ZMP
si:ch211-147h1.4
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to zebrafish pim-1 oncogene (Pim1) [Source:UniProtKB/TrEMBL;Acc:Q6ZM85]
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 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2647 | Nonsense | F2 line generated | Not yet available |
sa16385 | Nonsense | Available for shipment | Available now |
sa16035 | Nonsense | Available for shipment | Available now |
sa9231 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13039 | Essential Splice Site | Available for shipment | Available now |
sa22074 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa2647
Status:
F2 line generated
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057918 | Nonsense | 62 | 258 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 12 (position 19689853)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 18542014 |
GRCz11 | 12 | 18663888 |
KASP Assay ID:
554-3041.1 (used for ordering genotyping assays)
KASP Sequence:
AATGATGCTTAAGTTGATGAATGCTCCACAATGTCCAAACATCATCGAAT[T/G]ATACGACTGGGTTGAGAATGAAAAGAACTTCATTCTCAGTCTGGAGTACG
Long Flanking Sequence:
AATCTCCCTGCTTTTTTCTGTGTTTCAGGATTTGATCTGTCTCATTTTGAAGTAGAAAACTTGATTGGACAAGGAGCTTTTGGCCAGGTGTTTGTGGCATCTCACAAACTTCGTAAAAGTGAAAAGGTAGAGAACTAGTTTTTAAATTCAGTCAACATTTTCCTCCTGATTATTTATTATTAATAATTTGTTGTCTTTAATTTAATTAGTTGTTTTTTTCTCCGCAGGTTGCCCTGAAGTTTATCAACAAGCGTAAACAGGCCCACTATCTCAAGACTGTAAGTTGAATAATTCACACAACAATGAAAATGTGCTGACCATTTACTCATCCTTCACTTGTGTCGTACCTGTCTGGACCACCTTACTGGTTTTCAACATTCTTTGGTAATATCTTTGAAATCTGTTTTTTTTCTAGGATGGTCATTCCACACCTGTGCTTGCGGAAGTGGCAATGATGCTTAAGTTGATGAATGCTCCACAATGTCCAAACATCATCGAAT[T/G]ATACGACTGGGTTGAGAATGAAAAGAACTTCATTCTCAGTCTGGAGTACGCAGAGTCATGCCAGACCTTGTATGAGTACATCACAGATATATTTGAGATTGAAGAAAACCGAGCACGCCGGTTAATGCATCAGTTCATCCAAGCTGTAATGTTCTGCGCTGAGCGTGGAGTTTTCCATGGGGATATACACACAGAGAACATCCTGGTGACTAAACCCCGATCAGAGCTCAAATTGATCGACTTTGGTTGTGCTCAGCCAATTACCCACAAGCCTTTCAATAGCAATCAATATCGAGGTGAGTTGGCATTTTGTGTTAGTTTCTTTGGTCACAGTATTGTCTTATGAAATGACTGAATTCTGAAAACGTCTCTCTTACAGGAGTTGGATTTTACACGCCACCTGAGGTTTTTAGGCGTCGCACATTCCATGCTTACCCGGCATACGTCTGGACGATAGGCCTCGTGCTGTATGAAATAATGCATGGACGAATGGCTTTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16385
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 |
---|---|---|---|---|---|
ENSDART00000057918 | Nonsense | 106 | 258 | 2 | 5 |
ENSDART00000057918 | Nonsense | 106 | 258 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 12 (position 19689984)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 18542145 |
GRCz11 | 12 | 18664019 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCACAGATATATTTGAGATTGAAGAAAACCGAGCACGCCGGTTAATGCAT[C/T]AGTTCATCCAAGCTGTAATGTTCTGCKCTGAGCGTGGAGTTTTCCATGGS
Long Flanking Sequence:
GAACTAGTTTTTAAATTCAGTCAACATTTTCCTCCTGATTATTTATTATTAATAATTTGTTGTCTTTAATTTAATTAGTTGTTTTTTTCTCCGCAGGTTGCCCTGAAGTTTATCAACAAGCGTAAACAGGCCCACTATCTCAAGACTGTAAGTTGAATAATTCACACAACAATGAAAATGTGCTGACCATTTACTCATCCTTCACTTGTGTCGTACCTGTCTGGACCACCTTACTGGTTTTCAACATTCTTTGGTAATATCTTTGAAATCTGTTTTTTTTCTAGGATGGTCATTCCACACCTGTGCTTGCGGAAGTGGCAATGATGCTTAAGTTGATGAATGCTCCACAATGTCCAAACATCATCGAATTATACGACTGGGTTGAGAATGAAAAGAACTTCATTCTCAGTCTGGAGTACGCAGAGTCATGCCAGACCTTGTATGAGTACATCACAGATATATTTGAGATTGAAGAAAACCGAGCACGCCGGTTAATGCAT[C/T]AGTTCATCCAAGCTGTAATGTTCTGCGCTGAGCGTGGAGTTTTCCATGGGGATATACACACAGAGAACATCCTGGTGACTAAACCCCGATCAGAGCTCAAATTGATCGACTTTGGTTGTGCTCAGCCAATTACCCACAAGCCTTTCAATAGCAATCAATATCGAGGTGAGTTGGCATTTTGTGTTAGTTTCTTTGGTCACAGTATTGTCTTATGAAATGACTGAATTCTGAAAACGTCTCTCTTACAGGAGTTGGATTTTACACGCCACCTGAGGTTTTTAGGCGTCGCACATTCCATGCTTACCCGGCATACGTCTGGACGATAGGCCTCGTGCTGTATGAAATAATGCATGGACGAATGGCTTTTTATGACAGACAATCAATAATGTTTGGCTCCATTAGGATGGAATCCAGGTTATCTACAGGTAAGCAGACACCTCTGCACAATCTCAGCCTCAGTGACAATAAAATATGTCAGTCACGAGTAAAAAAGGATTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16035
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 |
---|---|---|---|---|---|
ENSDART00000057918 | Nonsense | 106 | 258 | 2 | 5 |
ENSDART00000057918 | Nonsense | 106 | 258 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 12 (position 19689984)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 18542145 |
GRCz11 | 12 | 18664019 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCACAGATATATTTGAGATTGAAGAAAACCGAGCACGCCGGTTAATGCAT[C/T]AGTTCATCCAAGCTGTAATGTTCTGCKCTGAGCGTGGAGTTTTCCATGGS
Long Flanking Sequence:
GAACTAGTTTTTAAATTCAGTCAACATTTTCCTCCTGATTATTTATTATTAATAATTTGTTGTCTTTAATTTAATTAGTTGTTTTTTTCTCCGCAGGTTGCCCTGAAGTTTATCAACAAGCGTAAACAGGCCCACTATCTCAAGACTGTAAGTTGAATAATTCACACAACAATGAAAATGTGCTGACCATTTACTCATCCTTCACTTGTGTCGTACCTGTCTGGACCACCTTACTGGTTTTCAACATTCTTTGGTAATATCTTTGAAATCTGTTTTTTTTCTAGGATGGTCATTCCACACCTGTGCTTGCGGAAGTGGCAATGATGCTTAAGTTGATGAATGCTCCACAATGTCCAAACATCATCGAATTATACGACTGGGTTGAGAATGAAAAGAACTTCATTCTCAGTCTGGAGTACGCAGAGTCATGCCAGACCTTGTATGAGTACATCACAGATATATTTGAGATTGAAGAAAACCGAGCACGCCGGTTAATGCAT[C/T]AGTTCATCCAAGCTGTAATGTTCTGCGCTGAGCGTGGAGTTTTCCATGGGGATATACACACAGAGAACATCCTGGTGACTAAACCCCGATCAGAGCTCAAATTGATCGACTTTGGTTGTGCTCAGCCAATTACCCACAAGCCTTTCAATAGCAATCAATATCGAGGTGAGTTGGCATTTTGTGTTAGTTTCTTTGGTCACAGTATTGTCTTATGAAATGACTGAATTCTGAAAACGTCTCTCTTACAGGAGTTGGATTTTACACGCCACCTGAGGTTTTTAGGCGTCGCACATTCCATGCTTACCCGGCATACGTCTGGACGATAGGCCTCGTGCTGTATGAAATAATGCATGGACGAATGGCTTTTTATGACAGACAATCAATAATGTTTGGCTCCATTAGGATGGAATCCAGGTTATCTACAGGTAAGCAGACACCTCTGCACAATCTCAGCCTCAGTGACAATAAAATATGTCAGTCACGAGTAAAAAAGGATTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9231
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 |
---|---|---|---|---|---|
ENSDART00000057918 | Essential Splice Site | 160 | 258 | 2 | 5 |
ENSDART00000057918 | Essential Splice Site | 160 | 258 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 12 (position 19690150)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 18542311 |
GRCz11 | 12 | 18664185 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTGCTCAGCCAATTACCCACAAGCCTTTCAATAGCAATCAATATCGAG[G/A]TGAGTTGGCRTTTTGTGTTAGTTTCTTTGGTCRCAGTATTGTCTWATGAA
Long Flanking Sequence:
CAACAATGAAAATGTGCTGACCATTTACTCATCCTTCACTTGTGTCGTACCTGTCTGGACCACCTTACTGGTTTTCAACATTCTTTGGTAATATCTTTGAAATCTGTTTTTTTTCTAGGATGGTCATTCCACACCTGTGCTTGCGGAAGTGGCAATGATGCTTAAGTTGATGAATGCTCCACAATGTCCAAACATCATCGAATTATACGACTGGGTTGAGAATGAAAAGAACTTCATTCTCAGTCTGGAGTACGCAGAGTCATGCCAGACCTTGTATGAGTACATCACAGATATATTTGAGATTGAAGAAAACCGAGCACGCCGGTTAATGCATCAGTTCATCCAAGCTGTAATGTTCTGCGCTGAGCGTGGAGTTTTCCATGGGGATATACACACAGAGAACATCCTGGTGACTAAACCCCGATCAGAGCTCAAATTGATCGACTTTGGTTGTGCTCAGCCAATTACCCACAAGCCTTTCAATAGCAATCAATATCGAG[G/A]TGAGTTGGCATTTTGTGTTAGTTTCTTTGGTCACAGTATTGTCTTATGAAATGACTGAATTCTGAAAACGTCTCTCTTACAGGAGTTGGATTTTACACGCCACCTGAGGTTTTTAGGCGTCGCACATTCCATGCTTACCCGGCATACGTCTGGACGATAGGCCTCGTGCTGTATGAAATAATGCATGGACGAATGGCTTTTTATGACAGACAATCAATAATGTTTGGCTCCATTAGGATGGAATCCAGGTTATCTACAGGTAAGCAGACACCTCTGCACAATCTCAGCCTCAGTGACAATAAAATATGTCAGTCACGAGTAAAAAAGGATTAAATATAATGGTTCCTTTAGATATAAAAGTTTTTTAATTGTGGATGTTTTGTAATTTGATGTAGTAAGATTTAAACAAATTCATGAATCTTGAGTATGCTGACATATTTCACATTCTCTGTGTCACTTTTCAGTATGCCAGGACCTGATTTCCCAGTGTTTAGTCCGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13039
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057918 | Essential Splice Site | 160 | 258 | 2 | 5 |
ENSDART00000057918 | Essential Splice Site | 160 | 258 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 12 (position 19690150)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 18542311 |
GRCz11 | 12 | 18664185 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTGCTCAGCCAATTACCCACAAGCCTTTCAATAGCAATCAATATCGAG[G/A]TGAGTTGGCRTTTTGTGTTAGTTTCTTTGGTCRCAGTATTGTCTWATGAA
Long Flanking Sequence:
CAACAATGAAAATGTGCTGACCATTTACTCATCCTTCACTTGTGTCGTACCTGTCTGGACCACCTTACTGGTTTTCAACATTCTTTGGTAATATCTTTGAAATCTGTTTTTTTTCTAGGATGGTCATTCCACACCTGTGCTTGCGGAAGTGGCAATGATGCTTAAGTTGATGAATGCTCCACAATGTCCAAACATCATCGAATTATACGACTGGGTTGAGAATGAAAAGAACTTCATTCTCAGTCTGGAGTACGCAGAGTCATGCCAGACCTTGTATGAGTACATCACAGATATATTTGAGATTGAAGAAAACCGAGCACGCCGGTTAATGCATCAGTTCATCCAAGCTGTAATGTTCTGCGCTGAGCGTGGAGTTTTCCATGGGGATATACACACAGAGAACATCCTGGTGACTAAACCCCGATCAGAGCTCAAATTGATCGACTTTGGTTGTGCTCAGCCAATTACCCACAAGCCTTTCAATAGCAATCAATATCGAG[G/A]TGAGTTGGCATTTTGTGTTAGTTTCTTTGGTCACAGTATTGTCTTATGAAATGACTGAATTCTGAAAACGTCTCTCTTACAGGAGTTGGATTTTACACGCCACCTGAGGTTTTTAGGCGTCGCACATTCCATGCTTACCCGGCATACGTCTGGACGATAGGCCTCGTGCTGTATGAAATAATGCATGGACGAATGGCTTTTTATGACAGACAATCAATAATGTTTGGCTCCATTAGGATGGAATCCAGGTTATCTACAGGTAAGCAGACACCTCTGCACAATCTCAGCCTCAGTGACAATAAAATATGTCAGTCACGAGTAAAAAAGGATTAAATATAATGGTTCCTTTAGATATAAAAGTTTTTTAATTGTGGATGTTTTGTAATTTGATGTAGTAAGATTTAAACAAATTCATGAATCTTGAGTATGCTGACATATTTCACATTCTCTGTGTCACTTTTCAGTATGCCAGGACCTGATTTCCCAGTGTTTAGTCCGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22074
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057918 | Essential Splice Site | None | 258 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 12 (position 19690770)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 18542931 |
GRCz11 | 12 | 18664805 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTGGAGCTGTAAGGCAAGAGGAGGTAGAGGAACACACCGAGCACAAAA[G/A]TACATCTTCATTTCTTTCTTTGCTTCATGCTATTCCTGTTGTTTTCTCTT
Long Flanking Sequence:
TCGCACATTCCATGCTTACCCGGCATACGTCTGGACGATAGGCCTCGTGCTGTATGAAATAATGCATGGACGAATGGCTTTTTATGACAGACAATCAATAATGTTTGGCTCCATTAGGATGGAATCCAGGTTATCTACAGGTAAGCAGACACCTCTGCACAATCTCAGCCTCAGTGACAATAAAATATGTCAGTCACGAGTAAAAAAGGATTAAATATAATGGTTCCTTTAGATATAAAAGTTTTTTAATTGTGGATGTTTTGTAATTTGATGTAGTAAGATTTAAACAAATTCATGAATCTTGAGTATGCTGACATATTTCACATTCTCTGTGTCACTTTTCAGTATGCCAGGACCTGATTTCCCAGTGTTTAGTCCGTGATCCAGTTAAACGAATAAAGTTACATCAGGTAGAAAAGCACCAATGGTTCAATCCAACGACCCCAGATCCTGTGGAGCTGTAAGGCAAGAGGAGGTAGAGGAACACACCGAGCACAAAA[G/A]TACATCTTCATTTCTTTCTTTGCTTCATGCTATTCCTGTTGTTTTCTCTTCTGCTCTTCTAGAGTCACAAGTCTTATTTGACAGCTCTTCATATCACTGCTTAAATAACTTTGTGTTATTTCTGAATGTTTTTCTTCATTTTAGAAAAAACTAAAGAAGCAAGAAAGAGGAGAGCAGCATTTCCAGAAATTTCACAAGACTGTTAAAGTTATTAATTACTCCCTCATGTCAATCCAAACCTCTAAGACCTTACTTTTCTTCTGTGTCAGTTCATGACGTGTGTTGACGAGAGCTCTGTCCTGCACTGTATGTGTGTCGCACTGCTGACGTTTACCTCAGATGTGCCCACGCTTTGTTTAAATGAGAGGAAGTCGCGCAGGCCTCGGGGTTAAACATCAGCAGTGCGACACACACAGTGCAGTACAGCACTTCTGAAGTCCTTATTTCTGTTTCATTATTTTTGTGTTTTTTTTTCTGCATTAAAGAAGTTTTGTTCCAAA
Associated Phenotype:
Not determined