Busch Lab

ZMP

araf

Ensembl ID:
ENSDARG00000054533
ZFIN ID:
ZDB-GENE-050102-2
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
sa40437 Nonsense Mutation detected in F1 DNA Not yet available
sa30859 Nonsense Mutation detected in F1 DNA Not yet available
sa13556 Nonsense Available for shipment Available now
sa20425 Nonsense Available for shipment Available now
sa33608 Nonsense Mutation detected in F1 DNA Not yet available
sa31438 Essential Splice Site Available for shipment Available now
sa31439 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa40437
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
ENSDART00000076687 Nonsense 10 605 1 17
ENSDART00000076696 Nonsense 10 604 1 17
ENSDART00000136342 Nonsense 10 265 1 6
ENSDART00000138182 Nonsense 10 608 1 15
ENSDART00000140081 Nonsense 10 604 1 15
ENSDART00000076687 Nonsense 10 605 1 17
ENSDART00000076696 Nonsense 10 604 1 17
ENSDART00000136342 Nonsense 10 265 1 6
ENSDART00000138182 Nonsense 10 608 1 15
ENSDART00000140081 Nonsense 10 604 1 15
Genomic Location (Zv9):
Chromosome 5 (position 28500926)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 26256224
GRCz11 5 26856377
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACTGCCCCATCGGAGACACCATGTCCAACACTTCCTCCTGTTCCTCCT[C/A]GGGGGAAACCAGCCCGGACGATACACCCCGAGGTGGAGGCACCATCCGCG
Long Flanking Sequence:
TCTTAATTTAGATTAGATTAAAGTTTGTAAATCCAAATCAAATCAAAAATCCTAATATAATTTACATTGTATATGGCTCATATTCAGCGTGAGCTTTGCACATTAGCATAACCATAGTTTGATATCACAGAACCCGTAATTAACTATTTCTAAAATAATTATTTGGAACAGTGCTAGGCATTTTACCATTCGTCTTTGTTTTTGTTTTTTTAAACCCTCAGTAATATCTTGTCATCATTCGTTTATCTATGCCCAACATTTTTTGCCTGACCTTTTAGTATTCACATCTGTTTAATGGACTTGTTTTTATGTCAACAGACATTAATGGAAGGTTTTATTTGTGTGTTTTGGCACTAACACAATGTTGTCCATCTCAGGCTCCAGATGAGGGCTTCCTCCTGCATTTGCCCCGCTGTGTAAATCTTTGTGAGTGTCAGTGCTGCCAGTCCCTCACTGCCCCATCGGAGACACCATGTCCAACACTTCCTCCTGTTCCTCCT[C/A]GGGGGAAACCAGCCCGGACGATACACCCCGAGGTGGAGGCACCATCCGCGTCTACCTCCCTAACAAGCAGCGGACGGTGGTGAGGCTTCTTTCACTCTTAATTGTTCTTCATAAATATTTGTAACAGCTTACATAACCTGTATATGTACAAATGTAGTTGTGTGCTTGTGATCATTCCCATCTTTGATTATGTTCAGGTAAACGTTCGGCCTGGGCAAACTGTGTATGATAGTTTAGATAAAGCCCTAAAAGTCCGAGGCCTAAGCCAGGATTGCTGTGCTGTCTTTCGCCTGCTTGAAGGGTATGTGTCCCTGGGATAGTAGCATTTAAAGTGACAAATTATTTGGTAAAGTTTCTGTTCAAGGGATATTTGTCTTTGTCTTTTGACAGCCGGAAGAGACTTACAGAATGGGACACTGACATCACACCCCTCGTGGGGGAAGAGCTACTGGTAGAAGTCCTGGATGATGTTCCCCTTACCATGCACAACTTTGTAAGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30859
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
ENSDART00000076687 Nonsense 10 605 1 17
ENSDART00000076696 Nonsense 10 604 1 17
ENSDART00000136342 Nonsense 10 265 1 6
ENSDART00000138182 Nonsense 10 608 1 15
ENSDART00000140081 Nonsense 10 604 1 15
ENSDART00000076687 Nonsense 10 605 1 17
ENSDART00000076696 Nonsense 10 604 1 17
ENSDART00000136342 Nonsense 10 265 1 6
ENSDART00000138182 Nonsense 10 608 1 15
ENSDART00000140081 Nonsense 10 604 1 15
Genomic Location (Zv9):
Chromosome 5 (position 28500926)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 26256224
GRCz11 5 26856377
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACTGCCCCATCGGAGACACCATGTCCAACACTTCCTCCTGTTCCTCCT[C/A]GGGGGAAACCAGCCCGGACGATACACCCCGAGGTGGAGGCACCATCCGCG
Long Flanking Sequence:
TCTTAATTTAGATTAGATTAAAGTTTGTAAATCCAAATCAAATCAAAAATCCTAATATAATTTACATTGTATATGGCTCATATTCAGCGTGAGCTTTGCACATTAGCATAACCATAGTTTGATATCACAGAACCCGTAATTAACTATTTCTAAAATAATTATTTGGAACAGTGCTAGGCATTTTACCATTCGTCTTTGTTTTTGTTTTTTTAAACCCTCAGTAATATCTTGTCATCATTCGTTTATCTATGCCCAACATTTTTTGCCTGACCTTTTAGTATTCACATCTGTTTAATGGACTTGTTTTTATGTCAACAGACATTAATGGAAGGTTTTATTTGTGTGTTTTGGCACTAACACAATGTTGTCCATCTCAGGCTCCAGATGAGGGCTTCCTCCTGCATTTGCCCCGCTGTGTAAATCTTTGTGAGTGTCAGTGCTGCCAGTCCCTCACTGCCCCATCGGAGACACCATGTCCAACACTTCCTCCTGTTCCTCCT[C/A]GGGGGAAACCAGCCCGGACGATACACCCCGAGGTGGAGGCACCATCCGCGTCTACCTCCCTAACAAGCAGCGGACGGTGGTGAGGCTTCTTTCACTCTTAATTGTTCTTCATAAATATTTGTAACAGCTTACATAACCTGTATATGTACAAATGTAGTTGTGTGCTTGTGATCATTCCCATCTTTGATTATGTTCAGGTAAACGTTCGGCCTGGGCAAACTGTGTATGATAGTTTAGATAAAGCCCTAAAAGTCCGAGGCCTAAGCCAGGATTGCTGTGCTGTCTTTCGCCTGCTTGAAGGGTATGTGTCCCTGGGATAGTAGCATTTAAAGTGACAAATTATTTGGTAAAGTTTCTGTTCAAGGGATATTTGTCTTTGTCTTTTGACAGCCGGAAGAGACTTACAGAATGGGACACTGACATCACACCCCTCGTGGGGGAAGAGCTACTGGTAGAAGTCCTGGATGATGTTCCCCTTACCATGCACAACTTTGTAAGTG
Associated Phenotype:
Not determined

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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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

This allele has been removed from public view.

Allele Name:
sa18801
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076687 Nonsense 171 605 5 17
ENSDART00000076696 Nonsense 171 604 5 17
ENSDART00000136342 Nonsense 171 265 5 6
ENSDART00000138182 Nonsense 171 608 5 15
ENSDART00000140081 Nonsense 171 604 5 15
Genomic Location (Zv9):
Chromosome 5 (position 28502432)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 26257730
GRCz11 5 26857883
KASP Assay ID:
2259-5861.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGTCAGGTGTGTTAATAATACAGAAGACTGCCCTGCGATATTGATATA[T/A]CCGGCCACCAATTCCATATCGCAGAGCGACCTACCTTTAACCTCAGATTC
Long Flanking Sequence:
AATCATTATCAAATGCTGACTAGAGGCTTAAGAAATCATTCTTTATTTTTGTCAATGTTATAAACGGTTATTCTGCTTAATATTTTATGATCCACATAATTTTGTAATGATTTGCTAAATAAAAAGAAACGTATAGAAGTTGAGATAATGTCAAATTAAATATCTTACTGTTGTTCACTTAGTCAGCCAATCAGCATCATCTTTAAATGTTTGTATTTACAGGTACGTAAAACGTTCTTTAAGTTAGCATACTGTGACTTCTGCCACAAGTTCTTATTCAACGGCTTCAGGTGTCAGACATGTGGATATAAATTTCACCAGCACTGCAGCAGTAAAGTCCCTACAGTATGTGTGGACATGGACACAATGACAAAACGGTATGTTATTCATGAAAGTTTCTGCCTTGATGTACACTTGTCTTCATTTTTGTCACTTAATTGATGTTCTTATCCTGTCAGGTGTGTTAATAATACAGAAGACTGCCCTGCGATATTGATATA[T/A]CCGGCCACCAATTCCATATCGCAGAGCGACCTACCTTTAACCTCAGATTCTCCTGGGTACACCTAATCTATTCTTACATTTATCTATTGATCCCCAAAGTGAAATGTAGAAATAACTTGCATATCCTCTTTTTGTTTTACTATTTTAGAGGGGAGCTGCCGTCTTCCCCGTCAAACTTCTGTTTGTTCATTCGAGGAGAGGACGGTCAGTCTCTCCAGAGGCATCGATCAACCTCAACACCCAATGTTCACATGGTCAGCACGCTGGAGCCTGGCGCTGCTGGCCTTTTGGAGGTTAGCAGCCAGACTAAAAGCTCAAATCCACATCTCTTGATGTTCTCTCATTTTGACATTGTTTTAAAGGAACAGTTCGCTTAAACATTATAGTCACTCTCAATGTTTTCTACTAAATCCAAAATGTGGTGTAAAGTAATGTTTTTTTTTCATATTCAAATTGCCATGTCTAAAAACAATAACAAAGACTATTAGCATATATTGTTT
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.
Availability:
Order Allele From ZIRC
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:
sa33608
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076687 Nonsense 282 605 8 17
ENSDART00000076696 Nonsense 278 604 8 17
ENSDART00000136342 None None 265 None 6
ENSDART00000138182 Nonsense 282 608 8 15
ENSDART00000140081 Nonsense 278 604 8 15
Genomic Location (Zv9):
Chromosome 5 (position 28503760)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 26259058
GRCz11 5 26859211
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGGGTCGCCAGGAAGAAAACCCCCCAAATCCCCTTCTGAACCCAAGGAA[C/T]GAAAGCAGTCCTCGTCTGATGATAAAAAGAAAGTGGTGTGTTTTTATTCA
Long Flanking Sequence:
CTGGTTTGGAACACAGTGAGTGTACATGCATTTTTAGGTGAACTGTCCCTGTACGCTACCAAATTAGACAAAACTTTACATCACAGAATGTGTCTATGGAGGTTCTGCATGCCTCCTTGATCATTTCTCCATTGCATGTATTTATTCATTTTTTCCCCCTCACTCTCATTCAGGAGCCATTCAAAATCAGCACAGTGGGTGAGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTACTTTGTTCAATTAACCATTGCTTAGAGCACATGTTTTTTTCTTTTTCCACACTCTCACATAACACTACAAAAAGTTTAGTTTGTTCTCCATTTCTGATCACAATGACGCATCAAATTACACTTCTATATAAATGTTTGTGTGTACTGGTTCTCATCTTCTAGCGTCGTCCACAGGGTACGAGTCCTCTCCCAAACCTTCCACTAGCCCACCCCACCTAGGGTCGCCAGGAAGAAAACCCCCCAAATCCCCTTCTGAACCCAAGGAA[C/T]GAAAGCAGTCCTCGTCTGATGATAAAAAGAAAGTGGTGTGTTTTTATTCATCTTTATTTTCTGATACAAAAATGATTCTGCTTATTTACAATCAGCCTTTTCAAACAAAAAAAATATATAATTGTGGTGTCATTGAAGCACCGGGGAGGTTACAGAGACTCCAGTTACTACTGGGAGGTGCACCCGCGGGAGGTGTCCATGTTAAAGAGGATTGGAGCAGGCTCTTTTGGGACCGTCTTTAAAGGCAAGTGGCATGGAGACGTGGCCATCAAAATTCTTAAAGTGACAGAGCCCACACCGGAGCAGCTCCAGGCCTTTAAAAATGAGATGCAGGTTTTACGGTGAGTCGTCAGTGGGATTTAGAGCTTCACAGAACATCTTTGATCATTAGTAAGCAGTAGTTTGCAGTAATGCTGCTTAGTTACAACAGTAATGTCTTTAGCTGCTACAACCATTGAGTGTTTCATTGACTATATATCTGTTTTGTTCTACAGAAAAAC
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.
Availability:
Order Allele From ZIRC
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.
Availability:
Order Allele From ZIRC
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