ZMP
BRSK2 (2 of 2)
Ensembl ID:
Description:
BR serine/threonine kinase 2 [Source:HGNC Symbol;Acc:11405]
Human Orthologue:
BRSK2
Human Description:
BR serine/threonine kinase 2 [Source:HGNC Symbol;Acc:11405]
Mouse Orthologue:
Brsk2
Mouse Description:
BR serine/threonine kinase 2 Gene [Source:MGI Symbol;Acc:MGI:1923020]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6805 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44312 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6805
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087570 | Nonsense | 138 | 673 | 5 | 18 |
Genomic Location (Zv9):
Chromosome 25 (position 25533179)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 24710061 |
GRCz11 | 25 | 24807609 |
KASP Assay ID:
554-5298.1 (used for ordering genotyping assays)
KASP Sequence:
GTGTTTTGACATTGTCTTCTKGYTGTTAGGGAGAAAAGTATGATGGAAGG[A/T]AAGCAGACGTTTGGAGCTGTGGGGTCATTTTGTTTGCTCTGTTGGTGGWG
Long Flanking Sequence:
AAACNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTAAATAAATAAATAAATAAATTATTTAAAATAGGTGGTTCATTCTGCTGTGGCAGCCCCTATTGAATAAAGGGACCAAGCCGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATATGTTAAAATAGGTATAGGAAAATAAATAAGATTATATATTTTCTATCAGTAACTACAGTTAATGTGATCTTTTCTCAGATCTCCTCATTACGCGTGTCCTGAAGTAATACGGGTGAGTATTGCTTTATTCATTTTTTTTTTTCATTGTAAAAGAACAAAAAAGAGAATTATAAATGAATGACCTGTTTTTAAATAAGAATTATTGTGTTTTGACATTGTCTTCTGGTTGTTAGGGAGAAAAGTATGATGGAAGG[A/T]AAGCAGACGTTTGGAGCTGTGGGGTCATTTTGTTTGCTCTGTTGGTGGTGAGTCATATCTAATTGCAAAGTCATTCCTGATTTTACCTTACAGGAACAGTTCACCCAAATGTAACTTTTTTTTTTCTTTTTTTTTTTCCAATGATTACTCACCTTCATGATTTTATTAACCTGTTTGACAGATGAAAAACAACTTTACATTCAGTGTATGGAAGATATATACAATTGAAGTCAGAATTATTAAACACTGTGTTTTTATATACAGGTATATTAGAACTTAGTAACTGATTTCATTTAGCTTTGCCATGATGACAGTACTTTAAAGGCTTAAATAGGTTAATTAGGTTAATTAGTCAAATTAGGGTAGCAAGTTATTGAATAACGGTGGCTTGTTCTGTAGTAGACAATCAAAATAAAAATGGCCTAAGGGGGCTCATAATATTGACTTTAAAATTGTTTAAAAAAACTTAAGTGAAGTTTATTTATAAACTAATTTTGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44312
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087570 | Nonsense | 286 | 673 | 9 | 18 |
Genomic Location (Zv9):
Chromosome 25 (position 25516569)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 24693476 |
GRCz11 | 25 | 24791024 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCAGGAGAAGATGATCTATTTTCTGCTGTTAGATCGTAAGGAGAGATA[C/A]CCCAGCCAAGAAGACCAGAACCTCCCTCCTCGCAATGATATAGGTAGAAA
Long Flanking Sequence:
ATCAAGTATGCCATGCTGCTCAAAATATTTAGTTTTAATTTCAAGTTTCATGACAGCCAACCACAAAAGTTTTTACTACAAAAAGTATGTTTGACATGACGAAACTTGCGATCTTAGTTGGCTAGCGATGGTTTTGGGAAACGCAACCCAGATTAGTTCATCCATACATTTTAATATAATTTGCAAACTTGAAGAACCAAGTTGGCTGGAAATCAGTTATCAAGATTAAAAGATCCAGGATCTGTCAAAGCATTTTAAGTTGTTTGAGTTGTGAAGAATGAACTCTTGAACTTACTGTTTTGAAAAAAACTATTTTAATTTTAAAGTTGAGCCAAAGCATTTGAGAAAAACTTTTTAAAAATACTTAAAGAGAGAATGTGGGATGACAATGTATTAATTGCATCTTATTATCTATATTGACTAATTCTCTATCTCTTTTTCATCAGTGAAAATCAGGAGAAGATGATCTATTTTCTGCTGTTAGATCGTAAGGAGAGATA[C/A]CCCAGCCAAGAAGACCAGAACCTCCCTCCTCGCAATGATATAGGTAGAAAACAGTCAATTCAGTTGTTGTCGCACTAATTACACAGTTTTTGGCAAGTGGTTTCAGTTTTGGATTTAATTGTATTCTGTCTTTGCTGTTACAATTGTTTATCTGTTTGTGCAGATCCACCACGGAAACGCGTAGACTCACCAATGCTGAACAGGCATGGGAAGAGAAGGCCAGAGAGAAAGTCTATGGAAGTGTTGAGTGTTACAGATGGAGGTTCACCTGTACCAGCAAGAAGAGCCATTGACATGACACAGCATGGACAGAGGTATGGAAAACACATACTACATCCATCAGAAGTTGAAATAATTAAGAATTTTTTTTTACATTAAACTAAAGACTTGTATGCTTACCAAGACTGCTGATGGATTGAATTCGTTCAAATATAAATAACTTTTGAAGATCTTAATATATATATATAAATATTTGTAGATATTTATATTATGCTATCTGA
Associated Phenotype:
Not determined