ZMP
cnksr2
Ensembl ID:
ZFIN ID:
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 |
---|---|---|---|
sa37902 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37903 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6772 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45832 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37902
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110241 | Nonsense | 442 | 1025 | 12 | 21 |
ENSDART00000142351 | Nonsense | 455 | 684 | 12 | 15 |
Genomic Location (Zv9):
Chromosome 24 (position 26094279)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 25419515 |
GRCz11 | 24 | 25564466 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGCTTTTAGGTCGTCTGAGGCCCATCTCAATGCCTGTGGAGTATAACT[G/A]GGTTCCTGACTATGAAGACCCAGCTAGAGTGAAGAGAGACGGTCGGAGAG
Long Flanking Sequence:
TTTTGAGGTTTCTAAAGCAAGCATGTCTATAACTAGTTTCCTGCGTAGGGAGCTGGTTTCAGATTTTTCTGTAATTAAACTCTAGGGAGCTGGGCTGCACTTTGTTGTGAGTATGTATGTGCGTTTGTTTGTGTAGCCTTATATCCAAAACCTGAGAACTCGGCACTAGTCGTTAAATGCCAGCGTGAGCCTCTGCAGTGGCACAGAACTGCTGACACACTCCATGCCCGCTGCTTCCCTAGAAAACGAGAGGACACATTAACTGTGACAGTTTGTCTTACACAAACACACACTCACACAGACTTACCTTGGCGTCTGTGGAGGAAATAGATTGTGAACTGTCATTTTACTTCCATCTATCCCCTATTTTCTATCCCCTGTCTTTCCACACACACACACACACACACACACACACACACACACACAATGTGATGTTTGAATGTGCTTTCTTGTGCTTTTAGGTCGTCTGAGGCCCATCTCAATGCCTGTGGAGTATAACT[G/A]GGTTCCTGACTATGAAGACCCAGCTAGAGTGAAGAGAGACGGTCGGAGAGGTGAGTTGGCATCAGTTACAGTACATGCATCTGCTTCTTCTCTTGTTTATGTTCAGAATTCTCTTTTTTGCTATGCAAAATATATCTTGGAAATTGAAAAATGTTGAAATAAAAATGTTTTAGAAAAGGTCAAAACTATGTAATTTTATACTCTGTTAAAATAGTTGGGTTAAAAATACCACAACATATAACCTAACTATAGGTTATTTTACCACCTTCCCGACTATGGGTTATGTTAACCCAATGCATTGGGTTATATAATCTAACCCAATGCATTGGGTTATTTTGATTAAATGTTATTTTTTCCATTCTGGTATTACTATTGAAGTACTACTATTATTTTCGAATTATGGCTGTGTAAATTAAAGAATGTCTCCTCTCGTCCCTAAAGGCGAGTATGACAGCCGAATATCCCAAATATGTGTATCATTTTATCCCGCTCCCTCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37903
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 |
---|---|---|---|---|---|
ENSDART00000110241 | Nonsense | 694 | 1025 | 18 | 21 |
ENSDART00000142351 | None | None | 684 | None | 15 |
Genomic Location (Zv9):
Chromosome 24 (position 26126857)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 25386937 |
GRCz11 | 24 | 25531888 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGGAGTGAAAGTGATCATGAAGACAATGAGACGCCCTCGACGCCCAAG[C/T]AAGACAGCCCACCACCCCCTTATGACACATACCCACGGCCACCCTCAGTG
Long Flanking Sequence:
GTACCTTCGGTTATATATTTCACAGTCTCCAGAAGTTAATGTAGACCTGGGTACGTATCTGCGATGAGCCTGGGTTGCAGAAAAGAAGGAAATGAGTCCTGTGACCTATGTACAACAAGCTGATAGACACAAATAAGTTATGCCCTTCTGGCGGATCATGCTACATACTAAGTTTCTCCAAAACATATTCATCCTTTTATCATTCAAAATTAGCCACTAATAAGAATTCAAAATGCTTTGTAAGTGTCTGACTCCTTTAGACGTCTTAAAATTAACCTTTCTTCTCCTGCTTTTGACATCACACCACAGTTGCAGACCTAGAGCAGCTCCTCACGGGAAAACCTACACATGATCTCAGAGGCTATAATTTAATAATTGTTTATTTTATGGAAATGTTTTGCAACAAGCTAATGACTCCCTGCATTCCCCTTCATCCCCTTCCAGCAGACTACTGGAGTGAAAGTGATCATGAAGACAATGAGACGCCCTCGACGCCCAAG[C/T]AAGACAGCCCACCACCCCCTTATGACACATACCCACGGCCACCCTCAGTGAGTCAGCATCCAGCACACACACACACAAACATAAACATGGCTCTTCTCGTTGTGTAATCCCACACAATGGCACGGCTTTATCATGCTTGACATTTGGCATTGGTAAAAGAGCTGTTTTGTAGTACCGTCCCTCAGACCTGGCCTTACCACGTCACTGCATGTGTGTGTGTGTGAATGAGTCAGACCACCTCATCTAAAAGCCCACTGTTGAGATGTGCTGAGATTGAGTCTTATCTCTAAGTCTCTCTACATATCTTTCAGTCTTTGTGAGTCACTGCTACTGTCGCTGATAGACAGTATCTGATATCGATTTCCTTTTTGGTGAGTCTCTCAAAATCTATCAAGGATCGAGTGATCACGCGATATTTCAATCCAAAGAATTTTTAAAAATACAAAAATTGCTATTTTCATTACTATAAATTAAAAATGAGGTTTGATGTAAATTATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6772
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 |
---|---|---|---|---|---|
ENSDART00000110241 | Nonsense | 933 | 1025 | 20 | 21 |
ENSDART00000142351 | Nonsense | 590 | 684 | 14 | 15 |
Genomic Location (Zv9):
Chromosome 24 (position 26144047)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 25369747 |
GRCz11 | 24 | 25514698 |
KASP Assay ID:
554-5163.1 (used for ordering genotyping assays)
KASP Sequence:
CCACTCGTCTGGAGTACAAACWTCTTTTCATCCGGCGTTGCAACGATCCA[C/T]AGCTAAATGACAAACTGCATCACCTTCGCATCCTGCAGAGCAYGCTAAAG
Long Flanking Sequence:
TCAATTGATACCAGCTAAAAACCGAGACAGCAAGAGGAGAATATCTTCCCGTATTTACATACATCTGAGCCTGATTAAGTATTTATCTATGCCAGCCAGACGAAAGACACTTTTTGTCCAAGTCTTTTGTCATTTATCTCATTTTATTTTCTAGATTCCAGACTAGCAAATGAAATAAATGAGCTGAGTATCATCAGCATACAAATGTCAGCCTACGCACCTGACTGAACATTAAAATGCAGAGTGTAAATGTTGCAATCTGTCTGTTTCTTTTCCATTCCCACTCAAAAATATGCTTTGCTGGTGGAGGCAGTCCTTTTTAACTCTGGCTTTCTGTGGCACCCCCCACAGGCGGGGAGCAGGACTACCAGGGGCAGACAGATTCGTTGGGGGACTTGTACAGAGCGCTGGAGCGTGCCCGTCTGACACCTATTGGTGAGCACCGCCTTTCCACTCGTCTGGAGTACAAACATCTTTTCATCCGGCGTTGCAACGATCCA[C/T]AGCTAAATGACAAACTGCATCACCTTCGCATCCTGCAGAGCACGCTAAAGGTATCCGAACTCTGCTGCCGCATGGGTCCCACTGCACCCTGTGTGCCTGTTTGTTTCATCTGTCCAGTCTGTCCGTCTGTCCTCTCCATCTGTCTGATGTCTGTGGGGTTCTGGGGACAGCAGTATTTATTGGTCTTTTTTAGTAGTCTATTTTGATATGGTTTCTTTCGCCAAACTGCTATCCCAGAATCCCATCCATGTTAGACGGAGTTCTCTGTCTGGTGTGGGAGGAGGGTATGGCCAAACTCTGCTCTGAACTCTGCCTCTCCGCGTGGGTTTAGGCTCTACCTGGTGCCAAGGGGTCTTCTTGTGGTGGGTCTGTGCAATTTCTGTGACCCCCTCTCCAAACTCCTTAACCCCATCTGCTGTGCTGTGTTCTTTATGTTGAGGCACAGCTTCCTGTTGGATTGTGGGTATAATAAACAGCTGGTTAGCAGCACCAAAAACAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45832
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110241 | None | None | 1025 | None | 21 |
ENSDART00000142351 | Essential Splice Site | 609 | 684 | 14 | 15 |
Genomic Location (Zv9):
Chromosome 24 (position 26144107)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 25369687 |
GRCz11 | 24 | 25514638 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAACTGCATCACCTTCGCATCCTGCAGAGCACGCTAAAGGTATCCGAA[C/T]TCTGCTGCCGCATGGGTCCCACTGCACCCTGTGTGCCTGTTTGTTTCATC
Long Flanking Sequence:
ACATCTGAGCCTGATTAAGTATTTATCTATGCCAGCCAGACGAAAGACACTTTTTGTCCAAGTCTTTTGTCATTTATCTCATTTTATTTTCTAGATTCCAGACTAGCAAATGAAATAAATGAGCTGAGTATCATCAGCATACAAATGTCAGCCTACGCACCTGACTGAACATTAAAATGCAGAGTGTAAATGTTGCAATCTGTCTGTTTCTTTTCCATTCCCACTCAAAAATATGCTTTGCTGGTGGAGGCAGTCCTTTTTAACTCTGGCTTTCTGTGGCACCCCCCACAGGCGGGGAGCAGGACTACCAGGGGCAGACAGATTCGTTGGGGGACTTGTACAGAGCGCTGGAGCGTGCCCGTCTGACACCTATTGGTGAGCACCGCCTTTCCACTCGTCTGGAGTACAAACATCTTTTCATCCGGCGTTGCAACGATCCACAGCTAAATGACAAACTGCATCACCTTCGCATCCTGCAGAGCACGCTAAAGGTATCCGAA[C/T]TCTGCTGCCGCATGGGTCCCACTGCACCCTGTGTGCCTGTTTGTTTCATCTGTCCAGTCTGTCCGTCTGTCCTCTCCATCTGTCTGATGTCTGTGGGGTTCTGGGGACAGCAGTATTTATTGGTCTTTTTTAGTAGTCTATTTTGATATGGTTTCTTTCGCCAAACTGCTATCCCAGAATCCCATCCATGTTAGACGGAGTTCTCTGTCTGGTGTGGGAGGAGGGTATGGCCAAACTCTGCTCTGAACTCTGCCTCTCCGCGTGGGTTTAGGCTCTACCTGGTGCCAAGGGGTCTTCTTGTGGTGGGTCTGTGCAATTTCTGTGACCCCCTCTCCAAACTCCTTAACCCCATCTGCTGTGCTGTGTTCTTTATGTTGAGGCACAGCTTCCTGTTGGATTGTGGGTATAATAAACAGCTGGTTAGCAGCACCAAAAACAAGGTTCCAACATTAAGTGAAGATAGACCATTCATAATGCACCAATGACAATCTTACACAAGT
Associated Phenotype:
Not determined