ZMP
raf1b
Ensembl ID:
ZFIN ID:
Description:
LOC557109 protein [Source:UniProtKB/TrEMBL;Acc:Q4V900]
Human Orthologue:
RAF1
Human Description:
v-raf-1 murine leukemia viral oncogene homolog 1 [Source:HGNC Symbol;Acc:9829]
Mouse Orthologue:
Raf1
Mouse Description:
v-raf-leukemia viral oncogene 1 Gene [Source:MGI Symbol;Acc:MGI:97847]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13517 | Nonsense | Available for shipment | Available now |
sa27701 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13517
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082519 | Nonsense | 71 | 685 | 3 | 18 |
Genomic Location (Zv9):
Chromosome 11 (position 506561)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 493298 |
GRCz11 | 11 | 519796 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCTCATTTCTATTGAATATGTTGAAATTGTGTTGAAATAGGTGAACGTG[C/T]GAGCAGGAATGACGCTGCGCAACTGTCTCATCAAAGCCCTGAAAGTTCGA
Long Flanking Sequence:
AAAGGGTAGTGAACAACTTCAACTGTATATATCACGAAAATAAACTCGAAATATTAGATTTTTCCAATATCGTGCAGACTTACTATGAAGCATTTTCTATAAAACCCAAAAGTATTGTCTTGTTTTCCGAAATAATATGCTAAGTTTTTCCTTACATCAAGCAAAACAATCTTATTTCAAAGCAAAAACCAGATTTATTTACCCTTTGCTCACTCCACTGGCAGATTATTGTGCTTTGCAGTGCACTCATTCTGATCTTATTTTCACTTCAGTCAGAACTTCAGGGAAAATGTTTGATTACTGATACAAGTAATAATTAAATAAACATTAATAAAATACTAATGCAAGCAAATGATTGCAGATCCACCAAAAATATGGCTAAATAAAACACAATGCCCTCTGCAATGTTGCTTTCATATCCATGTGTTGATCTGTGTAGCTCAGGATGCATGCTCATTTCTATTGAATATGTTGAAATTGTGTTGAAATAGGTGAACGTG[C/T]GAGCAGGAATGACGCTGCGCAACTGTCTCATCAAAGCCCTGAAAGTTCGAGGTCTTCAGCCTGAATGCTGTGCTGTTTTCAAGCTTCAGCGGGAACATTCTGCGTAAGTTCTGAAATATGAAATAAAATAATACAATGAGAGCGACCCACATGTGTGATATCATTAACAGCAGTGTCTATCATGCATTTACTGTTTGGATGAAGCCATCAACATGAAGGACGTAAACATTTATTAACCCCCCTGTAATAAATAATAAAATAAATACAATTGAACATTATATTAATAACAGATGTTTATGGCTGATGGATGCTCATTTTCCAGTATAGTACTCAGTTTCACTAGCTCATATATCAAAAATAAATTAGCCTAAAGGGGCTAATAAAATTGTCCCTAAATGGTGTTTAAAAAATTAAAAACTGCTTTTATTCTAACCAAAATAAAACAATTAGACTTTCTCTAGAAGAGAAAATGTTATCAGACATACTGTGAATATATATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27701
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 |
---|---|---|---|---|---|
ENSDART00000082519 | Essential Splice Site | 539 | 685 | 15 | 18 |
Genomic Location (Zv9):
Chromosome 11 (position 524249)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 510986 |
GRCz11 | 11 | 537484 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGATGACCGGAGAACTGCCTTATTCTATGATTGGAAACAGAGATCAGG[T/C]GAGAGGCCAGAGACCAAATGTCACGTGAAAATGTTTGGACACCCTCAACT
Long Flanking Sequence:
TTCCTGCACGAGGGTCTGACGGTGAAGATTGGAGACTTCGGTTTGGCCACAGTAAAGGCTCGCTGGAGCGGCTCTCATAGAGTCGAGCAGCCGTCTGGATCCATTCTGTGGATGGTGCGTTAATAACTCGCATTTTAATATGATGTGCATTCAAATGACTTTATATAGACTCGGTCTGTAAAGTGAGCACCAAACATCTCAGTTTTTCCTTGGAAACACTTTTAAAATGTTTGAAAATCCTTTATTAATCTTAATAGACCTGTTCTGCCCCTTTAACAGATGTGAATGCGTCTGTGATGAGTGTGTCGTCAAGTTTCAGCTCTAACAGCGATGCTTCAGTGTGTTGTGTGCTTGATGTTCTCCTCAGGCTCCTGAAGTGATCCGCATGCAGGATAATAACCCGTACAGCTTCCAGTCAGACGTGTACTCGTACGGGATCGTCCTGTATGAGCTGATGACCGGAGAACTGCCTTATTCTATGATTGGAAACAGAGATCAGG[T/C]GAGAGGCCAGAGACCAAATGTCACGTGAAAATGTTTGGACACCCTCAACTTAAGTGTGTGAAAAATTCTTGTGACCTCATTATATTCTTAAAGGGGCAGTTCACCCAAAACTGAAAATTCTGTCATCATTTAATTACTGTGTACCTGTGTCTTTCTCTCTGTGTGTGTGTGTGTGTGTGTGTGCAGATCATCTTTATGGTGGGTCGGGGTTATCTGTCTCCAGACCTCAGTAAGCTGTATAAGAGCTGTCCTAAAGCCATGAAGAGACTGGTGTCCGACTGCATCCAGAAGACCAAAGAGGAGCGCCCACTCTTCCCACAGGTCAGCAACAGCACACATACACACATAACACAACACACACACATAATGCAGCACAGCACTGAGAAGTAGTTTCATAGTGTGTATTTAAAAATAATATACAACTCCAATGGTGTGTGTATATATATATATATATATACACCACTTTATTAGGTTATTAGGTACACCTTAATAGTACCGGG
Associated Phenotype:
Not determined