ZMP
stk25b
Ensembl ID:
ZFIN ID:
Description:
serine/threonine-protein kinase 25 [Source:RefSeq peptide;Acc:NP_998473]
Human Orthologue:
STK25
Human Description:
serine/threonine kinase 25 [Source:HGNC Symbol;Acc:11404]
Mouse Orthologue:
Stk25
Mouse Description:
serine/threonine kinase 25 (yeast) Gene [Source:MGI Symbol;Acc:MGI:1891699]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32903 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa10029 | Nonsense | Available for shipment | Available now |
sa6836 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa852 | Nonsense | Available for shipment | Available now |
sa15243 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32903
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056963 | Essential Splice Site | 10 | 424 | 1 | 11 |
ENSDART00000146425 | None | None | 341 | None | 9 |
Genomic Location (Zv9):
Chromosome 2 (position 22093972)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 22980677 |
GRCz11 | 2 | 22636328 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGCTCTCATCCACTGAGATGGCGCACCTCCGCGACATGCAGAACCAGG[T/A]AAATCCGCAGCCCTGCCGAAGCTGCTCATCCTGCATCCACCCTGAGCTTT
Long Flanking Sequence:
ACATATTGACAAATGAGTTCACAAAGGTCTAACGTACAAGATAAATGGGAAAATAATTTGGATTTTAATTTCTGTCCAACTACAACTCCCACAATTCCTCATTCCTTGAATCATAATCTGCGCATGCGCTGTAGGTCCTATTATTTTGTTCTCCCGCAAGCAATAAATGAAGAGCCGCCCGAGCCTGCGTTGATCGTTATAAAACAATAACACGCGGAAAGCGGTTCGCTCGCACGCTGATGCTTTCATAAATGGAGTCACACGACACATAACTGTCATTCTCGCCAGGCTGCGGGGTCCGCCATCAGGGGATTGGAGGCCGAAAACGCGGCTGACGAACAGGACATGCAGAGGTGTTTTTGTATGTAAAAGCTAGCTAGCTAAGCAGGGGAACCAGAGTAAAACGTTGTAGAGTTTGTCAGCACCCCTTCTTTGGCAGAAAAGGCTACATCTGCTCTCATCCACTGAGATGGCGCACCTCCGCGACATGCAGAACCAGG[T/A]AAATCCGCAGCCCTGCCGAAGCTGCTCATCCTGCATCCACCCTGAGCTTTAATCTCGCTGTCTGTAGCATCACATTAACGTTTGGGGAGGCTGTCATGTCATGACATTTCTTTCTTTTAGTAATTAAAGCGGTCCTGACTTTATGTTGTCAAGATAACCGTTTAATGAAGCGTCTGCTTTTTGCTACGGCTTCAGTCCTGTTAAATTGTATAGATTAACGTGCTGTTTAGTGAAGCAGCTTTAGTTTGTGCAGATGTGATGTAGTCTGTGTTTTAAAGTGCCCACTGATTTATAACACAACATCTGTAATGGAGTTTTGTGTGTATTTGTATGCATGCATGCATGCATGCATGTGTGTGTGTGTGTGTGTGTATATGTGTTTGGTGTGTGTGTGTGTGTGTGTGTGTTTGTGTGTATCTGTGTGTGTATATATGTGTACTGTATATATGAGTGTTTGTTGTGTGTGTGTGTGTGTACGTAAATATGACAGGGCTTTTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10029
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 |
---|---|---|---|---|---|
ENSDART00000056963 | Nonsense | 189 | 424 | 5 | 11 |
ENSDART00000146425 | Nonsense | 100 | 341 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 2 (position 22087008)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 22973713 |
GRCz11 | 2 | 22629364 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAACACTTTCGTGGGGAYTCCTTTCTGGATGGCTCCTGAGGTCATCAAA[C/T]AGTCTGCGTATGACTTTAAGGTGAGGATATCCGGATGAATGATTCTGAGC
Long Flanking Sequence:
CACTGGTATTCATTTTTCTTGCTTGTATACGCTTCCTTCCACTCTTCTTACTGTAGCACCACAGTTTCAGCTAAAAACATCCTTTAATGCTCTATTGAAGAAAGAAAGCTGGACTCAGAAACTACTAAATCTTCTTCCTTTCCTCCACCCTTAGTTGAAACCAGGCCCGCTAGAAGAGACGTACATCGCCACTATACTGAGGGAGATTCTGAAGGGACTGGAATACTTGCATTCGGAAAGGAAGATTCACCGTGATATCAAAGGTGTGATCACCCACACGTCTGCCTACTCCATCAGGCTTCATTTTCGGTTGATCAGTTGTATTCAGTGCCGATGATTCACATTTGTGTCTTGTCGCCGCAGCTGCCAACGTGCTGCTGTCTGAGCAGGGTGACGTGAAGCTGGCAGACTTCGGGGTGGCAGGACAGCTCACAGACACCCAGATCAAGAGAAACACTTTCGTGGGGACTCCTTTCTGGATGGCTCCTGAGGTCATCAAA[C/T]AGTCTGCGTATGACTTTAAGGTGAGGATATCCGGATGAATGATTCTGAGCGTGTAGTAGAGCAAGCTGAATATTAATGAGGCTGCAGAGCTGTGAAAGCACACGTTCAGCAGAAAGGCTGGAGTGGTAAAACTGTTCATCAGTGCTTTTTTTTTTCTTAAAGTGGTAGGCATGGAAACCAATCAAAGTACGTTTTAGCATAGTAGCAGCTAATATTTTTTTTCTGGAATGTTTATGTAATGTTTATTTGTGGGAATTTTTCATGACATAAACAAAGATGGTTTGTTTTTTGACTGCAGGCAGACATTTGGTCCTTGGGAATTACAGCTATTGAACTGGCGAAGGGGGAACCCCCAAACTCGGACCTGCATCCAATGCGAGTTTTGTTTCTCATTCCCAAAAACACTCCTCCAACGCTGGAGGGCTCCTACAGCAAACCCTTCAAAGAGTTCGTTGAGGCTTGCCTCAATAAAGACCCTCGCTTTGTGAGTATTTCAGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6836
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056963 | Essential Splice Site | 196 | 424 | 6 | 11 |
ENSDART00000146425 | Essential Splice Site | 107 | 341 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 2 (position 22086711)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 22973416 |
GRCz11 | 2 | 22629067 |
KASP Assay ID:
554-4563.1 (used for ordering genotyping assays)
KASP Sequence:
TTGTGGGAATTTTTMATGACATAAACAAAGATGSTTTGTTTTTTGACTGC[A/T]GGCAGACATTTGGTCCTTGGGAAYTACAGCTATTGAACTGGYGAAGGGGG
Long Flanking Sequence:
GCTTCATTTTCGGTTGATCAGTTGTATTCAGTGCCGATGATTCACATTTGTGTCTTGTCGCCGCAGCTGCCAACGTGCTGCTGTCTGAGCAGGGTGACGTGAAGCTGGCAGACTTCGGGGTGGCAGGACAGCTCACAGACACCCAGATCAAGAGAAACACTTTCGTGGGGACTCCTTTCTGGATGGCTCCTGAGGTCATCAAACAGTCTGCGTATGACTTTAAGGTGAGGATATCCGGATGAATGATTCTGAGCGTGTAGTAGAGCAAGCTGAATATTAATGAGGCTGCAGAGCTGTGAAAGCACACGTTCAGCAGAAAGGCTGGAGTGGTAAAACTGTTCATCAGTGCTTTTTTTTTTCTTAAAGTGGTAGGCATGGAAACCAATCAAAGTACGTTTTAGCATAGTAGCAGCTAATATTTTTTTTCTGGAATGTTTATGTAATGTTTATTTGTGGGAATTTTTCATGACATAAACAAAGATGGTTTGTTTTTTGACTGC[A/T]GGCAGACATTTGGTCCTTGGGAATTACAGCTATTGAACTGGCGAAGGGGGAACCCCCAAACTCGGACCTGCATCCAATGCGAGTTTTGTTTCTCATTCCCAAAAACACTCCTCCAACGCTGGAGGGCTCCTACAGCAAACCCTTCAAAGAGTTCGTTGAGGCTTGCCTCAATAAAGACCCTCGCTTTGTGAGTATTTCAGTTATATGACAGGATTTCCCAATATGCAATACTGGCCAAATTTTTGATGAAGATTTGTTTTGCTAGCAAGATCTGGCTACAAGAGTGTGACATGCATTTAAAGGGATAGTTCACCCAAAAGTGTAAATTCCCTGTTAATTTTTTCATCCTCAGATCATCCGAGATGTAGTCTTTTTTCCAGTAAAACAACAAAGTTCTTGAGAAATCAAGATTTAAATTGAGAGGAAGGAGCCATTAATAGTGGGAAAGAAAAAGTGAATGGCTTTTTTTCTGCTTTTATTTAGACTTTTAATTCAGTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa852
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 |
---|---|---|---|---|---|
ENSDART00000056963 | Nonsense | 239 | 424 | 6 | 11 |
ENSDART00000146425 | Nonsense | 150 | 341 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 2 (position 22086578)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 22973283 |
GRCz11 | 2 | 22628934 |
KASP Assay ID:
554-0755.1 (used for ordering genotyping assays)
KASP Sequence:
GTTYTGTTTCTCATTCCCAAAAACACTCCTCCAACGCTGGAGGGCTCCTA[C/A]AGCAAACCCTTCAAAGAGTTCGTTGAGGCTTGCCTCAATAAAGACCCTCG
Long Flanking Sequence:
CACAGACACCCAGATCAAGAGAAACACTTTCGTGGGGACTCCTTTCTGGATGGCTCCTGAGGTCATCAAACAGTCTGCGTATGACTTTAAGGTGAGGATATCCGGATGAATGATTCTGAGCGTGTAGTAGAGCAAGCTGAATATTAATGAGGCTGCAGAGCTGTGAAAGCACACGTTCAGCAGAAAGGCTGGAGTGGTAAAACTGTTCATCAGTGCTTTTTTTTTTCTTAAAGTGGTAGGCATGGAAACCAATCAAAGTACGTTTTAGCATAGTAGCAGCTAATATTTTTTTTCTGGAATGTTTATGTAATGTTTATTTGTGGGAATTTTTCATGACATAAACAAAGATGGTTTGTTTTTTGACTGCAGGCAGACATTTGGTCCTTGGGAATTACAGCTATTGAACTGGCGAAGGGGGAACCCCCAAACTCGGACCTGCATCCAATGCGAGTTTTGTTTCTCATTCCCAAAAACACTCCTCCAACGCTGGAGGGCTCCTA[C/A]AGCAAACCCTTCAAAGAGTTCGTTGAGGCTTGCCTCAATAAAGACCCTCGCTTTGTGAGTATTTCAGTTATATGACAGGATTTCCCAATATGCAATACTGGCCAAATTTTTGATGAAGATTTGTTTTGCTAGCAAGATCTGGCTACAAGAGTGTGACATGCATTTAAAGGGATAGTTCACCCAAAAGTGTAAATTCCCTGTTAATTTTTTCATCCTCAGATCATCCGAGATGTAGTCTTTTTTCCAGTAAAACAACAAAGTTCTTGAGAAATCAAGATTTAAATTGAGAGGAAGGAGCCATTAATAGTGGGAAAGAAAAAGTGAATGGCTTTTTTTCTGCTTTTATTTAGACTTTTAATTCAGTGTTGATGTACTTGCAACTGAAACTGAATATTGAGTATGGGATGGGGCTTTCTTTTGCTCTTTGTTTTCTCATATGTGGCAAAAGTCATCAAACTGACATCAGCAGTGAAGGACCACCACTCCAAAATGCTGAAGCA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa15243
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 |
---|---|---|---|---|---|
ENSDART00000056963 | Nonsense | 287 | 424 | 7 | 11 |
ENSDART00000146425 | Nonsense | 198 | 341 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 2 (position 22084817)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 22971522 |
GRCz11 | 2 | 22627173 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACACGATACACCAAGAAAACGTCTTATCTGACAGAGCTGATCGACCGATA[C/A]CGCCGATGGAAGTCYGAGGGCCAYGGAGATGAGTCTAGCTCTGATGATTC
Long Flanking Sequence:
TTAAAATTTATTTTTCTCTCTGACTTTAATGTTCTACTGCAGAAAAAATAAAAAATGTTGGAAAAAAAGCAGCAATCGACATTCATACTAGGAACAAAACATACTATACAGGTTAATGGCAGTCTTTTCCGCAGCATTCTACAAAATATCTTCCTTTGTGTTCAACAGAATAAGGAAACTGAAACAGGTTTGGAACAAGTGGCAGATGAGTAAATGATGACAGGTTTTGGGTGAAGTATCCCTTTAAGATCTAAAACATCAAATGACAATCTTTTGACCAGTAATGTGGCTAATTTTTAAATTACATGATTAAGCGATGGTTATAGTTAGACATCTTAATATTTCCTAAATGAGGCCGTCATGACGTTGTGTATTCTGAGCATGGCATTACTGTGTTCTTGTTTTATGCAGCGGCCCACAGCCAAGGAATTATTAAAGCACAAATTCATCACACGATACACCAAGAAAACGTCTTATCTGACAGAGCTGATCGACCGATA[C/A]CGCCGATGGAAGTCTGAGGGCCACGGAGATGAGTCTAGCTCTGATGATTCTGACATGTACGCCGTCCATCCATTGTAATGCATATACTGAATGATCAATAACCGCACTGTAATTCATCATGATGTATTATTCATTATTTATTACATGACAACTGGCCTTTTAATTTGAGCTCTGCTATATTGATCCTCATAAGTTCTAGCTATGAATTGAAACCGTTCTCTGTTTCTCCTCGTACTCATACAGGGATGGTGATGGTGATGATAGAGACCACTGTCCTGTGTGGACGTTCCCCACAGTTCGGCCCAGCTCCATGAACAAGCTCCAGAAGGGCTACACAAACACAGACTCAGAGGTAGGGCTGTGCAATTTATCGAAAATCCGATTTCGATTTTGGCTTCTAACGATTATGAAAAATCATTAATCAAGATAAATGATTATTCCATTATTTACCACCCCCTTTCCAGTTCTCCTCACTTGTTGCTCTTAAAAGCGCGAAAGAC
Associated Phenotype:
Not determined