ZMP
stk36
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A2BFU1]
Human Orthologue:
STK36
Human Description:
serine/threonine kinase 36 [Source:HGNC Symbol;Acc:17209]
Mouse Orthologue:
Stk36
Mouse Description:
serine/threonine kinase 36 (fused homolog, Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1920831]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38479 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa11597 | Essential Splice Site | Available for shipment | Available now |
| sa25300 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38479
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 |
|---|---|---|---|---|---|
| ENSDART00000086765 | Essential Splice Site | 315 | 1231 | 7 | 20 |
| ENSDART00000136101 | None | None | 119 | None | 2 |
| ENSDART00000146167 | Essential Splice Site | 315 | 500 | 7 | 11 |
The following transcripts of ENSDARG00000061095 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 32038765)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29799595 |
| GRCz11 | 5 | 30399748 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCGGCAAAGCCAGAGAGCTTCGAGAGAAAGAGAAGACTAACAGACGGG[T/C]AAACTGAAACAACATCTGGAAACAACAGCAGGAACAAACAAAAACTGTAG
Long Flanking Sequence:
TGTGTATACTCTGTAATAAATTATTGTTACACAGAATTGTAGTTCATAGTAAAAATGCATGATATTCATTATTTTTGACAGAAAATATAATCTAACAGGACACATTATAAATAATGTAACAAGAAATAACTTTAAAGTTGTATTACAATTTTTGCTTTGATGCTTAAAAACACATTTGTCATATATATTTAAACATATGTAAACCTCTCATCAAATGGAACCCAAGAAAAAAACAGTTTTTACATACATTTTACATAATCTACATCAGTTTTACATGTCTTAATGACACTGTTTGGCTTTCTCTAAAGTGGTGATGTTGTTTGCTTTGACAGTGGTGTCAGATGAAGGTTCGAGTAACCCGCTCACTGTTCCACCCAGTCCAGACGTCCAGGCCCTCAAACACCAGCAGGTCGCAGAAAAAACAACAGTGCGCAGCGGAGAAGGCAAACTACTCGGCAAAGCCAGAGAGCTTCGAGAGAAAGAGAAGACTAACAGACGGG[T/C]AAACTGAAACAACATCTGGAAACAACAGCAGGAACAAACAAAAACTGTAGTCCTTCTTAGTTCTATGTATTAAATTGTTTTGAATCTGTTTTTTAGATGTCTTTCTGTCTGATTTCTAATTTATTTTTGCTCTAAGAAGTTTATGCAAATTAAATCAGTGCTATTGTTGTGATTTGTGCATATTAGACTATATATTGTTTACATTTATACAGAATTTGGAGAGGATGAGAGAAAATCCTGTATAGGTGTAATGTGTTTCTATGAAAATGTAATAAGAAATGTTGGCTGTTGATTAACTAGGAGGTTGCGAGTGGAAGTGCTGCTCGCTGTAAGACAGCTTCAGCTGGAGGAGCATCCAACACCGGCCATTCATTGGGCAGCACCTTTTCAGTGTATCAAAATTCATCTCAGCCAGCAACCAATCGGCATCAAGCAAATGACAACAGTGTTACCAGGTAGTATTTCCATCTAGAATTTGAATTTGAAAAACCTGCGGGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11597
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000086765 | Essential Splice Site | 613 | 1231 | 15 | 20 |
| ENSDART00000136101 | None | None | 119 | None | 2 |
| ENSDART00000146167 | None | None | 500 | None | 11 |
The following transcripts of ENSDARG00000061095 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 32044875)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29805705 |
| GRCz11 | 5 | 30405858 |
KASP Assay ID:
2259-5973.1 (used for ordering genotyping assays)
KASP Sequence:
GGGCCTGTGTGATGGCCTTCTGTCACTGATTCTCCACAGGCTAGCTGAGG[T/A]AATTTCTCTYTGATTAATTCCTCTCAAATCTGCGCTGGGCTAATTAGATA
Long Flanking Sequence:
TCTCTAGCTAAAAGGTTTTCTCTGAAACACTTTTAAACTGGGAAATAAAGCGGAGTACAGTAATCGTGGGATGTCTGCTTTCATTTGCATTACACTTGATTCTGTGGTCTCTCCTACAGCTTTTGGCAGCAGCAGTCTTAACCTTGTTCACACAGCGCGGTGTGTCTGTGAATGTCGGTATAGAAAAGCTCACGGCCGTTTTGGGGGATGTTTTGACATACACAGAGGTACAGTTCTATTATTTATCCTGTGAATAAGGGTTAACAGTGTTTGGAGTAATTAATGTCACTGATGTGATGAAATCCAGTGTAGTCAATTCCCACCTTCTCACTCTCTGCGTTTCTTTCCCTCTCCACCTCCCACCATCTGTCTGCTCTCTCTGTTTTTCTGTTTCTTTCTTTCTCTCTCTTTTTTTTTCCGATAGGCTCATAACCCCTTACCTGCAGGTTGGGGCCTGTGTGATGGCCTTCTGTCACTGATTCTCCACAGGCTAGCTGAGG[T/A]AATTTCTCTCTGATTAATTCCTCTCAAATCTGCGCTGGGCTAATTAGATACAGACAGATAATCGGTTTGGACAGTTGTCTAATATTGGATCTACGATAAATGGTGTAGTGTGAAATCTGAGGGAAACGCCACAGAGCAATGCTATTTAAAGAGCAAAGAACTGATGTAACTTTTTAAAATAGCAAGTGCTTATGAAGAAATGTTTAGCGGAACAAGGGTCGAAGATAAAACTGGCTTTTATTCATTCATCCATTTTCCTTTGGATTAGTCCCTTTATTAATCTGGGGTAGCCACAGTGGAATGAACCACCAACTTATCCAGCATATGTTTTACACAGCGGATGTCCTTCCAGGTGCAACCCAGTACTGGGAAACATCCATACACACTCATTCACACAAAATTTAGTTTATTCAATTTACTTCTCTTTGGACTGTGGGGGAAACCAAAGCACAGGGAGAACATGCAAACTCTACATAGAAATGCCAACTGACCCAGCTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25300
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000086765 | Essential Splice Site | 753 | 1231 | 18 | 20 |
| ENSDART00000136101 | None | None | 119 | None | 2 |
| ENSDART00000146167 | None | None | 500 | None | 11 |
The following transcripts of ENSDARG00000061095 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 32048006)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29808836 |
| GRCz11 | 5 | 30408989 |
KASP Assay ID:
554-7772.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTTCTCCAGTCATATCAAAGCTCAAATATTGTTGCAGGTCTAGTACAG[G/A]TATGGTTTATTAATATGCTCCACGATTTTCAGAAGTCATTTTGAGAAAAT
Long Flanking Sequence:
TGGTAGTGAACATGAAGAGAACATTCGTTTATTTCTCTAGTGCAACTTTGATATAACGTAATAACTTACACTTGTCTCTGTTTTCCTCTCAGGTCTGTATATGTTCCTCTCTCTGGCTTTATTGCTTTTCTCCAGCGATCCATACACCTGTGTGACTCTCCTATCAGATAACACCACAAACTGCTCCTCCACCCTCGGGCACCTTCTCACCACCAGTTGGTGAGCCTCAAACATAAAGCGCTTTTCTTTTTCTCTTATATTAGTATTCATTCAGAAGTGCTCCTCTCAGAGGTTTACAATGTATTTCTCATTTTATTCCTGACAGCAGCGCCTCATTGCTTGAACGTGGTCTTTTCTGGGGCGACTCAGAAATAAACAGCCTATCAGTGATGAGCTGTCATCTCCTCTGCATCCCCTTCTCTCTGGACTTGCCCCTGGAAAAACATCTGTCTGTTCTCCAGTCATATCAAAGCTCAAATATTGTTGCAGGTCTAGTACAG[G/A]TATGGTTTATTAATATGCTCCACGATTTTCAGAAGTCATTTTGAGAAAATGTCATTTTTATTTTTTTCTGCTGACTGGTCTTCTTGTTCAGATGATTCAGACTATTCCTATTGCCTTGGTGGAGCTTCCGTTGTGTCTTCTGAATCGTCTCCTGCTATCTGACCCACAACACACCACTCCGTGCCTTATCACTGCCGCCCAGGCCTCCGCTTTCCTCCCGCACGGCACAGAAAGCTCAGACAATGGAGCAGACCACACTCAGACTCAACTAAAGCACTCTGGGAATGGTGTTGAGCGAAGTAAGAGCAACGGAATTGTAAAGAAAACCAAGATTGATCATATCAAAGGAGACATCAAATCAAAAAAGAGCTTAGACCGACCCACAGGCGACGTAGATGCATCCAGGGACAAAAACAGTTCTCAAAACGCACCATCCAGAAATATTCGCCAAACCAAAGTCAAGAGTCAAGCCAAAACATATCCAACGAAGGCCATGGAGC
Associated Phenotype:
Not determined