Busch Lab

ZMP

si:ch211-67e16.5

Ensembl ID:
ENSDARG00000019316
ZFIN ID:
ZDB-GENE-070912-312
Human Orthologue:
FER1L6
Human Description:
fer-1-like 6 (C. elegans) [Source:HGNC Symbol;Acc:28065]
Mouse Orthologue:
Fer1l6
Mouse Description:
fer-1-like 6 (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:3645398]

Alleles

There are 12 alleles of this gene:

Allele Name Consequence Status Availability
sa34587 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa16199 Nonsense Available for shipment Available now
sa34586 Nonsense Available for shipment Available now
sa2511 Nonsense F2 line generated Not yet available
sa34585 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa18941 Nonsense Mutation detected in F1 DNA Not yet available
sa10809 Nonsense Available for shipment Available now
sa6110 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa11129 Nonsense Available for shipment Available now
sa27362 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa34587
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
ENSDART00000056105 Essential Splice Site 161 1810 6 42
ENSDART00000139898 None None 52 None 2
ENSDART00000141571 Essential Splice Site 65 322 2 7
ENSDART00000146449 None None 367 None 8
ENSDART00000146675 None None 576 None 12
Genomic Location (Zv9):
Chromosome 9 (position 14359992)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 14112557
GRCz11 9 14083760
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATATATTGCAATCAAGACATCTTTTTTGACAAAGTCATTAAACTATCA[G/A]TAAGTATTAACATGAACAATAGTTTATTAACATAACCTATAGAGCTCATA
Long Flanking Sequence:
TAGTGGAATGTGTTCATTCTTGTAAGTTTATATGTTCATCATTTTACTTTTTTTCTACTTTTAAAGATGTAAAGCTGTATCCAAGATCTTGGAAGGTGAAAGCAAACCACAAAATTTCCAGGTAGAATTTGTTACATTTACAATAAAAAAATAAGAATTTAACAGTTTTAGTGACCTCGCCAGTACCTAGAGATGCTAAAATATTTTCTTCCTAAGATTTCCATCAATATAACAGAGATCAGGCAGCTGGTTGGGGACAATATAGACCCTAGTGTTGTGATTGAAATTGGAGATGATAAAAAGCAGACATCGGTGAAAGAAGGAACCAACGCTCCCTTTTACAATGAGGTGATCATTCTCTTTAACTTTTGGACAATCGCTGAAATCAAAAGGCTTTACGGACAATTTTTAATACCCTTTGTTTTCTCACCCAACAGTATTTTGTGTTTGACATATATTGCAATCAAGACATCTTTTTTGACAAAGTCATTAAACTATCA[G/A]TAAGTATTAACATGAACAATAGTTTATTAACATAACCTATAGAGCTCATAATAATGTACTTCCCCCAAAGGTCATGCACTCAAAGATTATGAAGAGCTACTGTGTGGGAACGTTCAAGATTGATGTTGGGACAGTTTACTCTCAACCTGGTAACTATTTGGTTTGCAGTGTCAGAAGTTGGGGATTTTTTTATTTATTTATTTTTCGTTTTATAAGCAAATATCTTGTGCTTGTTGTCTCAGGGCATCAGTTCATCAATAAGTGGGCCACACTAACAGACCCTGCCGACATCCGTGTTGGGGTGAAAGGTTACCTGAAGTGTGATATCAGTGTGTCTGGAAAGGGAGATGTTGCACCACCATCTCAGAAATTCAGTGATGCCGAGGAACAAATTGATAAGTAAGATCTAGATGTTGAATGCATCTTTAAAAAAATTCTATGCTATTATTTTGGGTTTTCTGTAGCAGTCGTTAACCTATAATTCATTATATGCTTAGCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16199
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
ENSDART00000056105 Nonsense 237 1810 8 42
ENSDART00000139898 None None 52 None 2
ENSDART00000141571 Nonsense 141 322 4 7
ENSDART00000146449 None None 367 None 8
ENSDART00000146675 None None 576 None 12
Genomic Location (Zv9):
Chromosome 9 (position 14359603)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 14112168
GRCz11 9 14083371
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAAGGGAGATGTTGCACCACCATCTCAGAAATTCWGTGATGCCGAGGAA[C/T]AAATTGATAAGTAAGATNNCTNNNAGATGTTGAATGCMTCTTTAAAAAAAYTMTA
Long Flanking Sequence:
AAGGCTTTACGGACAATTTTTAATACCCTTTGTTTTCTCACCCAACAGTATTTTGTGTTTGACATATATTGCAATCAAGACATCTTTTTTGACAAAGTCATTAAACTATCAGTAAGTATTAACATGAACAATAGTTTATTAACATAACCTATAGAGCTCATAATAATGTACTTCCCCCAAAGGTCATGCACTCAAAGATTATGAAGAGCTACTGTGTGGGAACGTTCAAGATTGATGTTGGGACAGTTTACTCTCAACCTGGTAACTATTTGGTTTGCAGTGTCAGAAGTTGGGGATTTTTTTATTTATTTATTTTTCGTTTTATAAGCAAATATCTTGTGCTTGTTGTCTCAGGGCATCAGTTCATCAATAAGTGGGCCACACTAACAGACCCTGCCGACATCCGTGTTGGGGTGAAAGGTTACCTGAAGTGTGATATCAGTGTGTCTGGAAAGGGAGATGTTGCACCACCATCTCAGAAATTCAGTGATGCCGAGGAA[C/T]AAATTGATAAGTAAGATCTAGATGTTGAATGCATCTTTAAAAAAATTCTATGCTATTATTTTGGGTTTTCTGTAGCAGTCGTTAACCTATAATTCATTATATGCTTAGCCACTCTATTACATACTTAAAGCTATTCATTCCACACCCTCTCATTTTGTGAGATTGATTCAGTATCGTCTGTTTTAGACAAGAAAGATTTGAGTTGTAAAACTTGCTGGATGTTTTTATTGTACTTTGATCACTCACAACAGGGATGCCTAAACTCAGTCCTGGAAGGCCAGTGTCCAGCATAGTTCAGCTCCAACTTGCTTCAACACACCTATCTGGAAGTTTCTAGTATACCTAGAAAGAGCTTGATTAGCTAGTTCAGGAGTGTCTGAATAGGGTTGAAACTAAGGCTGTGCGATTAAACAAAATAGAATTGCAATTTAAAAGATTGCGATTAGTTAATCGCAAGAGGCTGCAATATGAAATATAAATGCATTATTTAACTTTCCCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34586
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
ENSDART00000056105 Nonsense 501 1810 12 42
ENSDART00000139898 Nonsense 28 52 1 2
ENSDART00000141571 None None 322 None 7
ENSDART00000146449 None None 367 None 8
ENSDART00000146675 None None 576 None 12
Genomic Location (Zv9):
Chromosome 9 (position 14356725)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 14109290
GRCz11 9 14080493
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAGGCATCCATGATCGACAGAAAAATTGGCGATAGACCAGTCACCCTA[G/T]AGTTTACGATTGGTAAATATCACATGAATTTTTTTATCTAGTTTGCTTAA
Long Flanking Sequence:
ATGGTTCTCTTCGAAATTCCACACTGGTGGATGACAGCCAGGAACTGAACGAAGGTGTTGGTGAAGGGGTGTCCTACAGAGGCAGACTCTACATAGAGCTGAGTGTAGAAATCCTGTCTGGAGGAGCTGCTGAATCCAAATCTCTGCTCTCAAAGTTCAGTCCAAAAGATGCCAAGGGTGGGAAAACTGGTACAGGAGCAGGAGGTGAAGAGGAGAAGTCCAAGATGATAGGACCTGAAGTGATCCCAGTGGAGCCCCCGCAGAAGGTGAAGTGTTTGCAGCAGTTCTTCTACTTTTTACTCTATACTTTTATTCTGTCCTCATTTTCCCCCATTGTTTGAAATACAACAAAAAGAAAGTAAGTACACAAAGTCAGTCAAGTGATGTTTTACCTTTTAATTTAGATGAGAGATGAAGACATGGAGACTTTCCTGCTCTTTGGTTGTGTATTTGAGGCATCCATGATCGACAGAAAAATTGGCGATAGACCAGTCACCCTA[G/T]AGTTTACGATTGGTAAATATCACATGAATTTTTTTATCTAGTTTGCTTAATCTTTAGAAAATTTTCATAGTAAGTCTGCCAAAAATATAGAGAGGATCCAGTAGAGATTGCCATAAAGTTTTATTGAATTAACAAGACAGAAAGTTCAAGTTTGTGGCAGCAGGTGGTAGCATGAATGTGACTGTACCCCTCCTCTTAAGAGCACCTCTTGGCACTATCAGAGGGTCTCTTACCTGTCAATTGAAATTAAATCACAGATAAGGGATAAGCATCTCTCCTCCAGGCCATAACCTTCTCAGAAGACCAAATACTGGAATCTACATCTCCTCTCAAGGCTCCAGTGCAGAAAATGTTTGACTGATTAAGTAGGCTGCCTATTTTCAAAATGTTACATTGGGGAACTGGAAGATGTGGATTAAAATGGGAATAAAAAACTTACTTTAATTCAGAAACATAAAAGAATAAAAAAAGGCTCATGTTTGCTGCAGCAGGTTTAAATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2511
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056105 Nonsense 580 1810 14 42
ENSDART00000139898 None None 52 None 2
ENSDART00000141571 None None 322 None 7
ENSDART00000146449 None None 367 None 8
ENSDART00000146675 None None 576 None 12
Genomic Location (Zv9):
Chromosome 9 (position 14353796)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 14106361
GRCz11 9 14077564
KASP Assay ID:
554-3185.1 (used for ordering genotyping assays)
KASP Sequence:
CCATCGCTGCACAGAAGCCCTGTGTGTATGTTTACAGTAGCTGGGAGGAT[C/T]GAGCGTACCGACTTCATCAYGCCAACATGCTAGACACAATTGCCCTCATG
Long Flanking Sequence:
TCGGTTTTAACCTCTTGCTTAGCAGTATAGAGCAGGGATCACCAAACTTGTTTCTGGAGGGCCGGTGTCCTGCAGATTTTAGCTTCAACCCTAATCAAACACACCTGAACAAGCGAATCAAAGTCTTACTAGGTATATTTGAAAGATCCAGGCAGGTTCGTTAAGGCAAGTTGGAGCTAAACCCCGCAGGGACACCGGCTCTCCAAGATTTTTGAACCCTGGTATAGAGTCCCGGTCACTCAACTGTGGCATTAGGACCCACACAGAACGCAGGTTGGATGTCCCCTGCTGGCAACCTAGCCTTCCCATGTGGTCTCCTATCCAAGCACTGACCGGGTGCAGCCCTGCTTAACTTTAGTGGGCGACCATGCGTTAGTTGCTGAGAGCTAGTTCTTGTCATGAACCAAACAAAACTGATAATCTTTTTTTGCAGGCATTATATGCATTTGCCCATCGCTGCACAGAAGCCCTGTGTGTATGTTTACAGTAGCTGGGAGGAT[C/T]GAGCGTACCGACTTCATCACGCCAACATGCTAGACACAATTGCCCTCATGTTTGTATGTGATCCTTCAATAAGTATTGTTTCAGAAAATTACTTTGTAATCGGTTAGTAGTTCATGCAGCCATTTTCCATTTTATGTTTGTCAGGAAGAGGGAGTCGCTAAGGTCACAGAGCTGGATAAAATGTTATCTCCGGAAGCATGGAGTCTCATGCACCACGTTCTTCGGGAATTCAGACGAGATGCCAAGTACGTTAATGGGGAATTCAAAGTTAAATAAAGAAATACCCAAAAATGGTAATTCTGTCATCATTTAGTCACCCTTGACTTGTTATAAATAAGTTTTGAGTTTTTTGTTGTGGTGAAAACAAAAGAAGATATTTTTAAGAATGTTACAAATCTGTAATCATTGACTTCCATAATATTTGCTTTTTGTACTTTTGTACTCAGTGGTTGCATGTTTCCAAACACACCTCAAAATATTTTAGTTTCAAGGGTCAATGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34585
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
ENSDART00000056105 Essential Splice Site 752 1810 18 42
ENSDART00000139898 None None 52 None 2
ENSDART00000141571 None None 322 None 7
ENSDART00000146449 Essential Splice Site 51 367 1 8
ENSDART00000146675 None None 576 None 12
Genomic Location (Zv9):
Chromosome 9 (position 14351947)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 14104512
GRCz11 9 14075715
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAGCAAAGAGGCAGAGACTGTGGGAAGATCAAGACACTGTTCCTCAAG[G/A]TCTGAACTCTATTAAATTCACAGTTTATAGGGTTTTATGTAGTACCGTAA
Long Flanking Sequence:
AAAGTGTCATTTAAAAATCAAAATGTTAATGTTGAAATGTTTTGAGATTGATAACATATTCATGTCAAGTGTATTTAAGCTTTGTCTGGTAGTAAATTCCTCCAATCTTTCCCTTTGTTTTCTTGAACTGCAGGAGAGTATGACTGAAATGGCAGGAGGACTTCTTGAGCCAAAGAGGAGATCTTTGACTGTGAAAGAAATGCTGCTGGAAGCTCAAAAAATTAAAAAGAAGCTGCGATTTCTGGTGGAGGAGGTTGTTATTATTTTGTCATTATGTAACATCCATATCCTCAACCTCTAAGTCTCCATATTTACTAATACTCATTTTTGTCTCACACTTATCTCAGCCTCAACACACTTTACCAGATGTGTTTGTGTGTCTGGTCAGTAATAACAAGCGTGTGGCGTATGCCAGAATCCCTGCTCGGGACCTGCTCTTCTCAGAGAGCCCAGAGCAAAGAGGCAGAGACTGTGGGAAGATCAAGACACTGTTCCTCAAG[G/A]TCTGAACTCTATTAAATTCACAGTTTATAGGGTTTTATGTAGTACCGTAAAGGGTTATCAACATTTGTCTACTACTAGTTTAACATTAAAATGTGTTGTTTAGCCTCCAGTGAAGCGTGCACCGGGATGGACTGTCCAGGCTAAACTTGATGTGTTCTTGTGGCTGGGAACTTGCGCAGAGTCATCCCGCATGTTGGACAATCTCCCGTCGGGCTTTGAACTTGTGTCCACCTCTTTTGAGGATAGGACTGGCGCTCCTCCTGAATATTTACTCTACACAGGCAAGACTGCTCAGCTAATATTGAAAATAGAACGTAATAGATACTTTTATTCAAGGTCGCTCACCTTGCATTGAAGGTGTACATTGTTTTTACCTCAATATCACCCTTTGTTGGTGAAATTCTCTACTGTTTGAATGGCAAGAAAGCTACAGAAATGTCAATTCTTCCTAAATGTAAGACACTGATTTGAATGTTTTTCTTGTTGACCCTATTTGTTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18941
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
ENSDART00000056105 Nonsense 1142 1810 27 42
ENSDART00000139898 None None 52 None 2
ENSDART00000141571 None None 322 None 7
ENSDART00000146449 None None 367 None 8
ENSDART00000146675 None None 576 None 12
ENSDART00000056105 Nonsense 1142 1810 27 42
ENSDART00000139898 None None 52 None 2
ENSDART00000141571 None None 322 None 7
ENSDART00000146449 None None 367 None 8
ENSDART00000146675 None None 576 None 12
Genomic Location (Zv9):
Chromosome 9 (position 14337658)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 14090223
GRCz11 9 14061426
KASP Assay ID:
2260-1615.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTGACTATAAAAACTGTCTATCAATGCCAGGTGTCAAAAAAGAGCAAA[C/T]GAAGATCTACAAAAAGGAAGAAACGCACCACGGCTGATGAGTCTGCAGAT
Long Flanking Sequence:
TTATCTTTCCTTCATATACCCTGAGCAAAGAATTGTCAAACATGAGTGAAAACCAAGCTCCAAAATCAGCTGAACATGAAAGCAGAGTTGAGGAGATAAAGTGGGGGAGAGGTACATTAACATACAATATCCTCCTCAGGCCATGACTCAACAATAGTAAACAGATTGTATATTGAAAAACATCATTGTTTCTGTTGATTTCATCACTACAACACTGAAATCATGAACTGAACACCAAACATGAAAAACTTACATGAAAAAAGATCACGAGCAGATTAATTGTGTATGGTGAAAAGCACATAGTTTCTGCAAGACAAATGGTAGAGATGTGTATTGGAGCTGTGAGGAACACTGCTACGCCAGGAGAACCCATCCTGTGGTTGGAATGTCCCAGTTTGTCCTTCATTAGCATAGAATAAATAGTCTCTAATATTTTCTCAGCTTAGAAATTGTTGACTATAAAAACTGTCTATCAATGCCAGGTGTCAAAAAAGAGCAAA[C/T]GAAGATCTACAAAAAGGAAGAAACGCACCACGGCTGATGAGTCTGCAGATAATGTCATCGATTGGTGGTCGAAGTACTATGCATCGATGGAGAAAATCAAACAGGTAACTAGTAAAAGCATTTCATTTGTTAGCCAGGGAGGTCGTTTTGCTTACTGATACTGATTTGTATCACAACTTCTGTCTTAGGCAAAGCAAAAAGAAGACAATCCTTTTCCACTGCTCTTTGAAAATAGTAAGTGATACCTGTATTTATGTCCTCTGCAACGTCTCGCTCCAGCTTTAGTCAAACATGCCCACGTTATGATGTATTTCAGTTACTCCTCTGGAGAACATTATTTCCGAAGGATTGATCAATCTGGGTAAGAATGACTGGGAAACTGCATGACTGCATGGCCTTCTTCTTTTGCTTTGGTCAACAGGATTGCAGAGTGTTTGGTCACTGTTCACAAGTCTTATTCATTTACATAACAGAGATGATGCGAAATTGAATCCATGTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10809
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
ENSDART00000056105 Nonsense 1142 1810 27 42
ENSDART00000139898 None None 52 None 2
ENSDART00000141571 None None 322 None 7
ENSDART00000146449 None None 367 None 8
ENSDART00000146675 None None 576 None 12
ENSDART00000056105 Nonsense 1142 1810 27 42
ENSDART00000139898 None None 52 None 2
ENSDART00000141571 None None 322 None 7
ENSDART00000146449 None None 367 None 8
ENSDART00000146675 None None 576 None 12
Genomic Location (Zv9):
Chromosome 9 (position 14337658)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 14090223
GRCz11 9 14061426
KASP Assay ID:
2260-1615.1 (used for ordering genotyping assays)
KASP Sequence:
TGTTGACTATAAAAACTGTCTATCAATGCCAGGTGTCWAAAAAGAGCAAA[C/T]GAAGATCTACAAAAAGGAAGAAACGCACCACGGYTGAKGAGTCTGCAGAT
Long Flanking Sequence:
TTATCTTTCCTTCATATACCCTGAGCAAAGAATTGTCAAACATGAGTGAAAACCAAGCTCCAAAATCAGCTGAACATGAAAGCAGAGTTGAGGAGATAAAGTGGGGGAGAGGTACATTAACATACAATATCCTCCTCAGGCCATGACTCAACAATAGTAAACAGATTGTATATTGAAAAACATCATTGTTTCTGTTGATTTCATCACTACAACACTGAAATCATGAACTGAACACCAAACATGAAAAACTTACATGAAAAAAGATCACGAGCAGATTAATTGTGTATGGTGAAAAGCACATAGTTTCTGCAAGACAAATGGTAGAGATGTGTATTGGAGCTGTGAGGAACACTGCTACGCCAGGAGAACCCATCCTGTGGTTGGAATGTCCCAGTTTGTCCTTCATTAGCATAGAATAAATAGTCTCTAATATTTTCTCAGCTTAGAAATTGTTGACTATAAAAACTGTCTATCAATGCCAGGTGTCAAAAAAGAGCAAA[C/T]GAAGATCTACAAAAAGGAAGAAACGCACCACGGCTGATGAGTCTGCAGATAATGTCATCGATTGGTGGTCGAAGTACTATGCATCGATGGAGAAAATCAAACAGGTAACTAGTAAAAGCATTTCATTTGTTAGCCAGGGAGGTCGTTTTGCTTACTGATACTGATTTGTATCACAACTTCTGTCTTAGGCAAAGCAAAAAGAAGACAATCCTTTTCCACTGCTCTTTGAAAATAGTAAGTGATACCTGTATTTATGTCCTCTGCAACGTCTCGCTCCAGCTTTAGTCAAACATGCCCACGTTATGATGTATTTCAGTTACTCCTCTGGAGAACATTATTTCCGAAGGATTGATCAATCTGGGTAAGAATGACTGGGAAACTGCATGACTGCATGGCCTTCTTCTTTTGCTTTGGTCAACAGGATTGCAGAGTGTTTGGTCACTGTTCACAAGTCTTATTCATTTACATAACAGAGATGATGCGAAATTGAATCCATGTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6110
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
ENSDART00000056105 Essential Splice Site 1365 1810 33 42
ENSDART00000139898 None None 52 None 2
ENSDART00000141571 None None 322 None 7
ENSDART00000146449 None None 367 None 8
ENSDART00000146675 Essential Splice Site 131 576 3 12
Genomic Location (Zv9):
Chromosome 9 (position 14330866)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 14083431
GRCz11 9 14054634
KASP Assay ID:
554-3926.1 (used for ordering genotyping assays)
KASP Sequence:
AAAGACAGAGACAATTACATMCCAAAGCAGCTCAACCCRGTGTTTGGAAG[G/A]TGAACAAGCAGATTGATTGAGAATTTATTTCTTCTAACTGCTCATTTTAT
Long Flanking Sequence:
TTTGCTTTTTAACTGACCCTGCATTTTGGGTCATAGACCCAAGTATGAAGTTATTGAAAAGTTTGGAGAAAGAAGTAGTTTTAATCAACAAGGATGAATTAATCAAAAGTGACTATAAGACATTTATAATTATAATTAGAAAATAATTCTATTGATTTCTAAGGTTTCAGTAAATGTATCTTGAATGCTATATTCTATCTAAATCTGAATTGAGTTTAGTTAAAGTAATTTAGTTTTTTTTTTTTAAAGTTTTATGATTTTTGATGACATACACACGGAATTTATGTACTTTAGCAAATCTTGGTGACCGGCTTTGCTGGTCTTAAACAGGATTTGCAACAGGTGTTTTCACAGTCTCTTATGCATTTTAAGGCCTTCAACCTGCACCCTGCAGACCCAGATGGCAAAGCAGACCCTTACATAGTGCTGAAACTTGGGAAAACTGAGATCAAAGACAGAGACAATTACATCCCAAAGCAGCTCAACCCAGTGTTTGGAAG[G/A]TGAACAAGCAGATTGATTGAGAATTTATTTCTTCTAACTGCTCATTTTATTAAGGTTCATTCATGACCTCCGTATTTCTCCCCTGATCAGATCTTTTGAATTTCAAGCCACTTTTCCCAAAGAATCCCTACTAACAATCCTAATCTATGACTATGACCTGGTTGGTGGTGATGATTTGATTGGAGAAACACAGATCGATTTGGAGAACCGGTTTTACAGCAGACATCGAGCAACCTGCAGCCTTCCTACTGAATATGCCATGTGAGTATTTATATTGTAACATTTATGGTCTTCTCAATTGAGTTCGATGCTCACTCTTGATCTGTCTCATGTCATCTAGTGAGGGTTATAATGCATGGAGGGACTGCATGAAGCCAGTAGACCTGCTGATTAAACTGTGTAAAGAAAACAGACTGGACAACCCTCAGTTTTCTCCAGGCCGTATTACCATCGGAAACAAAGTCTTTATGGGGAAAACGGTATTTCCAGATGAAGGTAGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11129
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056105 Nonsense 1375 1810 34 42
ENSDART00000139898 None None 52 None 2
ENSDART00000141571 None None 322 None 7
ENSDART00000146449 None None 367 None 8
ENSDART00000146675 Nonsense 141 576 4 12
Genomic Location (Zv9):
Chromosome 9 (position 14330747)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 14083312
GRCz11 9 14054515
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCGTATTTCTYCCCTGATCAGATCTTTTGAATTTCRAGCCACTTTTCCC[A/T]AAGAMTCCCTACTAACAATCCTAATCTATGACTATGACCTGGTTGGTGGT
Long Flanking Sequence:
ACATTTATAATTATAATTAGAAAATAATTCTATTGATTTCTAAGGTTTCAGTAAATGTATCTTGAATGCTATATTCTATCTAAATCTGAATTGAGTTTAGTTAAAGTAATTTAGTTTTTTTTTTTTAAAGTTTTATGATTTTTGATGACATACACACGGAATTTATGTACTTTAGCAAATCTTGGTGACCGGCTTTGCTGGTCTTAAACAGGATTTGCAACAGGTGTTTTCACAGTCTCTTATGCATTTTAAGGCCTTCAACCTGCACCCTGCAGACCCAGATGGCAAAGCAGACCCTTACATAGTGCTGAAACTTGGGAAAACTGAGATCAAAGACAGAGACAATTACATCCCAAAGCAGCTCAACCCAGTGTTTGGAAGGTGAACAAGCAGATTGATTGAGAATTTATTTCTTCTAACTGCTCATTTTATTAAGGTTCATTCATGACCTCCGTATTTCTCCCCTGATCAGATCTTTTGAATTTCAAGCCACTTTTCCC[A/T]AAGAATCCCTACTAACAATCCTAATCTATGACTATGACCTGGTTGGTGGTGATGATTTGATTGGAGAAACACAGATCGATTTGGAGAACCGGTTTTACAGCAGACATCGAGCAACCTGCAGCCTTCCTACTGAATATGCCATGTGAGTATTTATATTGTAACATTTATGGTCTTCTCAATTGAGTTCGATGCTCACTCTTGATCTGTCTCATGTCATCTAGTGAGGGTTATAATGCATGGAGGGACTGCATGAAGCCAGTAGACCTGCTGATTAAACTGTGTAAAGAAAACAGACTGGACAACCCTCAGTTTTCTCCAGGCCGTATTACCATCGGAAACAAAGTCTTTATGGGGAAAACGGTATTTCCAGATGAAGGTAGGTCATTCTTTTAGCTTTCAGCTTGGCATTGTTGATTTTAAAGGGATAGTTCACCCAAAAATGGTAATTTTCTGATTTACTTAACCTCAAAGTGGTTCCAAACCTTTATGAGTTTCTTGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27362
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056105 Essential Splice Site 1522 1810 37 42
ENSDART00000139898 None None 52 None 2
ENSDART00000141571 None None 322 None 7
ENSDART00000146449 None None 367 None 8
ENSDART00000146675 Essential Splice Site 288 576 7 12
Genomic Location (Zv9):
Chromosome 9 (position 14329161)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 14081726
GRCz11 9 14052929
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAGGATTGTTGGTGTGAATATTCTTAATTATTGATTTGTATGTTCCCC[A/T]GGGCCATTTGCAGATGTGGGTGGACATTTTTCCACTGGACATGCCTCACC
Long Flanking Sequence:
AACACTGATGTAAGTGATGCTGATACGGAGATTTATGGCTCTGTGTAAGAGAAAAAACTCTGAGAAAATGACCTTTAAAAAAATATAGTAATTGGAATCTACAGACAAATTGATTAATTGTGACAAAGGACATACTTAAGAGTGTATTTAGGAAGTAAAAAAATGTTTGCATGTTTTTGGCTTTATAGTCTCACTTTAACCCAATGAGCAATGCGCAATAAGTGTTTGCTGCCGATTCACAGATCAAATGGTGGAGTCGTATGAACACTTGGCTCTCAAGGTGCTTCACAGGTGGTCTGAGATGCCCAACGGAGGCTGTAAACTTGTCCCAGAGCATATTGAAACTCGCGCACTTTACCTCAAGGACAAACCAGGAATAGACCAGGTAACATGTTGATTAGTGACTTATGCAACCTTATGCACAATATACATAATACATTTAATATCAGTTTAAGGATTGTTGGTGTGAATATTCTTAATTATTGATTTGTATGTTCCCC[A/T]GGGCCATTTGCAGATGTGGGTGGACATTTTTCCACTGGACATGCCTCACCCTGGCCCACCTGTGGACATTTCCCCTCGCAAACCTAAAGGGTACAATGAAGAAACACTAAACCATCTTTCTGGGTTGTACAGTTACATTTAAAGGGGTCCTATGATGCAAAATCACATTTTATAAAGGATTTAAACACAGTTGTGTGGCAACAGTCTGTGAAATTAACCAGCTTCTAATGGTAAAATTGTATTCATTTTTTCTCTCCCTGATTAGCATAAGACATTAGTCTTGTTTTTGAATCTGTCACTATGCTGACACACAGGCATCCGTAGCTCCGCCCTCTTTTAAAAAAAGAAAACAATCTCATTTGAATTTAAACTGACAGTCACCAAAATGGCTCAAATAGGATCAAAGCCTAAAAGGGTCAGATTCAAAGAGTTATAAAACATTATTTGTGGGATATTGTAAGCTGAAATTTCACATACACACTCTAGGGACATCAGAGACT
Associated Phenotype:
Not determined