Busch Lab

ZMP

si:ch211-272f3.4

Ensembl ID:
ENSDARG00000061397
ZFIN ID:
ZDB-GENE-041111-262
Description:
Novel protein similar to vertebrate thyroid hormone receptor interactor 12 (TRIP12) [Source:UniProtK
Human Orthologue:
TRIP12
Human Description:
thyroid hormone receptor interactor 12 [Source:HGNC Symbol;Acc:12306]
Mouse Orthologue:
Trip12
Mouse Description:
thyroid hormone receptor interactor 12 Gene [Source:MGI Symbol;Acc:MGI:1309481]

Alleles

There are 11 alleles of this gene:

Allele Name Consequence Status Availability
sa23366 Essential Splice Site Available for shipment Available now
sa9891 Nonsense Available for shipment Available now
sa9786 Nonsense Available for shipment Available now
sa10603 Nonsense Available for shipment Available now
sa13854 Nonsense Available for shipment Available now
sa8943 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa17600 Essential Splice Site Available for shipment Available now
sa954 Nonsense F2 line generated Not yet available
sa29080 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa23366
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
ENSDART00000087566 Essential Splice Site 719 2095 13 41
ENSDART00000138552 None None 32 None 3
ENSDART00000145863 Essential Splice Site 677 2026 13 41
Genomic Location (Zv9):
Chromosome 18 (position 39614846)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 41284343
GRCz11 18 41274535
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCACTTGTCTCTGTTTTGCTAGGCTGGTGGACAACTTTCAGCATGAAGAG[G/A]TGAGAAGTATTGCTAAGCACAAATAGCTAATTATGCAAACCTTAAGAGGG
Long Flanking Sequence:
TAGGGTAATTAGGAAAGTTATTGTATAATGATTGTTTGTTCTGTAGACTATTGAAAAAAAATAGCTTAAAGGGGCTAATAATTTTGTCCTTAAAATGCTGTTTAAAAAAATTTAAAACTGCTTTTATTCTAGTCAAAACAAAACATATTAGACTTTTTCCAGAAGAAAAAACATTATCAAACACTCTGTGGAAATTTCCTTGCTCTGTTTAACATCATCTGGGAAATATTTAAAAAAGAGATACATATTCAAAGGGGGGCTAATAATTCTGACTCCTACTTTATACAAGAGCAGATGACCATAAATACACATAAAATGACATCTAGTTGAAGCTCTCTTTTTTGACAGACCTTTGGTGTAAACAATAAAAACATCAGTTTCTGTCTTAAATGAACCAGCACTTACTTGCTATTATGTCTTTTGTTTTATAGGATAAAAAGTCTGTGGAAAGCACTTGTCTCTGTTTTGCTAGGCTGGTGGACAACTTTCAGCATGAAGAG[G/A]TGAGAAGTATTGCTAAGCACAAATAGCTAATTATGCAAACCTTAAGAGGGAAAAATGTGTGTTTTTCTGTTTTTAACAGCTGTTTTTATATTATTCAGTAAGATAAATCAGCTTGTGAGTCATCTCTAAATGTTTTCAGGAATATTAAAGTATTAGTTTGTCCCAATGTTGTTGTTTTATTTATTTTGGGGCTCATCTGTGGGAACTAAAATCTAAACTTCTGATTGTGAAAAAGTGTCTGTTGAATCATTCAATGTAATTTCAGAATTTTTACATTCTGGCTTACAGCATTCCGAGAGACAGCTGCAAAATTAAAACTGAATTGTGTGCGGATATATGGATATATATTTTGGTATAAGCATGTTCATAATGTACAGCATAGACAACATAATTTAAAAACCTATCTTGCTAATGGTGAATTATACCTTAACTAACCCACTTTTTTTTTTACTTCGTTCTATTTTATGGCCACTTGAATCAATACATATAAGCAAATTAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9891
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087566 Nonsense 722 2095 14 41
ENSDART00000138552 None None 32 None 3
ENSDART00000145863 Nonsense 680 2026 14 41
Genomic Location (Zv9):
Chromosome 18 (position 39616927)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 41286424
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTGTGTGTGTGTCNNNNTGTCTGTCTGTCTGTCTGTCACAGAACCTGT[T/A]ACAGCAGGTGGCGTCACGGGACCTTCTGACCAACATTCAACAACTGCTAG
Long Flanking Sequence:
TAAACCACTTCTGATACCAAATGATCAACTAGAAGACAAGTTATTATTTAATTTAATAGTATTTATACAAGACTTTTGTCAGGTAGTGTAAAGTAGGGAAAACATATTGAAGCATTTTTAGAACCTATCATTCTTCAAAACATTACCTTTAGTTTTTAACAGATACAAGAAACACATTTACAAAAGTCAAGATAAGACTAAATAAATTGACAGTTTCAGTTTTTGGTGAACTCTCACTTTCAGTAGATTTTGCATTATGTAGATTTAGGATTATGATACAATAACTTGAAAAATATCTCTGATTTATTTCTAAATGCTATGTAAATCACTTAAAATTAATCACTGTGCTGTGTTTTGTTTGTTTGTTTGTTTGTTTGTGTGTTTGTGTGTTTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTGTTTGTCTGTCTGTCTGTCTGTCACAGAACCTGT[T/A]ACAGCAGGTGGCGTCACGGGACCTTCTGACCAACATTCAACAACTGCTAGTACTCACTCCACCTGTGCTCAGCTCTGGCATGTTCATCATGGTAGTGCGCATGTTTTCTCTCATGTGCTCCAACTGCCCATGTCTGGCTGTGCAGCTCATGAAGCAGAGTAAGTCACTCGCATACACACTCTAACCCTGCAGTTTACTATAACAAAAAGCACTATTAAAGAAAGCGTGTGGTTCTTAATTAAGGAGTAATTGACAAGAGGCCACTGACTTATTACGCCCGAGTACATTATTTTCTAGTTTTTCAACAGACCAGAGTCAATTATTCCACTTAAAGTATGGTTTAATACTTTAATAACACACCTAAAGCATTGCATTTTGAGATGTTTGTAAGTTTTTTTTTTTTTTGTTCTCTACTGTGTTTAGTACTAGTTTCTCATCCAAAGCTTGTTTATTTTCTATTATTGTTTTAGTTTATTTGTTATTATTATTTAAAAGAACTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9786
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
ENSDART00000087566 Nonsense 1101 2095 20 41
ENSDART00000138552 None None 32 None 3
ENSDART00000145863 Nonsense 1032 2026 20 41
Genomic Location (Zv9):
Chromosome 18 (position 39623221)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 41292718
GRCz11 18 41282910
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTCTCCAAGTTTCCAGCACAGCATGGACGACKCGCTGGACCTCAGTCCA[C/T]AGGGGTATAAAACCACTCTGACATACACAGTTATCGATCTAGAGTTTAAA
Long Flanking Sequence:
TGCTTGTCTTTAGTTAATTCTCATTCTGTAATTATGTTCAAATGTTTCTCTTCTGCTTGTGTGTAGCCACATAGCTTCCATGCTGTCCAGTCAGGACCTGAAGATTGTAGTGGGCTCTCTGCAGATGGCTGAGATCCTCATGCAAAAGCTACCAGATGTGTTCAGTGTTTATTTCAGACGAGAAGGTACTGGATCTGATTTTTATGAGCTAACTGAATTGTTCTGCAATTAAAGTGCAAACATCATTTACATCATCTTTAATTGCACTAATTCACCAAATGTCGCTCTTGTTCTGTTCAGGTGTGATGCACCAGGTAAAGAACTTGGCTGAATCTGAAGTGTTCCTCACCAGCCCTCCGAAAGCGTGCACAAGTGGCACAGCAAGTCTTTGCACCACCACCATCACCACAGCAACCACTACAGCTGCCTCTAACGTCACACCTGACCTGGGCTCTCCAAGTTTCCAGCACAGCATGGACGACTCGCTGGACCTCAGTCCA[C/T]AGGGGTATAAAACCACTCTGACATACACAGTTATCGATCTAGAGTTTAAACGCATGACATGAGTCACCTGGTTTGCAAAGTTTTAAAAATAGATCCGTCTTCTATAGTAGGTTGAGTGATGTTCTGAAAAGAAAACGCCTCCCTAAAAGAGGACCAAGGCGCCCCAAGTACTCGCCACCCAGAGATGATGACAAAGTGGATAATCAGGGTATGTGTTAAAAAAGAATTAGTACTTGGAATCTTCATGTTTTGTATTCGTATCATTTTAAGGGTGCTTTCACACATGTAGATTGATTCTTTTGTTCCGAAACAGGGATTAAAATTGTTAGTGTTTATTTTTGTTTTTGGTGTGGTTCGCTTTTATGCGGCAAAGTTTCTAAATGGACCAAAACAGCTAAAACAAGTCACGTGCGAGTAAACTCTCCTCACATTGGTCAGAGTCCCACTTAGCTGTCATGCGTACTTATTTTAATTTATGACGATCAGCAATAAGACAATAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10603
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
ENSDART00000087566 Nonsense 1339 2095 25 41
ENSDART00000138552 None None 32 None 3
ENSDART00000145863 Nonsense 1270 2026 25 41
Genomic Location (Zv9):
Chromosome 18 (position 39627799)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 41297296
GRCz11 18 41287488
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACTGCTTGCATTGGTGCACAAGATGAACAACTGCCTTAGTCAGATGGAA[C/T]AATTTCCTRTTAAAGTGCATGATTTCCCCAGTGGAAATGGCAACGGAAGC
Long Flanking Sequence:
AGAAGACTTTTTTATGAAAGGAACTCTTAAGGACATTTTTAACAAAGTGAAACCAGAAAAGATTTTAGAATTTTTATCATGTATTAACACAAAAAATCTTATTTAATATATGTTTTATTTTGTTTGTTGGTTTTTAAATTGTATATTTATTGTTGAAAGATTCCTGCCATGAAAATAGCCTTGGTTGCTGACATGGCATTAAATAAAAAAAAAACACATACATATAAATAAAATAAAAATAAATACACCTAGCAGCTCATAAGGGCTTGTAACAGTGGTTGGGTGTTACACTTTTCCTTTGTCACCGAATATATTTGACATGTTTATTGGGTCATTTTTTTTTAAATAGTAGTCATTGGTGTGATCAGTGTGACTCATTATTTATGCTATATGTGATTCAGATACCAGGGCAGGAACCTCCGGGACGTTTGGACCCAACAGAGAATGGCCCACTGCTTGCATTGGTGCACAAGATGAACAACTGCCTTAGTCAGATGGAA[C/T]AATTTCCTGTTAAAGTGCATGATTTCCCCAGTGGAAATGGCAACGGAAGCAGGTAATGACAACTGCACTTCACTCTTTAACCCTCCTGTTTTTATAAATGCATCAATTTATCTTTGACTGCCTCATTATGCAAACATTTTTTTCCATGTTATTTTTTCAACCTAGTTTCTTAACCTTTACCTCATATATACAGTATTTTTATATATGTTACTGCCTTCCAACTATGTGTCCGGGGTAGGAAATTACCCAGCTGTTCATAAGTTTGTTCTGAAACTAGGGGCTGGGTAACTACTAGCTAGTTTGTTACTAAATTTGTTCTTACTCTGGTTGAAGTTATTAGGTCGCAAAGTCTTGAGTAATTCAATATGTCTACGCGAATGATGTAATATCGGAAAAAAAAACCCATTAAAACATTAAACTGCTTTAAAATTCTGCAACTATTTTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13854
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
ENSDART00000087566 Nonsense 1372 2095 26 41
ENSDART00000138552 None None 32 None 3
ENSDART00000145863 Nonsense 1303 2026 26 41
Genomic Location (Zv9):
Chromosome 18 (position 39629730)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 41299227
GRCz11 18 41289419
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAGGGGTTCGCAGGCCCTGAAGTTCTTCAACACCCATCAGCTGAAATGC[C/T]AGCTGCAGAGACACCCAGACTGCACCAATGTCAAGCAGTGGAAGGGCGGC
Long Flanking Sequence:
CAATGAGCCATGGTCGACACAAGCTTAAACAGACTCCGTCGTCGTCTTCATGAACAAAATCTGCCGTGTCCTGTTGTTTGTTTTACGAGTCAGTCTAAAAACGCCAGCGTTTTCACTTTCTCCAGAGAGCTCCCATGCACTTGCTGTACGTCTATATTCGTTAGTTATTTACACATATTGCTAAAGAGCACACTCAAGACTTACAATACAAATGTGTTTATCATGTCAAAAACAAGCACATTTTACTGGGTTGTAGTATCTCTGCCCCTCTGCGGTACTTGTTTTAGTCTATTGCTACTCAATAGACTCGTTAATCCAAATTTAAAAACAATAAACATCATATTTAGTCAATTTTTTTTAAACAATTGAACCTGCTTTTCATCATGATTATAATTAGAAGCTGGCATGGCATTTCTGAGGGGGAAAATCTAATTATATTCTATTGTGTTTACAGGGGTTCGCAGGCCCTGAAGTTCTTCAACACCCATCAGCTGAAATGC[C/T]AGCTGCAGAGACACCCAGACTGCACCAATGTCAAGCAGTGGAAGGGCGGCCCGGTCAAAATTGACCCACTGGCCCTGGTGCAGGCCATTGAGAGATACCTTGTGGTTAGAGGTAAACTCACAAGAATCTAAACATAATTTTCCAGCTCTGTGGTTTTAGAGATCTCAGATGAGATGGTTGTTTTGTGCTGTTTCTACAGGATATGGAAGGATCAGGGAAGAGGATGAAGACAGTGATGATGATGGTTCTGATGATGAGATTGATGAATCTTTGGTATGGAGGTTTTCGTTTCATAATCATCTTCGGGCAGTAATTATTATAGCTGGATACTGGTTCAGAAGTCCTGATTTGCAAGCGCTCAATTATTATTTTTTCTTTCAATTTTTAAACAAACCAGACCATAAAACACTTTTAAACCGTAGCATAAAACAAAAAGACCTATAATACAAATTCCAAAATCACCAGATACAGTCTTATTTACAATTATAAGAATTTATGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8943
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
ENSDART00000087566 Essential Splice Site 1434 2095 28 41
ENSDART00000138552 None None 32 None 3
ENSDART00000145863 Essential Splice Site 1365 2026 28 41
Genomic Location (Zv9):
Chromosome 18 (position 39632050)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 41301547
GRCz11 18 41291739
KASP Assay ID:
2261-2526.1 (used for ordering genotyping assays)
KASP Sequence:
TGTTTTCTTCCTCAACATTAAAACTSTGGACCTCTAACCATTTTYCCAAA[G/A]GCTGCCCAGTTCCTGAATTCTGGGAGTGTACGACACAGGCTGCAGTTCTA
Long Flanking Sequence:
ACTCATGGTGCATTAACTAATGTTAACGAGCATGGACTTGGATGTTAATAATGCATTTGTAAATTCTCAATAATGATTAATAAATGCTGTACATGTGTTGTTCATGATAAGTTAATGTTAGTTAATGCATTAACTAATGAACCTTATTGTAAAGTGTTACCAAAATATTATAGTCTCTTTTTTATTATAAAAATGGTGAACTGTACACTGTTATTTGCCACTATTTACTTGCATTGAATATTCAGATAACCTGCTACATGATTTGTAAATAGCACATTTTTTGCGCAAATGTAACTAAATGTTAACTTTTAAAAAAATATGATTCATAGTTATAATACAGATGAAATTACTCTTCAGACTGGAAAAATGTTATAGCGTAGCATATACCTTACACTATTTGTAAAGTAGTTGACTAGCATTTCATTTTAAACTTCTCGGTAACCATCCCAGTGTTTTCTTCCTCAACATTAAAACTCTGGACCTCTAACCATTTTCCCAAA[G/A]GCTGCCCAGTTCCTGAATTCTGGGAGTGTACGACACAGGCTGCAGTTCTACATAGGGGAGCACCTGCTGCCGTACAACATGACTGTTTATCAGGCTGTCAGACAGTTTAGTTTGCAGGCCGAGGAAGAGAGAGAGAGCACAGATGATGAAGCGAACCCTCTGGGACGTGCTGGCATCTGGACCAAAACACACACTGTATGGTACGCAATTTACTAGCCTTTCACTCTTCAGAAGCGAAGAGCTTTTTCAGTGAATGCATCATTTCTGCAAGCTTTTTTGTACAGCTGCATGATCAATGGTTAAACAATAATAATCAAACACCCCATGTTATTAATTGTAAATAATTACAATTAGCATGGTTATTAGGGCTGCACAATATTTTGTTTCAGCATTGTTATCACAATGTGAGTGTCTGCAATAGTCACATTGGAATTATATTGGAATTATAGTTGATCAACAATTGAGAATACAAGAGAATTGTGGAGTCATTGCATATAACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17600
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087566 Essential Splice Site 1500 2095 28 41
ENSDART00000138552 None None 32 None 3
ENSDART00000145863 Essential Splice Site 1431 2026 28 41
Genomic Location (Zv9):
Chromosome 18 (position 39632252)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 41301749
GRCz11 18 41291941
KASP Assay ID:
2261-2527.1 (used for ordering genotyping assays)
KASP Sequence:
CGAACCCTCTGGGACGTGCWGGCATCTGGACCAAAACACACACTGTATGG[T/A]ACGCAATTTACTAGCCTTTCACTCTTCAGAAGCGAAGAGCTWTTTCAGTG
Long Flanking Sequence:
GTACACTGTTATTTGCCACTATTTACTTGCATTGAATATTCAGATAACCTGCTACATGATTTGTAAATAGCACATTTTTTGCGCAAATGTAACTAAATGTTAACTTTTAAAAAAATATGATTCATAGTTATAATACAGATGAAATTACTCTTCAGACTGGAAAAATGTTATAGCGTAGCATATACCTTACACTATTTGTAAAGTAGTTGACTAGCATTTCATTTTAAACTTCTCGGTAACCATCCCAGTGTTTTCTTCCTCAACATTAAAACTCTGGACCTCTAACCATTTTCCCAAAGGCTGCCCAGTTCCTGAATTCTGGGAGTGTACGACACAGGCTGCAGTTCTACATAGGGGAGCACCTGCTGCCGTACAACATGACTGTTTATCAGGCTGTCAGACAGTTTAGTTTGCAGGCCGAGGAAGAGAGAGAGAGCACAGATGATGAAGCGAACCCTCTGGGACGTGCTGGCATCTGGACCAAAACACACACTGTATGG[T/A]ACGCAATTTACTAGCCTTTCACTCTTCAGAAGCGAAGAGCTTTTTCAGTGAATGCATCATTTCTGCAAGCTTTTTTGTACAGCTGCATGATCAATGGTTAAACAATAATAATCAAACACCCCATGTTATTAATTGTAAATAATTACAATTAGCATGGTTATTAGGGCTGCACAATATTTTGTTTCAGCATTGTTATCACAATGTGAGTGTCTGCAATAGTCACATTGGAATTATATTGGAATTATAGTTGATCAACAATTGAGAATACAAGAGAATTGTGGAGTCATTGCATATAACCATATCAGACTGAAACTTTATAATTTGCATGTGTTTTAACGGCATTTTAAGAAAGTGAAGCATTCGGGCACAATAACGTACAACATTTGCAACTTTTAATAAAGAACATTAGTGAATTATTAATACAATGAAGTCTGTACAGTGTTATTTTACAGGACATTATCTGAATGCTGTTTGACTCTTCGGAAAACCATAAAGCACTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa954
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087566 Nonsense 1535 2095 29 41
ENSDART00000138552 None None 32 None 3
ENSDART00000145863 Nonsense 1466 2026 29 41
Genomic Location (Zv9):
Chromosome 18 (position 39634270)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 41303767
GRCz11 18 41293959
KASP Assay ID:
554-0859.1 (used for ordering genotyping assays)
KASP Sequence:
AGAGGGGTCGAGCACAGACGGCACCCACTAAAACCTCCCCTCGAAATGCC[A/T]AGAAACAGGACGAACTGTGGCATGGTATGGAGATATCNNNNNNNATTTTTAACAAAG
Long Flanking Sequence:
AGTTTTGTGTTACATATAAACACTAATGTCTGAAATTTAACTGCATCTTGACACTATAAATAAAGGTTTAATTATTGCGTCAGTAGGTGGCAACATTGAGTTATTAAAAAAATGAATAGGTCCTTCAAGCGATTCTTCTAGAAACACTGATTCATCCAGCAATATAAAAGTATCTCATTCATTTAAAGTGAAATTTAAAAAAATAATTGTAATAGCATAATTGTACATCTGCGTCAAAATAAATTGCGAGAAACCTTTATTAAATTAGTTATTTTTAATTTTTGTTTTCAATTGTGAGAAAATTGTGATTTCTATTTTAATTTAATTCAGTTTATCAAGAATCATGTGGCTCTACCTTTTTGCATTTGCAGTGTATGTCAATATGTGTATCTTGCAGGTATAAGCCAGTCAGAGAAGATGAAGAGGGCTGTAAAGACGCTGTAGGAGGGAAGAGGGGTCGAGCACAGACGGCACCCACTAAAACCTCCCCTCGAAATGCC[A/T]AGAAACAGGACGAACTGTGGCATGGTATGGAGATATCATTTTTAACAAAGATCAAATGTGTTTTGTTGTTTCGTAATGAACTGCTTTCAATCTTTTTTGCGTGTGTGTTTTTTCAGAGGGTGTGTGTCCCAGTGTGGCAAACCCATTAGAGACATACCTCATTTGTGATCCTCCAGAGGGCATCACTTTTGATGACCCTTCAATGGAGGTGATTCTGCTGCTGAGGGTCCTGCACTCCATCAGTAGATACTGGTTCTACCTGTACGATGTAAGTAAACCATGCTAGAGGATACAATTTAACTGTGTGAATCTCATGCTTCACCCCAGAAAAAATGAAAGATGTTAAACTTTACTAAAGAAAAAATTAACTTTTAGAGGCAATTTTTTGAGCACATTTAAAAAAAAAAAAAAAGAAATAGATTATTTTCATGATAAATAAATACAGACTGGTACAATCTTGATGCTGGAAAATGTCTAGTGAAAGTATACAATTATATATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa29080
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
ENSDART00000087566 Essential Splice Site 1593 2095 30 41
ENSDART00000138552 None None 32 None 3
ENSDART00000145863 Essential Splice Site 1524 2026 30 41
Genomic Location (Zv9):
Chromosome 18 (position 39634540)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 41304037
GRCz11 18 41294229
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGAGGGTCCTGCACTCCATCAGTAGATACTGGTTCTACCTGTACGATG[T/C]AAGTAAACCATGCTAGAGGATACAATTTAACTGTGTGAATCTCATGCTTC
Long Flanking Sequence:
ATTTTTAATTTTTGTTTTCAATTGTGAGAAAATTGTGATTTCTATTTTAATTTAATTCAGTTTATCAAGAATCATGTGGCTCTACCTTTTTGCATTTGCAGTGTATGTCAATATGTGTATCTTGCAGGTATAAGCCAGTCAGAGAAGATGAAGAGGGCTGTAAAGACGCTGTAGGAGGGAAGAGGGGTCGAGCACAGACGGCACCCACTAAAACCTCCCCTCGAAATGCCAAGAAACAGGACGAACTGTGGCATGGTATGGAGATATCATTTTTAACAAAGATCAAATGTGTTTTGTTGTTTCGTAATGAACTGCTTTCAATCTTTTTTGCGTGTGTGTTTTTTCAGAGGGTGTGTGTCCCAGTGTGGCAAACCCATTAGAGACATACCTCATTTGTGATCCTCCAGAGGGCATCACTTTTGATGACCCTTCAATGGAGGTGATTCTGCTGCTGAGGGTCCTGCACTCCATCAGTAGATACTGGTTCTACCTGTACGATG[T/C]AAGTAAACCATGCTAGAGGATACAATTTAACTGTGTGAATCTCATGCTTCACCCCAGAAAAAATGAAAGATGTTAAACTTTACTAAAGAAAAAATTAACTTTTAGAGGCAATTTTTTGAGCACATTTAAAAAAAAAAAAAAAGAAATAGATTATTTTCATGATAAATAAATACAGACTGGTACAATCTTGATGCTGGAAAATGTCTAGTGAAAGTATACAATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATTTTTAAAAAAATAATAAATATGTACACAGTTTTTTTAAATATAGTAATACAGGAAAAAGTGTTGAAACATTTATTAAAACCATTTATTTATTTTATTTTTTCCCAAATAAAACTATTATTTATCTTATTGTAAATAAACTTCTTATTGGAATAGATTCAGATATATTCATTAATGATGCAAAAATATGAAATGAGACTAAA
Associated Phenotype:
Not determined