Busch Lab

ZMP

inadl

Ensembl ID:
ENSDARG00000024964
ZFIN ID:
ZDB-GENE-030616-129
Description:
InaD-like [Source:RefSeq peptide;Acc:NP_001120657]
Human Orthologue:
INADL
Human Description:
InaD-like (Drosophila) [Source:HGNC Symbol;Acc:28881]
Mouse Orthologue:
Inadl
Mouse Description:
InaD-like (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1277960]

Alleles

There are 10 alleles of this gene:

Allele Name Consequence Status Availability
sa24137 Nonsense Available for shipment Available now
sa6702 Nonsense Mutation detected in F1 DNA Not yet available
sa37482 Nonsense Mutation detected in F1 DNA Not yet available
sa648 Nonsense F2 line generated Not yet available
sa24136 Nonsense Available for shipment Available now
sa32397 Essential Splice Site, Missense Available for shipment Available now
sa5970 Nonsense Mutation detected in F1 DNA Not yet available
sa43805 Nonsense Mutation detected in F1 DNA Not yet available
sa24135 Essential Splice Site Available for shipment Available now
sa43804 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa24137
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
ENSDART00000036467 Nonsense 111 1180 3 41
ENSDART00000132829 Nonsense 115 1831 4 45
ENSDART00000145208 None None 98 None 5
Genomic Location (Zv9):
Chromosome 22 (position 16971854)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 16723612
GRCz11 22 16749882
KASP Assay ID:
2261-6669.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGATCAGTTCTGTCCAATGGCACGGCTTTAACTAACGCCTCTTCTGAG[C/T]AGCTTCAGAGGTGGATACAGGCAGCTGCAAAGGTGAGGAGTTATTTCATG
Long Flanking Sequence:
AAAAGCACAATTAGGCCATTATTAATAAAATTAGTTGTAGTATTAATTGAAGTAGTGTTGTAATTTTGTCTTTTTGTTTTATATATTTAAAACCAATTTGTGATTTGTGTTGGTTTGGGTTTTTTTTATTTTTTTTTTAGTTGAAGCTGTTTGTTTTGTAGCTTGTCTTTTTTATTATTTATTTAACCATTTTTATTATTTTCCATTATTATTATTTGTTCTTTTTAATGTTAGAATTTATTTAAATCCATATTTATTGCAAGTAATATAAAGAGCTCCAGGTTTAAGTTTTGCTTGTAGTCATCGATGGATTTTTCTACATGTCTTTTAAAAATGTCTTTGTCTTCTTCTATCTGCAGTTGAACAGTTTGCCTCCGGACACATGCAGCGAGTTCAGTTTCTCCAGGAAGGGTCAGCTGATCGTCAGTGCCAGTCGGCCGTCCAGTAGTCTGGGATCAGTTCTGTCCAATGGCACGGCTTTAACTAACGCCTCTTCTGAG[C/T]AGCTTCAGAGGTGGATACAGGCAGCTGCAAAGGTGAGGAGTTATTTCATGTCAGCTTTTATTTCACAAATGCAGTTTCTACCATGCTTTGGCCTAGTTTGCATTAGTTAAGTCATTCTACAGGAATTACTTCCTTCGATAAAATACCTAAAAAATGTCTTTGCAAAAACCTTAAAGTCTTTGCAGCCATTAACCACTTTTAGCTACCTTTAGTCACACTTAACTGCACCACTCTTATTGCTGGTCTTGACTTGTGGTGCTCTTCAAGTTATGCTTGCGTCTCCATATTATACCGGCAATGTCCTTTCCTTCTGATATTGTTGAACCATGTATAATTTCCCTTCGTTGCCTTGGACAACAGAACACTTGACTGAGTTCATTGGTTAAATTGTCCTGGTTCTTCTTTCATACTTGTATTGAGCCTTGTTCTTACTGTAGCTCCCTTCAGCAACAAACGAGCAAGAGTCTTTTTTTTTTTTTTTACTGACTGGTTTATTTTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6702
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
ENSDART00000036467 Nonsense 248 1180 9 41
ENSDART00000132829 Nonsense 234 1831 7 45
ENSDART00000145208 None None 98 None 5
Genomic Location (Zv9):
Chromosome 22 (position 16959657)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 16711415
GRCz11 22 16737685
KASP Assay ID:
554-4601.1 (used for ordering genotyping assays)
KASP Sequence:
GACAAGTCAAGGGATTGAAARCGGTCCCCSGTGTGTGTCTTTTGCAGGAT[C/T]AGTGGGGACACGTGGAGGAGATCGAGCTGGTGAATGATGGATCCGGTCTG
Long Flanking Sequence:
CGGGATGAGCACTAGTGTAAAGCTTTGTTTCGAAAGAGCGACAAGGCGAACGACAGAGGAGGGGTTTCATTAGATAGTGAGAAAATTGCAGAGGTAGTCACCCGGCAGATAACGGCCAGGTAATAAGAGAACAGAAATGTACTGATTGTGGGTCATTTATATGAGCCCAAGGAGACTTGGGCGATTAGAAAGTGTGGCTGACGTGAGATCACAAAGACTCTCGTGGGCTTTCCTGACCCGGACATTGATCAGCCGCTGCAGGATCACACCGTTAACTTGTTCATTAGCATTCCCTGGCCTATTACCACTCCGTAGTCACAGGTCTTGGGTCGTCAATCGCTCCCTATTTGGACAATCAAAGGTGATTGAATGGATCTTTATTCTTTAAGTAGACAGTTTTGTGGCTCAAAGTAAAATATAGCTGACACTCGCTGACCTCTAAATGTACAAGACAAGTCAAGGGATTGAAAGCGGTCCCCGGTGTGTGTCTTTTGCAGGAT[C/T]AGTGGGGACACGTGGAGGAGATCGAGCTGGTGAATGATGGATCCGGTCTGGGATTTGGGATTGTCGGTGGAAAGACGACAGGGATGGTGGTCAGAACCGTGGTGCCAGGCAGCGTTGCAGATAAGGTTTGTGTTTGCATAATTTTACTGAACTATTAATGATGTTAATTTTAGAACCAAATTTCAGATGTTGAAAAAATACTTTTGAAGGTGTTCTCCCTAGGAAATTTTGCATTTCTTGCAATAATATTGAATTCCTTTGCAAAATATTCACAAATGTGTGTGCATTTTGCCATTTTAAAGCCGGTTTTGTAATTACTAGTAAATTTCCATACTTGTGAATGGGGTAGCGTTTACTACGTTGTACACTGATAAGCTATGCAAAATTGCATGTATAATCAAGCTATTGTGAGACCAAAGATAAGCATTCTGTGATTTAATGACAGCTGTGAAAGCAGTTAAATCTTCTCTTTATTAAGCGACTGCTATATGGATTTCCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37482
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000036467 Nonsense 516 1180 17 41
ENSDART00000132829 None None 1831 None 45
ENSDART00000145208 None None 98 None 5
Genomic Location (Zv9):
Chromosome 22 (position 16945552)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 16697310
GRCz11 22 16723580
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAGTGGTTTTGCTAAATTTCACCCGTCAATTTTATAGATAACAACCCT[G/T]GAAGTGCCATTAAAATTTATTTTGTGTCACGTAAAAGTTGACAAGCCCTG
Long Flanking Sequence:
GCTTAGCAGGCTTTGTTTCAGTCATGTTAGCCGGCAGATATAAATATGCAGATAGGCGAACTGGAAGCGGAAGAGCAGGCCTTGGCTGAAGCCGAAGCAGCCCGGAGCTCTGGTTACATTCTGCCCTAATTAATCCGGACAAGACCCGGTACCTGCCAAACTCCGAAATAAAGCGTTCTGTTGCGCTGGGCCAATACATGCCCGGGATAACAATGATTGGTTGTCAGGGACTCATTTCCCAAAGCTGGAATAGCAGCACGTGTAAAATGATAGCCGCCCTCAAGTCAAAACACACAGCGCTTTAATCATGCTTTCACCTCCCGACTCCTTTTTCCCTGCGGTCTTAAGAAATTACATTGCCATGTGAGCGTGTAGATGTTGAAATCTTTTTCTTCATGGATAATGCTCGGCTGTTTTGGTACATTGACGTGACATTCGATAAGCGCAAACTTGAGTGGTTTTGCTAAATTTCACCCGTCAATTTTATAGATAACAACCCT[G/T]GAAGTGCCATTAAAATTTATTTTGTGTCACGTAAAAGTTGACAAGCCCTGAAAACAGATGTGTTTCAGCCCATTATTATAAGAACGTGGATCAAAGTTGCATTTTTTCTTTCCCCAAGTTCTGTCATTGGACAGTAAATAAGTCAAGTTTGGTGAAAGAAAATCATGGTTAGGGGTTACAATTAGTAGCTCATTGGAAACATACACAATAGTGATTAATTTTCCACTGCACTATGCCTTTATATTCTATACTGTAGACCATTTTTGTTAAGAGACAAGACTTTTGTCTAAGCAAAGTCAGACATTACTGTCCTAATAAAATAATTAAAAATCAGGGCATCATCATATTTATTTATTTTTTGTAAATAAGCATAATCTAGAGGCTTTTTATCTTTTATAAGCCACATCTGTTTTCAAATGATCAACCAGAAGTCAAGTTTTTATTTTTTGTTCCTAAAACTTGGATAGGTGACAAGACTTTTGTCATGATTTCTTTTGTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa648
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
ENSDART00000036467 Nonsense 543 1180 18 41
ENSDART00000132829 Nonsense 526 1831 13 45
ENSDART00000145208 None None 98 None 5
Genomic Location (Zv9):
Chromosome 22 (position 16942443)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 16694201
GRCz11 22 16720471
KASP Assay ID:
554-0556.1 (used for ordering genotyping assays)
KASP Sequence:
TGCAAGAGCCGGCCTCGCTGACGGAGATGGAGCTTCGCGCTAAATGGGAG[C/T]AGGCTCTTGGTCCACATTACGATGTTATGGTAAGCAAAAACGAAGAGGAA
Long Flanking Sequence:
CTCACTGTCTCACCAAAAACCCCACCATATTCTGTTAAGTTATAGCTTAGGTTACAGAAAAAAACTTCTTTTACTATCCAGATCCCATTTTGTCTAAAACCCCCTCTATACTCACTCCATATCATAGTTAAGGGTCAAAAGTGCCCATAAAAGCTGTTCCACCCATTTATTTGCCTCCATTGCCCTTTGGGCTTCCAGCCGATACTGTTCCCAGGCGTCCCGTTGTCGTTTTCTGCAGGATCACTACTGACTCCTCTCTCAACTCTTGCCCTCAGCTCACTCTCAGCCCTCTGATTATATTCATCCGTCAGCTTGACATCAATCCCATGCTAGTATGCGGCACCTGACATTAATGTCATACGTTTCCACTCACTCTGTCATGGACAGTGGGCACCCAAATGGCGGTAATTGACTTTAAACGCTGCTCTCATTATTGTGTGTGTGTTGTAGTGCAAGAGCCGGCCTCGCTGACGGAGATGGAGCTTCGCGCTAAATGGGAG[C/T]AGGCTCTTGGTCCACATTACGATGTTATGGTAAGCAAAAACGAAGAGGAAGTAATGTTAACAGATGCTAAGTGCGGCTCTCAATTAAACATGAAGCAAACTGCACATCAGCAAGAACAGCCAGCACTTACGCATACTGTGATAAGAGATGTTCGATCGACCAGCTAAATCTGGCTGTAGATTGCCTCAGTTGACTCCTGTTGAATTTGGGTTCATGTGCTGACACTTTGTTGTTTGGGTTTATTTACCATAATAGGAGTGTAATGACCCCGTTCAGGTCACAACTGTGATTGAGATAAATATAAATAAATTATATAGTAAATAAAACAATTAAGATACTTTTTTTTTTTGTTTTTTTTGTTTTGTAGATTGTACAGCTTGACCCGGTCATAGAAGATGATATTGAGCTGCAGAAGTACTCCAAGGTAACATGGAAACAGCTGTCACAATTCATGATTCATTCATTCGTTCATTCATCTCCGTAGTAGGGCTGGGTAATCC
Associated Phenotype:
Normal
Stage Entity Quality Tag
Larval:Day 5
ZFS:0000037		 whole organism
ZFA:0001094		 quality
PATO:0000001		 normal
PATO:0000461

Mutation Details

Allele Name:
sa24136
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
ENSDART00000036467 Nonsense 648 1180 21 41
ENSDART00000132829 Nonsense 631 1831 16 45
ENSDART00000145208 None None 98 None 5
Genomic Location (Zv9):
Chromosome 22 (position 16940425)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 16692183
GRCz11 22 16718453
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGCTTTCCTTAGAGAAGTTCCTACTCCATTTACTTTGGTTTGCTGCAGA[C/T]GACTTGCTAAAGAGGACAACGAATATCACCCTGAATCTGAAGACTGGCAC
Long Flanking Sequence:
CTTTCAATATAACCAATATTCTTATGTACTCCTTTTGGCCTCATTTGATGCTTAAAAGCCTAATGATGCATGATGATGATGATGATGATGATGATGATGTGTGTGTGTGTGTATGGGAAAGGGTTATGTGATGACCATGGCTTCCCCTTGATTTGGGCAGATGGCACAGTGCCGCCCCCACTCACCATAGCAGCTCCAGGCTTGACCGCTCCTGGAAATGCCAATCAAAAATGGTCATTAGATGCCACAGAGACTATGGAATATAGTTACTTGCCTAATAAGCACTAAATGCGCATGTCCAAAATGTGCAAAAAAATAGGTGGATGGAAATGTAGCTATTGAGAAAATCCATATTCTGAGTTTTTGCATAATTTTCTATCAAACAATTCTGAATTTTAATTTTGCAGGTGAATGGTGTGCAGCTGTATGGGAAGTCTAGACGAGAGTCTGTAGCTTTCCTTAGAGAAGTTCCTACTCCATTTACTTTGGTTTGCTGCAGA[C/T]GACTTGCTAAAGAGGACAACGAATATCACCCTGAATCTGAAGACTGGCACTCATCCAGCTTACAGGAGCAGGTAACCGAGGAGTAATGAGTAAAAGCTGGCTTCGGCAAGTATTGGCTGATACTTTAAAGAGTACTACAAAACAATACATTCTCATTTAGTAATTATTCCACAGATTGAGCATAACCTCTCCATGTTGGCCAGAGATACAAGTCTACGCGACAGCATTAGGGAAGAGTTTCAGGTTTGTTCATGTTTTCTAATATAAAATTACTATTATATTGACAGTTATAGTGTTTATGATGGTGTTGCTTCAGGTTTTAAGTCAAACATATTTTTATTTTTTACTTCAATATGTTCAATTAAATGAAATGTAACATGACATAGATTTGTCCTATATGTGTGTTCACTGTTGGTTAACAAGAAAGTCGTCACTTCCTGATTAACTGGTGGCAAATTTTGAGATATTAAGCTTCAAAGTTTTTGCATTTCATAGCAAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32397
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:
Essential Splice Site, Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000036467 Essential Splice Site 650 1180 22 41
ENSDART00000132829 Missense 684 1831 18 45
ENSDART00000145208 None None 98 None 5
Genomic Location (Zv9):
Chromosome 22 (position 16939032)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 16690790
GRCz11 22 16717060
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCTCACCATGATTTGTACATTTCTTTTCAGGCCCGTCAGGCTTCGGCA[G/A]TAGAGCGGGAGGTTGACGATGAAGGAGAGCCCCTAGAGCCAATCAGCCCT
Long Flanking Sequence:
TCAATATTTTTTTATGTGCTTACCAAAAATGTGCATAAAAATAGGTTGATAGAAACGTAGCTAGTGAAATCAAAGTAATGTCTGTATTTCCACTTAAAGAAGCGACCACTTTCGACAGCAGCTATTTCAGCTCATGCTTATTAACTGACGTTTCAGTGGAAGACGTGATTTAAAAGAAGTATTTTTTTCCTTCTAAAAACTATCATTGTAATGTACAGTAAGTAACGCAATTACTTGACGCAATTAACTTGACTTAAGTGACTGTAATCGAATTACACAAATTTAAAATGTAATTCGTTACATTACTGCATTCCTCAGAAATGTAATTAGAATACAGTAATGGGTTACTGTGAAACGCCTTACTCCCAACTGTGTCTGATTGATTGATTAAGTGACCCCATCATAATAGACCCATTTTTGGGCCACAACCCACCAATTTAGAGCCACTCCTTGCTCACCATGATTTGTACATTTCTTTTCAGGCCCGTCAGGCTTCGGCA[G/A]TAGAGCGGGAGGTTGACGATGAAGGAGAGCCCCTAGAGCCAATCAGCCCTGAGAAAGAGCAGATGGACCAGGAGAATGATGATGACGACGAAGAGGAAGAGGAGGAGGATGAAGGAGAACTAGCTCTATGGTCTCCAAATGTGCAAGTGTTAGAACTAGAGAAAGCAGAGCGAGGTCTTGGCTTCAGTATACTAGACTATCAGGTAGGCAGTAATTTTTTTGCACTTTATATGCATCATTAAATTACTAAATGTATGCAGTAAAGCAATTTAGAAAAAGTCTTTAAGGAATACAGCTTTATTGCAAAAAAAAAAACTATAAATAGACAAAATAACAAACTTCAGAGCATAAACATAAGATTTGTTCTAAACGTCATCATTAAACTACGTTTACTGTAAAAAGTCAAGACAAGGAATCTGTTCACACATAATCTAGCTGAGGGGAAGGGGACCAGACTCAGTTAATCCCCATTGACTTTCCCAAAGTGCGATCACAGGAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5970
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
ENSDART00000036467 Nonsense 698 1180 22 41
ENSDART00000132829 Nonsense 732 1831 18 45
ENSDART00000145208 None None 98 None 5
Genomic Location (Zv9):
Chromosome 22 (position 16938888)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 16690646
GRCz11 22 16716916
KASP Assay ID:
554-3668.1 (used for ordering genotyping assays)
KASP Sequence:
AGGAAGAGGANNNNNNGGAGGATGAAGGAGAACTAGCWCTATGGTCTCCAAATGTG[C/T]AAGTGTTAGAACTAGAGAAAKCAGAGCGAGGTCTTGGCTTCAGTATACTA
Long Flanking Sequence:
CTGACGTTTCAGTGGAAGACGTGATTTAAAAGAAGTATTTTTTTCCTTCTAAAAACTATCATTGTAATGTACAGTAAGTAACGCAATTACTTGACGCAATTAACTTGACTTAAGTGACTGTAATCGAATTACACAAATTTAAAATGTAATTCGTTACATTACTGCATTCCTCAGAAATGTAATTAGAATACAGTAATGGGTTACTGTGAAACGCCTTACTCCCAACTGTGTCTGATTGATTGATTAAGTGACCCCATCATAATAGACCCATTTTTGGGCCACAACCCACCAATTTAGAGCCACTCCTTGCTCACCATGATTTGTACATTTCTTTTCAGGCCCGTCAGGCTTCGGCAGTAGAGCGGGAGGTTGACGATGAAGGAGAGCCCCTAGAGCCAATCAGCCCTGAGAAAGAGCAGATGGACCAGGAGAATGATGATGACGACGAAGAGGAAGAGGAGGAGGATGAAGGAGAACTAGCTCTATGGTCTCCAAATGTG[C/T]AAGTGTTAGAACTAGAGAAAGCAGAGCGAGGTCTTGGCTTCAGTATACTAGACTATCAGGTAGGCAGTAATTTTTTTGCACTTTATATGCATCATTAAATTACTAAATGTATGCAGTAAAGCAATTTAGAAAAAGTCTTTAAGGAATACAGCTTTATTGCAAAAAAAAAAACTATAAATAGACAAAATAACAAACTTCAGAGCATAAACATAAGATTTGTTCTAAACGTCATCATTAAACTACGTTTACTGTAAAAAGTCAAGACAAGGAATCTGTTCACACATAATCTAGCTGAGGGGAAGGGGACCAGACTCAGTTAATCCCCATTGACTTTCCCAAAGTGCGATCACAGGAAATGCGCATTGATGTCCCAAGTTGTTGAACATCGAACAAAAGAATGCAATGAAACCTTTCCGACTAGGGCCGCCGCTGTTTATCTGGCTCGGTGCCAACCGTCAAACCCTTTGCTCTGCTCACTTAGTACAAAAAGCTGCTTTCCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43805
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
ENSDART00000036467 Nonsense 934 1180 32 41
ENSDART00000132829 Nonsense 930 1831 21 45
ENSDART00000145208 None None 98 None 5
Genomic Location (Zv9):
Chromosome 22 (position 16923962)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 16675720
GRCz11 22 16701990
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGAGGACCAGCAGAGCTCTAAGGTCAATGACACCAGTCTGCCTTCATA[T/A]CTCAGTGAGAAGAGTCGCTCCTGGGAAGAACCAGCAACATCCAGCCGCTA
Long Flanking Sequence:
GACAATTTTAACATTTGTTCAAGGACAAAAGATGAAAAAATTCTAGTGCATTTGCAGTAATACTACTCAATGGACACTGTCAAATTTTGCAGCTACAGGGATAGTTTACCCAAAAATGCAGATTCTGCCCTCAATTACTCACCTTTGTGCCATTGCTTCTTCTGAAAAACACAACCTTAAATGTTTAGCTGAAAGCTCCTTTCCATATAATAATGGTAGAATTAATCTATGCTAAAATGCTAATCATACAAAGTGAAGCTAAGTCACTTTCTTTGTTTATAGGACTTTGTAAACGGCTCCATTTTATCTGACGACCTGGATGAGGAGCCAGAGCTGATCCTGGACGCAGAGCCGCGCTACGCCTCTCCCCTCACCACTGTTGACCTCCAGCCTGACGTAGAGAAAGAGATGGCTGTGGATGAGGAGGAGGAAGATGTAGACGTGAATGTCATGGAGGACCAGCAGAGCTCTAAGGTCAATGACACCAGTCTGCCTTCATA[T/A]CTCAGTGAGAAGAGTCGCTCCTGGGAAGAACCAGCAACATCCAGCCGCTACCATCTCAACACAGAGCCTGATTTACAAGAACAGGTGAAACTCCAATGATTTGACGGCTTTCCTAAAGTAATGTATACAGTTTTACAACTGTTGTGTTTCTGCTGTGGTTTGCAAAGGTGGACGACGATCTTTCCATGAATTTGGAGAAGATTCAACTGCAGCCATTGAAAATTCCTCTCGGTAAGTGTCTGTTAAAGCTTTTTAACACTTTCCAGGCTGTTGATAAGATTGAGTTTGTCAATTAAGAAGACTACACTTCCCCGCCATTGGGTTTTTACAGCAACACAAATTTCTGGTGTGTTATGGTAAGGAAAAACCCTAATGCATGGCAAGAACAGAACGCTAATCCATTGGTTCATATGAGCTGTCAATCACTCTGTTCCGATGACAGGGTGCCACAGCCGCAAAAATATAAAGGTCTGGATCTGAGAGAATAACAATAACACTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24135
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000036467 Essential Splice Site 977 1180 33 41
ENSDART00000132829 Essential Splice Site 979 1831 22 45
ENSDART00000145208 None None 98 None 5
Genomic Location (Zv9):
Chromosome 22 (position 16923730)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 16675488
GRCz11 22 16701758
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCATGAATTTGGAGAAGATTCAACTGCAGCCATTGAAAATTCCTCTCG[G/A]TAAGTGTCTGTTAAAGCTTTTTAACACTTTCCAGGCTGTTGATAAGATTG
Long Flanking Sequence:
TAAAATGCTAATCATACAAAGTGAAGCTAAGTCACTTTCTTTGTTTATAGGACTTTGTAAACGGCTCCATTTTATCTGACGACCTGGATGAGGAGCCAGAGCTGATCCTGGACGCAGAGCCGCGCTACGCCTCTCCCCTCACCACTGTTGACCTCCAGCCTGACGTAGAGAAAGAGATGGCTGTGGATGAGGAGGAGGAAGATGTAGACGTGAATGTCATGGAGGACCAGCAGAGCTCTAAGGTCAATGACACCAGTCTGCCTTCATATCTCAGTGAGAAGAGTCGCTCCTGGGAAGAACCAGCAACATCCAGCCGCTACCATCTCAACACAGAGCCTGATTTACAAGAACAGGTGAAACTCCAATGATTTGACGGCTTTCCTAAAGTAATGTATACAGTTTTACAACTGTTGTGTTTCTGCTGTGGTTTGCAAAGGTGGACGACGATCTTTCCATGAATTTGGAGAAGATTCAACTGCAGCCATTGAAAATTCCTCTCG[G/A]TAAGTGTCTGTTAAAGCTTTTTAACACTTTCCAGGCTGTTGATAAGATTGAGTTTGTCAATTAAGAAGACTACACTTCCCCGCCATTGGGTTTTTACAGCAACACAAATTTCTGGTGTGTTATGGTAAGGAAAAACCCTAATGCATGGCAAGAACAGAACGCTAATCCATTGGTTCATATGAGCTGTCAATCACTCTGTTCCGATGACAGGGTGCCACAGCCGCAAAAATATAAAGGTCTGGATCTGAGAGAATAACAATAACACTGACAGATTTAGTTTAAGAAACCAGCTAGAGTTACAATTATGACACATCTGATTAGTGATCATGTGCTGAATGTCAGTCCAGCATTTACACTTTTCGAAGAGTGGATAAAAGACTTCCCGCGTTTAAAGTCCGCTATGAATAAAGCATTCACTGTAAAGCCAGTAGGGCGGAGTTTTCAGGTAAGTGTTTGCCTCATCTACACATTTTAAGCACAGGATGTTCTAACGTTATTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43804
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
ENSDART00000036467 None None 1180 None 41
ENSDART00000132829 Essential Splice Site 1209 1831 29 45
ENSDART00000145208 None None 98 None 5
Genomic Location (Zv9):
Chromosome 22 (position 16906054)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 16657812
GRCz11 22 16684082
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTCAGGAGGAGGAGCATGAGCAGGAGGAGGAGGATGAGCAGGATACAG[G/A]TGAGAGACTGCTGGTCATTACACACTTGCTGTGTTTGGAGTCAAACTGAC
Long Flanking Sequence:
CACTTTGGAGGGCATCTGCTGCGTAAAACATATGCTGGACAAGTTGGCGGTTCATTCCGCTGTTGTGATTCCAGATTATTAAAGGGACTTAGCCGAAAAGAAAATGAATGAATGATCGCATATATAACTTTGTTTTTGTTCCAGTCACATACATTTAATGTTTAAATATCTATTACATATATGGTACTGCTTATATTATTTCACCATCTGTACACCAAAATAAGTAGTGAATGTGCGTGTCCGTGCATGGGGCTGTGTTGGTGTAGTAATGTGGGCTGGTGTGGCTACAGTGCCAGGGCTGATTTTTAGTCCCAGTCCGCCCCTGTTTGCATGTGTCCTGTGGCATTGTTCTCACTCTCGGTTTCTTTGGTTTTGTGCAAAGCAGAAAGCAGGACAGGGTGCTGCTCCTCCACCCATGCGTCTCCCCCCACCCTACAGACCCCCTAGTCAAGTTCAGGAGGAGGAGCATGAGCAGGAGGAGGAGGATGAGCAGGATACAG[G/A]TGAGAGACTGCTGGTCATTACACACTTGCTGTGTTTGGAGTCAAACTGACATTCTGTTGAGCATATTATGATTTTTTATATGCCTGAATAATTTACATGTGTTTGAGTGTATATGTTTGTTTGTGTTTACACATTTGTTGTGTTGTGTTGGTATTGGTGGTTTACAAGGACTCTCCATAGCCGTTAAATATTTTTATACTGTAAAAATCGTTTTATTCAACCGCTATCTCTAAAACCCAACCACCTCAAAGGAAACCTGTGGCAAATTTTGAATGTGAAAAGAGCCTCTTAAGTATAATTTTTAAGCATTTAGATTTACAAAACACAAGGTTTGTCCTCATAAACCACCTCAATTTTGTAATACCTAGAGCATACCCATGTGATTATACAAATTTCTGTTTTAAACAGTACACACACACACACTCTACCATTGTTCTAAAGTTTTTAGAATTTTTGAAAAATTTTATTTAATTTTTTTGTTTAAAGAGTACTTTTCTGCT
Associated Phenotype:
Not determined