGCGGAGCACTGCATGTATATGTACTGGCCACTGATACACAAGAAATTAACTTTTTCTGATTTTGTCTGAAGTGTAATAACATTCCCGCTTTGTAAAGCAACTTTGTATTGTATTGTTGTGAAAAGCTCTATATAATCAAAATTTAATGGAATTTGTAACTCACAGGACATCAAACGCCAAAAGAAAACCCTGAAAAAGACTCGCAAGTTTTTGGTCGACGGGGTGGAAGTCAGTGTCACCACATCCAAGATTGTCACAGACAATGACACCAAGAGTGAGGAACTGAGATTCCTGAGGTATCTGAAATAACATCAGTTACTCTTTCTAGTCAATTTGCAAATGATGAATTTGATAATGCATGAATAACAATATATATTAGTTGAAAAGTTTATAAAGAGTTATTTGTTGTTCTGTAGGCGCCAAGAGCTACGAGAACTGAGGCTGCTGCAAAAAGAGGAGCAAAGGGCTCAACAGCAGCTCAGCAATAAACTGCAGCAG[C/T]AGAAAGAGCAACTCTTCAGACGCTTTGAGCAGGAAATGTCGGTCAGCAGCCTCATTCCTATACTAGATTTGTTTCCATTCAACATCTTAATCTGCTGTTGACTGTTTAATGTACACTCAGACAAGGCATGATGAAAATTTAAGAGCATAACAAGCAATGTTTGTGTTATGTTAATATTATTTTGCGATTTGTGGATGCACCCAATCAAGTTTTCCTGCTCCAAAATTTGGCTTCTTTGCTAAAGGAACTTTTGATTTTTGAAAATAAGCTCATTCAAGAAGCCCTTTCGAGTTAAACTTTTGAATTTTTTATATTTTTAAAAATTCATTCAGTCTTCAACAGAAAATTTCCCTGATTATTATTTCAGAATAAGAGTATACTTCCCCTAGACATATTGAACAAAAAAATAGCAACCTTTCATTTCTAACCCTTTTTTATACACAAACAAGCACAGAATAATTATCAAAACTCTTTTTTTATTATTTGTTTTGTTTTTGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5860
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 |
---|---|---|---|---|---|
ENSDART00000087786 | Nonsense | 1117 | 1206 | 17 | 19 |
ENSDART00000136177 | None | None | 121 | None | 3 |
ENSDART00000142745 | Nonsense | 1112 | 1201 | 16 | 18 |
The following transcripts of ENSDARG00000061525 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 25009612)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 24655272 |
GRCz11 | 13 | 24785722 |
KASP Assay ID:
554-3862.1 (used for ordering genotyping assays)
KASP Sequence:
ACCAGATGAGAGACCTGCAGCTGCAGTGCGACTCCAACATCAGAGAACTT[C/T]AGCAGATGCAGGTCTGCAACATTACCTTGTGCTCGCMTGTTTGAGTTCTT
Long Flanking Sequence:
TGAACTAATAGTTCATTATTCTAAAATCCAATATCAATGACAATATTGGTCATTACTTGTCCACAATTTCTTTACACCATTTCCATAGAAAACCCCATTTTCCATTATTTTAGTTTTTAAAAGAATATTCAGGTTTGCATCCTTAATATCTCCATTGCAGCTGCTTTCCAGTGTTCTAGTGTGGGTGAATTCAGCTAAAGTCATTCATGGGTATTATATTTTTTGGCTGTGACCTAAAATATTCTCCACAAATTTGTAAAAAATGGTTTTGGAAAAAAGTCTTTGAAAATTGAGTTTTTAATTTTAAATGCACCCAGTATGTGAAAATAATACACATGATTTGGGAGAGGGTTAATCTTCTGGGGTGTTTTTCACTTTTTCAACAGTTTGCAGTTCAGGAGGACAAGAGACAGAAGAATGAGAGACTTCATCAGCATCAAAAACATGAGAACCAGATGAGAGACCTGCAGCTGCAGTGCGACTCCAACATCAGAGAACTT[C/T]AGCAGATGCAGGTCTGCAACATTACCTTGTGCTCGCATGTTTGAGTTCTTTCCCTCTTCTGTTCTGGCTTATCTTAAATTGCATCATCTGGTTGATTGTCTTGTTGCCATCAGAATGAGAAATGTCACCTGCTGATTGAGCATGAGACTCAGAAGCTGAAGGAGCTTGATGAGGAACACAGTCAGGAGCTAAAAGAATGGAGGGAGAAGCTTCGGCCACGGAAGAAGGTAGAGTAACAACATTATTTACCTTTTCAGTGCATCTAATCAAACCTGATCATTAAATTTGAATGCTGCATTTTCCCCCATGTCATATATTGTGGGTTTCCAGACAAGCTCTTAGAAGGAGAGAAAAAATCTGTCCTGCACACTGTGCTAAGGTAGTGTGAGTGTCAAAGTTCACTCTGGCCACCCTAGTTACAACGCTGTCTGTCTTCTTAGCTCCAGCACTGAGAGCATCAAAATTCGCTACATTGATCTCATATTTAAAGCAGCTGTTGA
Associated Phenotype:
Not determined