Busch Lab

ZMP

si:ch211-194i4.1

Ensembl ID:
ENSDARG00000079725
ZFIN ID:
ZDB-GENE-070912-171
Description:
Novel protein similar to vertebrate DEAH (Asp-Glu-Ala-His) box polypeptide 9 (DHX9) [Source:UniProtK
Human Orthologue:
DHX9
Human Description:
DEAH (Asp-Glu-Ala-His) box polypeptide 9 [Source:HGNC Symbol;Acc:2750]
Mouse Orthologue:
Dhx9
Mouse Description:
DEAH (Asp-Glu-Ala-His) box polypeptide 9 Gene [Source:MGI Symbol;Acc:MGI:108177]

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa19813 Nonsense Available for shipment Available now
sa32962 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa13148 Nonsense Available for shipment Available now
sa39873 Nonsense Mutation detected in F1 DNA Not yet available
sa8582 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa39874 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa45108 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa18641 Essential Splice Site Available for shipment Available now
sa39875 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa19813
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111661 Nonsense 109 1271 3 27
ENSDART00000134918 Nonsense 109 1271 4 28
Genomic Location (Zv9):
Chromosome 2 (position 35576389)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 35873099
GRCz11 2 35855556
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGGAGGTAATGATGATGGTGGCGGATTTGGAAATCTCCCGTCTAACTG[T/A]CCACTGCCTCCACATCTGGCTGTGAAGAAGGAGTTAGGTGAGAGAATGGC
Long Flanking Sequence:
TTCCATAAAAGGGAAAATAAATACTATAGAAGTCGATGGTTCAGCTTTCTTCAAAATATCTTCTTTTGTGTTTAACAGCAGAAAGAAATTTAAACAGGTTTTAAGTAAAAGGTGGGTAGATGATTGCAAAAATTTCATTTCTGGGTGAAATATAACTTTGAATTGGGAATTGTTTTAGGAAAACTGCATTAAATGTTTTATTTTTGTAGGTGCGTGTGGAGAGTTACAGTTACATCGGTATGGGAAACTCCACCAACAAGAAGGATGCTCAGTCCAATGCCGCCCGAGATTTTGTGAATTATCTAGTGCGGACAAAAGAAATAAGTCCTGGTGAAGTCCCTGCTCTCGGGGTCAGTATTAGCACATCTGATGCTCATATATGATGTTTTGGGGTGAATGTCTTAATATCAGGTTCATAATTTTCAGGTCAGTGTTCCTGATGGACCGAGTGAAGGAGGTAATGATGATGGTGGCGGATTTGGAAATCTCCCGTCTAACTG[T/A]CCACTGCCTCCACATCTGGCTGTGAAGAAGGAGTTAGGTGAGAGAATGGCTGAAAGTGCTGGTTCACCCTAAAAGGGAAATCTTTTCATCATTAGCTATGTTTCCATCCAAAATTGCGAATAAAGCAGTGTTTCCATCCAGCGAGTCAAAGAGAAATAAAGATTTGAAGATGTGAGATTCTGGAGACACTCTTGATTCTGGAGGTCCTTAATAATACAATAACACTAATACTGAAATAGTTAAGGTGTTTTAGAATGACAGGAACAACATTTTAGATGTTTTACAATGTGCTCAGCCTGCTGGTTCATCCATTCATACACATTTTTGTCATCACATAATCTCATAACCAAATCACATGACATTTTTTAATGCGTATGCTGGAATTTGTTCGGTAAAGGTGTTTCCATTGTAGTTTATCTGCATCTTTTCCTATAGAATAAAAGGCTTATTCTATTCAGTTATAAAATATAAAATTATATTCATATATAATTAATGCGCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32962
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
ENSDART00000111661 Essential Splice Site 121 1271 3 27
ENSDART00000134918 Essential Splice Site 121 1271 4 28
Genomic Location (Zv9):
Chromosome 2 (position 35576427)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 35873137
GRCz11 2 35855594
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCGTCTAACTGTCCACTGCCTCCACATCTGGCTGTGAAGAAGGAGTTAG[G/A]TGAGAGAATGGCTGAAAGTGCTGGTTCACCCTAAAAGGGAAATCTTTTCA
Long Flanking Sequence:
GTTCAGCTTTCTTCAAAATATCTTCTTTTGTGTTTAACAGCAGAAAGAAATTTAAACAGGTTTTAAGTAAAAGGTGGGTAGATGATTGCAAAAATTTCATTTCTGGGTGAAATATAACTTTGAATTGGGAATTGTTTTAGGAAAACTGCATTAAATGTTTTATTTTTGTAGGTGCGTGTGGAGAGTTACAGTTACATCGGTATGGGAAACTCCACCAACAAGAAGGATGCTCAGTCCAATGCCGCCCGAGATTTTGTGAATTATCTAGTGCGGACAAAAGAAATAAGTCCTGGTGAAGTCCCTGCTCTCGGGGTCAGTATTAGCACATCTGATGCTCATATATGATGTTTTGGGGTGAATGTCTTAATATCAGGTTCATAATTTTCAGGTCAGTGTTCCTGATGGACCGAGTGAAGGAGGTAATGATGATGGTGGCGGATTTGGAAATCTCCCGTCTAACTGTCCACTGCCTCCACATCTGGCTGTGAAGAAGGAGTTAG[G/A]TGAGAGAATGGCTGAAAGTGCTGGTTCACCCTAAAAGGGAAATCTTTTCATCATTAGCTATGTTTCCATCCAAAATTGCGAATAAAGCAGTGTTTCCATCCAGCGAGTCAAAGAGAAATAAAGATTTGAAGATGTGAGATTCTGGAGACACTCTTGATTCTGGAGGTCCTTAATAATACAATAACACTAATACTGAAATAGTTAAGGTGTTTTAGAATGACAGGAACAACATTTTAGATGTTTTACAATGTGCTCAGCCTGCTGGTTCATCCATTCATACACATTTTTGTCATCACATAATCTCATAACCAAATCACATGACATTTTTTAATGCGTATGCTGGAATTTGTTCGGTAAAGGTGTTTCCATTGTAGTTTATCTGCATCTTTTCCTATAGAATAAAAGGCTTATTCTATTCAGTTATAAAATATAAAATTATATTCATATATAATTAATGCGCATTTTCAAAGTTGATGCTTATCTTGGTGTTTTAATCAACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13148
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111661 Nonsense 168 1271 5 27
ENSDART00000134918 Nonsense 168 1271 6 28
Genomic Location (Zv9):
Chromosome 2 (position 35577809)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 35874519
GRCz11 2 35856976
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTAAGTTTCTGAGAATGAATTKTTCTTTTTWTAATACCSAAAAGACRTA[T/G]GAATCAGAGGAAGTTGATCTGAATGCTGGCCTGCATGGGAACTGGACTCT
Long Flanking Sequence:
AGAAGATGAATTGGTACATTTTTGCAATGTGTTTTAATTTTTTAGCTTTAATAAAAAAAAACTATTATTTTAATTATTTCTTAGTTTTTATAATCTTGGCTTTGATTTGTCTAGTCTTAATGCATCTACGATGGCATGTATATTTTACCTCTGTGTTCTTATGGAAAGAGCTTTGAGATGATACTTTTAAAGGCTCTATATAAAATAAAGTTTATTATGATTTTAAAAATGTGTACTTTACTAAACCGTCCAAAATCTTTGTGTCTCAGAATCTTGTGAGGGTTCTGCACCTGTCCCTGGAGTCACAGGTTTAGGCTACTCAGGACGTAATAATGCACCATGGGAGAGAGGAGCTAACCTGCAGGAGTATTACTCCAAGAAAGAGGAGCAGGATGCAAAAGCAGTAGGTCTTTTGTTTAGGCAGTTTGCTGTCTAATAAATAGAACTGTAGTTAAGTTTCTGAGAATGAATTGTTCTTTTTTTAATACCGAAAAGACATA[T/G]GAATCAGAGGAAGTTGATCTGAATGCTGGCCTGCATGGGAACTGGACTCTGGATAATGCAAAGGCCCGTCTGAACCAGTTCTTTCAGAAGGAGAAAAATCAAACCGACTACAAGTATAGCCAAGTGGGCCCTGACCACAACAGGTCAGACTTCCATTTACTGTAACAGCTTATGTCACATGTTAAGGGTTTGTTTTTCTGCTGGACTGAAACAGTGACAGAGAACTCCTTGATGTGTATCTAACCTCAAGGAGATCTCAGATGACAAATCACGGATGTTACTTTTAAAACAAAATCACCAGTGTCATATGAGTGAATCTCACAAAACTCATCAAGAACATGTCCAGGTCATATTTCACTCCAGAGTTGTAAGAATGAATAATGGTAATTAAAATGGATGGGAATAATATACTTAATATCACAGTGCATCTAAAAGCAGAGTTAACTATTGATAAATAAAGATGGCTAGCTTTATTTTCAGGACATTAAAATATATAATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39873
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
ENSDART00000111661 Nonsense 294 1271 8 27
ENSDART00000134918 Nonsense 294 1271 9 28
Genomic Location (Zv9):
Chromosome 2 (position 35579485)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 35876195
GRCz11 2 35858652
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAGATGTTTATCCAGTTAATGTCAATGATGATGTCCAACACCAGCTGTA[C/A]AGTGTTGTGCAGGAACTTGGCATCCACATCCCTCCTCCTGTAAGTGTTGG
Long Flanking Sequence:
AAAAGGTCAGTTTTTTTGCGCTACATTGTTAAAGACAAATGTAGGCTAAATAGGACATTTTCATGCTAACCTTTGCTTTGTTGTAGGAGTTTTATTGCTGAGATGACAATCTTTGTTAGACAGCTGGGTAGAAGTAAGTATCAGAATGCTTTTATGTACAATAATATATTCCTATAATAAATGGTAATGTCAAGCAGTTTCAGTCTGTTAATATCTGTTTTACTTTTCCAGGGGTTACTGCTCGTGAGCACGGCTCTACAAAGAAGCTGGCTGCCCAGTCTTGCGCTCTCTCTCTTGTCCGTCAGCTGTACCATTTGGGGGTTATAGAAGCTTACACAGGACAAACTAAGAAAAAAGAAGGAGAAAGCGTGAGTTGAACAGTCTAGTTCAACTATCTTTGAGGCCTGTGTGTTTGACACATCTAACTTTCTGTTTTGGTTGCTATGACAGGTAGATGTTTATCCAGTTAATGTCAATGATGATGTCCAACACCAGCTGTA[C/A]AGTGTTGTGCAGGAACTTGGCATCCACATCCCTCCTCCTGTAAGTGTTGGACTGTAATCTTACTTGACTTTTACAAGAATAATATGTGCTTTCAATTTTGCTGTGTGTCTTGTTTTAGCCTCAAGACCCCAACAGTCCAGTGTCTCTGGTGCAAGGGAAATTGGCTCATTTTGAACCCTCTCAAAGGCAGAGCATGGCAGGTGTGGTGCCGTGGTCTCCACCACAGGTCAACTGGAACCCTTGGACCAGCTCCAACATTGACGAAGGACCACTAGCATTTGTGAGTTTGCTTTTCTGCATCGATCTTTTCAATTGGTGTTTGCAAGCAAATTTGGGGTGGTCGATTTCATAACAATAAAAATGTTTTGTTCTTGTTTTTGGCTGCAGTGCACCCCAGAACAGATCAGCAATGACCTTCTGAATGAGCTCAACTATCAGCTTGAACAGGACCAAAATCTGCAGACGGTGAGATAAAAATGCCACTTTAAGACTCCATGAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8582
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
ENSDART00000111661 Essential Splice Site 361 1271 9 27
ENSDART00000134918 Essential Splice Site 361 1271 10 28
Genomic Location (Zv9):
Chromosome 2 (position 35579767)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 35876477
GRCz11 2 35858934
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGAACCCTTGGACCAGCTCCAACATTGACGAAGGACCACTAGCATTTG[T/C]GAGTYTGCTTTTCTGCATCGAKCTTTTCAATTGGTGTTTGCAAGCAAATT
Long Flanking Sequence:
GCGCTCTCTCTCTTGTCCGTCAGCTGTACCATTTGGGGGTTATAGAAGCTTACACAGGACAAACTAAGAAAAAAGAAGGAGAAAGCGTGAGTTGAACAGTCTAGTTCAACTATCTTTGAGGCCTGTGTGTTTGACACATCTAACTTTCTGTTTTGGTTGCTATGACAGGTAGATGTTTATCCAGTTAATGTCAATGATGATGTCCAACACCAGCTGTACAGTGTTGTGCAGGAACTTGGCATCCACATCCCTCCTCCTGTAAGTGTTGGACTGTAATCTTACTTGACTTTTACAAGAATAATATGTGCTTTCAATTTTGCTGTGTGTCTTGTTTTAGCCTCAAGACCCCAACAGTCCAGTGTCTCTGGTGCAAGGGAAATTGGCTCATTTTGAACCCTCTCAAAGGCAGAGCATGGCAGGTGTGGTGCCGTGGTCTCCACCACAGGTCAACTGGAACCCTTGGACCAGCTCCAACATTGACGAAGGACCACTAGCATTTG[T/C]GAGTTTGCTTTTCTGCATCGATCTTTTCAATTGGTGTTTGCAAGCAAATTTGGGGTGGTCGATTTCATAACAATAAAAATGTTTTGTTCTTGTTTTTGGCTGCAGTGCACCCCAGAACAGATCAGCAATGACCTTCTGAATGAGCTCAACTATCAGCTTGAACAGGACCAAAATCTGCAGACGGTGAGATAAAAATGCCACTTTAAGACTCCATGAAATCAAATAGAAAATTTCAACGTGGTGATGTCATTGGCCATTGAACATTTCCTGACTGTTGTCAACCTAATTCATATATGTAACAAGAGGCGATTCAATCATAACTTAATGTTGTAACAGCTATCATAACATTATTTGAAATTTGAAATGTAAAAGGAAATACATCAGGACCATTGTAATTATTACATCCCTCAAAATGATCTATATGAATTCTGTGTGTTTTAGTACGTGTATTAGATTTGATGCCATTTAGGCCCATTTTACACTTGCTATTTAAATATGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39874
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111661 Essential Splice Site 387 1271 10 27
ENSDART00000134918 Essential Splice Site 387 1271 11 28
Genomic Location (Zv9):
Chromosome 2 (position 35579951)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 35876661
GRCz11 2 35859118
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTGAATGAGCTCAACTATCAGCTTGAACAGGACCAAAATCTGCAGACG[G/T]TGAGATAAAAATGCCACTTTAAGACTCCATGAAATCAAATAGAAAATTTC
Long Flanking Sequence:
TTAATGTCAATGATGATGTCCAACACCAGCTGTACAGTGTTGTGCAGGAACTTGGCATCCACATCCCTCCTCCTGTAAGTGTTGGACTGTAATCTTACTTGACTTTTACAAGAATAATATGTGCTTTCAATTTTGCTGTGTGTCTTGTTTTAGCCTCAAGACCCCAACAGTCCAGTGTCTCTGGTGCAAGGGAAATTGGCTCATTTTGAACCCTCTCAAAGGCAGAGCATGGCAGGTGTGGTGCCGTGGTCTCCACCACAGGTCAACTGGAACCCTTGGACCAGCTCCAACATTGACGAAGGACCACTAGCATTTGTGAGTTTGCTTTTCTGCATCGATCTTTTCAATTGGTGTTTGCAAGCAAATTTGGGGTGGTCGATTTCATAACAATAAAAATGTTTTGTTCTTGTTTTTGGCTGCAGTGCACCCCAGAACAGATCAGCAATGACCTTCTGAATGAGCTCAACTATCAGCTTGAACAGGACCAAAATCTGCAGACG[G/T]TGAGATAAAAATGCCACTTTAAGACTCCATGAAATCAAATAGAAAATTTCAACGTGGTGATGTCATTGGCCATTGAACATTTCCTGACTGTTGTCAACCTAATTCATATATGTAACAAGAGGCGATTCAATCATAACTTAATGTTGTAACAGCTATCATAACATTATTTGAAATTTGAAATGTAAAAGGAAATACATCAGGACCATTGTAATTATTACATCCCTCAAAATGATCTATATGAATTCTGTGTGTTTTAGTACGTGTATTAGATTTGATGCCATTTAGGCCCATTTTACACTTGCTATTTAAATATGTTTTTTTTTGTTTAGTTTTTTTTTAATCAGATCAGAGAAATGGTCATAACAAAATCTTGAACACATAAGAGATGCAGAATTCATAATAATTGCATGTTTTATTTAAAATAACATGTTCTAGAATAATAGTTATGTAAGTGTGCACCGTATTTTATCCCATTTTTATGTTCTATGTTACACCTTAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45108
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
ENSDART00000111661 Essential Splice Site 499 1271 12 27
ENSDART00000134918 Essential Splice Site 499 1271 13 28
Genomic Location (Zv9):
Chromosome 2 (position 35582461)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 35879171
GRCz11 2 35861628
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTCTTTCCTGCCCAGACCTCATGCCAGCATCCTCTTCTGCACAGTTGG[T/C]ACGTTCTAGTTTTTTAAATCCTTTACTCTGTAACACAAAAGCACTTGGTG
Long Flanking Sequence:
TCGTTTATGGTGAAAATGGATATAAAGTTTCAATAGTCTGGTACTGAACATTAAGCATGTTCTTCTTACAGATTCTAACGGAACGAAGTCAGCTACCAGTCAAGAACTTTCAGGAGCAAATCATGTCCACCATTTACAATAATCCAGTGGTCATCATCCGTGGAGCTACCGGCTGTGGAAAGACCACTCAGGTTCCTCAGTACATCCTGGACGAGTTCATTAAGGGAGGCAGAGCTTCCGATTGCAATATCGTTGTTACTCAGGTCAGTCCGGTGAAATGGTCATTTATTTTGTGCGTTGGCATACCACAAGGAGATCGCCTGTGTGACTTCCCTCTGCTGTTATTCCTCCTCCTAGCCAAGACGTATCAGTGCTGTTTCAGTGGCAGAACGCGTGTCTTTCGAGAGAGGTGAAGATGTGGGCAAAAGCTGTGGCTACAGTGTGCGCTTTGAGTCTTTCCTGCCCAGACCTCATGCCAGCATCCTCTTCTGCACAGTTGG[T/C]ACGTTCTAGTTTTTTAAATCCTTTACTCTGTAACACAAAAGCACTTGGTGATGTTGCTAAAAGACTTTTATTCACAGGGGTGTTACTGAGGAAGCTAGAGTCTGGTATCCGTGGGATTAGTCACGTGATCGTGGATGAAATCCATGAGAGGGACATAAATGTAAGACCATACCATTTGTTTTTAAAGGGAGAGTCAACCCAAACTAAAAATGTGCTCATTTTAATAGTTTCTTTTTTTCTGTTGAGCACAAAAGAAGATATTTTGAAGTATGTTTGTAGCTATTGATTTCCATTGTATGAAAAAATACTATGGAAATCAACAGCTGCTAATTTTCCACATTAATCAAAGTATCTGTTCAACATGAGATAAAGGTAAAGGGGAGTTACTCATGACATAATTTTTATTATTGGGTGAACTTTTCTTTTAAGTTAGTTACAGAGATGTGTGTTCGGTTTCACCAAATTCACACAAAAAAATTTTTCCCGTCTAGACTGATTTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18641
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111661 Essential Splice Site 790 1271 19 27
ENSDART00000134918 Essential Splice Site 790 1271 20 28
Genomic Location (Zv9):
Chromosome 2 (position 35587194)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 35883904
GRCz11 2 35866361
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGACCAGGCTTCTGCTTTCACCTGTGCAGTCGGGCTCGTTTTGAAAAG[T/C]ATGAAATCTCATTCTTYRTCTTAGTCTCCAAGTCAAACAGTATATGAAGT
Long Flanking Sequence:
ATTAATATGCTAGCATATAAAAATAAATCAGTATTTTATGCAATATTTAATGTGTCAGACACAAAATAGACACTTCAATTTGTTTAATATAAAATTAATAGTAATCTGACCAGTTAACCGTTAATAACCGATTAATGAGCAGCGGTTGTCGGTTAGCAAAATTAACTGAAATGAGCATCCCTACTGTCTACACTAATATTAGGTTAATAACAATTGGAACACAAAATTGCAAGTGCATTTGACATTTGTGTATGAGATTTTGAAATTGGCATTGTATCTTTTTACAGTGTATATGTCCTGTTTTGTCCACAAATGACTTGACAAATTTCAAACTTGTTTCATTCAGGCAGAAGGTGAAGCTGTTCACTTCTCACAACAATATGACAAACTACGCCACTGTGTGGGCCTCAAAAACCAACCTCGAGCAGAGGAAAGGGCGTGCTGGCCGAGTCAGACCAGGCTTCTGCTTTCACCTGTGCAGTCGGGCTCGTTTTGAAAAG[T/C]ATGAAATCTCATTCTTTATCTTAGTCTCCAAGTCAAACAGTATATGAAGTTCTTACTGTAATATTTGTCGTGCAGACTGGAGACCCACATGACTCCAGAGATCTTCCGTACGCCGCTGCATGAGGTGGCGCTCAGCATTAAATTACTGAGGCTTGGAGGCATTGGGAATTTCCTGTCCAAAGCCATCGAGCCACCACCATTGGATGCCGTTATTGAGGCTGAACATACTCTGAGAGGTAGAACTTCTGCTGCTTTTTTTTTTTTTCATACCAGTGATGTTCAGGTAAACAAAATCCAACAAGCAAATGTTGTTCCCCAGAGCTGGATGCTTTAGACAGTAATGATGAGCTCACTCCACTGGGACGCATTCTGGCCAAACTGCCCATCGAACCACGACTGGGGAAGATGATGATCATGGGATGCATTTTTAAGTAAGTTTCTTTATCCAGCGTTTTCTGTTTGTGAACTGGAGGAATATTTATGATGCAATCCTGTCATAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39875
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111661 Essential Splice Site 844 1271 20 27
ENSDART00000134918 Essential Splice Site 844 1271 21 28
Genomic Location (Zv9):
Chromosome 2 (position 35587432)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 35884142
GRCz11 2 35866599
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCCACCACCATTGGATGCCGTTATTGAGGCTGAACATACTCTGAGAGG[T/G]AGAACTTCTGCTGCTTTTTTTTTTTTTCATACCAGTGATGTTCAGGTAAA
Long Flanking Sequence:
TTGACATTTGTGTATGAGATTTTGAAATTGGCATTGTATCTTTTTACAGTGTATATGTCCTGTTTTGTCCACAAATGACTTGACAAATTTCAAACTTGTTTCATTCAGGCAGAAGGTGAAGCTGTTCACTTCTCACAACAATATGACAAACTACGCCACTGTGTGGGCCTCAAAAACCAACCTCGAGCAGAGGAAAGGGCGTGCTGGCCGAGTCAGACCAGGCTTCTGCTTTCACCTGTGCAGTCGGGCTCGTTTTGAAAAGTATGAAATCTCATTCTTTATCTTAGTCTCCAAGTCAAACAGTATATGAAGTTCTTACTGTAATATTTGTCGTGCAGACTGGAGACCCACATGACTCCAGAGATCTTCCGTACGCCGCTGCATGAGGTGGCGCTCAGCATTAAATTACTGAGGCTTGGAGGCATTGGGAATTTCCTGTCCAAAGCCATCGAGCCACCACCATTGGATGCCGTTATTGAGGCTGAACATACTCTGAGAGG[T/G]AGAACTTCTGCTGCTTTTTTTTTTTTTCATACCAGTGATGTTCAGGTAAACAAAATCCAACAAGCAAATGTTGTTCCCCAGAGCTGGATGCTTTAGACAGTAATGATGAGCTCACTCCACTGGGACGCATTCTGGCCAAACTGCCCATCGAACCACGACTGGGGAAGATGATGATCATGGGATGCATTTTTAAGTAAGTTTCTTTATCCAGCGTTTTCTGTTTGTGAACTGGAGGAATATTTATGATGCAATCCTGTCATATTTATCTCTGAAATTTAAAATTGAGAAACCAGTAATATATAATTATGAATACATAATAGTTTAGACTTTTTCAAAGCAAGTGAAGATCACAAAGGCTTCTAATTTATCAAAAGTACTGTACATATGTTAATACAGTGAGATGTAATAACAAAATACATTTTCATTAATAGATTATCATATTAAAAAGCTCTATTTAAAGGTCATATTGCAGGCCCATAATACTGATTGTTTTTTTTACA
Associated Phenotype:
Not determined