Busch Lab

ZMP

fryb

Ensembl ID:
ENSDARG00000056001
ZFIN ID:
ZDB-GENE-080215-5
Human Orthologue:
FRY
Human Description:
furry homolog (Drosophila) [Source:HGNC Symbol;Acc:20367]
Mouse Orthologue:
Fry
Mouse Description:
furry homolog (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2443895]

Alleles

There are 21 alleles of this gene:

Allele Name Consequence Status Availability
sa34945 Nonsense Mutation detected in F1 DNA Not yet available
sa5830 Nonsense Mutation detected in F1 DNA Not yet available
sa24880 Nonsense Mutation detected in F1 DNA Not yet available
sa21770 Essential Splice Site Available for shipment Available now
sa10244 Nonsense Available for shipment Available now
sa21771 Nonsense Available for shipment Available now
sa24881 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa41695 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa41696 Nonsense Mutation detected in F1 DNA Not yet available
sa12198 Nonsense Available for shipment Available now
sa44728 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa41697 Splice Site, Nonsense Mutation detected in F1 DNA Not yet available
sa13238 Splice Site, Nonsense Available for shipment Available now
sa27638 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa31789 Essential Splice Site, Missense Available for shipment Available now
sa5586 Essential Splice Site F2 line generated Not yet available
sa41698 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa12244 Splice Site, Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa34945
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000044294 Nonsense 249 2973 8 62
ENSDART00000138547 None None 162 None 4
ENSDART00000142881 Nonsense 297 3080 9 61
Genomic Location (Zv9):
Chromosome 10 (position 34945406)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 33973264
GRCz11 10 33917124
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTTCAAAAACACTTCTACTGTTATGTGTTTATAGGAGTGTGCTCAGTA[T/A]TTCTTGGAGGTGAAAGATAAGGACATTAAACATTCTCTTGCTGGACTCTT
Long Flanking Sequence:
TACAGTATTACACAAGTATGAATAAATAAGCACCAGTTTACAGTATCTTGTCAGCCATTGCAGAATGATGGGAATCAACCCAAAGCTTTTTATTCATTCAAAGTTTTAAATATATCTAAATATTATTATTAAAATATTTTTATTATTATATTTTTTTATTTAATGTAATTTAATATATTTAAAATATATAATTTTTTAAAAATAAACATTAATCCCTCTCTAATCTTCACAGGTTTCCTGCAGTGAGGAAGAAGTTCATCTCCGAGTTAAAGGAGCTCAGGCAAAAAGAGCAAAGCCCATATGTGGTCCAAAGCACCATCAGCCTCATTATGGGGGTCAAGTTTTTTCGCATCAAGATGTACCCGGTGGAAGATTTTGAAGCCTCTTTCCAGTTTATGCAGGTACACAGTGCTGCAACTACTAAGTTTGTCATTTGAATCTCTTTTCTTTATTTTCAAAAACACTTCTACTGTTATGTGTTTATAGGAGTGTGCTCAGTA[T/A]TTCTTGGAGGTGAAAGATAAGGACATTAAACATTCTCTTGCTGGACTCTTTGTAGAGATACTCGTCCCTGTAGCCGCAGTAAGTATAGCCATGTCTGATTTATTTATTTTTTTTCTCAATAATTTAATTAGATTCATTACAAAAGGAGGGATACATTTTTATGATAGCCCCCTTTAAATATTATGTTGACCAATAAGTACTTTTGCAATTACATGTCACCTAACAGAAATAGGGGGAAAAATAAACAGGAGGGCTAATAATTCTGACTTCAACCGTACATGTCATGTATAAACTGTAATTCACACTTGTGATGTTTTTTTAGACGGTGAAGAATGAAGTGAATGTGCCCTGTTTGAGGAATTTTGTGGAAACCCTCTACGACACAACTTTAGACCTGTCGTCCAGGAAGAAGCACTCTCTGGCAAGTCTCGCTGTCCTTTCCCACACTAAAGTGATGCATCTAATTGGCTCATAGCTGGAATGCTTTTGCTGTCTGTGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5830
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
ENSDART00000044294 Nonsense 366 2973 11 62
ENSDART00000138547 None None 162 None 4
ENSDART00000142881 Nonsense 424 3080 12 61
Genomic Location (Zv9):
Chromosome 10 (position 34949941)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 33977799
GRCz11 10 33921659
KASP Assay ID:
554-3890.1 (used for ordering genotyping assays)
KASP Sequence:
CCCGAGTGGCACTTGAATCCCTCTATCGKYTGCTGTGGGTCTACATGATC[C/T]GAATCAAATGTGAAAGCAACACTGCAACACAAAGGTAGTGTACTAAAATA
Long Flanking Sequence:
GAAATGAACCGCCAACTTATCCAGCATGTTTTTACGCAGCGGATGCCCTTCCAGCTGCAACCCATCTCTGGGAAAATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATCATTAAAGCAGAGAAGCACAAAGCAAGAATGAATAAAAATAGATGATAAACAGCTGAAATGATTGTAACTATTATTATTATTATTATTATTATTATTATTGTCTTAATTGGTATGTGTATTGCATTATTCAAGATATGGTCTAGAAAGGTATTATACTCAAATAAATGTTGTTAGATTTTTTATTTATTTATATATATATATTTTTTTTTGGTAAACTGGAATTATCTGAAAATAAACAGAAATATGCAAATGTAACCATAATTTAATAAGAACTTTTCTTGCAGAACAAAGACCACAAAATGGCCCGAGTGGCACTTGAATCCCTCTATCGTTTGCTGTGGGTCTACATGATC[C/T]GAATCAAATGTGAAAGCAACACTGCAACACAAAGGTAGTGTACTAAAATATTCAAACATACAAACCCATTTTAAGAAATATATTTAGAATTAAAGAAATGTCATAGGTTTTCTGTAACACGTTTCAAATGCGTAGACAGTACTGTCAAAGAATGAGAAATGATCATGTTGATTGTGATGATGATTGACATCCGCTAAAAGTACTTTCTTTTTATCTGTTCCAGCCGACTCACCTCAATCATATCAACACTGTTTCCCAAGGGTTCACGAAGCGTTGTTCCTAGAGACATGCCACTTAACATCTTTGTCAAGATCATTCAATTCATTGCCCAGGTTTGACAGAACTCACACCCATAGATGTCTGATACACACTTAAGACAACATTCCACTTCTTATGTTTTCTTGTGCCCTTTTGAAAGCCTTACATTTTAAGTAGCCGTTCACACAGAACATGTTTTTTCAATAGGCCTTGAAATGTGTTTTTAAAATAATTTATTTCAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24880
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
ENSDART00000044294 Nonsense 505 2973 15 62
ENSDART00000138547 None None 162 None 4
ENSDART00000142881 Nonsense 563 3080 16 61
Genomic Location (Zv9):
Chromosome 10 (position 34952750)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 33980608
GRCz11 10 33924468
KASP Assay ID:
554-7556.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTCGCTTACAGTATGGATTGTGTATGCTTCAGGTATGGCACTGTATTA[C/A]TCGCAAGTCAGGAAAGCCATGGATAACATCCTGAGGCATCTGGATAAGGA
Long Flanking Sequence:
CACACCAGTATGCTTAGTTCAAATGTTCTGTTTTTATTTAAAGCTAGTTTAAGAGTATGATATAATATGTGTTCAACATTATATAAAAATAGAAATATAATTACTGAATTGTGTTGCAAAAAAACTGTACATTCATTTAAACACATCTCAATGTTCCATCTGATCTTGTAATGACTGAATATTTGATGTATTTTTGTGGTGTATATCCAGAGGATGAACATCGCTCTAAGAGCCTTCCTTGTCATAGCCGATAACCTGCAGCAGAAAGACGGAGAACCACCCATGCCGAACACAGGGGCCACTTTGCCTTCTGGGAACACACTAAAGAAGAAAAAAACTTACCTCAGCAAAACTCTAACCGAGGAGGAAGCAAAACTTATAGGTCAGATTTGCTTTGCTATTTCCGACACCTGGCTGTGTATTAGAGTTTGACATTGTTGTACAATTTTACAGTCGCTTACAGTATGGATTGTGTATGCTTCAGGTATGGCACTGTATTA[C/A]TCGCAAGTCAGGAAAGCCATGGATAACATCCTGAGGCATCTGGATAAGGAAGTCGGCCGCTGTATGATGCTCACAAATGCCCAGATGCTCAACAAGGAACCTGAGGACATGATCACGTAAACAGCTTTTCATTTTTTCACCTATTATTTTAGTGTAACATGAGCGTGTGAAGAGAACGCTCAGAGCCAGACAACTTTTTATGAGTCAAGTTCAGCCCACACACCCTGTTTAGACAGTTTGGCATTCTCTTTATTCCTGTTTCCTTGTGTTTCTTTGCCTTTCTCTTTGTTTATTTTTGCTCAACTCTTTCCTTCTCTCTTTTGTCAGGGGTGAAAGAAAACCCAAAATTGACTTGTTCCGGACATGTGTTGCGGCCATTCCTCGTATTCTGCCTGACGGCCTGTCCAAAATTGAGCTCATCGATCTTTTAGCCAGGTGAGGTTCACCACGAATCCTTTGACTATTCAAAGAAAACAGAAAAAAAGTAAAATAAGATTTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21770
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000044294 Essential Splice Site 659 2973 18 62
ENSDART00000138547 None None 162 None 4
ENSDART00000142881 Essential Splice Site 717 3080 19 61
Genomic Location (Zv9):
Chromosome 10 (position 34956594)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 33984452
GRCz11 10 33928312
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATGGGAGCTGTGTACCCAATCACCTGTTTTTGTATGTTTGTTGAGCTC[A/T]GATGGGATCCCAGAGCAGCGGAAGCTCCAGGCTGGCGCCTGATCGCAGTC
Long Flanking Sequence:
TTGCTCTGTTAAACATCACTTAGGAAATATTAAAAAAATTGAATAAACATTTCTCAGAAGGGCTAATAATTATGTCTTCAACTGTGCATATATAGTTTTTAAAGCTCATTGGTCTTTTGCACTTTGAAATAAAAGCATAAAACTTTGTCATTGATTTGTTTATGTTTCATATTTAGGCTGACGGTCCACATGGACGATGAACTCAGACTCATTGCTCAGAATTCCCTGCAGAGTTTGCTGCTGGACTTCTCTGATTGGCGAGAGGATGTGTTGTTCGGGTACACAAACTTCTTACTGCGTGAGGTGCAGGACACACAGCAGGGCCTGCAAGACTCTTCCGTTAAACTGCTGCTGCATTTCCTGACACAGTGGAGGCTGGCAATTCAAGCGCCTGGAAAACGCTCAGCGGAGGTATCAGCGGGATCATTTTCTTTACCGGTTATACAATGTAAATGGGAGCTGTGTACCCAATCACCTGTTTTTGTATGTTTGTTGAGCTC[A/T]GATGGGATCCCAGAGCAGCGGAAGCTCCAGGCTGGCGCCTGATCGCAGTCCTCACTCTACTGTCCTGCACGCTGTGGAGGGTCTGGCCCTGCTGCTGCTGTGTTCCTGCCAGACCAGCACCCGAAAACTGGCCGTTTCAGTCCTCAGAGAGATACGCTTGCTGTTTACAGCCATCGGACAAGCCGAGGTGAGAAACATAACTAAAACTGAATTCCATAAAAAGACAATATAATGGAATACGATGTATTAAGTGTAGTTTCATAAACTAATTTTGAGAGGAGCACTTGATATGATTACGGCTGGTCTCTCATCCATAATCAGCAGTAATCAGATTGATCCAAGCCTACAATAAATAGACTGATTTCTCCTTACTGCCTAATCTTCATATCGGAAAAATCCCCCCTTCCACCCCATCTCCTCCTTTTTCTTCTTTACCAGGGGAAGCTCTCGTGACCTACCTGATTTCAGACCCCTTACATGCTAATTGACTAGGCGGGGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10244
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000044294 Nonsense 819 2973 20 62
ENSDART00000138547 None None 162 None 4
ENSDART00000142881 Nonsense 891 3080 21 61
Genomic Location (Zv9):
Chromosome 10 (position 34959031)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 33986889
GRCz11 10 33930749
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGGCCAGAGCATCTACCCAAACACTGTCCTACAGCGCKCAGCTATGCCT[G/A]GCCCTACGCCTTTACTCGCCTACAGCTGCTKATGCCAYTTGTAGACCCAA
Long Flanking Sequence:
ATACTGATCAGTATGAGATCTGTTAGTGCAGCATAAACATTCAGCAACCCTTCTGCTGTCATGTTTCTGCTTACAGGATGACGACAAGTCCATGATTGAGGTTATGGATCAGCTTGCCCCCAGTGTGCTGGACAGTTTTGTTCATGTGGCCGTCTCTGACTCGGTAAGAATTTCCCAATGGATGTGTTTCTGTCTTTTTATCCATATTTTTATGCGTTTATGCCACAAGACACCAAATGTCTGCCTGTAGAGTCATGATCCTCATTTTAACCTGTTGAAATCTTCTGTGAAGGCCACTCTTCCCCTGAGTCATCACGTGGACCTGCAGTGGCTGGTAGAGTGGAACGCCCGTCTGGTTAACAGCCACTACGACGTAAAGAGCCCTTCTCACGTGTGGATCTTCGCCCAGTCTGTGAAGGACCCATGGGTGCTGTGTCTGTATAGCTTCCTTAGGCCAGAGCATCTACCCAAACACTGTCCTACAGCGCTCAGCTATGCCT[G/A]GCCCTACGCCTTTACTCGCCTACAGCTGCTTATGCCACTTGTAGACCCAAAGTGAGTACTCCTAAAAGATGATTATCATGAGTCTCTTTTAAAGGGATAGTTTACCCAAAACTGAAAATTCTGCCATCTTTACTCGCTCCTTTACTTCTTCTGAACCTGTTGGACATTCTGTCTTCTGTTGAGCACAAAAGAAGATATTTTGAAAAATGCTGCAAACCTGTAATCAATGACGTTTATAGTATTTGTTTATCCTACTTACTGGTACTACTTACTTACTTACTTACAGGTTACTGGTTTCCAGTTTTATTCAAAATATTTTCTTTTGTATTCAACAGAATAAAGAAGCTACTATAGCTTGGTAACCCCCTGAAAGCATGTAAACAGGGAAAACATTTTCATTTTTGGGAGAACTAATTTTTAATCTGAAGCAAGTCTTACACAAGGTGCATGGAAACAAATAACATGTAAAAATATTGGGGGGAATGGGGAAAATTTAAATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21771
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
ENSDART00000044294 Nonsense 884 2973 21 62
ENSDART00000138547 None None 162 None 4
ENSDART00000142881 Nonsense 956 3080 22 61
Genomic Location (Zv9):
Chromosome 10 (position 34961169)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 33989027
GRCz11 10 33932887
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCCAAGCCCAGCATCATGAGCCCAGGTCACCTGAGAGCCTCTACACCT[G/T]AAATAATGGCTACCACCCCTGATGGCAGTGTCACGTACGATAACAAGGTC
Long Flanking Sequence:
TTAAAGAGCAGACGCGAATGGCACTCGAGAGAAATTTGAGATCTCAAAAAGCTTACACAGTGAGCTATGGTGGATTTGCAAAAACAAAAACGCAAAAAATGTAGCTCTTGGAATGTATTTGGCGCTCTCCAGAATCAATATTATAGATGTGGTGGGAATAATTTTTTAACAATTTTAAACTACATATTTATTAATATATTTATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTGCACTTTTGATATCTGAGTCACTTTCTCTGGTACGCCCTTGCAGCAGTCCTGTTTATGCCAAAAAGACCAGCACGCCAGGCTCAGCTGATGGCTATGTGACGCTCTGGAGGAACTATTTGATAATGTGCCTCGGTGTTGCCAAGCCCAGCATCATGAGCCCAGGTCACCTGAGAGCCTCTACACCT[G/T]AAATAATGGCTACCACCCCTGATGGCAGTGTCACGTACGATAACAAGGTCAGTTACACACATATTCTGATATCTATGATTCAGAAAATGAAAGAAATTGTGGCGTAATGAGTGCATTTGTGTGTTTATAACCAGGTGATAGGCACACCATCAGTGGCGTGGCTTCTGAAACAGCTGGTTCCCCTCATGAGATCAGAGAGTTTAGAGATCACAGAGTCTCTAGTCCTCGGTTTTGGACGAACTAATTCCCTGGTGTTCAGGTATTTTTTTATTTTCACCAAACATGCTCCTTTCTCATCGTAAATGACTGGATTTCATAGTTTTAATTAAGTTATTTTCTAAATCAGGGCACATTTACAGCATATACACAGTCCCAATGTACTCTGGCATCCACATTGGTCACATTGGGTTTTTGACTATGGCGAATGAAAAAAGCATTAAGTAATGTGTTTGCCAAACTAAATAGCAGAGATTAGTGTCATTCCATTCTGACGTGTGCCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24881
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000044294 Essential Splice Site 941 2973 23 62
ENSDART00000138547 None None 162 None 4
ENSDART00000142881 Essential Splice Site 1013 3080 24 61
Genomic Location (Zv9):
Chromosome 10 (position 34962822)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 33990680
GRCz11 10 33934540
KASP Assay ID:
554-7733.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTCTGCTGTTTTTTATTTCATGACTGTTTCTTACATGTGTGTTTAATT[A/C]GGGAGCTGGTGGAAGAACTTCATCCACTAATGAAAGAAGCTCTGGAAAGA
Long Flanking Sequence:
CACTATGGCCAATTTAGTTGCTTAATAAAGTGTCTTCAGCCTAGGGGGGGGAGCGGTGCACCTGGAGGAAACTCATGCAAACACGGGGAGAACATGCAAACTCCACACAGAAATGCCAACTGAACCAGCAACCTTTTTGCTGTGAGGCGATAGTGCTAACCCTAATCCAAATTTGCTGTCAATAATTTGTTTAATCATCAAACTTTTTCACTTGAAACTATTTAAACTAGGGTGACGCTTAATGAAGCTTTACTGGCCCCCTAGGTTGGGAACTGCTGATATAAAGAATTCTAAAACTTTACTGAGCACAGGCTATTTGATGTAACCTATAAAAAGCACAGACCTACATGTTTGAATTAAAATTTGGACTCTGTATACAGTTATGACTTCATGGTGGTACATTGCGTAATTTTGATTATTTGTGGTTTTGTACAAAACATTCAAAAAAAATTCTCTGCTGTTTTTTATTTCATGACTGTTTCTTACATGTGTGTTTAATT[A/C]GGGAGCTGGTGGAAGAACTTCATCCACTAATGAAAGAAGCTCTGGAAAGAAGGCCTGAGGTGAGATGCAGATCTTTGAAAACTAAATATTAAATTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGGTAGTATTTGCTTTAATGAATTTAAATAGAGTCTGTTTCTTTGTTGCTCCCTCTGTAGAACAAGAAGCGCAGAGAGAGGAGAGATCTGCTCCGGCTGCAGCTGCTGCGCATCTTTGAGCTTCTTGCTGACTCTGGGGTCATCAGTGACAGGTGAAGTCATGTAGTCAAATCCTGGGTTTAACTGTTTAATCTGATCTTCTTTCACAACAAAGCAAGTCTTTGACCTTTGTGGAATTCAAGTGAAAATGGAAAGTCTTGTAAAAATCCTGTGCACCTGTTTTTTTTTCATCTTCATTGTAGTACTAATGGAGCATTGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41695
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000044294 Essential Splice Site 991 2973 24 62
ENSDART00000138547 None None 162 None 4
ENSDART00000142881 Essential Splice Site 1063 3080 25 61
Genomic Location (Zv9):
Chromosome 10 (position 34963156)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 33991014
GRCz11 10 33934874
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTGCGCATCTTTGAGCTTCTTGCTGACTCTGGGGTCATCAGTGACAGG[T/C]GAAGTCATGTAGTCAAATCCTGGGTTTAACTGTTTAATCTGATCTTCTTT
Long Flanking Sequence:
AGCACAGACCTACATGTTTGAATTAAAATTTGGACTCTGTATACAGTTATGACTTCATGGTGGTACATTGCGTAATTTTGATTATTTGTGGTTTTGTACAAAACATTCAAAAAAAATTCTCTGCTGTTTTTTATTTCATGACTGTTTCTTACATGTGTGTTTAATTAGGGAGCTGGTGGAAGAACTTCATCCACTAATGAAAGAAGCTCTGGAAAGAAGGCCTGAGGTGAGATGCAGATCTTTGAAAACTAAATATTAAATTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGGTAGTATTTGCTTTAATGAATTTAAATAGAGTCTGTTTCTTTGTTGCTCCCTCTGTAGAACAAGAAGCGCAGAGAGAGGAGAGATCTGCTCCGGCTGCAGCTGCTGCGCATCTTTGAGCTTCTTGCTGACTCTGGGGTCATCAGTGACAGG[T/C]GAAGTCATGTAGTCAAATCCTGGGTTTAACTGTTTAATCTGATCTTCTTTCACAACAAAGCAAGTCTTTGACCTTTGTGGAATTCAAGTGAAAATGGAAAGTCTTGTAAAAATCCTGTGCACCTGTTTTTTTTTCATCTTCATTGTAGTACTAATGGAGCATTGGAACGAGATTCTCTGGCTCTGGGAGCCCTTTTCCTGGAGTATGTCGATCTGACCCGAATGCTCTTAGAAGCAGAGAATGACAAAGAGTTGGACATTTTGAAGGACATGAGAGCTCATTTTAGTGGAATGGTGGCCAATCTCATCCAGTGTGTTCCAGGTAATCAATGGCATTTTTTCTAAAAAAATAAAAAAAAATAAAAAGTCCTATTAGTGTAAACATTTTATAATTTAATCCAGAAATCATGAAAATTAGATATCATTTGAAACCAAAGTATTAAATCTAATGGCAAAGACCACAATAATAGAGCAGGTGAGATATTTTAGCTGGCATAATAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41696
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000044294 Nonsense 1061 2973 26 62
ENSDART00000138547 None None 162 None 4
ENSDART00000142881 Nonsense 1133 3080 27 61
Genomic Location (Zv9):
Chromosome 10 (position 34965606)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 33993464
GRCz11 10 33937324
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTTTCTCTGTAGTCCACAACAGGCGGTTATTGTTCCCCCAGCAGAGCT[T/A]GAGGCATCACCTCTTCATTCTCTTCAGCCAGTGGGCCGGTCCCTTCAGTG
Long Flanking Sequence:
CTGATATGAAATGAGGACTCTTGACTGCAAATCAAATCTACCTTCGGGTATAAATAAAGCAACCTAACCTAATGATATGTAATGATATATGATGGCATATGTATATAGGAATAGTGAATACTGAACACTAGAATAAAAAAATTCAACATACATAAAGATAGAAAACTATTTTAAATAGTAATGGCATATTAAAATATAATATAATTATATAATTATGTTATTTTTACTATTATATTAAAAGTAGCCTTGTTTATTATAAAAACTTTTTTTTTTAAAGCAGCCCCTGAATATTTGAACGTTTGTTTACATACTTTTACATACTTTACATACCCTTGGTAATTTTACAATTCATGTTGCCTGACCAAACACATTTCACATTGTAGCTTGCTCTGAGCACTTTTTTGTTTTGTTTTTGAGACTGGATTAATTTTTGTGTTGAGTCTCATTCATGTTTTTCTCTGTAGTCCACAACAGGCGGTTATTGTTCCCCCAGCAGAGCT[T/A]GAGGCATCACCTCTTCATTCTCTTCAGCCAGTGGGCCGGTCCCTTCAGTGTCATGTTCACACCTCTGGACCGCTACAGTGACCGCAACCACCAGATCACACGCTACCAATACTGCGCTTTGAAGGTAAACCTGGATAAAAACTCAATTAATCTAGTCATTGACGTTTTAGAGGATCATATTTTAATGAATAACACTGTGTTGCCTCATACTTGGCATGTATAAATGTCCTGTATTTTAAGAACAGAGGAAGTTTTGAATTTACCTTCATAGTCCATTGACTGTTTGGCTCGAGTCATTGAAAGGAAGAATGATACAGTCATGTCAGCAGTGCTAAATCAAGTAAAAATGTCTGAAATCCAATCTGGAAAGTACCTATTTGCTCAATTAACAACTGGTAGATGTCTTGTGGAAAATTCCCAAAGCTCTCTGCACTCTCTTTGTCCAAACAAGCATGCAGTTGGCAGGCATCAAGTGCACTGATCTTTCTTTTTTATAGGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12198
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000044294 Nonsense 1178 2973 28 62
ENSDART00000138547 None None 162 None 4
ENSDART00000142881 Nonsense 1250 3080 29 61
Genomic Location (Zv9):
Chromosome 10 (position 34970497)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 33998355
GRCz11 10 33942215
KASP Assay ID:
2260-3456.1 (used for ordering genotyping assays)
KASP Sequence:
GTTTAACTGGGCTGTGGATCGCTGTTTCACTGGATCATACCAGCTYGCTT[C/A]AGGATGTTTCAAAGCTATCGCTACTGTGTGCGGTAGCAGGTAATCAGAGC
Long Flanking Sequence:
GTGGGCCTTTCTACAGACGGATACCTGTACAAGTGGCTGGACAATATCTTAGCCTGCCATGATCTCCGAGTAAGCACACTTGCTCTTTTTTTATTGCTGGAAGGATCAGCTTTAGTCCTTGTTATAACCTGCTGATGCTGAACAGACTTCCTGTTTAAATCTTTTGTCAGATTTAATAACCATCATTAAAACTAAACCAGCAAGCCTGACAGGATTAGCTTGAGAGGGATATTTGTATTATTAGCTTTATGAGTAATCTTGTTTGTTTAGGTCTGCCGTTAAACTATAATGACTAGTGTAATGTTGACGTTTGGATTGTCAGTTTTGATTGAAGGAAAAGCACCCATTTAAATACTCATGTTTATATCACCGCCTTGGGATACAGGTGCATCGGCTTGGCTGTGAGGTTGTCATTTTGCTCCTGGAGCTCAACCCAGATCAGGTGAATCTGTTTAACTGGGCTGTGGATCGCTGTTTCACTGGATCATACCAGCTCGCTT[C/A]AGGATGTTTCAAAGCTATCGCTACTGTGTGCGGTAGCAGGTAATCAGAGCTCATGTCATCATTGCCATGGTGTTACTTAATGAAGTTTGAAGGTTTTTATTATCAGACAAAACCTATTTATTTTTCTCTCTTCTTTTTAGGAATTATCCATGTGACATTGTGACTCTTTTGAATCTGGTGCTGTTCAAGTCATCTGACACAAGCAGAGAGATTTATGAGATATCCATGCAGCTCATGCAGGTACGTTTAGTTGCAGTTTTAAGAAAAGGAATCTACAGTGCTCAGCCTATATAAGTACACCCCTCACAAATCTCTCTTTTTAATTCATCCCAGCAGGCACACAACATTATTAGACGTTAATATTAGGTTAGATATAGGTCATGACTTCAGGTGACCAAAATTCAATGTCTAGCGTTTAAGGACAACATTATTTTGACGTCCAATAACGACGCCAAATTATGTTGATATTTGGTTGATTTTAGGTTGTGTTGGAGAGTGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44728
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
ENSDART00000044294 Essential Splice Site 1224 2973 29 62
ENSDART00000138547 None None 162 None 4
ENSDART00000142881 Essential Splice Site 1296 3080 30 61
Genomic Location (Zv9):
Chromosome 10 (position 34970738)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 33998596
GRCz11 10 33942456
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCTGACACAAGCAGAGAGATTTATGAGATATCCATGCAGCTCATGCAG[G/A]TACGTTTAGTTGCAGTTTTAAGAAAAGGAATCTACAGTGCTCAGCCTATA
Long Flanking Sequence:
TAGCTTTATGAGTAATCTTGTTTGTTTAGGTCTGCCGTTAAACTATAATGACTAGTGTAATGTTGACGTTTGGATTGTCAGTTTTGATTGAAGGAAAAGCACCCATTTAAATACTCATGTTTATATCACCGCCTTGGGATACAGGTGCATCGGCTTGGCTGTGAGGTTGTCATTTTGCTCCTGGAGCTCAACCCAGATCAGGTGAATCTGTTTAACTGGGCTGTGGATCGCTGTTTCACTGGATCATACCAGCTCGCTTCAGGATGTTTCAAAGCTATCGCTACTGTGTGCGGTAGCAGGTAATCAGAGCTCATGTCATCATTGCCATGGTGTTACTTAATGAAGTTTGAAGGTTTTTATTATCAGACAAAACCTATTTATTTTTCTCTCTTCTTTTTAGGAATTATCCATGTGACATTGTGACTCTTTTGAATCTGGTGCTGTTCAAGTCATCTGACACAAGCAGAGAGATTTATGAGATATCCATGCAGCTCATGCAG[G/A]TACGTTTAGTTGCAGTTTTAAGAAAAGGAATCTACAGTGCTCAGCCTATATAAGTACACCCCTCACAAATCTCTCTTTTTAATTCATCCCAGCAGGCACACAACATTATTAGACGTTAATATTAGGTTAGATATAGGTCATGACTTCAGGTGACCAAAATTCAATGTCTAGCGTTTAAGGACAACATTATTTTGACGTCCAATAACGACGCCAAATTATGTTGATATTTGGTTGATTTTAGGTTGTGTTGGAGAGTGACCAAAATCCAACGTCTGATAGATGTCATAGTGGTAACGTTCATACAGTGTCAAGGTGTAACATGATTAGACGTTGATATTGAGTTCATTTTAGGTTGATTTCGGTTGGATGTTTGACATTGATGTCGGCATGACATTGGGTTCTGATGTCAACCCGATTTTCATTTTCAGACAAAATTCAACGTTCCCACAACGTTGGGGCACACATCAGTATAACGTCATGTTAACATCCTGTGCCTGCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41697
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:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000044294 Splice Site None 2973 None 62
ENSDART00000138547 None None 162 None 4
ENSDART00000142881 Nonsense 1473 3080 33 61
Genomic Location (Zv9):
Chromosome 10 (position 34972855)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 34000713
GRCz11 10 33944573
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAAATTTCATCAAACGACTCGGACATCATTTTCTGTATGGTTTCTCTA[C/T]AGTATGGGGATGAAGTCCCTGGTCCTGAGATGGAGAACGCCTGGAATGCT
Long Flanking Sequence:
CAACATTTACTTAAGTGCACAATGTTCTTCCTATTGCAAGATGTTCTGGTCATCTTTAATCAAGGTTTAAGAAACATGCTTGTAATGTGTTAAGTCATGCTAGCAACATGGAAAACAGGATAGCATGATATGCTAAACATCCTAGCAGTGTGATAAATATTGTGTAATATTCTTACATTTTAAATCATTTAACAATATGCTAAAATTTACTAGCAATGTGCTAAATAGTACTAGAGCAAAAGTGAGCATGCTAGACACAGCAGGCTAAAACATGCTAGCAATATTCAAAATCATAAGCCTTCAAACTGTATGCTTTTATGAAGTTATTTTAAGCTTCAACAGTTATTTATAATCAAACTTTACTTGTGTACATGACATTAAAGCAAGATGTGTTGTTATAGGTGGACTATGGAAAAACACAATGCTATGAACGTATTAGAAATCACCCCTTTAAAATTTCATCAAACGACTCGGACATCATTTTCTGTATGGTTTCTCTA[C/T]AGTATGGGGATGAAGTCCCTGGTCCTGAGATGGAGAACGCCTGGAATGCTCTTGTGTCCAATGACAAGTGGAGTAACAACCTGAGAATAACACTGCAGTTCCTCATTAGCCTGTGCGGAGTCAGCAGCGACACCACACTGCTGCCATATGTGAGCCATACAGACACACTTAGCCCACATTCAATTTATTAGCTCTGTATAATAGACTAAACTTGTATCTGACTGTTTTTAGATTAAGAAAGTGGTGATATATCTGTGTCGGAACAACACCATTCAGACCATGGAGGAGCTGCTTTTTGAGCTTCAGCAGACAGACCCAGTAAACCCAGTTGTCCTACACTGCGACAACCCACCATTCTACCGCTTCGCTGCCAGCAACAAGACCTCTGTTGTGGCTTCAGGTAAATCAAATAATAATGTTTGACGCAAGGTATTAGGAGAAACTGTAACACTTTATTTTAAGTACCAATTCTCACTATGAACTAGTGGCTTATTACATGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13238
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:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000044294 Splice Site, Nonsense 1416 2973 32 62
ENSDART00000138547 None None 162 None 4
ENSDART00000142881 Splice Site, Nonsense 1522 3080 33 61
Genomic Location (Zv9):
Chromosome 10 (position 34973004)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 34000862
GRCz11 10 33944722
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCCTCATTAGCCTGTGCGGAGTCAGCAGCGACACCACACTGCTGCCATA[T/G]GTGAGCCWTACAGACACACTYAGCCCACATTCAATTTATTAGCTCTRTAT
Long Flanking Sequence:
GTGATAAATATTGTGTAATATTCTTACATTTTAAATCATTTAACAATATGCTAAAATTTACTAGCAATGTGCTAAATAGTACTAGAGCAAAAGTGAGCATGCTAGACACAGCAGGCTAAAACATGCTAGCAATATTCAAAATCATAAGCCTTCAAACTGTATGCTTTTATGAAGTTATTTTAAGCTTCAACAGTTATTTATAATCAAACTTTACTTGTGTACATGACATTAAAGCAAGATGTGTTGTTATAGGTGGACTATGGAAAAACACAATGCTATGAACGTATTAGAAATCACCCCTTTAAAATTTCATCAAACGACTCGGACATCATTTTCTGTATGGTTTCTCTACAGTATGGGGATGAAGTCCCTGGTCCTGAGATGGAGAACGCCTGGAATGCTCTTGTGTCCAATGACAAGTGGAGTAACAACCTGAGAATAACACTGCAGTTCCTCATTAGCCTGTGCGGAGTCAGCAGCGACACCACACTGCTGCCATA[T/G]GTGAGCCATACAGACACACTTAGCCCACATTCAATTTATTAGCTCTGTATAATAGACTAAACTTGTATCTGACTGTTTTTAGATTAAGAAAGTGGTGATATATCTGTGTCGGAACAACACCATTCAGACCATGGAGGAGCTGCTTTTTGAGCTTCAGCAGACAGACCCAGTAAACCCAGTTGTCCTACACTGCGACAACCCACCATTCTACCGCTTCGCTGCCAGCAACAAGACCTCTGTTGTGGCTTCAGGTAAATCAAATAATAATGTTTGACGCAAGGTATTAGGAGAAACTGTAACACTTTATTTTAAGTACCAATTCTCACTATGAACTAGTGGCTTATTACATGCCTAATATTAGGATTATTAGACCGTTTATTAGTAATTAAAAAGTAGTACATATTCTGCATGATCATATTCAGTACTCCTAATTCTAAACATATAAGCGTAAGCATTAATGAGAAGCTAATTAGGAGTTTATTGAGGCAAAAGTCATAGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27638
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000044294 Essential Splice Site 1531 2973 35 62
ENSDART00000138547 None None 162 None 4
ENSDART00000142881 Essential Splice Site 1637 3080 36 61
Genomic Location (Zv9):
Chromosome 10 (position 34974943)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 34002801
GRCz11 10 33946661
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAATCACGTTACAGCAACAGCTCTGGAGGTTCTTACGATGAGGAGAAGAG[T/A]AAGTTCTGTATGATAATTAATTTAGTAGCAGATTATTTTGTGGTTCAGAA
Long Flanking Sequence:
AGGTACAACATCTAGCAGTAACACAGTAGTGGCTGGGCAAGAAAACTTCCAGGACACAGATGAGGCAAAAATCACCAGAGAGACTGAAGAAAGGTGCGACTTTCTTTATAGAACTTGGATTTTTTTTTTTTTAATGGAGAAACAGCTTGATTGCTTATTTATTTATGTTTTTATTCATTTATTTATTTATTTGTTTGTTTGTTTGTTTGTTCATCCATTCATTGGCAGATTTTTTTGTGATCGCTAAATTCTCAACCACATATGGGCTTTAATATTCTCCTCCACTGTATACATGCTAATTTGGCAGCTACTTGGTTGTCAAACAGCCAATGAAAAAAAAAAGTCAATATATTATGTGCTTTAAAGCGCATGCATGTTTATGTCCCCTAATATAGTTTGTGTACATGTTTCCTCAGGTTAAGCAGTGCTGCCAGGGCTCACAACCGTCTGGAATCACGTTACAGCAACAGCTCTGGAGGTTCTTACGATGAGGAGAAGAG[T/A]AAGTTCTGTATGATAATTAATTTAGTAGCAGATTATTTTGTGGTTCAGAAGCCCTATGTGCACTTCCACCACACATGATAGGTTACTGTCAGTAATCCTCCAGATTACAAGAACAGAGCAACAGGTGTTTCATAGCTATCGATTCACTGATTGATACATACAAGTGAGGATACATTTACATTTATTGTTTTACAGCTATACATTTTATCAGCTGATATCTGTACATGTGGCTCACCATTTCACAGATTGTGTATATACTACCAGCACTACATGCTCACTAGCATTGCTTGTTCATATTAAGGAATTACTGCATGCATGTAATTGTATGTCATCCAGTTGTGCTTGTAAAATTGTTTGCTTTTGGTGTGAGAGCTGCCAGCTTTTGTCTGCTTACATACCTGTCATGACAGCAGATTGACGGGTTGCAGGATAGAATGTATGACTTGATGATGTGCTCAGAATTATTGCACATTGGCTTGACAGACTGAAAAATATTAATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31789
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:
A > T
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000044294 Essential Splice Site 1745 2973 None 62
ENSDART00000138547 None None 162 None 4
ENSDART00000142881 Missense 1861 3080 41 61
Genomic Location (Zv9):
Chromosome 10 (position 34985985)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 34013843
GRCz11 10 33957703
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGGTGGTGGTGGTGGTACAGTGCATGGAGTACTGTCCTGTCCTTACTC[A/T]GGGCTTTCGGACCGCTTTGGTGCCATGAAGACATCACTCCGAAGAATCTC
Long Flanking Sequence:
AAATTTCCATTTATTTCAAGCTCCAAATGTTTATATCGTATCTCAAAAGAAGAACAATATATGTAAATAAAAATAAAAAGATATGTGAACAAACAAGTTTTGTTAATTTATGATCCTTATTATACAACATGTATTGCCCTTTGCAGGAAATGTATGCAGATGCATGTATGCAGAATTATAAAATGGAACACTTAGCAGTTTAGCATATTGCATTCATACTCTAGCTGAATCTGATCACCTGTAAATAGTTAGCATGAGATGAAAACTGAATTTGATTGTTTAATATCACTTTCTTACCACAATAATACATAGTACAAACCTGATGAAAAAATTAAATGGTGTTATTGGAGGAAAATCTCGAGTGTGATGTCACGTGGAAACTATGAATCAGGCCATTTCCCGCATCATTAGGTCAAGTTAGTGAGCAGTAGTTGATGTATTTGTGATTCTGGTGGTGGTGGTGGTGGTACAGTGCATGGAGTACTGTCCTGTCCTTACTC[A/T]GGGCTTTCGGACCGCTTTGGTGCCATGAAGACATCACTCCGAAGAATCTCAACTCTAAGAGTGCTGAGCAGCTCACCAATTTCCTGCGACATGTCGTCTCTGTATTCAAAGAATCCAAATCAGGTAATAATCATTTATGTGTCATCCTCAATACAAAAACATATCCATCTTTTTCTGCATGTGATGACTGAGTTTTAAATTTTGAGTTGAGCTTTTACAACTTTCTTTCACAATATTAAAGTTATGTGCTATGAATTTTCCACATATATATATACACACATACATATATATGAAAGTTAGGGAGAGGTACATCTAGTTCTGTGCTGTATATTTTTTATCCATCATGAAAATTGTGTTACATTTGATATTTTAACTTGAATTTTATATCACACATTTATATGTGTCCAAAACTATTTTGAGTTATTTATATACTGTATATTATTTATAGTGTTTATATTTATTTTGATTTGTTTATAGTAGTTATTTATGGTATATTATTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5586
Status:
F2 line generated
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
ENSDART00000044294 Essential Splice Site 2284 2973 47 62
ENSDART00000138547 None None 162 None 4
ENSDART00000142881 Essential Splice Site 2400 3080 48 61
ENSDART00000044294 Essential Splice Site 2284 2973 47 62
ENSDART00000138547 None None 162 None 4
ENSDART00000142881 Essential Splice Site 2400 3080 48 61
Genomic Location (Zv9):
Chromosome 10 (position 35003261)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 34031119
GRCz11 10 33974979
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAAAGCCCTGCCAGGAAAGACGATGGAATTCCATTTCGATATATCTGAGG[T/C]ATATTGTTGCTCAATTGTTCACATTCRTGTGTGACACTGTATTTTTGCTC
Long Flanking Sequence:
TAACTTACAAAATGGTATGTAAAATTGCATGCAAAGAACAGTGTTGTAATGCTAGCTGATCTTTCTTCACAGTTGCTAGATAAAGGATTACCCAGCATGCAACAGCCCCTGCTGCAGATCATCTATAGTCTGCTAAGCCACATGGATTTGGCAGGAATTCAGGTCAAACCTTTCAATGTTGAGGTGCTAAAGACCATTGAGAAATTTGTACAGGTGAGATTCTTACTGAATGAGGATTCATTTGGTCATTTTTAAGCATCTCGATCTGATTTGATAAACCAATATGTGTGTGTGTTTGTGTGTGTGTGTGTCCTAGACGGTCCACTGGAAAGAAGCTCTGAACATTTTGAAGCTCGTCGTTTCCCGTTCAGCTAGTTTATCACTGCCATCTTACACCCATGGTGATCTAGCCCACCTGGAGGTTAGCCGTATGATGTGGGATGGCTCATCTAAAGCCCTGCCAGGAAAGACGATGGAATTCCATTTCGATATATCTGAGG[T/C]ATATTGTTGCTCAATTGTTCACATTCATGTGTGACACTGTATTTTTGCTCTTGAAAATGTCAGTTTTCAGTGAGATCACACACCTTTTCTGACTCATTCAACTCTTGAGGTGTGGCCCTGTTGTTGTTTTGACTATGCATTTGTTATCAGATCCCATGAAGGGTGCAGCCACTTTTCCTTTGTTTTTAGTGCATAATAGGCCAAAGGAGAGTCACTCAAGTTTTCAGTTCACTTTCAGCTGGAGAAATGGGGGTGATAGTCAACAGAAGTTTAGAGAGAAGTTTTAACTGCATTTAGAATTATAACCTCTCATCATACAGTATTATATAATCCAGAATGATCGCATGCTTTTGTACGTTATGTTTGACATTTAAATAAGTAAAAAAAATCATAAATTATTAACTAAATCATAACTCTCTGTTATGTTATATGAAAGTTTCCTAAATCATCTATCCAATCAATCTATCCAAGGTCCTGTTTACATGCACCAATTTTCGTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41698
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000044294 Essential Splice Site 2777 2973 58 62
ENSDART00000138547 None None 162 None 4
ENSDART00000142881 Essential Splice Site 2890 3080 58 61
Genomic Location (Zv9):
Chromosome 10 (position 35018110)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 34045968
GRCz11 10 33989828
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCCGACGATGGAGTGATAACCTGTCAGCCTGGAGACTCAGAGGAAAAGG[T/A]GAAAACAGCTGTCTGTGTTCACTCGACATTATTTACATTAATCCAATTAT
Long Flanking Sequence:
CCAGTAGATCAGCAGTTTCTGAAATACTCAGACCAGCCCGTCTGGCACCAACCGTGCCACGTTCAAAGTCACTTAAATCACCTATCTTCCCTATTCTGATGCTCGGTTTAAATTGCAGCAGATCATCTTGACCATGTCTACATGCCTAAATGCATTGAGTTGCTGCCATACTGATTTTAAATTTTTTGTTAACAAGCAGTTGGACAGGTGTACCTTATAAAGTGGCCGGTGAATGTATTTATGCTCAGTGGAAACAAGGCACCACTGAAAGCACATTTATAAGGTAGTTTGTGCCATGCATAAGATAATTTTGCAAGTTATTAAGGCTTTTGCATGATGGATGTTTTAAAATAAATACCATCAGCTTACACTGAAAGACGTTTCTTGCTCATATTCTCTTCTCATCTTTCAACAGTGGTTGCAGAACTGTAAGGCCACATTTCCCAGGTTTCCCGACGATGGAGTGATAACCTGTCAGCCTGGAGACTCAGAGGAAAAGG[T/A]GAAAACAGCTGTCTGTGTTCACTCGACATTATTTACATTAATCCAATTATACACAGTAGTTTCTAATAGATTAGAGTGGGATTATTGAGTGGGTCAGGTGGCCATATATACACTATCATTCAAAGGTTTGTGGTCTGTGAGATTATTAATGTGTCTTTCTTTATTTTGAAATCGTACTCATTATGGGTGCATTTATTTGATAAAAGTAGAGCAAATAAAATTTTATTGATTTTATTTCCTTTTTTATTAATATATAGCTTAAAATAAAGTTAAAGCAGCCGTTACGTCCTGTTTTAGTGTAGTTTTGATACATCAGATACTGTAACATTCTTATGTGCTGATTTGCTGATATATGCAAAATACAGTAATACTGGACAGCATTTTAAAAAAATTAATGTATAAAAAGCTGTTGTTTAAAATCATTTGTAACATTATCAGTGTCATTTTCAATTTTCACTCATTGTAATGAATCCTTGCATGACTCCAAACTTTAAAATGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12244
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:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000044294 Splice Site, Nonsense 2784 2973 60 62
ENSDART00000138547 Splice Site, Nonsense 9 162 2 4
ENSDART00000142881 Splice Site, Nonsense 2891 3080 59 61
Genomic Location (Zv9):
Chromosome 10 (position 35019150)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 34047008
GRCz11 10 33990868
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGTGATTCCTTTATTGTCATGTGACTAAACTATTCATATCTTCCACAG[C/T]AATTGGAGTTGTGTCAGCGACTATACAAACTTCACTTCCAGCTCCTTCTG
Long Flanking Sequence:
TTACACCTGATTTTCTTGTGCACTTTCACCTGTTCTGCATGATTTATACGGGTTGCTTCTTGGGTTGAATCTGACTGGCACTAATCCTCTAATTATGTTAATGGGATTTCTGAGCTGACATTCGGTCTCACAGATTGCATGCTGGGAATTAATGCTGTCTATTTCTCCCTTGTCAACTCTTTTCTGTTTTATGACATGCTTGCTCTGCAGCAAATGGAAACTCTGGCTGTAAGTTTGAAACTAAAGAACCGTTCTCTTTCTTTGTCTTCTGCTAGAGCGAGTGTTTTATAGTTTAGTACATGCATTCAATTCAGAGCGTTTATATGCACATTCCTACACAACCTTAACCACTTCTATTATTGAAATTTATATTTTAATTGTTTTTGTGCATATAAACACCCTCATTGATGTATATTTGAGTTGTGTATTTACTGTTTGTGGCTGTGCATATGTGTGATTCCTTTATTGTCATGTGACTAAACTATTCATATCTTCCACAG[C/T]AATTGGAGTTGTGTCAGCGACTATACAAACTTCACTTCCAGCTCCTTCTGCTGTTTCAGTCCTATTGTAAACTTATCGGACAAGTGAACACCATCAGCTCTGTGCCGGAGGTATACTCTTTTGAATGGTTTTTAAATTTGAATCAAAATTAATGGTCACACTTTATTTTGATGGTGTGTTTGTTGAATTTAAGTTACATTGCATCTACATGACTAATTCTCATTAGATTATAAGTAGACTGTTAGGTTGGGGTTGGGGTTAGGGTTAGTGTAAATTGAAATGTACTTGCAAAGTTTTCTGCAAAGTCAGTTAATTGTCTGTTGAAGGAGCAGTACCAACAGATATTAAGCAGACAGTCTACTAATACTCAAGTGGACCATCAAAATAATGTGTTACAAAGCAAATTTTTCAATGTGAGCAGATTTGGAAAACAATTATTTGACCACCAGTTTCTTTAGATTGATTAGGTATGGTTAATGTATAGTGTGTGTCTTTTTTCT
Associated Phenotype:
Not determined