Busch Lab

ZMP

ENSDARG00000058782

Ensembl ID:
ENSDARG00000058782

Alleles

There are 13 alleles of this gene:

Allele Name Consequence Status Availability
sa22993 Nonsense Available for shipment Available now
sa36307 Nonsense Mutation detected in F1 DNA Not yet available
sa17887 Nonsense Available for shipment Available now
sa39142 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa22994 Essential Splice Site Available for shipment Available now
sa42865 Nonsense Mutation detected in F1 DNA Not yet available
sa45591 Nonsense Mutation detected in F1 DNA Not yet available
sa36308 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa36309 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa36310 Nonsense Mutation detected in F1 DNA Not yet available
sa39143 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa22993
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000081721 Nonsense 142 1871 4 40
Genomic Location (Zv9):
Chromosome 17 (position 6618210)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 6697146
GRCz11 17 6854376
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGTTTTGTCTCCTGAAGGATTCCGATCTTCATAAAGTGACCGATGCTT[T/G]AAAGCAGCTCATTACATCAGTTTGCCAACCAGAAGCTTCATCCCTTAAAG
Long Flanking Sequence:
TGTTTATGGAGTCTTCTCTACTAGTATAGCTGTTTAACCATGTGGATGGATGATAACAGCCTTCTGAGCCAACCAGTAAACGCAGATGGCCCCTACTGGCCCATATCTATAAGCTAATAACTACTGATAATACCCATTCAATCGAATGATAACATTCGAAGTAGGTGAACCAATGCTGAGCAGTCATTAGCAAAAATATTGTTCACTGTTAACGAATGCAGGATAATGCATTATAGGAATAGTTCATCCAAAAACTAAAATATTCGCATCATTTACTCACCCTCAAGTGCTTCCAATCCTTTATGAGTTAATTTATTCTGTCAAACACAAAAGAAGATATTTTGAAATATGTTAGAAAGCAAATACTCTGGAAGTCAGTGCTTTCATGTGAATGTTGGTCATTTTAAGTAACAGTGGAATTAGTCCTGTATCCAGCATTGCTCCACTGATGCTGTTTTGTCTCCTGAAGGATTCCGATCTTCATAAAGTGACCGATGCTT[T/G]AAAGCAGCTCATTACATCAGTTTGCCAACCAGAAGCTTCATCCCTTAAAGATACCTCTGATGTGTGGAGAAACATTTATAACACAGCAAACATGCTTCAGGTGAGTATCAGTAGAGAAATAGATGCTTTAAAATTATATTCTCAAGATCAACATAAAAGCACACTCAGTTTTTAAATACACGGTCCTATTGTGTTTTGTTTTTGGTTTAACGGTTCATTTAAAGCAGAGATGCCCAAAGGTGGCCCATGTTAACCTTTCATTTGGCATGCCATCCAATTGTCTTGTCAATTTTAATGTAATTTTTTTAATAAATGCTGAGCTACAAAAAATAGCCACTCTGTCACTTGACTGAAAGATGCAGAAGAAATGCAAAAGAAATTCGTGAGCAAATTAAGCCACAGATCAACTAGTAGTGTATTCCACTTTGGGATTATTTCTGTTTTTAGTGCAGTAATTTCATTATAAAATGATACCGCATTATTACTTAATATGATTTAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36307
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
ENSDART00000081721 Nonsense 151 1871 4 40
Genomic Location (Zv9):
Chromosome 17 (position 6618236)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 6697172
GRCz11 17 6854402
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTTCATAAAGTGACCGATGCTTTAAAGCAGCTCATTACATCAGTTTGC[C/T]AACCAGAAGCTTCATCCCTTAAAGATACCTCTGATGTGTGGAGAAACATT
Long Flanking Sequence:
TAGCTGTTTAACCATGTGGATGGATGATAACAGCCTTCTGAGCCAACCAGTAAACGCAGATGGCCCCTACTGGCCCATATCTATAAGCTAATAACTACTGATAATACCCATTCAATCGAATGATAACATTCGAAGTAGGTGAACCAATGCTGAGCAGTCATTAGCAAAAATATTGTTCACTGTTAACGAATGCAGGATAATGCATTATAGGAATAGTTCATCCAAAAACTAAAATATTCGCATCATTTACTCACCCTCAAGTGCTTCCAATCCTTTATGAGTTAATTTATTCTGTCAAACACAAAAGAAGATATTTTGAAATATGTTAGAAAGCAAATACTCTGGAAGTCAGTGCTTTCATGTGAATGTTGGTCATTTTAAGTAACAGTGGAATTAGTCCTGTATCCAGCATTGCTCCACTGATGCTGTTTTGTCTCCTGAAGGATTCCGATCTTCATAAAGTGACCGATGCTTTAAAGCAGCTCATTACATCAGTTTGC[C/T]AACCAGAAGCTTCATCCCTTAAAGATACCTCTGATGTGTGGAGAAACATTTATAACACAGCAAACATGCTTCAGGTGAGTATCAGTAGAGAAATAGATGCTTTAAAATTATATTCTCAAGATCAACATAAAAGCACACTCAGTTTTTAAATACACGGTCCTATTGTGTTTTGTTTTTGGTTTAACGGTTCATTTAAAGCAGAGATGCCCAAAGGTGGCCCATGTTAACCTTTCATTTGGCATGCCATCCAATTGTCTTGTCAATTTTAATGTAATTTTTTTAATAAATGCTGAGCTACAAAAAATAGCCACTCTGTCACTTGACTGAAAGATGCAGAAGAAATGCAAAAGAAATTCGTGAGCAAATTAAGCCACAGATCAACTAGTAGTGTATTCCACTTTGGGATTATTTCTGTTTTTAGTGCAGTAATTTCATTATAAAATGATACCGCATTATTACTTAATATGATTTAAAGCAACGTTTTCTAGTTATTTTTAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17887
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
ENSDART00000081721 Nonsense 168 1871 4 40
Genomic Location (Zv9):
Chromosome 17 (position 6618289)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 6697225
GRCz11 17 6854455
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAGAAGCTTCATCCCTKAAAGATACCTCTGATGTGTGGAGAAACATTTA[T/G]AACACAGCAAACATGYTYCAGGTGAGTATCAGTAGAGAAATAGATGCTTT
Long Flanking Sequence:
ACGCAGATGGCCCCTACTGGCCCATATCTATAAGCTAATAACTACTGATAATACCCATTCAATCGAATGATAACATTCGAAGTAGGTGAACCAATGCTGAGCAGTCATTAGCAAAAATATTGTTCACTGTTAACGAATGCAGGATAATGCATTATAGGAATAGTTCATCCAAAAACTAAAATATTCGCATCATTTACTCACCCTCAAGTGCTTCCAATCCTTTATGAGTTAATTTATTCTGTCAAACACAAAAGAAGATATTTTGAAATATGTTAGAAAGCAAATACTCTGGAAGTCAGTGCTTTCATGTGAATGTTGGTCATTTTAAGTAACAGTGGAATTAGTCCTGTATCCAGCATTGCTCCACTGATGCTGTTTTGTCTCCTGAAGGATTCCGATCTTCATAAAGTGACCGATGCTTTAAAGCAGCTCATTACATCAGTTTGCCAACCAGAAGCTTCATCCCTTAAAGATACCTCTGATGTGTGGAGAAACATTTA[T/G]AACACAGCAAACATGCTTCAGGTGAGTATCAGTAGAGAAATAGATGCTTTAAAATTATATTCTCAAGATCAACATAAAAGCACACTCAGTTTTTAAATACACGGTCCTATTGTGTTTTGTTTTTGGTTTAACGGTTCATTTAAAGCAGAGATGCCCAAAGGTGGCCCATGTTAACCTTTCATTTGGCATGCCATCCAATTGTCTTGTCAATTTTAATGTAATTTTTTTAATAAATGCTGAGCTACAAAAAATAGCCACTCTGTCACTTGACTGAAAGATGCAGAAGAAATGCAAAAGAAATTCGTGAGCAAATTAAGCCACAGATCAACTAGTAGTGTATTCCACTTTGGGATTATTTCTGTTTTTAGTGCAGTAATTTCATTATAAAATGATACCGCATTATTACTTAATATGATTTAAAGCAACGTTTTCTAGTTATTTTTAAATATTTGCAAATAAATTAGGAAATTACGAATGGTAAATTTAATGTAATACAGTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39142
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
ENSDART00000081721 Essential Splice Site 199 1871 5 40
Genomic Location (Zv9):
Chromosome 17 (position 6620429)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 6699365
GRCz11 17 6856595
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTACCCAAATATGCAGATCAGAGGCCCTCTGAGAGAAAGAGTGAAGGG[T/G]AATTTTAGGCCCAAAAAGGCTTTTCTTACTTAGAGTTTTTGTCTTGTTTC
Long Flanking Sequence:
ATCACTTCATAATTCAGAAAATAGTGCAAACAGGAAAGTAAATGTAATTTCAACATTTCATTGTGAAATAAAATGTTGTATAATCAGACAAATAACATACTGTATGAACATATCACTGTGTAAAAACCCTCAGAAAAGATAGATCTGAATAAAATAGTGAAGCCTGGTGTTTGTAAGTGTGGCTGAAATAAAAATTTAGAGAAAATACGCATTTTGTAAAAATAAATTTAAAATCTTCAGCCACAAACTGATCAACTCTGAATAAATATACACTTAAAAGTTTATTCTAAGTGCATTTTTTCTTTCCATCACACTGGAAAATCACTTTATGAAGGGCCAAAATCTCAAAACTGACACATGCATGAAAACAGTATTTCTCAACTTTTTAAATTCAATTTTTTTAATGGTTGTGTGCATTTTTTTTTCAGGTGACTACTGGACAAATGATTCGTTTACCCAAATATGCAGATCAGAGGCCCTCTGAGAGAAAGAGTGAAGGG[T/G]AATTTTAGGCCCAAAAAGGCTTTTCTTACTTAGAGTTTTTGTCTTGTTTCTAGTTCAAATATCTAAAAATTATTAAATTAATAAGTATTATCTCAACAAGCAAAGCATATTGTCTGGTTTAAAGAAGCAATGTGCCAAAATAAGTGAGTTTTTCCATTAAGCAAGCAAAATAAAGGAAAGTAATCAACATAGGTTCATTCTGAAAACGTAGCCCTATGTACATTTTTGGAGATCGCGAATTATGTAGCCACAAGTATGTGTGGCTGCATTTTGTCTATAAAATGCACTCTATGAGGCGGTATGATGCTGTTTCTTTTCGCACTCACCGGCTGACCGCTTACCTAAGTATGGATGGCTTTTCCGCTGTTACCAGTTTGTCCAGTGGCTCGCCGCGTACGTTGGCGAACTTGAGACGCAGAGAGGAGTTGACCGTATTGACGGGGTTCGAGTCTGGTTAAGAACAGTTCCAGAAAGCAGGAAAGACGAAAACAAATCCAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22994
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000081721 Essential Splice Site 715 1871 15 40
Genomic Location (Zv9):
Chromosome 17 (position 6641707)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 6720643
GRCz11 17 6877873
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAGTTGGAAAATACATTCTTGTTGATTTTGGCTTCTTTCTTTTTTTCT[A/G]GGTTTATCCCAAACAGTCTTCCTCTTGCTGTTCAGGAACTTGATGAAAAT
Long Flanking Sequence:
ACTAGCTTATAGAGATCCTTAAAACTAACATACTGATACTAATGTCTACAAAAAAACTTTATCTTAATTTCATGGAACCTTTAAAACCAACCAACTACAGTAGGTGTTTTGCAGCCTCAATGCTGTAATCAGTAGTTGTTTTCAAGTCCAGGATGAGTATTTAACAAGATTTAGGAGCCGTTCACTTTTACACTTTTCACGCTTTTACTGTTAACATACCTAATTCTTTAAAAACTTTGTGTAAATGTGCTCTAGGAAATATTTTTTAATTATTCGTACTAATTTATTTTGTGCCTTTTGCTATTTTTCCTTCATATTCTGTGAGCAGCTACTATACCAAAATGAGGTAGCATAATCAAAAGCTGTTCATTTGAGGTACTTGAGCTCAATCACTCAAACATCGAATACAATTTTTTTCAAAGCACTTCACAGGACCTTTAAGTTTTCTTGAACAGTTGGAAAATACATTCTTGTTGATTTTGGCTTCTTTCTTTTTTTCT[A/G]GGTTTATCCCAAACAGTCTTCCTCTTGCTGTTCAGGAACTTGATGAAAATCATATCTGCAAATTCAGCTTTCGATCGAAAGAAGCAGTTTTACAGGTAATTACACAATGATTGACAACACAGGTCTGTGTCTGGGAAGAAAATCTGATGATGTTTCAAACAAAACAAAGCAAAATTTTGTTTCTAAACTTGCATGAGTTTCTTTTTTCTGCTAAAACCAAAAGAAAATATTCTGAAGAATGTTGGAAACCAAAAAAATGCATGGTCCTCACTGACTTTCATAGTAAGTGACTAAAAATACCATTTCAGTCAAAAGGGGACCAACAACTGTGTGCTTTCCAACATTCTTCGAAATAACTTCTTTTGTGTTTTTTTATTTTTATTTTTAATTGTAGCATCCCTACAAGTGATTAATATTTCTCCATCTTTTTAAAAAGGCCACAAAATGCCATATATTGTGAGGAATTTCATGAAGAACAAAGCAGTTATGATTATTGGAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42865
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000081721 Nonsense 923 1871 19 40
Genomic Location (Zv9):
Chromosome 17 (position 6648246)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 6727182
GRCz11 17 6884412
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATAATGGGCAAACCTGAAGACCCCCGAGCAGACCTGCAGGCCGAGGGC[A/T]GACCAAGTCCTGATCCCAGGTGAACATGTGGAGGGAAATTAGGTGATATT
Long Flanking Sequence:
GAAGCATTCGACTACTTTAGTAACTGTTTGTGCTCGTTTAAGAGAAAATTATCCACAAAGTGGCACAAATGGATTTGCCATTTAAACAATGTGGTGCAAAACTTGAAAATTTACAGTTGTGCTGGTCTGAAAATAGCAACAAATCACGCCAAACACATCTTGCTCCTTTTTGTGACGGGTATATGATAGGGCCCCAAGCCCAAAAGGTAAGGAAAGTAACACGAAAGTAACTCAAAGTAACGTAACGCATTACTTATCATAAAAGTAACTATGTACTAGTTTAGGGAGTAACTCAACATTGTATTGCATTACTTTATGTACTGCATTACTTTGTGTCTTGCAGGTTTAATGAGCGTGTATGTGAGTGTTTTGTTCGAGGGCAGCTGATCTCTCTAACCTTCAGTCTCTTGTCACTGCTGCGTGAGGTGCCACACATCAGAGACCAGCACTTCATAATGGGCAAACCTGAAGACCCCCGAGCAGACCTGCAGGCCGAGGGC[A/T]GACCAAGTCCTGATCCCAGGTGAACATGTGGAGGGAAATTAGGTGATATTGAAGAAAAATTTGATATGCCAAGAGCATGTTAAATAATTTGATTCTTAAATAATGCAATATTTGTAAAAAAATAAATAAAAAAATAAGCAAAAACAATGATGTAACATATAGTTAAAGTCTTTCAATTATTACTAATGATACACACACACACTGGCCACTTTATTAGGTACACTTGTCCAACTGCTCGTTATCCCAAATTTCTAATCAGCCAATCGCATGGCAGTAACCCACAGCATTTAGGCATGTAGACATGGTCAGGATGATCTGCTGCAGGTCAAACCGAGCATCAGAATGCGGAAGAAAGGTGATTTAAGTGACTTTGAACGGGGCATGGTTGTTGGTGCAAACAGGCTGGTTTGAGTATTTCAGAAACTGCTGATCTACTCGGATTTTCACGCTCACCCATCTCTAGGGTTAACAGAGAATGGTCCGTAAAAGAGGAAATATCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45591
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000081721 Nonsense 1123 1871 24 40
Genomic Location (Zv9):
Chromosome 17 (position 6658818)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 6737754
GRCz11 17 6894984
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTGAATTTTGCTTCAATTCCGTTTGTGGTTTCAGGCCCAAAAATTATA[T/G]CCATGGAGATCTTTCCTTGCAATTCATGGATTACATCCCTTGGTCATGTG
Long Flanking Sequence:
CCTGGAGAAAGTCTTATTATTATTATATTTTTTGCTAGAATAAAAGCAGTTTTTAATTTTTAAAAACCATATTAAGGTCAATATTATTAGCCCCTTTAAGCTATATATATTTTCTGATAGTCTACAGAACAAACTATCATTATACAATAACTTGCCTAATTACTCCAACATGCCTAGTTAACCTAATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGGTGTAAAGAAGTGTCTTGAAAAATATCTAGTCAAATATTATGTGCTGTCATCATGGCAAAGATAAAATAAATTGGTTATTAAAAATCAGTTATTATTATGTTTAGAAATGTGTTGAAGAAATCTTCTCTCCGGTAAACAGCAATTGGAGAAAAATAAAAAGGGGTGATTAATTCAGGTGGGCTAATAATTCTGACTTCAGCTTTATGTCTGCCAAATCATAACTGGATTCCAGTGAATTTTGCTTCAATTCCGTTTGTGGTTTCAGGCCCAAAAATTATA[T/G]CCATGGAGATCTTTCCTTGCAATTCATGGATTACATCCCTTGGTCATGTGGGACGTCTCACCCATTGAACATTACATGCAGGTGTGTTACTTTATAAATGTGAACATTGTACTCATTATACTGTACTTTGTATACTATACTACTAATTACTGTTATTATCTTCACTATTATTGATATCAGTGTTGCCTTCATCACAAAATTTTTAATATACCTTATCTACAGAATTTCACCAACCTTATTATTATTATTGTTATCATCATCTTTATTAATATTTTTATTGATATTATTATAATTATAATTATTGATATTATTATCATCATTATTATTATTATCTTTATTATTATTATTATTATTATTGTTGTTATTATTATTAATGATATTATTTACATTATTATTGTTATTAGTATTATTATTATTATTATTATTGATATTATAAGTATTGATATTATTATCATTATTATTATCTTTATTATTATTATTATTATTGTTATTATTATTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36308
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
ENSDART00000081721 Essential Splice Site 1273 1871 26 40
Genomic Location (Zv9):
Chromosome 17 (position 6665249)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 6744185
GRCz11 17 6901415
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAACCATCAACACACCAGCGCTGTTTAAGCACTTCTCTCAGCTCTACAG[G/A]TCAATAACATTTATTCGTTCACTCTTAAAAACATTAGAGGTTTGTACAGT
Long Flanking Sequence:
GACTCACGAAATCACATCACTTGAGTGCGTGAGATCAATCGAGGATCAAAACATGACCTCTCTGGACAGAAATTTAAAACATAGATCAATCGCTCGCTTTTTTATACTGTATGTCTAATTATCTTGTTTAATCCCGCCCCTTTTCGCAGCGCCATACAACAGAATTTCGCAAGCTCAAACACTAGCGTGACCACAGCTTAAGTGTGTTGAAGCAGGGCTGGAACTAAACTCTGGAGGGCTGCAGAGTTTGACACCACTGGTTTAAACCATTATTCTCATGTCATATTTCAGCTTCTTGATGACGGCATGGCAAACAATAAGAAAAAAGCAGAGTGTGTGTGTCAAGCTGAAGATGCGTTTCAGAGCCTGTTGAAGCAGAAGGGTTTTCTGCTGCTCTGGAAGCAGATGGAGGTCTTTAAAGAGAGCTGGACTCAACGACAGACCAGTTTCAAAACCATCAACACACCAGCGCTGTTTAAGCACTTCTCTCAGCTCTACAG[G/A]TCAATAACATTTATTCGTTCACTCTTAAAAACATTAGAGGTTTGTACAGTTAAAGTCACAATTATTAGCCCTCCTTTAAATATGTTTTTCTTTTTTTGAATATTTCCCAAATGATGTTTGACAGAGCAAGGAAATTTTCACAGTATGTCTGATAATATTTTTTTTTTTTCGGAGAAAGTCTTATTTGTTTTATTTCGGCTAGAATAAAAGCAGTTTTAAATTTTTTAAAAGCCATTTTAAGGTCAAAAGTATTAGCCACTTTAAGTTATATTTTTTTCAATAGTCTACAGAACAAACCATTGTCATACAATAACTTGCCTAATTACCCTAACCTGCCTAGTTAACCTAATTAACCTAGTTAAGCCTTTAAATGTCACTGTAAGCTGTATAGAAGTGTCTTGAAAAATATCAAGTCAAATATTATTTACTGTCATCATGACAATGAGAAAATAAATCACTTATTAGAAATGAGTTATTAAAACTATTAAGTCAATTCTGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36309
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
ENSDART00000081721 Essential Splice Site 1319 1871 27 40
Genomic Location (Zv9):
Chromosome 17 (position 6666732)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 6745668
GRCz11 17 6902898
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGCTTCCACCTCCTGGAGCTGCAGAAGTCGACATCAAAGCATGGCAGG[T/C]AATAAAAATAAAAATAAAATCAGGATTATTACTGGTATGGAAAACTCATA
Long Flanking Sequence:
TTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGCGTGCATGGAGTTTGTGTTTGTGCATGATTATGTACAGTATATATATTTATATATTTATGTGTGTGTCTGTGTGTCTGTGTGTGTGGTACTGTATGTGTGTGTTTGTGCATGCATGGGGTTTGTGTTTGTGTACTTGAGTGTGTGAGTATGTGTTATGTATGTGTGGTGTTTACTGTATATGGTGTTTATGTATATGTCTTTATATATGGGTGTGCTTATAAGGTGTGTGTGTGTGTGTATATGTGTTACTCTGACCCATGATGCTGTGTTGTAGGGTGGAGATTTTCTTTCCCAGCATGCAGGCTCTGGCTCAGCAGATGGACGTGGAGAAAGAGTACCAGATTCTGCTTTCTCAGACTCAAACTGTGCTTCCACCTCCTGGAGCTGCAGAAGTCGACATCAAAGCATGGCAGG[T/C]AATAAAAATAAAAATAAAATCAGGATTATTACTGGTATGGAAAACTCATACTATTAAAAACTAATTGTTAAATGAAATGAAGCTGAAGTAAAATATATTAACAGAGAAACTTGGACATTGCAGCGTGCTGAAAGTATAACTTAAAAAAATCCATAAAATTATTAATATTTAAAAATCTAAATATGTAGTGGTGGCGCAGTGGGTAGCACAATCACCTCACAGCATGAAGGTTGCCAATTTGAGCTGGGTCAGTTGGCATTTACATGTGGAGTTTGCATGTTCTTCCCGCGTGGATTTCCTCTGGGTGCTCCGGTTTCCCCCACTATCAAAAGAGATGCAATATAGGAGAATTTAATTTACTAAATTGGCTGCAGTGTATGTGTGGAAATGTGAGAGTGTATGGGTGTTTCCCAGTGCTGGGTTGCAGCTGGAAGGGCATCCGTTGCGTAAAACATATGCTGGATTAGTTGGTGGTTCATTCCACTATGGCGAACCCAGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36310
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000081721 Nonsense 1373 1871 29 40
Genomic Location (Zv9):
Chromosome 17 (position 6669834)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 6748770
GRCz11 17 6906000
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTGATAAAGATCTGTGGAAAAGACCATCAGCGAAACACAGCGTATCTT[T/G]AGAGAGACCGCAGATTGTGGAGGATTTTATCCAGAGACTGATGAGCGCTG
Long Flanking Sequence:
TAAGTTTACAAGTGTGATTATTTATCTTGACATGCACTAACAGACTGAAATTTGTCTGTGGTGTGTGTTGTAGCTCCTGAGACTCCTGGAGATGACGGAGGTTGACATGATCCGTGCGCTTCAGAACAGGATTAACACTGAAATGACTCTAGTGATGTCTGAGCGCTCGCGACACGACATGCAGATCCCTGCAGGTACCAAAGATCGTTGTGGAAAGAGATGAGACGAGTCTGGATGCAGTGCAGTCTGAGCTGCATTCAATACTTTTGTCATTGTGAGGGGTGGGGTTAGGTGAGCGCAATTTCAAACAGAAATTAAGGTAAAAGTATATAAAATAATTCAAATTTAACACGAGGGTTAGCAATTATGACTGCAACTGTATATTTGGACAGATAACAACAGTCCTTTCTAGATTGGTTTGTTCATCTCAGTCTTGTTTGGTGTTTTCACATGTGATAAAGATCTGTGGAAAAGACCATCAGCGAAACACAGCGTATCTT[T/G]AGAGAGACCGCAGATTGTGGAGGATTTTATCCAGAGACTGATGAGCGCTGAGGAGAGACAGACTGATGGACAGGTGAACAGTTCCCTCTATAGGCAAAAACTGCTTTTCATACAAATATCAGTTTTACAGTTTTGGGCTGTTTGACGTTTGTGTACACTTTTCCTATTTATGTATAGAATGGCATCCACAGCATAAAACATATGCTGGAATCGTTGGTGGTTCATTCAGCTGTGGGGACCTCTGATAAATCAGAGACTAAGCTAAAGAAAAAGGATTGAATTTTACATATGTATTGTGAATATATATTGGTATGTAATGAATAATTAGAGTATTTTCTAGGTGACGTTCTCCACTGCTCATCTGCAAGATTGTTTGACTGAGCTGTCCTGTGCTGTAATGAATCGTGAGAAAAGCGTCTTCCAGCGGTATTCGCAGTTTTATGAGCACATCCTCCAACAGCAGGAGCAACTGCTTTACCAGAGAGAGCAGGTACATCACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39143
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
ENSDART00000081721 Nonsense 1429 1871 30 40
Genomic Location (Zv9):
Chromosome 17 (position 6670268)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 6749204
GRCz11 17 6906434
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCCTGTGCTGTAATGAATCGTGAGAAAAGCGTCTTCCAGCGGTATTCG[C/T]AGTTTTATGAGCACATCCTCCAACAGCAGGAGCAACTGCTTTACCAGAGA
Long Flanking Sequence:
TGTTTGGTGTTTTCACATGTGATAAAGATCTGTGGAAAAGACCATCAGCGAAACACAGCGTATCTTTAGAGAGACCGCAGATTGTGGAGGATTTTATCCAGAGACTGATGAGCGCTGAGGAGAGACAGACTGATGGACAGGTGAACAGTTCCCTCTATAGGCAAAAACTGCTTTTCATACAAATATCAGTTTTACAGTTTTGGGCTGTTTGACGTTTGTGTACACTTTTCCTATTTATGTATAGAATGGCATCCACAGCATAAAACATATGCTGGAATCGTTGGTGGTTCATTCAGCTGTGGGGACCTCTGATAAATCAGAGACTAAGCTAAAGAAAAAGGATTGAATTTTACATATGTATTGTGAATATATATTGGTATGTAATGAATAATTAGAGTATTTTCTAGGTGACGTTCTCCACTGCTCATCTGCAAGATTGTTTGACTGAGCTGTCCTGTGCTGTAATGAATCGTGAGAAAAGCGTCTTCCAGCGGTATTCG[C/T]AGTTTTATGAGCACATCCTCCAACAGCAGGAGCAACTGCTTTACCAGAGAGAGCAGGTACATCACCTAAACATGCATTTATTTCATTAGTAATACTGGAAACTGATGTGCTTTCTGTTTGAATATACAGTGAATATGAATATACAGTGCTCAACATAAATGACTACAACTAATTTTAAAAATGATTATTTTTATCCATTTCTCAGTGAATATAGGCCATATATTTTGGTGCATTTAAACAAAACAGATTTATTAAACAGGAATACTTATTAAAACAATATTTTAATCAACGAACATCTTTGAAATAGAAAGTTGATATAGTTAAATTCGTGTTAAATATTGAAAAAATTTAAAAACTACAAAATTTCAGCAAAATTTTATACATTTTTTGTTTCTCTTGATTTTGTTCTTTTTTATATATGTTTATTTTTCCCTAACATATAAATTTAGGTGTACTAGTTTTCGACTGATATAAGTTATTTTGTTAGAATAGCTCCAGAT
Associated Phenotype:
Not determined