Busch Lab

ZMP

myo7aa

Ensembl ID:
ENSDARG00000061937
ZFIN ID:
ZDB-GENE-020709-1
Description:
myosin-VIIa [Source:RefSeq peptide;Acc:NP_694515]
Human Orthologue:
MYO7A
Human Description:
myosin VIIA [Source:HGNC Symbol;Acc:7606]
Mouse Orthologue:
Myo7a
Mouse Description:
myosin VIIA Gene [Source:MGI Symbol;Acc:MGI:104510]

Alleles

There are 10 alleles of this gene:

Allele Name Consequence Status Availability
sa44881 Nonsense Mutation detected in F1 DNA Not yet available
sa36566 Nonsense Available for shipment Available now
sa28974 Nonsense Mutation detected in F1 DNA Not yet available
sa11378 Nonsense Available for shipment Available now
sa28973 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa23224 Essential Splice Site Available for shipment Available now
sa16521 Nonsense Available for shipment Available now
sa36565 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa39188 Nonsense Mutation detected in F1 DNA Not yet available
sa44880 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa44881
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
ENSDART00000088945 Nonsense 34 2179 2 47
Genomic Location (Zv9):
Chromosome 18 (position 6530289)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 3109871
GRCz11 18 3442699
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCATGAGTTTGAGGTCCCGATCGGAGCTGTGGTGAAGCTCTGTGATTCT[G/T]GACAGATTCAAGTTCTGGATGATGAAGGAAATGTAAGTTAATGGCCACTG
Long Flanking Sequence:
GTAGATTTTGACCTTGTGGGGACTTCTTTTGGTATCCATGATGAAAAGGGCTCATAAATCACACAGAATGAAGTACTTTGAAACATGTTTCAAATGTTTCATATGTTGCAGATTGTTTCCTGTAAGATTTGGGTTTAGGGGAAAGAGGAGAGAATATACAGTTTGTACAGTAAATAATTATAATCAACTCACTAAAAAAAAAGTGGACAGAAAAAAAAGTATTTAGAATTGCTTATATTGCAAAAATGCTTAGATATCCATCCATAAATGTGTTGAATTATTTGATTATCCATTCTATTTTATTCTAAGGAATATATTTGTTTATTTATTTTTTTTTTTACATTTTTAAAATAACGCTTAGTGATGTCTGATAATGTGATGGCTGCACTGACATTAACAATGTCTGCACTGTGTTTCAGGGGGATTATGTCTGGCTGGACCTGAAGACGGGTCATGAGTTTGAGGTCCCGATCGGAGCTGTGGTGAAGCTCTGTGATTCT[G/T]GACAGATTCAAGTTCTGGATGATGAAGGAAATGTAAGTTAATGGCCACTGAACGCTGCTTTTTTCATATATGCACAACATTTATGTCAGTACTGGGATGTGTTTTTTCTCCTCGCTTAAATGATGTAAGATGATTGGGCAGATCCTGGATCTGTTAATCCTAATAACTCATCTCTCACTAATCTGGTTCTTCAAATAAGTTTGCAAATCAAATTAAAATATCTGGATGAATTGAAGGTGGCACAGTGGCTCAGTGGTTAGCATTGTCGCCTTACAGCAAGAAGGTTGCTGGTTCGAGTCCTGGCTGGGTCAGTTGTCATTTCTGTGTTTGGATGTTCCCCCCGTGTTGGTGTGGGTTTCCTCCGGGTGCTCCGGTTTCCCCCACAATCCAAACACATGCGCTATAGGGGAATTGAATAAATTGGTCGTAGTGTATATGTGTGTGTATGAATGTGAGAGTGTATGGGTGTTTCCCATTTCTGGGTTGCAGCTGGAAGGGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36566
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
ENSDART00000088945 Nonsense 1066 2179 23 47
Genomic Location (Zv9):
Chromosome 18 (position 6493270)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 3146890
GRCz11 18 3405680
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGTGACCTTCCCGAACCCAAATACCACACGGCCATCAGCGACGGCAGC[G/T]AGAAGATCCCTGTCATGACCAAAATCTACGAGACACTCGGAAAGAAAACC
Long Flanking Sequence:
ATATATATATATATATATATATATATATATATATATATACAGAGTAAAAAAAAAGTAAGTTTGTTGTTTTTTGTCTTACTTTAAAGTATTAGGATTATAGATTTTAATCAATTTTAGTAAATTAAATTGAAAAATAATCTTCTGCTTGGCAACTAGCATAAATAAAACAAGTCTAATTAATAAAACTATTTTAATTATCTGTTAACTATAAGAACCCTGCACATAGTGTTTACTGTATAATACTGTATGCAGTTGGAAGATTTGTTTTTGTCAAATTGAGTACTACTTTCTGAATACTGTCCAAATAAAAGCTTATCATAGAGAGCTTTAACTGACCTGATTATTTCAGATGTTTCTTTGACCGTTTCTTCATTCATGTAGAAGTGTTTAATGTAGATCTGCTGGTTCTGCAGGCGGCTCTGGCCGTGTGGATCACCGTCCTGCGCTTCATGGGTGACCTTCCCGAACCCAAATACCACACGGCCATCAGCGACGGCAGC[G/T]AGAAGATCCCTGTCATGACCAAAATCTACGAGACACTCGGAAAGAAAACCTACAAGAGGGAACTGCAGGCACTGCAGGGAGAAGGAGAGGTGCGTTCAGATGAGAAACAGTCAATAGCTTGTGTTTCCATACAAAGATGTGAATTAAACGTATGCACAAAACTGGAATATGGCATAAAACATTTGCACATAAAGCAACTTTCCCATCCAGCGAGTGAAAGAGAACAAAATCATCACTTGCTGATAAACTGGGAAGTGTTTTTTTGTGCAGTAGACGAAGCCACTGTGGTCTTTTTTCTTCTCTAATAAACGCATTGCGCCTCAGAAGATGTACATGAAATTCAATCAAAGCTATGCGGTGGCTTTTGGAGGCATGAGACGCTCTTTGGGAGGCGTAAACAGATGCTCAAGACAGTTTTGGAGGGAATAATAATATAATACTGAACTACTGTGATGAAGGACTGATGGCTGAGGGGTTTTAGAAATGAGAAAAACAACATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa28974
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
ENSDART00000088945 Nonsense 1396 2179 30 47
Genomic Location (Zv9):
Chromosome 18 (position 6483974)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 3156186
GRCz11 18 3396384
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTTCCGGGTGAAGGAGGATCTGGCGGAGCTGGCGTCGCAGCAGTATTA[T/A]GTAGATTACGGCTCTGAGATCCTCGTTGAGAGACTGTTGAGTCTGATTCC
Long Flanking Sequence:
AAAAAAACTATAAAATAGCAGTTTTGGACACCAATCAATCTGGTTTCAAAAGTAGACACAACACTGAGACTGCACTAAGAAACGGTTGTCTGTGTTTTTGGACCGCTTAACTTTTCTATTTGACATGGCATCACACGGTGTGTCATTCAGAAACATGTAACGATGTCAGGATATCGATATGTCTGACAGATATTTTTTTTAGATGATGCACTTGTCACATTCGACTAAAGTTTTGTTCAGCAAACACAGACAATGCAGAAATCACATTAGGCAGATTCATTTGGTCACCTTCAGGGAGACCAGTACATAAGCAAAGTGCTATTTTGGGTCTTTTGAAACGCCATACCAAAAGTTTTCACTCACCCGCTGTATGTCTAATGTGGGGATATTATCTTTCTCTTGTTTGTTTTTTTACATTGATTTTTCCTTCTCTATCTATCCGTCTTGTGTGTTTTCCGGGTGAAGGAGGATCTGGCGGAGCTGGCGTCGCAGCAGTATTA[T/A]GTAGATTACGGCTCTGAGATCCTCGTTGAGAGACTGTTGAGTCTGATTCCCTCCTACATCCCGGACAGAGAGATCAGCTCGGCCAAGACTGTGGAGAGATGGGCTCAGTTCATCATGGCTGCGCACAAGAAGGTGCCAAAACTTAATCTTAAACCTTGTGGAATTGAACATGTGTGTATTGTGTAGAATAATTAATAACACTGAATGCTGGATGCATTATTTAAATGCAATGCAAAATATTACAAATAGTTTTAGGCTAAGTTGGATTTCAGTATTCTTGTTCATAAAATGCCGTCAAATTAAGAATTGTTTTTTTAAAAATTAAGTTAAAACTCTGATAAAAAAAAAAAAATGCACTAAGATAAAAAAAGAAGAACCTGAGCATAATATAAATGGTCATGAAAAAGTAACATATGTAAACATATAGGTAGGTCCAGACGGAATCTGCGGACATTTTTTGCCATTTCTGCTGAGAATTTTGGAATTATAATTTTCCAATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11378
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
ENSDART00000088945 Nonsense 1415 2179 30 47
Genomic Location (Zv9):
Chromosome 18 (position 6483917)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 3156243
GRCz11 18 3396327
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACGGCTCTGAGATCCTCGTTGAGAGACTGTTRAGTCTGATTCCCTCCYA[C/A]ATCCCGGACAGAGAGATCAGCTCGGCCAAGACTGTGGAGAGATGGGCTCA
Long Flanking Sequence:
ACAACACTGAGACTGCACTAAGAAACGGTTGTCTGTGTTTTTGGACCGCTTAACTTTTCTATTTGACATGGCATCACACGGTGTGTCATTCAGAAACATGTAACGATGTCAGGATATCGATATGTCTGACAGATATTTTTTTTAGATGATGCACTTGTCACATTCGACTAAAGTTTTGTTCAGCAAACACAGACAATGCAGAAATCACATTAGGCAGATTCATTTGGTCACCTTCAGGGAGACCAGTACATAAGCAAAGTGCTATTTTGGGTCTTTTGAAACGCCATACCAAAAGTTTTCACTCACCCGCTGTATGTCTAATGTGGGGATATTATCTTTCTCTTGTTTGTTTTTTTACATTGATTTTTCCTTCTCTATCTATCCGTCTTGTGTGTTTTCCGGGTGAAGGAGGATCTGGCGGAGCTGGCGTCGCAGCAGTATTATGTAGATTACGGCTCTGAGATCCTCGTTGAGAGACTGTTGAGTCTGATTCCCTCCTA[C/A]ATCCCGGACAGAGAGATCAGCTCGGCCAAGACTGTGGAGAGATGGGCTCAGTTCATCATGGCTGCGCACAAGAAGGTGCCAAAACTTAATCTTAAACCTTGTGGAATTGAACATGTGTGTATTGTGTAGAATAATTAATAACACTGAATGCTGGATGCATTATTTAAATGCAATGCAAAATATTACAAATAGTTTTAGGCTAAGTTGGATTTCAGTATTCTTGTTCATAAAATGCCGTCAAATTAAGAATTGTTTTTTTAAAAATTAAGTTAAAACTCTGATAAAAAAAAAAAAATGCACTAAGATAAAAAAAGAAGAACCTGAGCATAATATAAATGGTCATGAAAAAGTAACATATGTAAACATATAGGTAGGTCCAGACGGAATCTGCGGACATTTTTTGCCATTTCTGCTGAGAATTTTGGAATTATAATTTTCCAATTATTTTGGAAGTATCACAACTAAAACCTTAATATGTGATTATAATAAAATCTTTTAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa28973
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
ENSDART00000088945 Essential Splice Site 1480 2179 31 47
Genomic Location (Zv9):
Chromosome 18 (position 6482227)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 3157933
GRCz11 18 3394637
KASP Assay ID:
2261-1802.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTGGCCTTTATTATTCTCCAGATTCTACGAGGCCTTCAAGTTTTCAGG[T/A]ATTTATTTTTTCGTTATGTCAGATTAATGTGAGAAACTGCAGGCAAAAAC
Long Flanking Sequence:
ACTGCGTAAAAAAACGTGCTGGATAAGTTGGCGGTTGATTCTGCTGTGGCGACCCCAGATTAATAAAGGGACTAAGCCGAGAAGAAAATGAATTAATGGATGACGTAAAATTGTAAATAAATGAACAAAATCATCTTTAAATTATACTGATAAATTGCATTTTTTTATATCCCACAATAAAAACATTGAAATAAGACACCACATTCATGTTATAATTGTACTTTTATTAAACAAAAAGCAGCCTTAGGGTGCAGAAGGCATAAAGAATGTATTTTCAAACTTTTGCCTCGCACTGTAGAGTAAATAAACACAATGAAGCCGAAATGAACCATGTAATTTGATTGTTGCAATGAAATCAATAGAGTTGTGTTTGATTTGTAGGGCGTCTACACTCAGAAGAGGGTGGATCCTCAGAAAGTCAAGGAGGAAGTTGTTGATTTTGCACGTTATAAGTGGCCTTTATTATTCTCCAGATTCTACGAGGCCTTCAAGTTTTCAGG[T/A]ATTTATTTTTTCGTTATGTCAGATTAATGTGAGAAACTGCAGGCAAAAACTTTTCATTCACCAGTCCGGTTTGAGTTTTGCTTTTTTCTCTTCTTTTCCTCATTGTGTTTTTCTGTATAATATATATAAAACAACTAAAATCATCATAATTCTCCACTTTAGAAGCTTTTACATACACCAGACTTCACAGTTTTATTCATACATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTCTGAAGGTTTTTACTGAGGGATTTGTTCAAAAATAATAAGCATTTAATGCACAAAAAGGTTCTGTCTGCTCACAGTATTTCCTGAGTTATAAAGTGATAAAAGGTAATTTTTAAAATCCACTTTTAAAAATATTTAAAAATCCAATATATATCCAATATAAGTGCATATTTAATGACTGAATATCTCATTTGCATAGTTACACAACATTGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23224
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088945 Essential Splice Site 1522 2179 32 47
Genomic Location (Zv9):
Chromosome 18 (position 6481398)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 3158762
GRCz11 18 3393808
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTTCTGGAGCTCTCCTTCCCAGAGATCACAGCCGTGTCCAGCAGCAAG[T/C]ACGACTTTAATACTGTGATTTACCTGCAGGGATTATACAGCTGAAGAGAA
Long Flanking Sequence:
CATTTAATGCACAAAAAGGTTCTGTCTGCTCACAGTATTTCCTGAGTTATAAAGTGATAAAAGGTAATTTTTAAAATCCACTTTTAAAAATATTTAAAAATCCAATATATATCCAATATAAGTGCATATTTAATGACTGAATATCTCATTTGCATAGTTACACAACATTGTAGATATCTTCTAATATAAAAACTTAAACATGGGCAATATTCTGCTCGTTTTGCAACTCATCCGTATAGTGCGTAATATTCAATCTCTGTCCACTGATTGGTTGATTGTGTTACTATTTGTCTATGTTTTAGTTCTTACAGAAATATTGCAGGTTTTATGGCTGTATGTTTGTGTGATGGGCTTGCCGTATTGTGTTTTTAGGTCCTAGTTTACCCAAGAATGATGTGATCGTGGCTGTAAACTGGACCGGTGTGTATTTTGTGGACGAGCAGGAGCAGGTTCTTCTGGAGCTCTCCTTCCCAGAGATCACAGCCGTGTCCAGCAGCAAG[T/C]ACGACTTTAATACTGTGATTTACCTGCAGGGATTATACAGCTGAAGAGAACATTATTAGCATTTTTTACACCCATTTTATTTAATGTTTCAAACATTTACCAAGTGCTGTTTAACAGTACAAGGAATTTTTTCTCAGTATTTTGTATTATAATTTACTTTTGGAGAATTATTTTTTTTTCCTTTTAGTTTGGCTGGAATAAAAAAAATAAATATGATATTAATTAATATTAATTATATAATATTATTAGAACTCTTAAGAGATTATATTTTTTGATTGGCTACAGAACAAACCACTGTTGTCTAGTGACTTGCCTAATTAGCCTAAATTGCCTAGTTAACTCTTTTCCCACCGTTGATAATTTTTGAGAGTTTGTGTTTTAGGTAGATAATGGTAAGGGAAGCCCTAACATATGTCATGGGTGAGTTTCAGGACTTCTGGTTCTCCTGTGAGCGAGATAAAAGACAATCAGAGAAAGTAAAATCAGATTGCATGTAAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16521
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088945 Nonsense 1742 2179 37 47
Genomic Location (Zv9):
Chromosome 18 (position 6472160)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 3168000
GRCz11 18 3384570
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTGTGTWTGATYCTCCTTGACCGTKTKTCCTGCACCAGTAATGAAGTA[T/A]ATGGGTGATTATCCGTCTAAACGCACACGCTCAGTGAACGARCTCACGGA
Long Flanking Sequence:
ACCCACGCGAACACAGGGAGAACATGCAAACTCCACACAGAAACGCCAACTGAGCCGAGGATCGAACCAGCAACCCAGCGACCTTCTAGCTATGTGGCGACAGCACTACCTACTGCGCCACTGCTTCGCCCTATATTATATTATATCATATAATAAATAAATATTTGATTTTTAAAAATATATATTTTTTAATAATAATCATTTTATATTTTTTCTTCATGTCTGGCTGACCTAGACCAGAAAATACTTTATGAAAAGCATACTTTAGTATATTTTTCAAATTAATTTTATTTGTATGTTAAATGATGCTTGCTTCTTCCACTTAATGCAACAAACACTTTCATATTTGTATTTATTTATATTAATTATGGGCTTAAATTACCTGGTCTCCCAAAAAGTTTTTTTTTTCCTTCAAATTAAGCTCTAAAATATCCTTTAATTTGCAGTGTATTGTGTGTTTGATCCTCCTTGACCGTGTGTCCTGCACCAGTAATGAAGTA[T/A]ATGGGTGATTATCCGTCTAAACGCACACGCTCAGTGAACGAGCTCACGGATCAGATCTTTGAAGGAGCGCTGAAGGCTGAACCACTCAAAGACGAGATTTACTGTCAGATCCTTAAACAGCTGACAGAAAACCACATCAAGTACGTCATTTATAAACACTCTATAGTGGTCAAAAGCTTACACTAAAAAATTTAGTATTCTAGTCCAAATATCTACAAATTCGTAAATCAAGACATATTTTCCAGACAAGCAAAAGAATATTGCCTTGTTTTCAGAAATAATATGTCAAAATGAAGTGAGTTTTTCTTTAAATAAGCAACATTAATCTGCCAGTGGGGTCAGCAAAATAATCTTTGATCTCAATTTGAAGTAAGATTATTTTCCTGACCGCATTGACAGATTATTTTGCTTGTTTTGGAGAAAAACTCACTTCATTTTGACATATTATTTCTGAAAACAAGACAAATTGTTCTTTTTGCTTGTCTAGAAAATATATTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36565
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
ENSDART00000088945 Essential Splice Site 1789 2179 37 47
Genomic Location (Zv9):
Chromosome 18 (position 6472019)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 3168141
GRCz11 18 3384429
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACGAGATTTACTGTCAGATCCTTAAACAGCTGACAGAAAACCACATCAA[G/T]TACGTCATTTATAAACACTCTATAGTGGTCAAAAGCTTACACTAAAAAAT
Long Flanking Sequence:
TATATCATATAATAAATAAATATTTGATTTTTAAAAATATATATTTTTTAATAATAATCATTTTATATTTTTTCTTCATGTCTGGCTGACCTAGACCAGAAAATACTTTATGAAAAGCATACTTTAGTATATTTTTCAAATTAATTTTATTTGTATGTTAAATGATGCTTGCTTCTTCCACTTAATGCAACAAACACTTTCATATTTGTATTTATTTATATTAATTATGGGCTTAAATTACCTGGTCTCCCAAAAAGTTTTTTTTTTCCTTCAAATTAAGCTCTAAAATATCCTTTAATTTGCAGTGTATTGTGTGTTTGATCCTCCTTGACCGTGTGTCCTGCACCAGTAATGAAGTATATGGGTGATTATCCGTCTAAACGCACACGCTCAGTGAACGAGCTCACGGATCAGATCTTTGAAGGAGCGCTGAAGGCTGAACCACTCAAAGACGAGATTTACTGTCAGATCCTTAAACAGCTGACAGAAAACCACATCAA[G/T]TACGTCATTTATAAACACTCTATAGTGGTCAAAAGCTTACACTAAAAAATTTAGTATTCTAGTCCAAATATCTACAAATTCGTAAATCAAGACATATTTTCCAGACAAGCAAAAGAATATTGCCTTGTTTTCAGAAATAATATGTCAAAATGAAGTGAGTTTTTCTTTAAATAAGCAACATTAATCTGCCAGTGGGGTCAGCAAAATAATCTTTGATCTCAATTTGAAGTAAGATTATTTTCCTGACCGCATTGACAGATTATTTTGCTTGTTTTGGAGAAAAACTCACTTCATTTTGACATATTATTTCTGAAAACAAGACAAATTGTTCTTTTTGCTTGTCTAGAAAATATATTTTTATTTAAGAATTTTTTGTGTGTGTATTTGTGTGAGTTTGTGACTGTGTGTATGTGTGTTTATCCATGTTTGTGATGTGTTTTGGTGCATGTATGTGTGCTAATTGTTAACACACGTACACATTTGTTTTGTTTGTTTTATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39188
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
ENSDART00000088945 Nonsense 1817 2179 38 47
Genomic Location (Zv9):
Chromosome 18 (position 6471196)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 3168964
GRCz11 18 3383606
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTGTGTGTTGGTCTCTTTCCTCCCAGTAATGTCCTCTTACCACACGTC[C/T]AGCGCTTTCTACAGTCCAAGAAACATCATCCTCTGGCTCTGGACTGCATG
Long Flanking Sequence:
AAATTGTTCTTTTTGCTTGTCTAGAAAATATATTTTTATTTAAGAATTTTTTGTGTGTGTATTTGTGTGAGTTTGTGACTGTGTGTATGTGTGTTTATCCATGTTTGTGATGTGTTTTGGTGCATGTATGTGTGCTAATTGTTAACACACGTACACATTTGTTTTGTTTGTTTTATTTAAATTCATTTTGAGATATACTGTAAATATTTATATATATTTTGACATATTCTGTGTCTGTCTGTCTGTCTGTCTGTCTCTTTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTTTGTCTGTCTGTCTGTCTGTCTGTTTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTTTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTATGTGTGCAGGTACAGTGAGGAGAAGGGCTGGGAGCTGCTCTGGCTGTGTGTTGGTCTCTTTCCTCCCAGTAATGTCCTCTTACCACACGTC[C/T]AGCGCTTTCTACAGTCCAAGAAACATCATCCTCTGGCTCTGGACTGCATGCAAAGACTACAAAAAGCCTTACGGTGAACACACACACACACACACACCAGCCGTGGAGTTGTTCTTCAGTAGGAATTTAGCAGAGACATCTGCATTACACTGAACTAAGCTGCAACAGTGACATTTATACTGAAACCGTTTCAGCAAAAAAAATATATATATTATTATAGCTGTTACTCTCTTTTCTTCATCTATGTTATCCTCTTAACAGCCCAAGCTGTTTTTAACATGCATTTTTTATTTCTCTTTGCTTTTTGGGCTTATTGGAACCTAATAAGAATATAACCTACGAATCATCTTTTGATATGATGTACTTTTAGAGAAAAATGATGTCCATATATGTGGACTCGTGGTCTGAATTTCCATATAACACAATAAAGTCACCTTTGTGAAAACGCTTTATTTCTGCCTTGAACACAGCAGTTTTTTTCCTGATTGTTTTTAATGCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44880
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
ENSDART00000088945 Essential Splice Site 1876 2179 39 47
Genomic Location (Zv9):
Chromosome 18 (position 6467395)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 3172765
GRCz11 18 3379805
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCACGCAGATCTTTCACAAGGTTTACTTCCCTGATGACACAGATGAGG[T/G]CAGACTCGTTCATCTGCACAGGACAGATTGAGCTTTTCATGTGGTTCTGA
Long Flanking Sequence:
TGGGTTTGGACTGGCCCAGCCGGGATTCGAACCAGCAAACATCTTACTGTGAAGCAACAGCTCTGTAGAATATTCAAATGCCATTTTAGATCAACTTTGAGATGCAGAAATCAAAAATTTACATTAATTTTAGTTCAGGTTTGAGAAAATTGGTTGTATTGTCATTTATATTAGTTCAAAGATGTCCTTTTAACAGTATAATCTTTTTAGTTTAGTTGTAGTTGTTAGAACTACTTTTTGAAATGTAGTATTAGTTGTTGAGTGTTTTTCCAGTTTTTTCTTTTGTCTGTCGGCTCCCAGTGAATACAAGTCTTTAATGGAGTTGTTATCTGGTTCTGTTGAATATGAAGGACAGCATGACTCATCATAAACTCTGTATGTCTATCTGTGCAGGAACGGCTCCAGGAAATATCCTCCTCACCTAGTGGAGGTGGAGGCCATTCAACACAAAACCACGCAGATCTTTCACAAGGTTTACTTCCCTGATGACACAGATGAGG[T/G]CAGACTCGTTCATCTGCACAGGACAGATTGAGCTTTTCATGTGGTTCTGATGTGACGCTTATTAATGGGACGTCTTGATATTTAAGAACGCTAACGTGACTATCGTTACATGAAATAAGAGCTTCACATTTCTGCTTTTAACCCTGCAGGATGTAATCGATCAAATAATTGACTAAAGCCGCCTTTCCACTGCACGCGACATTTGGACACGACTGTCAAAATACGCCCCCTTGTGGCAGTCGCACAGTATTTTCAGTGTTGTCATGCACCATGGGAGAGATTCTCAAGCTGCGTCAAATGGCACACTATACACTATGCACTCATGCACTCATGCACTATGTACTTATGCACTTACACACTCAACAGGATAGTATATGTTTTAGTATAGTGTTGTCCCAAATGGCACACTAATGTTTTTTTACTAAGCGAAAATTCAAACCGTTTCCCTGATGACGTTTGACGGTTGCCAAATCAGTGAAATAAATGAGCAAACTATCAAA
Associated Phenotype:
Not determined