ZMP
si:ch211-26b3.4
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate connector enhancer of kinase suppressor of Ras 2 (CNKSR2) [Sourc
Human Orthologue:
CNKSR2
Human Description:
connector enhancer of kinase suppressor of Ras 2 [Source:HGNC Symbol;Acc:19701]
Mouse Orthologue:
Cnksr2
Mouse Description:
connector enhancer of kinase suppressor of Ras 2 Gene [Source:MGI Symbol;Acc:MGI:2661175]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa18798 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa6972 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa9214 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18798
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111146 | Essential Splice Site | 22 | 1031 | 2 | 23 |
| ENSDART00000132612 | None | 1 | 411 | 1 | 11 |
| ENSDART00000134394 | None | None | 179 | None | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 24708531)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 22421403 |
| GRCz11 | 5 | 22925203 |
KASP Assay ID:
2259-5711.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAATTACGATCACATGATTGTGATTTTCTCTCCGTGTCTCTTTCTCTC[A/G]GGGCTGGATGACTGTTTGCTGCAGTATATGAGGACGTTTGAGCGGGAACA
Long Flanking Sequence:
AGCTGAAGGACATCCTACACACACACACACACACACAAACATAATGGTAAAACAACACACAGGATGTCTTGAGTGTGTGTGTGTATATGAGACTACAGAGCAGGTTATGAAGGACACTGAGCTTGTGTGTATCTGCAAGTTCAGAATGTTCCATCTGAAGAGCCTCTCAACCTCATCCTCTAAATGTGTGTGTGTGTCGCCGCCTTGCGAAATGCAGGTGTGTGTGTCTTTCAGAGAGACGTGTCTGCAATCTATAAGTGGCTTATCTTCTTTTTTGGGGCACAAAGTGTTAGTGGAATCAGCCACTTGACATCATTTGCAGGTTTACGGTGTGCTTGTGCATTACGTTGTGTGTTTGTGTGTGAGCGGTGTGTATTAATCATCTTAATGACTGCGTGGAGAGGCACACCATTACACCAGCTCGCGTTTTAAGTTTATTACACAGCATAAATGAATTACGATCACATGATTGTGATTTTCTCTCCGTGTCTCTTTCTCTC[A/G]GGGCTGGATGACTGTTTGCTGCAGTATATGAGGACGTTTGAGCGGGAACAGATAACCGGAGAGCAGCTGCTGCACATCACCCATCAGGAGCTGGAAGAGCTTGGCGTGACCCGCATCGGACACCAGGAGCTCATTCTGGAGGCTGTGGACTTACTCTGTGCACTGGTGTGTGTGTGTGTGTGTGTGTGTGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGAGAGAGACTGGCTGTGATAATGATGTGTTTGTTTTCTATTAATGACACAACAGACATTTTAATCAAACTCCGCTTAACACTGAATGATTAGCACCCAGCGGGAGTCTTCCAACCAGTACTAGCACACACAAAAAAGAAGGTATAGAGAATGTGTTTGTGTAGGGGAGGGATGGTGTGTTTTGGATTCTGATTGGCTGCTGCTGGAGGAGTTTATGCATCATAGAATGAGAGGAGGAGCTAGATGTCAGTCTAACTCTGCTTGAGCAGGGGTTCAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6972
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 |
|---|---|---|---|---|---|
| ENSDART00000111146 | Nonsense | 866 | 1031 | 22 | 23 |
| ENSDART00000132612 | None | None | 411 | None | 11 |
| ENSDART00000134394 | None | None | 179 | None | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 24660040)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 22372912 |
| GRCz11 | 5 | 22876712 |
KASP Assay ID:
554-5341.1 (used for ordering genotyping assays)
KASP Sequence:
CGCACCGCAGCACTCGTACACACATGCACACGCATGGTACTCTGAGGCCA[C/T]GAACTCACCTYCATGAGGAAGATGAGGAAGAAGAGGAGGAGAAACATGTG
Long Flanking Sequence:
ATCACTGCATCTCTCTGACCATCATCAAATATCACTGAGCATCAGCAATGGTAATGAGCGGTGATTCTATTTGTCTTCAGGCAACTTCAACCAGTCCATTTCCTGAGCGACATTTTTCCAGCGGTTCCACATTCTCACATTCCTCTGCCGAGGAGTCCCATTCTTCTTGCCGATCCTCCCATCGGGAACGCCGCTCATGGCAGGACCTGATTGAAACACCTTTGACCAGCACAGGATTACACTACCTGCAGACCGCAGAAGAGGAGGAACCAGGGCTGCTGTCACCTGACCAGCTGCGGCAAGCCACGCTCCCCGCTCAGCGTCGGCGTCCTCTAGAGCGGGACGGGCCTTTTCCATTGACGGACAGCGAGGAGTCCAGACCCCGGCATCACACTCACAAGCAGCGCAGCCAGAGCCTCCCTCGCCACCGTGACACGCACGGAGGACACTCGCACCGCAGCACTCGTACACACATGCACACGCATGGTACTCTGAGGCCA[C/T]GAACTCACCTCCATGAGGAAGATGAGGAAGAAGAGGAGGAGAAACATGTGCGGAAAGCCAGCAGCAGGAGGCCTGAGAGTGACGAGAAAGCTTCCGATGGCACCGATGGCCTTCAGGAGCTGTACAAATCGCTGGAACAGGCCAGTCTGTCTGCTTTCGGCCAGCAGAGGCCTTCCACCAAACAAGAGTTTAGACGATCCTTCATCAAACGCAGTAATGACCCTGCCACGAATGAGCGACTACACCGCATACGGGTTCTCCGCTCCACACTCAAGGTACGCAGACTCAATGAGGAATATACACTCCTCTCACTAAAATGTGGAAGTAAACTGTAACAGTGTGGACGTCTACTAAAAAGTCTAGAGCAGTACTGGTATTTTTACTTGTTTCATTATTTACTCCTTTCTTCTGTTGGATTCAATAGATGATATTTTAAAGAATGTCTAACTAAAAAATTGTTGGCGACCAAAGTATGGAGTAATATATGATGGATTCAGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9214
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 |
|---|---|---|---|---|---|
| ENSDART00000111146 | Essential Splice Site | 957 | 1031 | 22 | 23 |
| ENSDART00000132612 | None | None | 411 | None | 11 |
| ENSDART00000134394 | None | None | 179 | None | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 24659764)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 22372636 |
| GRCz11 | 5 | 22876436 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCACGAATGAGMGACTACACCGCATACGGGTTCTCCGCTCCACWCTCAAG[G/A]TACGCAGACTCAATRAGGAATATACACTCCTCTCACTAAAATGTGGAAKT
Long Flanking Sequence:
TGCTGTCACCTGACCAGCTGCGGCAAGCCACGCTCCCCGCTCAGCGTCGGCGTCCTCTAGAGCGGGACGGGCCTTTTCCATTGACGGACAGCGAGGAGTCCAGACCCCGGCATCACACTCACAAGCAGCGCAGCCAGAGCCTCCCTCGCCACCGTGACACGCACGGAGGACACTCGCACCGCAGCACTCGTACACACATGCACACGCATGGTACTCTGAGGCCACGAACTCACCTCCATGAGGAAGATGAGGAAGAAGAGGAGGAGAAACATGTGCGGAAAGCCAGCAGCAGGAGGCCTGAGAGTGACGAGAAAGCTTCCGATGGCACCGATGGCCTTCAGGAGCTGTACAAATCGCTGGAACAGGCCAGTCTGTCTGCTTTCGGCCAGCAGAGGCCTTCCACCAAACAAGAGTTTAGACGATCCTTCATCAAACGCAGTAATGACCCTGCCACGAATGAGCGACTACACCGCATACGGGTTCTCCGCTCCACACTCAAG[G/A]TACGCAGACTCAATGAGGAATATACACTCCTCTCACTAAAATGTGGAAGTAAACTGTAACAGTGTGGACGTCTACTAAAAAGTCTAGAGCAGTACTGGTATTTTTACTTGTTTCATTATTTACTCCTTTCTTCTGTTGGATTCAATAGATGATATTTTAAAGAATGTCTAACTAAAAAATTGTTGGCGACCAAAGTATGGAGTAATATATGATGGATTCAGCAGGGACTACAAACCACATTTTTTTTTTGTTCTGCAGAAGAAAGAATTTCATACAGGTCTGGAATGAATGATGCCAGAACCTAAATGCTTGTGTGAATTATTCCTTTAAAAGCACAGTATATCATTTTCACCACTAGAGGGTGCATATTCACAACAAATAAAGACGTATTATGATGACAGTGTAACTTAGGGTGGAATCATGGGTGTTGTCGTCTTCATTACATGGACCATACAGAAATCATACTCATGGATGAGCTAAAGTATTTAAACTTATTATCA
Associated Phenotype:
Not determined