ZMP
si:busm1-122b7.1
Ensembl ID:
ZFIN ID:
Description:
Si:busm1-122b7.1 protein [Source:UniProtKB/TrEMBL;Acc:A8E5P2]
Human Orthologue:
KSR1
Human Description:
kinase suppressor of ras 1 [Source:HGNC Symbol;Acc:6465]
Mouse Orthologue:
Ksr1
Mouse Description:
kinase suppressor of ras 1 Gene [Source:MGI Symbol;Acc:MGI:105051]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42576 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa17165 | Essential Splice Site | Available for shipment | Available now |
sa39058 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42576
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000048103 | Essential Splice Site | 560 | 982 | 11 | 20 |
Genomic Location (Zv9):
Chromosome 15 (position 30381902)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 31203609 |
GRCz11 | 15 | 31084350 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATTAGCTGCCTGCTACTTTCAGCATAGACAACAGTTTGTCTTCCCTGG[T/C]AAGTTAAGAATTCTCCCCACAACAAAACTCTGTGATTTTTCTCTTCAGTA
Long Flanking Sequence:
TAAGAACAGTTTTGTAGAAGTTGCCATTATTTATAATTAGGCATATTATGTATGAGCTTATCCATTGATAAAAACTTTTAGAATACAAATCTGATGAAAACTGAACATTTTTGTATGTTAGTGTTGCTGATTGCTTATTTTAAAAGTAGACATTTATTATTAAGTGCAGGAGAGGAAAAGCTCATTCAGACTTTAACAACATCTAATGTAATTGTAAAACTCTGATTAAAGTAGGAAAAACAATTACTTAAATAAGTTTTTTTAGGGGAAATAACACTTCATAAAAAAAGCCAAAATAGCAAAAAATAAAATTAAATAAAAAATTAGTTACAGGTGCATTAAAAAACAGCCTGCTGTATCTTGCCTTCTGGAGCTTTCTGATGCTTAACTAACAAATTGTTTAACCCGGTCTTTCTCTTGTCCTTGTGGACATCTGTCTGTTTGCCCTGTTCATTAGCTGCCTGCTACTTTCAGCATAGACAACAGTTTGTCTTCCCTGG[T/C]AAGTTAAGAATTCTCCCCACAACAAAACTCTGTGATTTTTCTCTTCAGTAGTGTTGTGTTGAGTTCTTCACGAGTGCTTCATCATAGCTTCAGTTGTGTTTGAATGTTAGCAATTCTCCTGCTGCATTGTACCGCCACCTAGTGCTCATCTATGGGAATAGCTTTTTCCTCTTTTGCTTTTAACCATCTGTGTGCAAAAAATAATAATAATAATAAGCAACACATATATTCTGGTATTAAAATAATTGCATAAAAGAATTAGTGATAATACAAAATAATAATAGAAATTTTAAGTGATACAAATTAAGAAATTTTAGTGATTTGATGGATGGTGGCGATTTTAATTTAAAGTGACAATTATGAATGACAACTTGTGATTTAAAATGACAATTTATTTACATTTTGTTTTTATAATATTTCACTAAATGATTCTTGTAAATATGGCAGACAAGATTTTTTTCTATATAAACAAATGTATCACTTTTAGTGGGTGTCTTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17165
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000048103 | Essential Splice Site | 801 | 982 | 16 | 20 |
Genomic Location (Zv9):
Chromosome 15 (position 30373002)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 31194709 |
GRCz11 | 15 | 31075450 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCACAGATTTTGGCCTKTTTGGGATGTCTGGAGTGGTTCAAGAGGACAGG[T/C]ACAGAGTCAGTCTATTATAATAAATCAATTAACCCTATTATGGAGCCAAA
Long Flanking Sequence:
TCTGTGCTGCACTGCATAACTATAGATGTGTAAAAATTTGCGTCCTGATCGAGATGTAATGTCCTGAGTCTGAAACTGCGTGATCGGGCCCGATTTCCTATCACGTGATCAGACTAGAATCCTACAACTAGGATCTGCTTGTTTTGATATTGTTTAGAATATGTGGCTAAGAAATAACTAATTAGAATTTTTTAATGGTTGGGAACAATAGAACAAAACCCTTAACATTTCTCTTAGAATAAGTCTGAAATTTTATTCGTAATGGTCTTAAAATGTCCATAACGGGTCTTAATTTTGACTTGATTGAACCTGCTGAAACCCTGTTCATCAGTTGTTGTTGTTTTTTTTGTGTTTGCCTTCTTCAGGGAATGGGTTACCTCCATGCAAAGGGAATCGTACACAAAGACTTAAAGTCCAAGAATGTCTTTTACGATTCAAACAAAGTAGTCATCACAGATTTTGGCCTGTTTGGGATGTCTGGAGTGGTTCAAGAGGACAGG[T/C]ACAGAGTCAGTCTATTATAATAAATCAATTAACCCTATTATGGAGCCAAAATGCTTCATTTATGCCTATCTTGTGTGTGTAGGAGAGAAAATGAGCTGAAGCTGCCACGAGGATGGATCTATTACTTGGCTCCAGAGATTGTGCGAAAGATTGGACCAGGAAACCAAGAAGACTGTCTGCCCTTTTCAAAAGCTGCTGATGTTTACGCCTTTGGGTAAAAAAAAATTCAGTTTCCATGTCTGCATCTCAAAAGAAAAGTGTATAATGCGGATGTGTTGTTTAGGTGGTTGTTTCATATCTGCCTTTTGTCCTATACAAAGTAAAACTAACCTGATATTTTCATTAAATTTTTCCGTTTGATAATATTTTTAAATAGATTTTGCATGGTGCCACTGAAGTTGGTTATTTGACTGTAAATGTGTCTGTTTTAGCACTATCTGGTATGAACTCCAGGCCAAAGCCTGGCCAATCATCAACCAGCCGACTCAAGTGTTGATCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39058
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000048103 | Nonsense | 849 | 982 | 18 | 20 |
Genomic Location (Zv9):
Chromosome 15 (position 30372558)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 31194265 |
GRCz11 | 15 | 31075006 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGTTGGTTATTTGACTGTAAATGTGTCTGTTTTAGCACTATCTGGTA[T/G]GAACTCCAGGCCAAAGCCTGGCCAATCATCAACCAGCCGACTCAAGTGTT
Long Flanking Sequence:
TAGTCATCACAGATTTTGGCCTGTTTGGGATGTCTGGAGTGGTTCAAGAGGACAGGTACAGAGTCAGTCTATTATAATAAATCAATTAACCCTATTATGGAGCCAAAATGCTTCATTTATGCCTATCTTGTGTGTGTAGGAGAGAAAATGAGCTGAAGCTGCCACGAGGATGGATCTATTACTTGGCTCCAGAGATTGTGCGAAAGATTGGACCAGGAAACCAAGAAGACTGTCTGCCCTTTTCAAAAGCTGCTGATGTTTACGCCTTTGGGTAAAAAAAAATTCAGTTTCCATGTCTGCATCTCAAAAGAAAAGTGTATAATGCGGATGTGTTGTTTAGGTGGTTGTTTCATATCTGCCTTTTGTCCTATACAAAGTAAAACTAACCTGATATTTTCATTAAATTTTTCCGTTTGATAATATTTTTAAATAGATTTTGCATGGTGCCACTGAAGTTGGTTATTTGACTGTAAATGTGTCTGTTTTAGCACTATCTGGTA[T/G]GAACTCCAGGCCAAAGCCTGGCCAATCATCAACCAGCCGACTCAAGTGTTGATCTATCAGCTGGGAAGTGGAGAAGGAATCAGATCTTTATTGACTACTAAGGGTACTAGCTTGGGCAAGGAGGTCACGGTGAGTCCAACCCTGCCATTTTTAAGTACTAAAAAGCACCTATAGTATATAATTTAGTGTAATTGTAGATTTGCGTTACATTGTATAATTAACACATAGACATATTACTATTATCATTATTATTTATAAATAATTATGATCATAAATTTATTAGATACATATCATAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATTAATTATTATAGTGGATTGAGAAATCATCATTTTATTCCATTTTAATTTGCATTATATAGAAATTTTATATTTAATCACTCACAATATTAAAAAATGAAATAACTATATCATATAAATG
Associated Phenotype:
Not determined