Busch Lab

ZMP

ENSDARG00000017425

Ensembl ID:
ENSDARG00000017425
Human Orthologue:
AC104809.3

Alleles

There are 11 alleles of this gene:

Allele Name Consequence Status Availability
sa20707 Nonsense Available for shipment Available now
sa40698 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa26751 Nonsense Mutation detected in F1 DNA Not yet available
sa20708 Nonsense Available for shipment Available now
sa33873 Essential Splice Site Available for shipment Available now
sa33874 Nonsense Mutation detected in F1 DNA Not yet available
sa5752 Nonsense F2 line generated Not yet available
sa2292 Nonsense Available for shipment Available now
sa20709 Essential Splice Site Available for shipment Available now
sa25339 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa20707
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
ENSDART00000065238 Nonsense 272 1959 8 37
Genomic Location (Zv9):
Chromosome 6 (position 27118754)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 27419965
GRCz11 6 27410526
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACCTGCCGACCATATGTCCATATCATCATTCTGCAGATGAATACCTCC[C/T]GAAACAGCCGCGAACAAGTCCGTGTACGATCTTTGTGGCGTCAAGTTGCC
Long Flanking Sequence:
GGAAGGAAGGAGAGATCTGTAGTGTATGTTTTTATCCAAATCCACAGTTTAAGGAAAATCTCTTCTTAATCCAACCCAATGAAACTCAACTCTGGAACTTGTGGAATTCCACCCTGGTGCCTGTTTTGTCAGTCTGGACCCTGTCTTTGTTTTAAATCATTGTTGTGATTTTCTCAGCTGTTGTTTCCTGTGAAAACATTCCAGTTGATTGGAAAAAAGAGTAAGAATTCATTGCTCTGTGCAAACATCTGGTGATATGGTGGAACTCGTTTCGTTTTTAGTCACATTCAGAATAGGTTAAGGTACTATTTGTGCATGCGAGTCTATGTGGGTGTCTGCGCCGATCGGTTTAAATGTGTGCTCGTGTGGGTGCATTCATTATTTTTCATATGTGTGCATTAAAATGGAGACGTCTTTAACCTTATGCTCTTAATCCCACCCCTCTTTACTAAACCTGCCGACCATATGTCCATATCATCATTCTGCAGATGAATACCTCC[C/T]GAAACAGCCGCGAACAAGTCCGTGTACGATCTTTGTGGCGTCAAGTTGCCTTCCTGCGGAGCTCTTTCACCCAGCTGCGGGCCTTTGCTGACAGGTGAGTCTAGCTTGCGGCAAAAAACTTACTTCCAAACCAACCACCATTTATCCCTGTTTGAGATCAAAGCTTGGTGGGTCACCTGGGTCAGCCCTCACCCATCCTGTCTACATCGTCCAGGGAAATGTGATGGTTAGATTGCCCTATAGATTAGCCTTGAGTTATCCATCAGAGCCAAGCTTGATGAGGGCTCAACCTGTGTAAATGCTGTGATCATTGTTGAGTAATTTGCAGTAATGTGGATTACTCAACACATGGACAGCAGAGAAAGTATTCACGACCCTTACTCAGACACGACACCGTTCAAAGAGTTTATTCCCACACCACAATAAACTTTCGGCCATCTGGCTCTCGTCACTTGTGAATGAAACACAATTTCTAGGGAATGTAGGAGAACAAGAATTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40698
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000065238 Essential Splice Site 483 1959 13 37
Genomic Location (Zv9):
Chromosome 6 (position 27123369)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 27424580
GRCz11 6 27415141
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTATGTAATTTCAGTTCATTTAACAAAATCACAATATCTATCCACCCAA[A/T]GGATCTGCAAGCATGTCTGGAAGCTTCCCAAGAGCAGGTTGTCACTTTGC
Long Flanking Sequence:
GTCAGTGGAGAGGTTTCCCGAGACTGCTCATCCAAACATGAGCACTCTTTTATTTCTGCAGGATCTATATCCTCATCTCAACGAGAGGGTCCACTGATAGCTGTGCAAAAAGCACTGTTACAGCGGCAGACACAAACTGAGGTTTGCAACAAACCTTCAACATACCAACCTAAATGATACAGTTGTCATGACTGTTATATTAAGGGTGAAGTAAATTTTCAGAAGAAATCCTTGTTATTGCTATCCGTACATAGCAACACTGGCTCAACCAAGGGTTTGGGCAGGGCTATGTATTTGTCCAACCAATTGATGACAGGTGGAATGTTCTGGAAATACATTTTTATTTTCCGTTTGGCAACATTTGTAGAACTTAAATCACACACATCACCTTTAAAAATGCTTTCATATCACTTTATTAGATCACTAATCTTATCTCCTGCTATCGAGAAGAGTATGTAATTTCAGTTCATTTAACAAAATCACAATATCTATCCACCCAA[A/T]GGATCTGCAAGCATGTCTGGAAGCTTCCCAAGAGCAGGTTGTCACTTTGCAAAAGCAGCTGCATGTGGAAGAAGATAAAACCAGAACCCTGGAAAAAAGACTCCAAGAACTGCAGCAAGAGAACCAGCTATTGGAAAGAGCTGAGGAGGACAGCACTAGAGATGCTGAGAGATACCGCAACTCTCTGGGAATAATAACCAGGTCTGCTACTGATCAAACCTGGCACTTCAATACTATTTCCACTGTTAAATTTGAACCCTCTACTTTTACATCAGCATTCTTTTACAGAGCTCTTATGACATTAGTCGGCCAATTCAGAAGGCAAATAACTTAAAGATTTGTCCTGACTTTACATGCATCAAAAGTTATAACATGCTACATTATAATTCTAATTAATCATATCAAAGATGTAGTTCTAATCCTAATCTAGCAGACTTATTGGCTCAAAGTATTTCCCTCTATTTTTAGTACTACCATATATCCTGAACAGTCACATACTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26751
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
ENSDART00000065238 Nonsense 557 1959 14 37
Genomic Location (Zv9):
Chromosome 6 (position 27123927)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 27425138
GRCz11 6 27415699
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACAATTGCTACTGTCTTTCTTTCTAGTGAAAAAGGAGAGCTTGAGAGG[C/T]AGCTCTCAGCCATGCAGCAGCAGCTGGAATGCACACAAACAGAGCAGGAA
Long Flanking Sequence:
GCTGCATGTGGAAGAAGATAAAACCAGAACCCTGGAAAAAAGACTCCAAGAACTGCAGCAAGAGAACCAGCTATTGGAAAGAGCTGAGGAGGACAGCACTAGAGATGCTGAGAGATACCGCAACTCTCTGGGAATAATAACCAGGTCTGCTACTGATCAAACCTGGCACTTCAATACTATTTCCACTGTTAAATTTGAACCCTCTACTTTTACATCAGCATTCTTTTACAGAGCTCTTATGACATTAGTCGGCCAATTCAGAAGGCAAATAACTTAAAGATTTGTCCTGACTTTACATGCATCAAAAGTTATAACATGCTACATTATAATTCTAATTAATCATATCAAAGATGTAGTTCTAATCCTAATCTAGCAGACTTATTGGCTCAAAGTATTTCCCTCTATTTTTAGTACTACCATATATCCTGAACAGTCACATACTGTACCACACAACAATTGCTACTGTCTTTCTTTCTAGTGAAAAAGGAGAGCTTGAGAGG[C/T]AGCTCTCAGCCATGCAGCAGCAGCTGGAATGCACACAAACAGAGCAGGAAGGTTTGAGAAGTTCCTCTCTGGATGTTCAGAGGCAGAGAGACCTCCTCAGGCAGCAGAGGGAGGACCTGGAGAGGCAGCTGGCCCGAGAACGCTCTGAATCCGAGAGGGGGTATGACATTGCGAAACCTCAAACCCTTTGACTTCTTTCTTGGCCCTTGTTTATTTCCCTGTCCTATTGTTTACTGTCAGTATCACTAGCACATGTTGTCCTTAAAGTAGCCTTGAATTAATCCAGAATAGTATTGTTTACAAAGTCCATCAAAGATGAAGACGGATAATGCATTTAGTTTACTTGTTAGGTTAAAGGTAACAACCCTGATCTTGTTGTTTCCATGTCCGATCATTATGTACTGTATATTAGTAATATTATGCACTGTAAAAAAAACAAAAAAAAAAAACTTAATTTTACGGTTTATTTCCGGCAGCTGGGATGCCGGAAAAAAAAAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20708
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
ENSDART00000065238 Nonsense 585 1959 14 37
Genomic Location (Zv9):
Chromosome 6 (position 27124011)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 27425222
GRCz11 6 27415783
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAAACAGAGCAGGAAGGTTTGAGAAGTTCCTCTCTGGATGTTCAGAGG[C/T]AGAGAGACCTCCTCAGGCAGCAGAGGGAGGACCTGGAGAGGCAGCTGGCC
Long Flanking Sequence:
TGAGGAGGACAGCACTAGAGATGCTGAGAGATACCGCAACTCTCTGGGAATAATAACCAGGTCTGCTACTGATCAAACCTGGCACTTCAATACTATTTCCACTGTTAAATTTGAACCCTCTACTTTTACATCAGCATTCTTTTACAGAGCTCTTATGACATTAGTCGGCCAATTCAGAAGGCAAATAACTTAAAGATTTGTCCTGACTTTACATGCATCAAAAGTTATAACATGCTACATTATAATTCTAATTAATCATATCAAAGATGTAGTTCTAATCCTAATCTAGCAGACTTATTGGCTCAAAGTATTTCCCTCTATTTTTAGTACTACCATATATCCTGAACAGTCACATACTGTACCACACAACAATTGCTACTGTCTTTCTTTCTAGTGAAAAAGGAGAGCTTGAGAGGCAGCTCTCAGCCATGCAGCAGCAGCTGGAATGCACACAAACAGAGCAGGAAGGTTTGAGAAGTTCCTCTCTGGATGTTCAGAGG[C/T]AGAGAGACCTCCTCAGGCAGCAGAGGGAGGACCTGGAGAGGCAGCTGGCCCGAGAACGCTCTGAATCCGAGAGGGGGTATGACATTGCGAAACCTCAAACCCTTTGACTTCTTTCTTGGCCCTTGTTTATTTCCCTGTCCTATTGTTTACTGTCAGTATCACTAGCACATGTTGTCCTTAAAGTAGCCTTGAATTAATCCAGAATAGTATTGTTTACAAAGTCCATCAAAGATGAAGACGGATAATGCATTTAGTTTACTTGTTAGGTTAAAGGTAACAACCCTGATCTTGTTGTTTCCATGTCCGATCATTATGTACTGTATATTAGTAATATTATGCACTGTAAAAAAAACAAAAAAAAAAAACTTAATTTTACGGTTTATTTCCGGCAGCTGGGATGCCGGAAAAAAAAAAATCAAATAACGGCTGTTAAATTACAGAAATTTACTGTAAAAAAACTGAGGTTGAATAACAGATATTTACCAGAAATTTGAATTTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33873
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
ENSDART00000065238 Essential Splice Site 707 1959 16 37
Genomic Location (Zv9):
Chromosome 6 (position 27126832)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 27428043
GRCz11 6 27418604
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGAGGGATTGGCTAAAGACAAGGTTGAATTAAACCGTCTTCTCCTACAG[G/A]TCAGGGTCATGGAATTGGATTGTGTGCGTAGAATGTTTCAACTTTTTACA
Long Flanking Sequence:
TTTCCCCCTGTCAAATGTCCAAGTCAGTTGTTGAATTACTGGAAACTCGGTTTACTTTGACCTTGGGTGAGTTATGTAGCTCTGCTTATTTGTAGTGGTTGAGATTTACCATGCAAAACTGCCTTTGCAAGATTCTTCATCACTTGATCTGTCTAACTTACAGTTTTTCCGCACTTCCCAAGGTCATTCTGGGGACAAAATGTAATGGTTAAGTGGAAGTGCTATTAAACAGCTCTGCAAACATATTTTACCCTGACCGCTGATTACAAAATAAATGGTGGTTATGTGAACTTGGTAGCTAATGATTGTATGTAGCTATGCTTCCCACTGATGTTTGTAATGCCTCCCTATAGGCGGAGGCCCAGAATGCAGAGCAGGAACTGGCGCTCACTAAACTACGAAGTGAAGATGCAGGGCTACAGGACTCCCTGGCCAAGATGGGAGCCCTAAGTGAGGGATTGGCTAAAGACAAGGTTGAATTAAACCGTCTTCTCCTACAG[G/A]TCAGGGTCATGGAATTGGATTGTGTGCGTAGAATGTTTCAACTTTTTACATTTCAATTCCTTTAGGGGAGAATACTGATTACGGTATTTAATTTTAATTGCATGATGTACTACATTACATCATGATCACAAGCCTCTTCAACCACATTAAAGTCTATTGTTACAATATTCAAACAAGCAATTAAAATGAAGGATTTGAAGCCTATGTGATAGCATCATAGTGCTGCTTTACGCAAGCATAACCTTTTTTGTTTTGCTGTCTTCAGTTATTTTATTTCAATTAAATTCATGTTTATTTCTATAATGCTTTTACAATGTAGATTGTGTAAAGGCAGCTTAACATAGACCTTCTAGTAGATTGAAACTGTCAGTCCTGTTTTCAGAGTTGAAGTTCAGTTCAGTGTGGTTTAATTTTTACTGCTGAAAGTCCAAACCCTGAAGAGCAAATCCTTGGATGGGCAGCTCCACAAGTCCCAAACCAAGCAAGCCAGTGGCAACAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33874
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
ENSDART00000065238 Nonsense 795 1959 18 37
Genomic Location (Zv9):
Chromosome 6 (position 27130414)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 27431625
GRCz11 6 27422186
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTGTGTGTTTTTTGTAGGCCAGTAAGCAGAAACAAGCTGTGCAGGAA[C/T]AGTTAAATGCATGTCATAGAGAAATGGAGCTGAGCGCTGCCTTGCTGCAG
Long Flanking Sequence:
TCATCGAGTGTCAGAATGTTGTGGGACTACTATACAGAAGTTATTATTAGGGATCATATATAGCGAAATTTTTATTTATTTATTTTTTTACGTTTTTTAAAGTACGACCGTAAAACACAAACGCTGTTATGAATGTATTAAAACATGAGCTTGTTTGTTGTAAAAAATTTGTTATAATGCCAAAAAAATACTATTTTGTGCATCTCCCTAATTCTGGAAAATTTTCGTACCCCTGGTTTTGAGTGTAGTCCTGAAAAAACTCTGTTTAGTCCTTCCCCTTAACCCTATGCCTTCAAGCCAAAGAGAATTTGGTCACCGCTACCCCTTCACGTGAGCACCCAAAAAGGAAGGGCTAAGGGGTAGAATTGGGATTGTACCTTACTAATAGCAAACACTGGATTTTCTTTGCATTTATTCTGAATGAAAATCACGAAAACCCATGTGTGTGTGTGTGTGTGTGTTTTTTGTAGGCCAGTAAGCAGAAACAAGCTGTGCAGGAA[C/T]AGTTAAATGCATGTCATAGAGAAATGGAGCTGAGCGCTGCCTTGCTGCAGAAGACTTACAAAGAGAGAGATGAACTGGCAAGAGACAAAGCCAATCTCACAGTGCAACTCACCTCAGAGCAACGTAAATCCAAGGCTCTGGCCCAAGACCTAGCCGCTCTGCGGTGAGTCAGTGTGTTAGTGTTTTAGTGCGAGTAGGATTTGGTGCATTAATGTGTTTATATGGGCTAAGTGTTTGTATTTATGTTGGAGTTTGACCCTGGCGAGCAAAGTAAAACACCTGTGTTTTCAGCATGTTTTTTTTTTTTGAGTAATTATCAATTGGGCCTTTTCAATCATGTAACTCTTCCTAGTTTCACTTAGTCTGTTTTGCGAGAGAATCACCATGAGGTTAAGCCTCTGTTTTGCTGTATAAATCATCTCCTTAGAACATCTCATCTGTCCCGAACGATGTTAGCTAAAGAAACAACCATTTAAAGACGTTCATTATCTACACAAAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5752
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
ENSDART00000065238 Nonsense 873 1959 19 37
ENSDART00000065238 Nonsense 873 1959 19 37
Genomic Location (Zv9):
Chromosome 6 (position 27131043)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 27432254
GRCz11 6 27422815
KASP Assay ID:
554-2612.1 (used for ordering genotyping assays)
KASP Sequence:
AGTCAAGCCTGTTGGACAGGCAGGAACTGGCCTCATCTCTAGAGGCCATA[C/T]GAGATAGACTAGATGGAGAGAATGCTAGTCTACAGCAGGCTAACAAGTCC
Long Flanking Sequence:
TCCAAGGCTCTGGCCCAAGACCTAGCCGCTCTGCGGTGAGTCAGTGTGTTAGTGTTTTAGTGCGAGTAGGATTTGGTGCATTAATGTGTTTATATGGGCTAAGTGTTTGTATTTATGTTGGAGTTTGACCCTGGCGAGCAAAGTAAAACACCTGTGTTTTCAGCATGTTTTTTTTTTTTGAGTAATTATCAATTGGGCCTTTTCAATCATGTAACTCTTCCTAGTTTCACTTAGTCTGTTTTGCGAGAGAATCACCATGAGGTTAAGCCTCTGTTTTGCTGTATAAATCATCTCCTTAGAACATCTCATCTGTCCCGAACGATGTTAGCTAAAGAAACAACCATTTAAAGACGTTCATTATCTACACAAAACTCAACCTATTTTTCTTTGTATTCCCTTACCATCTCTCTTGCTTTTTCCTCTTGCTCAGGGCTGAGAGAGAGTCTCTAGAGTCAAGCCTGTTGGACAGGCAGGAACTGGCCTCATCTCTAGAGGCCATA[C/T]GAGATAGACTAGATGGAGAGAATGCTAGTCTACAGCAGGCTAACAAGTCCTTGACGCGTGAGTTTCTCTCCAGGGAGCCTTTATCCTACTCTCATTGACTTGGCTGGGTGTACTGGCCACTGGGCCCCAGCTATAGTCCACAAGGGGCTCATATTTTTACTCGGAACTGGGGAACAGCTGAGAGGTCGGTCGAGGATTTCTCTAGAGCTTAACAAAGTCCCCTCTCAGATATCATCCACACTGTACTATTTATGTGTTGTGCTGTCATCATATATTGTGTAATGATGATTCTTAAGAGCATTTATAATTTCAGGTTTCCAGCATGCTGGAACCGAGTGTGTCCCTAATGTATATTTTCATTACAAAGCATATTTCTCCTCTGTGTGTTTACTTGTTCTTCCCTCTGCACAGGTGAACTTTCTAGTGTTCAAAGTGAACTAGAGCAGCAAATGTCCCGGGCTTTGCAGGAGAAACAGGCTTTAGAGTTAAAGCTTGCTCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2292
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
ENSDART00000065238 Nonsense 873 1959 19 37
ENSDART00000065238 Nonsense 873 1959 19 37
Genomic Location (Zv9):
Chromosome 6 (position 27131043)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 27432254
GRCz11 6 27422815
KASP Assay ID:
554-2612.1 (used for ordering genotyping assays)
KASP Sequence:
AGTCAAGCCTGTTGGACAGGCAGGAACTGGCCTCATCTCTAGAGGCCATA[C/T]GAGATAGACTAGATGGAGAGAATGCTAGTCTACAGCAGGCTAACAAGTCC
Long Flanking Sequence:
TCCAAGGCTCTGGCCCAAGACCTAGCCGCTCTGCGGTGAGTCAGTGTGTTAGTGTTTTAGTGCGAGTAGGATTTGGTGCATTAATGTGTTTATATGGGCTAAGTGTTTGTATTTATGTTGGAGTTTGACCCTGGCGAGCAAAGTAAAACACCTGTGTTTTCAGCATGTTTTTTTTTTTTGAGTAATTATCAATTGGGCCTTTTCAATCATGTAACTCTTCCTAGTTTCACTTAGTCTGTTTTGCGAGAGAATCACCATGAGGTTAAGCCTCTGTTTTGCTGTATAAATCATCTCCTTAGAACATCTCATCTGTCCCGAACGATGTTAGCTAAAGAAACAACCATTTAAAGACGTTCATTATCTACACAAAACTCAACCTATTTTTCTTTGTATTCCCTTACCATCTCTCTTGCTTTTTCCTCTTGCTCAGGGCTGAGAGAGAGTCTCTAGAGTCAAGCCTGTTGGACAGGCAGGAACTGGCCTCATCTCTAGAGGCCATA[C/T]GAGATAGACTAGATGGAGAGAATGCTAGTCTACAGCAGGCTAACAAGTCCTTGACGCGTGAGTTTCTCTCCAGGGAGCCTTTATCCTACTCTCATTGACTTGGCTGGGTGTACTGGCCACTGGGCCCCAGCTATAGTCCACAAGGGGCTCATATTTTTACTCGGAACTGGGGAACAGCTGAGAGGTCGGTCGAGGATTTCTCTAGAGCTTAACAAAGTCCCCTCTCAGATATCATCCACACTGTACTATTTATGTGTTGTGCTGTCATCATATATTGTGTAATGATGATTCTTAAGAGCATTTATAATTTCAGGTTTCCAGCATGCTGGAACCGAGTGTGTCCCTAATGTATATTTTCATTACAAAGCATATTTCTCCTCTGTGTGTTTACTTGTTCTTCCCTCTGCACAGGTGAACTTTCTAGTGTTCAAAGTGAACTAGAGCAGCAAATGTCCCGGGCTTTGCAGGAGAAACAGGCTTTAGAGTTAAAGCTTGCTCAG
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:
sa20709
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000065238 Essential Splice Site 891 1959 19 37
Genomic Location (Zv9):
Chromosome 6 (position 27131101)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 27432312
GRCz11 6 27422873
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTAGATGGAGAGAATGCTAGTCTACAGCAGGCTAACAAGTCCTTGACGC[G/T]TGAGTTTCTCTCCAGGGAGCCTTTATCCTACTCTCATTGACTTGGCTGGG
Long Flanking Sequence:
AGTGCGAGTAGGATTTGGTGCATTAATGTGTTTATATGGGCTAAGTGTTTGTATTTATGTTGGAGTTTGACCCTGGCGAGCAAAGTAAAACACCTGTGTTTTCAGCATGTTTTTTTTTTTTGAGTAATTATCAATTGGGCCTTTTCAATCATGTAACTCTTCCTAGTTTCACTTAGTCTGTTTTGCGAGAGAATCACCATGAGGTTAAGCCTCTGTTTTGCTGTATAAATCATCTCCTTAGAACATCTCATCTGTCCCGAACGATGTTAGCTAAAGAAACAACCATTTAAAGACGTTCATTATCTACACAAAACTCAACCTATTTTTCTTTGTATTCCCTTACCATCTCTCTTGCTTTTTCCTCTTGCTCAGGGCTGAGAGAGAGTCTCTAGAGTCAAGCCTGTTGGACAGGCAGGAACTGGCCTCATCTCTAGAGGCCATACGAGATAGACTAGATGGAGAGAATGCTAGTCTACAGCAGGCTAACAAGTCCTTGACGC[G/T]TGAGTTTCTCTCCAGGGAGCCTTTATCCTACTCTCATTGACTTGGCTGGGTGTACTGGCCACTGGGCCCCAGCTATAGTCCACAAGGGGCTCATATTTTTACTCGGAACTGGGGAACAGCTGAGAGGTCGGTCGAGGATTTCTCTAGAGCTTAACAAAGTCCCCTCTCAGATATCATCCACACTGTACTATTTATGTGTTGTGCTGTCATCATATATTGTGTAATGATGATTCTTAAGAGCATTTATAATTTCAGGTTTCCAGCATGCTGGAACCGAGTGTGTCCCTAATGTATATTTTCATTACAAAGCATATTTCTCCTCTGTGTGTTTACTTGTTCTTCCCTCTGCACAGGTGAACTTTCTAGTGTTCAAAGTGAACTAGAGCAGCAAATGTCCCGGGCTTTGCAGGAGAAACAGGCTTTAGAGTTAAAGCTTGCTCAGGCAGAAAGAAACGCACAAGAAATGCTCATTACAACACAGCAAAGCCATCAGGAGCAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25339
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
ENSDART00000065238 Nonsense 1398 1959 27 37
Genomic Location (Zv9):
Chromosome 6 (position 27140705)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 27441916
GRCz11 6 27432477
KASP Assay ID:
554-7543.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCAATTCTACTTTGAGACGTACACTCGGATCCAGGCGTGGAAGGCAAT[C/A]ACCCACACCTGGGGAACGAGGACGGAGCCCCTCGCCATGGAGAACTCGCT
Long Flanking Sequence:
GAGCAGAGAGAAGAGGAAATGAGAAAGGAGACCTTTACCCTTAGACAAAAAGTACTGGAAAGTGAAGCTGGAAAAGAAGCGGCCCTGAAGGAGGTATACCAAACAACTGACATAAATTGATCCATACACACATACAATAGCATGCTTCAACAGCTGCAAATGCTCTGTGTGTGAACAGGCAGCAGGTTTGCAGCGTCATATAGCAGAACTGGAAGAAGCACATCAACAGGAGAAAGAGTTGCAGCAACAACGGGATGCCAGTCTTCAGGATAGCCAATTGAAGCAGCGTGAAGAGGTTGCACGCTTGGAGGGGGCACTGCAAGAATCTCAGGCCCAGCTCAGGGAATTTGGGCTATCGGTCAATCTTGCAGAGGCCCGTGCCCAAGGGCTGGAAGAGCAGCTAGCACAGAATGATGCCAAACGGAGAGATCTTGAGCACAGATTGAATGTTCTCAATTCTACTTTGAGACGTACACTCGGATCCAGGCGTGGAAGGCAAT[C/A]ACCCACACCTGGGGAACGAGGACGGAGCCCCTCGCCATGGAGAACTCGCTCACCTGTAAAAGGTAATGTATTCTTAGTCCAATAATGAATCAGGTCTCTGTAGCAAAGGTTAGTGTAGAGTTAAGAAGAAGATCATCTCTCATATTACAAAGGATTGTTTTCTTCAAGGCTATTAGTAACTTCAAGCTTATTAAACAATGTGCGGCTCTAACTTACAAGGTGCTCTTGCTTACATGTCAGATGATTTAAATGAAAACTGTGTGTATGCCCTCAGGTGAAATCATATCAGATGAGACTGGGGTGGGTGGGTTGCCAGTGTGTTCTCTGTCCCCCTCCCGCAGGGAAGATGGCGAGTTGGATCTGGATGCAGTTCAGATGTTACTGCATAGCTTCCAGCAAGAGCTCAGGGACACACAGAAAGAACGGGTACTTGACACCTTTACATCAGCATAAGGGACACACATTCACCATTAAAAAAGTAGTCCACATCCCTATACTGT
Associated Phenotype:
Not determined