Busch Lab

ZMP

ARAP2

Ensembl ID:
ENSDARG00000056389
Description:
ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 2 [Source:HGNC Symbol;Acc:16924]
Human Orthologue:
ARAP2
Human Description:
ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 2 [Source:HGNC Symbol;Acc:16924]
Mouse Orthologue:
Arap2
Mouse Description:
ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 2 Gene [Source:MGI Symbol;Acc:MGI:2684416]

Alleles

There are 10 alleles of this gene:

Allele Name Consequence Status Availability
sa12743 Nonsense Available for shipment Available now
sa17957 Essential Splice Site Available for shipment Available now
sa34218 Nonsense Mutation detected in F1 DNA Not yet available
sa9517 Essential Splice Site Available for shipment Available now
sa7098 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa41062 Nonsense Mutation detected in F1 DNA Not yet available
sa21116 Splice Site, Nonsense Available for shipment Available now
sa41063 Nonsense Mutation detected in F1 DNA Not yet available
sa11046 Nonsense Available for shipment Available now
sa34219 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa12743
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
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078816 Nonsense 306 1612 5 32
Genomic Location (Zv9):
Chromosome 7 (position 64318151)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 64114685
GRCz11 7 64531313
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTTCACTCTACTATTTGTTTATTTATTTTTTTCAGACACAWGCAGACA[C/T]AAGCCAAAGAAAAAGTACATTATAACAACAAGCAAGACCTTTCCAAGCAA
Long Flanking Sequence:
GGTCTAATGAAAAATCTATTTTAGTTTCTCAAAATAGCAACGCGCCAGCAGTGCGCCTCAGAACGCCTTCCTCTTTAGACTAGAATGCCTATGGGCACACATATGAGCGCAAATGCATTTGCTGTTTAAAGAGCGTGGCGCAATGCCTCAAAATGACTCTTGCGCCAAGCTGAAACTAGCAAACAAGTATTGCGCCGCACCTTGCGCCACATTGCGCCGGTTGTATGATAGGGCCTCAAGTTCATCTTAGTAAATACATTAACTAACATTAACATATTAAACCTTATTGTAAAGTGTGACCAAAATGTGTACAGAAATGTTACCCAAACTTTTTTTTAAATTATAATTAGTGTCCAAACGAAGCTATTTGTTAATATTTAGCCTTGTTAAAATGTGTTTAACAATTTTTTGCTTAGTGCTCTTTCACTCTACTATTTGTTTCATTCTACATTTTTCACTCTACTATTTGTTTATTTATTTTTTTCAGACACAAGCAGACA[C/T]AAGCCAAAGAAAAAGTACATTATAACAACAAGCAAGACCTTTCCAAGCAACACATCGATGATGATAAGAATGTTGATGAAAATGATTATGATGATTACTCTACTGTCCAAGCATCCAGCTTTTGTCAGCAAATTACTAATGAACATCCCACACCTCCTACTCTTCTCTCTAGCACTGGACCCTCAGCTGTGTCAGCCCAGTCACAAGCAGATGTAAATGTTATATACAGTTTGGCACACGATGACCAACCAGGTCTCCTGAAACCCAGCGTTCCTCCTCGAACTGACCTGTCCATTTCTCCATACGCCTGCTTCTATGGGATCTGTAAGACTGCAACCAAAGCCGGCTGGCTGGACAAACTCTCCCCTCAAGGGTAAAGAATATGCAAAAAGCTCTGTTTCTTTATTTGCAATTTTTTTGCACTGATTTTAATATTATTCTTGACAATAGGCACAGGAATCTTTAGAAATTTCACAATTATTGTTACATACTGTATATCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17957
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
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Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078816 Essential Splice Site 430 1612 5 32
Genomic Location (Zv9):
Chromosome 7 (position 64318526)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 64114310
GRCz11 7 64530938
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTAAGACTGCAACYAAAGCCGGCTGGCTGGACAAACTCTCCCCTCAAGGG[T/C]AAAGAATATGYAAAAAGCNNNNNNTCTTTATTTGCAATTTTTTTGCACTG
Long Flanking Sequence:
ATTTAGCCTTGTTAAAATGTGTTTAACAATTTTTTGCTTAGTGCTCTTTCACTCTACTATTTGTTTCATTCTACATTTTTCACTCTACTATTTGTTTATTTATTTTTTTCAGACACAAGCAGACACAAGCCAAAGAAAAAGTACATTATAACAACAAGCAAGACCTTTCCAAGCAACACATCGATGATGATAAGAATGTTGATGAAAATGATTATGATGATTACTCTACTGTCCAAGCATCCAGCTTTTGTCAGCAAATTACTAATGAACATCCCACACCTCCTACTCTTCTCTCTAGCACTGGACCCTCAGCTGTGTCAGCCCAGTCACAAGCAGATGTAAATGTTATATACAGTTTGGCACACGATGACCAACCAGGTCTCCTGAAACCCAGCGTTCCTCCTCGAACTGACCTGTCCATTTCTCCATACGCCTGCTTCTATGGGATCTGTAAGACTGCAACCAAAGCCGGCTGGCTGGACAAACTCTCCCCTCAAGGG[T/C]AAAGAATATGCAAAAAGCTCTGTTTCTTTATTTGCAATTTTTTTGCACTGATTTTAATATTATTCTTGACAATAGGCACAGGAATCTTTAGAAATTTCACAATTATTGTTACATACTGTATATCTTAACTTTATTTTAATGGTCCATTTGAGTATTAGTAGACAGTCTGCTTAATATCGGTTGATACTGCTTTGCAAGTACATGTCAACTTACACTAACCCTAACCCAAACATTACAGTCTACTTGTAATCAAATGAGAATTAGTTAGCATGTAGATCATAATAAAGTGTGACCAAATATATAAACACATTTAGACATGTTTTTGTGCAAAAGCGTCAACTTTTTTAACTTTGGTGAGTTTTTTTTTTTACATCTTTCAAAATGGTTTCATCTTTTAGCCTAGACAACGGTGATCACAACAATATAAGAGTTTACGTTCATACTTTCACATTTTTTTTAAGAATAAAAAAAATATTCATTATGATAAAAATACTTTTATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34218
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078816 Nonsense 616 1612 10 32
Genomic Location (Zv9):
Chromosome 7 (position 64377481)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 64055355
GRCz11 7 64471983
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTGGATCGAGGCTGTTCAGGAGTCCATCGTAGAGACGTTGTGCAATTA[T/G]GAGGTGCTGGAGAAAGTTTGGTTCAACAAGTCCAACAGGAAGTGTGCCGA
Long Flanking Sequence:
CAAACAACCCCATGGCGTTCATATGAAGTTAATAAACAAATAAAATTTGTAAAATGTATCCTTTTTCAAACATTAATGAACTTTTGAAAAGTTTTTATGAATGTTTATTTAATAGTTTCACAGAATTGAACTGAATTGGTCTGGCTTTTTAAAACGGCCCCAGAGTCTAAACTGGCCCATTGTAAAAAAGAAATAATAATAATTGCACACTACTGTTTTAACTTCTATAAGGATAATTTCAAGTAGTAAGAAGTGACCTTAAAATCTTGAAATTTAGAAAATGGTAATTTGTAGCTACAATGCAGCTCTAATTTAGTTCTCCACTGAAGCTAAAAAAAACATTTCAATTATGGACTGCAAAAGTTAAAATGTAACCAGTCTTATTAAAATTTGTAAGAATTTTGTTTCATTTGTGTTAGTTTTACAGTGGAGTCGGAGCATGAGAGAGATGAGTGGATCGAGGCTGTTCAGGAGTCCATCGTAGAGACGTTGTGCAATTA[T/G]GAGGTGCTGGAGAAAGTTTGGTTCAACAAGTCCAACAGGAAGTGTGCCGATTGTCAGGCACCTGAGCCTGAATGGGCCTCCATTAACCTCTGTGTGGTCATCTGCAAGAACTGTGCTGGTAAGAAACTAACATGAACACTAACAACTGACAAATACAAACACACTGTACAGTTTGCTGTCAACACGCACTGTGCTCGTGAGTCTGTGGGTTTAAAAAATAATAAAAATTTTATATACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGTTGAAGTCAGAATTATTATCCCCCCTTTAATTTTTTTTTTTGCTTTTTAAATATTTCTTAAATGATGTTTAACAGAGTAAGGGGATTTTCTGGTGGGCGGCGTGCGTTGGCTAGAGGCTGCAGGCCGAGTGCCTTAGTGTTCCACCAGTGATAATATACAGCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9517
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
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Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078816 Essential Splice Site 928 1612 16 32
Genomic Location (Zv9):
Chromosome 7 (position 64415818)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 64017018
GRCz11 7 64433646
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTGGAGACCTCGGACGCACACCAAGATTGGACAAACGCCATAGCCAAGG[T/G]CACACACATAGACACACACAYACATACATTTGTTTTTGTGAAYTGTGGGG
Long Flanking Sequence:
TTTAATGAATGTTTGCGCTTGAGCACCTTCTGTGGGTTAGAGGTTACAGAAAGAGTTTCAGATGTAAGTTTCTATTCACTAACAAACACAAAGAAATGAGAGCAAACTGACGTGTAGAGCAACCTCTAACCCGATTAGCGCGACTGTTGGGGAAATCTCTCGCTACCTTAACAAAAATATCCCATCCACAAAAAATGTGGGCCACAAATCAGAGCTGTTAAAGCCATTAAGAGAGTGACCTTTCCCCCTGGATTAATCTCCTGCGTTCAGCTGTTTATTGTAAGAGCAAAAGACTAACAGAGATTAATCACCATCCTTTCTGTTGCACAGCTGTGAGCATGTGTGTGTTTCAGTCATTGTGTGTGTGTTAATTGTACTGTTTCACACCTCCCTCAGGCCAGTGTTCACCTTTGAGTTGTACCTGCGCTCTCAAAGAGTGCTGGTGTTCGGAGTGGAGACCTCGGACGCACACCAAGATTGGACAAACGCCATAGCCAAGG[T/G]CACACACATAGACACACACATACATACATTTGTTTTTGTGAATTGTGGGGACATTTCATATGTTTCCATTAATTTTAAGACCATAAAAGCTGTATTTGCTAACGCTAAACCCCAAGTATGTTCCTTAACACCCCTCAACCCTCACAGGAAACTGTGTGCAGTTTTACTTTCTGGAAAAAAAACAAAACAAAAAAAAAAAACTGTTGTATTATTTATAAGCCTTTCGGCAATGAAGTCACCTTTTCCTTGTAATATTTTTGTCATACCCATGTCATACAAATTTGTGACCTGATATGTCAATAAAACACACACACACAAACACACAATTTACACAGATTGTTATTGGTGGTTTATTTATATTTTTAACCATTCTATTTGTAATTGATAATCTTTAGCTTGTCGATCTAATTCCAATTTTTGATCAAGTTTAAGTTTTTCATATTCGATTTTGTGCTGTTTTAGTAACTCCATAAATCTTGCTAATTCAACCTCCTTATAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7098
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078816 Essential Splice Site 1275 1612 25 32
Genomic Location (Zv9):
Chromosome 7 (position 64445934)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 63986906
GRCz11 7 64403534
KASP Assay ID:
554-4998.1 (used for ordering genotyping assays)
KASP Sequence:
AAGTCTTGAACTTTCAAAACACTGAATGATGCTGATGTGCGTTTCTTTTA[G/A]ATCTCTCCGAATATGAGGTCAGATGAACTTGCCGTCAGCACTCTGGAGAT
Long Flanking Sequence:
AAAGGTGTGTGTTTTGTCACTGTGTCCGTCTGTGTTTGCAGTTCTCTCCTGCTGGTGACCTGATATTTGAAGCCTACCTGGAGAAAAAGGAGCCAGAGAAGTGCTGTTTAATCAAGGTTTGTTTCCCTCGCTCTCATCTCTCTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCAAACCTAGAGGGTATTCTGCCACAAACTAAATCAAACTGCAGTTAATCAAAGGCATGTTTGATTTAATTGTGAGAGTAATTGTGTTTTATCAGTAGTCAAGGTAAACCTCAGTTAATAGAGGTTGTTTCAGAGCATTTTTTTCCTCTCTCTTGACGCTTTTGATATCTTCTTCCTCTCATTTTTTTCCTCCAGCAAAAGTAGATAAATCATTTTGCACAAGGAAATGAAGTCTTGAACTTTCAAAACACTGAATGATGCTGATGTGCGTTTCTTTTA[G/A]ATCTCTCCGAATATGAGGTCAGATGAACTTGCCGTCAGCACTCTGGAGATGAAGGGCATGGAGGTCAAAGCTCAAGATCTCTGGACCACGTTTGAGGTCATTGAAAATGGAGAAATGGGTAGGACTCACACTGTTGAGGTTTAAAACGATGCTTAAATGTACTGTTTAAATGAATGACTTCATAAAGTCTTTTTTTAAAGTTTAAGCTGATTATTAGAGCATTTAATGATGTTCCTCTAAGGCTTACGCACACATTTAAATGCTTCAGTCACTAAGTGAATGCGCATGAATAGTACTATTATTATTTGATGGCAGTTATGAGAAACTATTAACAGATTGCGATGGCATTGGAGGGAGGGGGAGACAGGTGGTGTAAGAGTAATTTTTGCCAATAGCGAGCATTGTGTTTTTCCTTTTTTACAAATTACAACTTGATAATGGATCTATTTTGCACTTGAGTGTGTTTTCTAATCATAGTCAGATTGGCTGGCGATAATTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41062
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
ENSDART00000078816 Nonsense 1376 1612 27 32
Genomic Location (Zv9):
Chromosome 7 (position 64449578)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 63983262
GRCz11 7 64399890
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGGATTTCATTAAAGGAGAGCATCTCAAATTCAAAGACGGTTCTTCC[A/T]AACTGCTATTGGGGAATAAGTTTCAGGACCGCTACTTGGTACTACAAGAC
Long Flanking Sequence:
TGGATGGAGCACTTGCAGAAAAGCTAAAGTTTTCTTTTCTATTTACACCCTCTTTCCCGTCCCACTGAAATCATCAGTAATGGCAGCCAGAAATCATCATTTTTGTACCTGCGCTGAGTAATAGCTTCTCTGCATGCCTCACTAAAGATATTAATATATATTAAGCGGTGATGGGAGGCAAAAGTGTATTCATGTGGCAGGATGTGTATGTGCTAGACTCTCAAATGTGTTAAGCAGTAAATGTGTTTTGCGGCACTTCAGGTGCTTTTCTATACAACTTTAGACATTTTTAAAAATGTATGATATCTCGCTGCAGTCTGAAGCGGCAGGGGGCCACACTGGTGCAAAGCTACAGCATATGTGTAGTTTTTATGTTGCGTCTCTCATAAATAGTTCATGCTATGACTCAATGTGTTTTGTTGTGTTCTTCTGTGCTTGTGACAGATAAACTGAAGGATTTCATTAAAGGAGAGCATCTCAAATTCAAAGACGGTTCTTCC[A/T]AACTGCTATTGGGGAATAAGTTTCAGGACCGCTACTTGGTACTACAAGACAAAAAACTGCTGCTGTACAAAGACATAAAAGTACGTCTCCTACATCTTCACTTTTAATTCCAAGTCGACTTTTTTTCAAGTCAAATCAAAATGATTTGCTGGTCTTTTAAGTGCCTCTACCCATGGTAATATTTACCCCTCCCCAACCCTGCTGTTCACCAAGCTCAGCCTTTGCATGATATAACTGTTCGCCAGTGGCCCTGCAGCACTCGCCAGTTTAACAATTTAGATTTTGCAGCGTGGCGTTTCATATTAGCTCTGTTTGTTTTCTTAGCGTGCGTTTACAGATGAAATAGTTATTAAAAAACACAGCGGATGTAAAATTACCTGCTTTGGGCCAATCGCAGGGGCCCGCTTGTAATAAGCATGGAAGGAAAAGGAAACAAATAAAGCCATAATGGCTATTTTCATTTTGAATTAAAGTAATGTGGGACTTCTCATACCCCCTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21116
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 > A
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078816 Splice Site, Nonsense 1442 1612 30 32
Genomic Location (Zv9):
Chromosome 7 (position 64459377)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 63973463
GRCz11 7 64390091
KASP Assay ID:
2259-9692.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGTTCACTTGAGTGCTTCAGTGTTCACCTTTGCATCGTCTCTGAAACAG[G/A]TATTTCTGCTGTAAAGGGAATGATTCTCAGCAGGACTGGGTCACCTCCAT
Long Flanking Sequence:
TAGGTAAGCAGAAAATCTCAAAACAGACCATTTGTTTTTGTTATTCCAGTCAGCTGTCTGTGTAAATTAAGCTGAATTTAATGGTATCTTAGCACTTTAGAGGTTCAGCTTGTGGCACCATCAGGAAAAGCTGAATATAGCTGTAAATTGATGTGGAGAACCTGTATGAAATGCTGTGAAACTAATGGAATTCTTTTTTTGTTGTTGTTTTTCTGACAAATTTTCAACAGTTGGGGATTTACTGTTTATACTGAAAAGCAGCAGTGGTAAGTGCAATTAACTCTGTTCCTAATTACATAGTCAATCTCACGCTTCAGTACTGTTTTTAGGAAAAACATTTTGCTGGGACTGGGTAATATGTGCCTTTTTAATATTTCAGTCTGAAACTTATAAAGGCTTTTTGGTACAGCTTAATACATGAAGTACAGAACTGAAGGACTGCATTTCAAATAGTTCACTTGAGTGCTTCAGTGTTCACCTTTGCATCGTCTCTGAAACAG[G/A]TATTTCTGCTGTAAAGGGAATGATTCTCAGCAGGACTGGGTCACCTCCATTATCAGAATGAAGGTGAGCTTTTTCCTTTTCAGATGATGTGCAGTTAACATTCTTACAAATGGGCTGGTTTTTGTAATGCAATTTTAACATTTGATAATGTTTCACTTATTTTGAATTGAACAATCAAAAAAATAATAATTGCATTTCTCTTTCTTTGTATAAACAACGCATTCACTCACTGGCCACTTTATTAGATACACCTGTCCAACTGCTCGTTAATGCAAATTTCTAATCAGCCAATGACCTCATGAATAGCACAGGCCTCACCAAAATTATACAATAGAAGATTGAAAAAGCGATGCCTGTTCTGTCTCAAGTCTCGATTTCTGCTGCAACATTCGGATTGTAGGGTCAGAATTTGGCGTCAACAACATGAAAGCATGGATCCATCCTGCCTCGTATCAATGGTTCAGGCTGGTGATGGTGGTGGTGTTATGGTGTGGGGGATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41063
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
ENSDART00000078816 Nonsense 1520 1612 32 32
Genomic Location (Zv9):
Chromosome 7 (position 64471119)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 63961721
GRCz11 7 64378349
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTTAAAGGAAAGTCGGTGCTTACTACTAGTACAGAAGATTCAAATACA[C/T]AAAACCAAATGGCCGCAGATGAGGGCATCCGACCGGACTCGCTGCATAAA
Long Flanking Sequence:
AAAACTCCAAAATCATTCACAAATTCAGTATTGAAGAAAAAAAAAAGCATCTGTCTAACAAATAAACATTCATCTTTTTGCAGCACGGCAGTGACTTATGGCCTAGGGACCTAAAGCAGAGCACATCTCTACCTTATAACCTGAGCAGAAGGAGAACCTCCACTCAGAGCACCACACAGTCCAGCAATAAAAACCAAAGAGAGGTCAGCTCCAACGCTCACATAAACATCACAAACATTTAACAAACCACTTCATTTATTACTACTTAATGAATTTTTGCTTCAGTGAACACCTCTAAATGCCAGCACAGATCGCTGTTCTCCATCTTTGTTGACAGTTAAGCCAAATCCATGTCCTTTTAACCCACAAAACAGTTGTTAGAATTGGGCATCCAGTCTGTTCACTGCATACAAAACAACCGCTGACTATGATACACTTCCTTTTTTGTGCAGGTTAAAGGAAAGTCGGTGCTTACTACTAGTACAGAAGATTCAAATACA[C/T]AAAACCAAATGGCCGCAGATGAGGGCATCCGACCGGACTCGCTGCATAAATTGGCAAGTGCTGAAGGAACTCCGGGTGTCTCCAGGCTTGAAATGGTGATTGATGACACACTCCAGTCCCAACGAAGGGCATCACTTCAACAAGACACTGCCACTCTAACCCAGATTTCACAAAGGAAAGCCGCTATTCCCGGCAGAGGAGTGCAGTTGCCTCAAAACCTCATTAATGAGCTAAGTACTGTTCTCAACAAAACAGGACGCTCTCAGAAAGAAGCCGATTAGGAGAGACAGAAAGACAAGAGTCTTGTCCATTACACTTCCATGGTGCAAGAGGAAAATCAAACTCAGACCAAACCCAAAGTAAAGCTGCCTCTAAGTAAGCATAGTGCTATATGCATTGAAGATTTAAAGCATCTATGTTTAAGCTATGTAAGTATATGTAAGTATTAGCAGCTTTTTTTTAGTCAAAATGTATGAACAGAACTTTAAAACATAGATTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11046
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078816 Nonsense 1561 1612 32 32
Genomic Location (Zv9):
Chromosome 7 (position 64471242)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 63961598
GRCz11 7 64378226
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGGTGTCTCCAGGCTTGAAATGGTGATTGATGACACACTCCAGTCCCAA[C/T]GAAGGGCATCACTTCAACAAGACACTGCCACTCTAACCCAGATTTCACAA
Long Flanking Sequence:
CATCTCTACCTTATAACCTGAGCAGAAGGAGAACCTCCACTCAGAGCACCACACAGTCCAGCAATAAAAACCAAAGAGAGGTCAGCTCCAACGCTCACATAAACATCACAAACATTTAACAAACCACTTCATTTATTACTACTTAATGAATTTTTGCTTCAGTGAACACCTCTAAATGCCAGCACAGATCGCTGTTCTCCATCTTTGTTGACAGTTAAGCCAAATCCATGTCCTTTTAACCCACAAAACAGTTGTTAGAATTGGGCATCCAGTCTGTTCACTGCATACAAAACAACCGCTGACTATGATACACTTCCTTTTTTGTGCAGGTTAAAGGAAAGTCGGTGCTTACTACTAGTACAGAAGATTCAAATACACAAAACCAAATGGCCGCAGATGAGGGCATCCGACCGGACTCGCTGCATAAATTGGCAAGTGCTGAAGGAACTCCGGGTGTCTCCAGGCTTGAAATGGTGATTGATGACACACTCCAGTCCCAA[C/T]GAAGGGCATCACTTCAACAAGACACTGCCACTCTAACCCAGATTTCACAAAGGAAAGCCGCTATTCCCGGCAGAGGAGTGCAGTTGCCTCAAAACCTCATTAATGAGCTAAGTACTGTTCTCAACAAAACAGGACGCTCTCAGAAAGAAGCCGATTAGGAGAGACAGAAAGACAAGAGTCTTGTCCATTACACTTCCATGGTGCAAGAGGAAAATCAAACTCAGACCAAACCCAAAGTAAAGCTGCCTCTAAGTAAGCATAGTGCTATATGCATTGAAGATTTAAAGCATCTATGTTTAAGCTATGTAAGTATATGTAAGTATTAGCAGCTTTTTTTTAGTCAAAATGTATGAACAGAACTTTAAAACATAGATTTGCTTGAACGGGGTGTTCATTAGACTGGGTCACACTTTATTGTGATGGTCTGTTTGTTTAATTTAAGTTACTTTGCAACTTATTTTCATTAGAATATAAGTACACTGTTAGGTTGGGGTTAAGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34219
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
ENSDART00000078816 Nonsense 1574 1612 32 32
Genomic Location (Zv9):
Chromosome 7 (position 64471281)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 63961559
GRCz11 7 64378187
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCAGTCCCAACGAAGGGCATCACTTCAACAAGACACTGCCACTCTAACC[C/T]AGATTTCACAAAGGAAAGCCGCTATTCCCGGCAGAGGAGTGCAGTTGCCT
Long Flanking Sequence:
CTCAGAGCACCACACAGTCCAGCAATAAAAACCAAAGAGAGGTCAGCTCCAACGCTCACATAAACATCACAAACATTTAACAAACCACTTCATTTATTACTACTTAATGAATTTTTGCTTCAGTGAACACCTCTAAATGCCAGCACAGATCGCTGTTCTCCATCTTTGTTGACAGTTAAGCCAAATCCATGTCCTTTTAACCCACAAAACAGTTGTTAGAATTGGGCATCCAGTCTGTTCACTGCATACAAAACAACCGCTGACTATGATACACTTCCTTTTTTGTGCAGGTTAAAGGAAAGTCGGTGCTTACTACTAGTACAGAAGATTCAAATACACAAAACCAAATGGCCGCAGATGAGGGCATCCGACCGGACTCGCTGCATAAATTGGCAAGTGCTGAAGGAACTCCGGGTGTCTCCAGGCTTGAAATGGTGATTGATGACACACTCCAGTCCCAACGAAGGGCATCACTTCAACAAGACACTGCCACTCTAACC[C/T]AGATTTCACAAAGGAAAGCCGCTATTCCCGGCAGAGGAGTGCAGTTGCCTCAAAACCTCATTAATGAGCTAAGTACTGTTCTCAACAAAACAGGACGCTCTCAGAAAGAAGCCGATTAGGAGAGACAGAAAGACAAGAGTCTTGTCCATTACACTTCCATGGTGCAAGAGGAAAATCAAACTCAGACCAAACCCAAAGTAAAGCTGCCTCTAAGTAAGCATAGTGCTATATGCATTGAAGATTTAAAGCATCTATGTTTAAGCTATGTAAGTATATGTAAGTATTAGCAGCTTTTTTTTAGTCAAAATGTATGAACAGAACTTTAAAACATAGATTTGCTTGAACGGGGTGTTCATTAGACTGGGTCACACTTTATTGTGATGGTCTGTTTGTTTAATTTAAGTTACTTTGCAACTTATTTTCATTAGAATATAAGTACACTGTTAGGTTGGGGTTAAGGTTTGTATAAGTTGACATGTACTTGCAAAGGTCAGTTTAAT
Associated Phenotype:
Not determined