ZMP
araf
Ensembl ID:
ZFIN ID:
Description:
serine/threonine-protein kinase A-Raf [Source:RefSeq peptide;Acc:NP_991306]
Human Orthologue:
ARAF
Human Description:
v-raf murine sarcoma 3611 viral oncogene homolog [Source:HGNC Symbol;Acc:646]
Mouse Orthologue:
Araf
Mouse Description:
v-raf murine sarcoma 3611 viral oncogene homolog Gene [Source:MGI Symbol;Acc:MGI:88065]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13556 | Nonsense | Available for shipment | Available now |
sa20425 | Nonsense | Available for shipment | Available now |
sa31438 | Essential Splice Site | Available for shipment | Available now |
sa31439 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13556
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000076687 | Nonsense | 46 | 605 | 2 | 17 |
ENSDART00000076696 | Nonsense | 46 | 604 | 2 | 17 |
ENSDART00000136342 | Nonsense | 46 | 265 | 2 | 6 |
ENSDART00000138182 | Nonsense | 46 | 608 | 2 | 15 |
ENSDART00000140081 | Nonsense | 46 | 604 | 2 | 15 |
Genomic Location (Zv9):
Chromosome 5 (position 28501153)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 26256451 |
GRCz11 | 5 | 26856604 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCATCTTTGATTATGTTCAGGYAAACGTTCGGCCTGGGCAAACTGTGTA[T/G]GATAGTTTAGATAAAGCCCTAAAAGTCMGWGGCCTAAGCCARGATTGCTG
Long Flanking Sequence:
CTTGTCATCATTCGTTTATCTATGCCCAACATTTTTTGCCTGACCTTTTAGTATTCACATCTGTTTAATGGACTTGTTTTTATGTCAACAGACATTAATGGAAGGTTTTATTTGTGTGTTTTGGCACTAACACAATGTTGTCCATCTCAGGCTCCAGATGAGGGCTTCCTCCTGCATTTGCCCCGCTGTGTAAATCTTTGTGAGTGTCAGTGCTGCCAGTCCCTCACTGCCCCATCGGAGACACCATGTCCAACACTTCCTCCTGTTCCTCCTCGGGGGAAACCAGCCCGGACGATACACCCCGAGGTGGAGGCACCATCCGCGTCTACCTCCCTAACAAGCAGCGGACGGTGGTGAGGCTTCTTTCACTCTTAATTGTTCTTCATAAATATTTGTAACAGCTTACATAACCTGTATATGTACAAATGTAGTTGTGTGCTTGTGATCATTCCCATCTTTGATTATGTTCAGGTAAACGTTCGGCCTGGGCAAACTGTGTA[T/G]GATAGTTTAGATAAAGCCCTAAAAGTCCGAGGCCTAAGCCAGGATTGCTGTGCTGTCTTTCGCCTGCTTGAAGGGTATGTGTCCCTGGGATAGTAGCATTTAAAGTGACAAATTATTTGGTAAAGTTTCTGTTCAAGGGATATTTGTCTTTGTCTTTTGACAGCCGGAAGAGACTTACAGAATGGGACACTGACATCACACCCCTCGTGGGGGAAGAGCTACTGGTAGAAGTCCTGGATGATGTTCCCCTTACCATGCACAACTTTGTAAGTGTACTTACTTCATGAATTGAACCAGTTAGGATACATTTTCATTGTTAAGTCTATTTTTTTTTCAAATTAGTTAGAATTTTAAGGACTGTTTAATTTGTTAATATTACATTTAGTCTTATGCATTACATTTGGTATTTTAAAATAATACAAATAAACAATGTTTTTGCCCTGCATCTATTAACCTTTACTATTAATACTGTGTGTGCTATACTGATTTACTTATATAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20425
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 |
---|---|---|---|---|---|
ENSDART00000076687 | None | None | 605 | None | 17 |
ENSDART00000076696 | None | None | 604 | None | 17 |
ENSDART00000136342 | Nonsense | 263 | 265 | 6 | 6 |
ENSDART00000138182 | None | None | 608 | None | 15 |
ENSDART00000140081 | None | None | 604 | None | 15 |
Genomic Location (Zv9):
Chromosome 5 (position 28502798)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 26258096 |
GRCz11 | 5 | 26858249 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAATCCACATCTCTTGATGTTCTCTCATTTTGACATTGTTTTAAAGGAA[C/T]AGTTCGCTTAAACATTATAGTCACTCTCAATGTTTTCTACTAAATCCAAA
Long Flanking Sequence:
ATGACAAAACGGTATGTTATTCATGAAAGTTTCTGCCTTGATGTACACTTGTCTTCATTTTTGTCACTTAATTGATGTTCTTATCCTGTCAGGTGTGTTAATAATACAGAAGACTGCCCTGCGATATTGATATATCCGGCCACCAATTCCATATCGCAGAGCGACCTACCTTTAACCTCAGATTCTCCTGGGTACACCTAATCTATTCTTACATTTATCTATTGATCCCCAAAGTGAAATGTAGAAATAACTTGCATATCCTCTTTTTGTTTTACTATTTTAGAGGGGAGCTGCCGTCTTCCCCGTCAAACTTCTGTTTGTTCATTCGAGGAGAGGACGGTCAGTCTCTCCAGAGGCATCGATCAACCTCAACACCCAATGTTCACATGGTCAGCACGCTGGAGCCTGGCGCTGCTGGCCTTTTGGAGGTTAGCAGCCAGACTAAAAGCTCAAATCCACATCTCTTGATGTTCTCTCATTTTGACATTGTTTTAAAGGAA[C/T]AGTTCGCTTAAACATTATAGTCACTCTCAATGTTTTCTACTAAATCCAAAATGTGGTGTAAAGTAATGTTTTTTTTTCATATTCAAATTGCCATGTCTAAAAACAATAACAAAGACTATTAGCATATATTGTTTGGAAAAGAGCATTGTCGACTTTGTGCAACACTTCCGTTTTTGTGTCGTATTAAAGATGGGGTGTCATACAAATTTGAAATTACAAGAACGTCAAGAGGATTTTAAAAGGGATAGATTTCTTTACACCTATCATAACTTTTATTTTTTGTACCTTCATCTGCATCATGAATTAAACATGCTCAATGAATCATAATATTCAAACATCCTTCATTCTGAACTAATATATATATATATATATATATATATATTAACGGCCAGTTCTGAGCACTTTGTTTTTGACCTTTTTTTTCTCTGACCATGACTGCTCTTACCCTGAGGCATGTTTATCTGGTTTGGAACACAGTGAGTGTACATGCATTTTTAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31438
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000076687 | Essential Splice Site | 361 | 605 | 9 | 17 |
ENSDART00000076696 | Essential Splice Site | 357 | 604 | 9 | 17 |
ENSDART00000136342 | None | None | 265 | None | 6 |
ENSDART00000138182 | Essential Splice Site | 361 | 608 | 9 | 15 |
ENSDART00000140081 | Essential Splice Site | 357 | 604 | 9 | 15 |
Genomic Location (Zv9):
Chromosome 5 (position 28504103)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 26259401 |
GRCz11 | 5 | 26859554 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACACCGGAGCAGCTCCAGGCCTTTAAAAATGAGATGCAGGTTTTACGG[T/G]GAGTCGTCAGTGGGATTTAGAGCTTCACAGAACATCTTTGATCATTAGTA
Long Flanking Sequence:
ATCAAATTACACTTCTATATAAATGTTTGTGTGTACTGGTTCTCATCTTCTAGCGTCGTCCACAGGGTACGAGTCCTCTCCCAAACCTTCCACTAGCCCACCCCACCTAGGGTCGCCAGGAAGAAAACCCCCCAAATCCCCTTCTGAACCCAAGGAACGAAAGCAGTCCTCGTCTGATGATAAAAAGAAAGTGGTGTGTTTTTATTCATCTTTATTTTCTGATACAAAAATGATTCTGCTTATTTACAATCAGCCTTTTCAAACAAAAAAAATATATAATTGTGGTGTCATTGAAGCACCGGGGAGGTTACAGAGACTCCAGTTACTACTGGGAGGTGCACCCGCGGGAGGTGTCCATGTTAAAGAGGATTGGAGCAGGCTCTTTTGGGACCGTCTTTAAAGGCAAGTGGCATGGAGACGTGGCCATCAAAATTCTTAAAGTGACAGAGCCCACACCGGAGCAGCTCCAGGCCTTTAAAAATGAGATGCAGGTTTTACGG[T/G]GAGTCGTCAGTGGGATTTAGAGCTTCACAGAACATCTTTGATCATTAGTAAGCAGTAGTTTGCAGTAATGCTGCTTAGTTACAACAGTAATGTCTTTAGCTGCTACAACCATTGAGTGTTTCATTGACTATATATCTGTTTTGTTCTACAGAAAAACACGCCATGTAAACATTCTGCTGTTTATGGGCTTCATGACAAGGCCTAATTTTGCCATTATCACACAGTGGTGTGAAGGCAGCAGTCTGTATCGCCATCTGCATGTCACTGAGACCAAGTTTGACACCATGCGGCGCATTGATGTTGCTCGCCAAACAGCACAGGGCATGGAGTAAGAATATTAAATTGTTTTCTTTTTTTTCTTCATTTCAGCAGTATAAGTTTAGTTCTTATCTTGCATGCAGAATCTTTGCTCTTTAAAAAGGCAATAAAATGTGATATTTTAAGTACATTTAAGTAAGACTTTAAAAATGCTTTTTTTTTTGGGCAAATCATATTTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31439
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000076687 | Nonsense | 592 | 605 | 17 | 17 |
ENSDART00000076696 | Nonsense | 591 | 604 | 15 | 17 |
ENSDART00000136342 | None | None | 265 | None | 6 |
ENSDART00000138182 | Nonsense | 595 | 608 | 15 | 15 |
ENSDART00000140081 | Nonsense | 591 | 604 | 15 | 15 |
Genomic Location (Zv9):
Chromosome 5 (position 28509010)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 26264308 |
GRCz11 | 5 | 26864461 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATCGAGCGGAGTGCCTCTGAGCCCTCTCTACACCGTGCTGTACATGCC[G/T]AGGACCTGAATCCGCTTCTCCTTCACACCACGCGCTTCCTGTGAGACTCC
Long Flanking Sequence:
AATCTGACATTAACCTGACGAGAGGTGAAGTGTGAAACACACCAAACCAACTAGCCAGATGCAACTTAACGACCGACCATTGACCATTGGTGTCCCGGTCCTAAAAAAAAGCATCATTGCTATTTAACTTTTTTTTGACTTTAGAATAAATTTGCAGTTTTTTTTTTTTTTTTTTTTTTTAAAGGCAATGCAAAATGTTTTCAAATAACCCAGTATTTGCAAGGAATTTGCAGAAATGAGTATGGATTAATTATTAATCTGATTTTGTCACGGTAATTTGCATGGTTTTTGTGTGTTAATTTTAGATGTAACAGTAAATTTGTTTTGTGTAGTTCCATTTTGTGAGTGTGTGGGTTGGTAAAGGCAAATTAAGCAACAACCTCTTGTGTATCATCCCTGCTGTTCCTCAGATCCTGGTGAGCATTGAGCAGGTCCAGGAATTGTTGCCAAAAATCGAGCGGAGTGCCTCTGAGCCCTCTCTACACCGTGCTGTACATGCC[G/T]AGGACCTGAATCCGCTTCTCCTTCACACCACGCGCTTCCTGTGAGACTCCCGGAGACCATCCTCTCTTCTGAAAGCCGTGCAGCATCATTCCCAGCATGAAATCCCGAGTTCCTCTCTTTTATTCCACACATTCCTGAGAGCACCCTAGTTAGGCTACTTTATTGGTCCCAAATACAGTCAAGCACACACATATAACATTTATTGCTCTCGCCCTCCTCTTTCCAACTTCCGAAAGCTGCCAGTAGAGAATGTCAGTTTGTATCTGGACCCAACTGCTTTCTAAAAAGGAAGCAGGACATAAACCGTGCTCCATTACTACATTTATTGGATTACCATATCCAAGCATCATATCGGCACAATCTTAATAACCTCCTTTTTTGAGGTGTATTTCAAAATGTGTATGGTTGCTTACGTTACTTTTTTACTTTGAGATGAAAGTAGCTTTTTATTTTTTCATAGAACAAGCAAACCAGCTTGGAGATTTCCTTTTTTTTTGTCT
Associated Phenotype:
Not determined