Busch Lab

ZMP

BRSK2 (2 of 2)

Ensembl ID:
ENSDARG00000061421
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.
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.
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