Busch Lab

ZMP

ITPR1 (2 of 2)

Ensembl ID:
ENSDARG00000014655
Description:
inositol 1,4,5-triphosphate receptor, type 1 [Source:HGNC Symbol;Acc:6180]
Human Orthologue:
ITPR1
Human Description:
inositol 1,4,5-triphosphate receptor, type 1 [Source:HGNC Symbol;Acc:6180]
Mouse Orthologue:
Itpr1
Mouse Description:
inositol 1,4,5-triphosphate receptor 1 Gene [Source:MGI Symbol;Acc:MGI:96623]

Alleles

There are 11 alleles of this gene:

Allele Name Consequence Status Availability
sa9229 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa20768 Nonsense Available for shipment Available now
sa40754 Nonsense Mutation detected in F1 DNA Not yet available
sa20769 Nonsense Available for shipment Available now
sa7044 Nonsense Mutation detected in F1 DNA Not yet available
sa20770 Nonsense Available for shipment Available now
sa10338 Nonsense Available for shipment Available now
sa1340 Nonsense Available for shipment Available now
sa38569 Nonsense Mutation detected in F1 DNA Not yet available
sa2315 Essential Splice Site F2 line generated Not yet available

Mutation Details

Allele Name:
sa9229
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
ENSDART00000065092 Essential Splice Site 733 2727 20 64
Genomic Location (Zv9):
Chromosome 6 (position 39882253)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 39953853
GRCz11 6 39951389
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGCAAAAGATGGACATACAGAGGACCAGGAAGTCATCAATTATTACAGG[T/A]AAGGACAAAAACACCTACTTGTAAATAGGATGGAGTGATGMGGAATGTTT
Long Flanking Sequence:
AAATGACTCATTTCTTTTTATATTCTGTGGTAAAATTATTGATTAGTACATTGAGAAGCCTTCTAACTGGATCACAGTTGCACAGTGTTTTTGTGGGTTTCTAAATATATGCAGTTGAAAATTAAAGCCCTGATTTATTTGGCAAGTAATATCACCCAAACCTTAAGCATGTGTGCAATTAGACCAACAATACTGTGTGAAGAGCCAAAAAAGTGATGAAACACATGAGGAATTTAAAAGAGTTAGAAAGTCTGGAAGTCTGTTTGTGTGTTATTTGTGAGTGATTGTGTGTGTTTTGTGTCAGGCTTGTGTTGTCACGGTTTGAGGTGGCAGGAACGGTGTTGGGTGAAGGTGCGGAGGAGGAAGAGGAGGATGAAGAGGAGGTCTGGCTGTTCTGGAAGGACAGTGGAGGAGAGGTGAAGAGTAAAAGCATACGAGAGCTTGCACAGGACGCAAAAGATGGACATACAGAGGACCAGGAAGTCATCAATTATTACAGG[T/A]AAGGACAAAAACACCTACTTGTAAATAGGATGGAGTGATGCGGAATGTTTCATTTAATATTATGTAATTATAACTAGAGACGCACTAAATTTTTTCCCTTGTAAAAATAAATAAAGATGTGTTGTACTGCCTTGCAGTTTTCAGCGGAAAATAAATTTCTGCTCAAATAACATGCCGACAGGACATTACTCTATAGCAGGGGTGCTCAACCCTGTTTCTGGAGATCTACCTTCCTGCAGATTTCAGTTGCTACCCATATCAAACATACCTAAACCAATTAATTAGGACCTGAAAACCATGTGATAATTACAGGCAGGTGTATTTGATACTATTATAATTGAAATCTACAGGAAGGTAGATCTCCAGGAACAGGGTTGAGCACCCCTGCTCTATAGTATACTTGTTCCTGCTGCTAGTGTTCTGTCATAGCAACAATCTCGACTCTCGGATCTTCATTCATTTATTCATCCATTTTACTTTGGCTTAGTCCCTTTATTTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20768
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000065092 Nonsense 781 2727 21 64
Genomic Location (Zv9):
Chromosome 6 (position 39883458)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 39955058
GRCz11 6 39952594
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCTGCATGTCAGATGAAGATTTGCCCTTTGACCTCAGAGCATCGTTCTG[C/A]CGCATGATGCTGCACATGCATGTAGACCGTGACCCTCAGGAGCAGGTCAC
Long Flanking Sequence:
CCAACTGGCCCAGCTGGGACTCGAACCAGCAACCTTCTTACTGTGAGGAGACAGTGCTAACCACTGAATCACTGTCACCTCTCAACTCATTTACTTTTGGTTAAATTTTACTGTCAATATAATGTGGTAATTTTATTGGCTTAAGTTTTTTAATAAATAACATTTTTAAGTTGTTGAGTTAAATTTAGAAAGTGGTACAAAATTTTATATATTATTCAATTAAATAATAAATAATGATTATTTCAAATCTATTTAAAAAAAAAGATTGTTTTTGGTCAAATGCATCCAGAATTGTAGTTTTTGGCCCAGAATGTTTATTTCAGTGGATGACTAACATAGTGACTTGTCTCTGTCAGATATCAGCTGAATTTGTTTGCTCGGATGTGTCTGGATCGACAGTATCTTGCGATTAACAAGATATCAGCACAGCTGGATGTGGATCTGATTCTGCGCTGCATGTCAGATGAAGATTTGCCCTTTGACCTCAGAGCATCGTTCTG[C/A]CGCATGATGCTGCACATGCATGTAGACCGTGACCCTCAGGAGCAGGTCACCCCGGTCAAATATGCTCGACTGTGGTCTGAAATCCCATCACAAATTTCCATTGATGAGTGAGTGCGTTATTGCTGTGAAATAACACAACGTTAATGAGTGATCTGTTCATTAGCCCGTCTGTTTGCTGTTTCTTGAGCAGTTATGATAATGATGGGACGTCAAGTGATGAAGTGAAAGAGCGCTTCTCTCAGACGATGGAGTTTGTGGAGAATTACCTGAGGGATGTTGTCTGCCAGAGTTTCCCGTTCTCTGATAAGGAGAAAAACAAACTCACTTTTGAGGTGTGTATTCTCACTGAGATGTTCACTAAACAGTCATTTTGCATCAGATTCACTAAGCATGAATGACTTTTTAGGTCACATTTTATTCAGTAGAATTTTAAAAACATTTGTAAATAAAATTTATGTTGATTTGATTCATGCAAGTCATTGGCCCTTTGGCAGTCAGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40754
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
ENSDART00000065092 Nonsense 1220 2727 30 64
Genomic Location (Zv9):
Chromosome 6 (position 39890144)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 39961744
GRCz11 6 39959280
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAACATGGGAGCTCACAGTGTGGTCCTCGAACTGTTGCAAATCCCTTA[T/A]GAGAAGGTGCGGGTCAGCCATTGGAGGAATACATTTGGAAAATTATTCTG
Long Flanking Sequence:
AAATCAGAGTTGTGGGTGTATAAGAGACAAGGCTCAGACTCAGGACTGGATGCTGGAGAAGTCACCCCTGAAGCCCACCACAAGGTCAGGATGTACCTCTAAATAAATATAATAAAAACCCAAGAAGCAACATAATAGCTCTTTTCCAAATTGTAGTGAATTATATGTTAAATAGAAGCTTTTTCCTGCTTTAACAGGGTGTCATCAACTCGAGTAGATCAAACAAACCCAAAGTGGAAAGTACCAGCAGCTCGAACTACAGAGTCGTGAAAGAGGTGCAGTGTTTTTTTATGGAGATTTATAAGAAAATTGGATGTTCTTTTGAAGTAAATCTTATGTTTGAAAGAATTCCAACGCTTGTGTGTGTAGATCCTGCTGAGGCTGAGCAAACTGTGTGTTTTGGAGGGCATCTCTGGCAAGAAGAATAAGAAACAGCAGCAGCGGCTCCTCAGGAACATGGGAGCTCACAGTGTGGTCCTCGAACTGTTGCAAATCCCTTA[T/A]GAGAAGGTGCGGGTCAGCCATTGGAGGAATACATTTGGAAAATTATTCTGTGCTACTTTGAAACAAGTGTTCAGGCATACTAGTGCAACAGAATTAATCAGAGCTAATGCAGAATTAAACAGATAGCCAAAATGCACCTGTTATGTTGCATCTAACTTAGATTTGTAGACTAAATTTTGCAATTTAAATGAAATTGATCAAATTTGACTGGAAACAATCTTCTTGCTCATGTTAGTTTCAGGTTTGATGTTCACTGAGCATCAGCCTCTTATTCTTTAAGGACCATCTAGCAATTGCATACATTCCAAAACATGTAAATGATGTCAAATAAATAATATTTAGAAGGTTGTAGTAAATATCTTGTGGTCGCACTGGCTTTATATGTATACAGTACGTAAATTAATTTATAAAAAGGCATCTTATTCTTTTTCATCATGCTTGTGTGTGTTTTTTGACTATTTAGGGGGAGGATGTCCAGATGCAGGAGATCATGACCTTAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20769
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000065092 Nonsense 1255 2727 31 64
Genomic Location (Zv9):
Chromosome 6 (position 39890704)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 39962304
GRCz11 6 39959840
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTTCAAAACTTCTGTGCTGGAAATCAGCAGAACCAGGCACTTCTACAC[A/T]AACACATCAACCTGTTCCTCAACCCTGGGGTAAGAACACACAAACATACT
Long Flanking Sequence:
GAAACAAGTGTTCAGGCATACTAGTGCAACAGAATTAATCAGAGCTAATGCAGAATTAAACAGATAGCCAAAATGCACCTGTTATGTTGCATCTAACTTAGATTTGTAGACTAAATTTTGCAATTTAAATGAAATTGATCAAATTTGACTGGAAACAATCTTCTTGCTCATGTTAGTTTCAGGTTTGATGTTCACTGAGCATCAGCCTCTTATTCTTTAAGGACCATCTAGCAATTGCATACATTCCAAAACATGTAAATGATGTCAAATAAATAATATTTAGAAGGTTGTAGTAAATATCTTGTGGTCGCACTGGCTTTATATGTATACAGTACGTAAATTAATTTATAAAAAGGCATCTTATTCTTTTTCATCATGCTTGTGTGTGTTTTTTGACTATTTAGGGGGAGGATGTCCAGATGCAGGAGATCATGACCTTAGCACATCAGTTCCTTCAAAACTTCTGTGCTGGAAATCAGCAGAACCAGGCACTTCTACAC[A/T]AACACATCAACCTGTTCCTCAACCCTGGGGTAAGAACACACAAACATACTTTGGTGTTTATGAAGACTCTTGATTTGCATTTTATACTGTATTTAACCACTTAAACTCTGCTGCTATTTGGGGATTTCCGCCTGGATTTTGCCTACCCAAATTTAAAAGCTTCCCAAATCCACATGCAGAGGTGTAAATGCAAAAATTTGGTATCATTTTAAAGAAAACCCTTTGAATTTTCATAAAACACTATTGGAAGTGTTTAAAATAACTGTATATGTTGTCTGTTTTATAATAAACACCTTAAAAAAAGAGGCACTTTTTTTTTTTTTTATAAACTCAAAATTGAAAGTGTACCTTTTAGGTTCTGTGTGGTCTAGGGTGCTGTAATTAATTTTGGTGGTTCCTGCACATGTCTGTAATCATAGGAAAAAAGAAAAAGGTCTACCATAATCTATGCAAAAGTTATTGTATTCCAACTGATGAGATGTCCTATACAAGCCACAGGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7044
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
ENSDART00000065092 Nonsense 1371 2727 34 64
Genomic Location (Zv9):
Chromosome 6 (position 39892786)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 39964386
GRCz11 6 39961922
KASP Assay ID:
554-5078.1 (used for ordering genotyping assays)
KASP Sequence:
TGCRKACTTGTTGTTGTCATTATAAGACTTCATGCTSACTCTTACAGGTA[T/A]CACATTCAYCTGGTGGAGTTGCTGGCTGTGTGCACTGAAGGCAAGAACGT
Long Flanking Sequence:
CTGCTGAAATACACAGAGTATTACTTAGTAAATATGTTTTATGTGTGTGTTTGTGTAGCTGGTGACTGCAGGTGAGGATGTGCTGGTGTTCTATAATGACCGGGCGTCTTTTCAGTCATTGGTTCAGATGATGCGTCTTGAGCGGGAACGACTTGATGAGAGCAGTGCACTCAGGTTCGGAGATAAAACTGCCCAAACACGTCTTGTCTCTACAATATTACAATATAGATTGTTACTGTATCTATTTAACGTTGAAAACTGCACTGAATCATGCTAGTATGAACTGAACAAATGTCAATATTTGTTCAATTTGTTGAAGTTGGTGCAGAATATCTTGTTTTATGATTGTAAATATCTGTGCTCTGCCTCTGAATTTTTCAGTTTTCAGCACTCACAATGAGGTTACAATGACATCTCTCATTTGCATTTAAAAAGTCAGAAAAGGTTTGTTGCGTACTTGTTGTTGTCATTATAAGACTTCATGCTCACTCTTACAGGTA[T/A]CACATTCACCTGGTGGAGTTGCTGGCTGTGTGCACTGAAGGCAAGAACGTCTACACTGAGATCAAATGCAACTCGCTGCTCCCTCTCGATGATATTGTACGTGTGGTCACACATGAGGACTGCATCCCTGAGGTGTGTGCACTTTTTGGATTGCTTCACAACCTAAAGTAAATTGTTGGTCTGATGCTGCACAGTCCATAAACAAATAATTGTCTATAACAAATTGTAATATGTTAAACTGGATATTGCTAATCTACTTTTTCTAGTTGAATTCAGACTCTTAATGACTAATGTTTCCCACAACACATTAAATAGGTAAATAGCTTTGATAAACGACTAACATTGTGGATACGATGGTTAATCGTATAGAGGTTGTATCTGGGATTGAATGAATAATGATTAAAATCTAAACCTGATGTTAACTATTTATTTCATGTTATCTGGATTATATTCCGTCTGCAACAGTATTTTAAAAGTTTTATAAACATGTATCTGCATGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20770
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
ENSDART00000065092 Nonsense 1779 2727 43 64
Genomic Location (Zv9):
Chromosome 6 (position 39902956)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 39974556
GRCz11 6 39972092
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGTGTGTTCGTTTGATTTCAGGGGGGTTGAGCAGGGCTGAGATGTCAT[T/A]AATGGAGGTGCAGTGTCATCTAGACCGTGAAGGGGCATCGGATCTTGTCA
Long Flanking Sequence:
TCCGCTCTGCTCACTCACTCAGGTGGTGGATATCAGTCTGCCACCCAAACAGCAGGAGGATCGGCAGAGGGTAGGTCACTAACATCACGCTATCTTCACCTAACGCAGCTCTCTAACAACACATCTCAACCTTTCAACTGCCTTAATTCAATTTCACAACAACTTTAATTATCCATTTCTTGATATGCCACTTTTTTATGATGGATACTTACTGGACAACAAACAAATCAAATAAAAAGCTGTAAAAAATAACATGACCACTCTCATGACAGGGGGAGGCCCTTCGGCAGCTGCTCGTCAATCGTTACTATGGCTTCAGGAGTGGTGGGCGGAGAGAAAGTCTGACCTCGTTTGGTAACTCCACCCTAACTCCTGTCGGGCCAATCAAGAGCCAGCCAGGTAAGTACATTGTAACCTCTGGGAGCATTTGTAATGCAATTTAATCATTTTTATGTGTGTTCGTTTGATTTCAGGGGGGTTGAGCAGGGCTGAGATGTCAT[T/A]AATGGAGGTGCAGTGTCATCTAGACCGTGAAGGGGCATCGGATCTTGTCATTGATCTCATCATGAACACTACCAGCGACCGCGTCTTCCATGAAAGCATTCTGTTGGCCATCGCACTGTTGGAGGGCGGAAACACCATCATACAGGTCAGATAGGCCTGCCAGTGAAATGATAGTTCAGTTTAAAATAAGTGTTGTGTATGTACATTTATGATTTAAGTCATTCTGACATACTAATATGATCAGTTTTTATTGTTACTTACTCATTAAAGGTTCTATGTAATTAAAATAAAAAATGTTTAGATTTTAGTATCAGTATGTTAGTTTTAAAGATATACATGGTGGGCCATTTATATGGATACACCATCATAAAATGGGAATGGTTGGTGAAGATACAAGATGTGCAGCACCTGTAGCTAAGCATACTGGAAGCCTGTGCTGGCATTTCTCCTGTGGTGTTGCTATCAGTGTGGGAAGAGTGGGAGAAGAGGCTTGCATTGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10338
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
ENSDART00000065092 Nonsense 1885 2727 44 64
Genomic Location (Zv9):
Chromosome 6 (position 39904668)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 39976268
GRCz11 6 39973804
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTYGGCAACAAGCGGCGTGACGACAACACTCCAGACAAAGATACTCCA[C/T]AACGCCGCAGAGGTCTNGACTGGCAGTKTTTRATTAGCTCTGAGCAGATR
Long Flanking Sequence:
AAGTCATACAGAAACACAGGTCACTGCAAAGTCACAAGGAAGCGAGGGCTTTCTCCTGCTCAGTTTTTCAAGGTTACATTATAGACCTGCTTTACTTTTACACACAAGACAAAGAAATTAACAAAAAAAATCATAAATCTCATGCTAAGGCCCTGAAACCACATCTTTAGACAGAAACACAATATTTCATAAGCATTTAAGTTTGGTAAAAGTTCTTTTTTCCTCCACTCCTTTATTGATGGTTTTTAGTATTCTGTACAAGACTTTTTCCTATTTTCAAACTTGCAACACATTGATGGAGTCATGTTTGTGTTTTTATCTGGTTGCAGCATTCCTTCTTCAAACGTTTAACAGAAGACAAAAATTCAGAGAAGTTTTTCAGGGTGTTTTATGACAGAATGAAAGTGGCTCAGGTGGAGATCAAAGCCACGGTTACTGTCAACACTAGTGACCTCGGCAACAAGCGGCGTGACGACAACACTCCAGACAAAGATACTCCA[C/T]AACGCCGCAGAGGTCTGGACTGGCAGTTTTTAATTAGCTCTGAGCAGATACTGTCTTTATTTGCACTTAATCTCAACGTACAGTTACTGAAAAAAATCGAGAGACCAACTGAAAATTCTGTTTCGGTAGAATAATAAATTTGGCTTGCGTTTGAGTAAAAAGTTAAGATGTTTTGTTTCAATACTGATTACATTTTTTATGCATGTTTATGTATATTTTTTTGGCAACATATTAATAATGATGTAACTTTGGAAAAGTTAAGAATTCAGTATTTACTGGAAAAACCCTGATTTCAGTCAAAACAAATGAAAAAATCTTTTATTCTGGCCAATTGTGATTTTCAGTAGAAAACACTCTAAATTACTTTTCTTATTTGTAAATTTTTTGTTTTAGATCTTTACAAAACAAAACTTACAAATTAACATATTATTCAAACTCATACCTAATAAATTTCCAGAGAAACTGTCTCTTAATTATTGCCATAGTTTTATATTTGTGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1340
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
ENSDART00000065092 Nonsense 1985 2727 46 64
Genomic Location (Zv9):
Chromosome 6 (position 39906614)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 39978214
GRCz11 6 39975750
KASP Assay ID:
554-1254.1 (used for ordering genotyping assays)
KASP Sequence:
CTCTTTTCCCCACAGAATTTTCTGCGCTGTCAGAACAATAAAAACAACTA[T/G]AAYCTGGTGTGTGAGACGCTGCAGTTCCTGGACTGTATCTGTGGCAGCAC
Long Flanking Sequence:
TATTTCTTAAAAAAAAACTGATTTATAAAATATAGCTTAAGGGGGCTAATAATATCGACCTTAAAATGGTTTTAAAACTGCTTTTATTTTAGCTAAAATAAAACAGTTAAGACTTAAGAAAAACATTATTGGAAATACTGTGAAAAATTCCTTGCTCTTTATTCCTACAAACATTATTTAGGAAATATTTAAATAAAGAAATCAATTTACAGGAGGCCTAATAATTTTGACTTTATTTTACATTATACATCTGTTATTTTGTTTTAAGAAATCTGCAAACACCTGAGAGAAAGTCACTCCTCAAACCGATTTTGTAAAATTACCTCTGAGAACTGTCTTGCACATTTGTTTTCTTAAACATCAGGAACCTGAAACCAGTCACATGACAGAGTAAATTATTGGGTGTGTTGTATACCGTTGAGTATGGTCAAATTCAGCCTATAATTTCTCCTCTTTTCCCCACAGAATTTTCTGCGCTGTCAGAACAATAAAAACAACTA[T/G]AATCTGGTGTGTGAGACGCTGCAGTTCCTGGACTGTATCTGTGGCAGCACAACAGGAGGCCTGGGGCTGTTAGGACTCTACATCAACCAGCATAACGTAGCGCTCATTAATCAGACTGTAGAGAGCCTCACTGAATACTGTCAAGGTCCCTGCCATGACAATCAGGCATGTACTCACACTTCAATTTTTCAGTTATTTCACATATTTCTATCACTCATACTTACCATATTCAACAGAATTGCATTGCCACCCATGAGTCTAATGGCATCGACATCATTATTGCACTGATTCTGAATGATATTAATCCACTGGGCAGGAAGAGAATGGATCTGGTTCTAGAACTAAAGGTATATCATTTTACACTCAATTGACAAAGTAACAATACTTTTCAGTTGTAGTTTCTGAAGTTTGTGTAATTTTAAAGACTTGTAAAGCAGAAATTTTTCAGACGTTTTGAATTTTTTTTAAGGCTTTCAAGATATTTCTGGAAGATCTGTAAT
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:
sa38569
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
ENSDART00000065092 Nonsense 2129 2727 49 64
Genomic Location (Zv9):
Chromosome 6 (position 39907648)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 39979248
GRCz11 6 39976784
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATGAAAATGGCCTACCAGCAGGGGGAGGCAGAGTTTGAGGATGAGGAA[C/T]AGGAGAATGGAGAGGATCATGCAGCATCGCCTCGCAATGTTGGACACAAC
Long Flanking Sequence:
ACAAAAACTAGGATTTATGCTATATTAAAATTAACAAATAATATTATTATAAATATTTAAATTCCATAATTCTAGAATGTTTTTGTAATAATATTATTTCAGTAAAATATTGTGTTTCAATAATATTTAATTTTATTTATTTTAATATATCTGTTAAATATTCAGTTTTTGAAATATTCAGATATTTTTTAAAATTGTATCTTGTGAACCATCATTTGTCTTAATTCTTCAGAATAATGCATCTAAGCTGCTGCTGGCCATCATGGAGAGCCGTCATGACAGTGAGAATGCAGAAAGAATTCTGTACAACATGAGACCAAAAGAACTAGTGAGTTATCACTGTACATTCTGTTGCACTCATTGTGCTAACTGAAATCATACTATGTAAGCAGATGGTAAGTCACAACAGCATTTATACAATCCTGACTGTGTTCATGTTTAAGGTGGAGGTGATGAAAATGGCCTACCAGCAGGGGGAGGCAGAGTTTGAGGATGAGGAA[C/T]AGGAGAATGGAGAGGATCATGCAGCATCGCCTCGCAATGTTGGACACAACATCTATATTCTTGCACATCAGGTACACACATACAATCACATCTGTACATAAGAACTTTTTGTGGTATATGATTTTCCACAGTTTTCACATAGTCTGTTAAATCCACAATAAATTTATGTTTAATATATTAGAGCATTTTGTTTACAAGAGTCATATTATTATTTGTTTGTACACTAGTTTGAACTATCTTGAATGTTGCTGCTGCTTTTGCTGAATGTAATTCCCAGTGGTTGAAAGTCCTTAAAAAATCATACTTAAGTAAAAGTGCCATTACTTACAAGTAGAGTAAAAGTATCTGCTGTAAATATTACTCAAAGTATGAGTAAAGAGTAGACCTTTCAAAAGTATTCAGGAGTAGTGAGCAGTGAGTATTATGCTGTAAAAAGCTGATGCATTTCAGTGTAATTTGAGGATGTGTCTAAACTTAACATTCTGCACACTATGTCATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2315
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000065092 Essential Splice Site 2184 2727 50 64
Genomic Location (Zv9):
Chromosome 6 (position 39909716)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 39981316
GRCz11 6 39978852
KASP Assay ID:
554-3164.1 (used for ordering genotyping assays)
KASP Sequence:
AGAGGACCAGGMCCTGGAGTATTACACAAAACACACCTCACAGATAGAGG[T/C]AGYACAAACACCTTTAACTGATCAAMYTTTTAAAGTCCACTCTTTACATT
Long Flanking Sequence:
TATAATATCATTCAGAATTTTCTAAACAAAAAATGTAAACTAGGCTTAAAAATGGATTCAGGTTTTGTTTGTTGTGCTGGGGTATCTGAAGTATGTGCTGTAAAGCCACTGCCCTCTTCTGGAAAGAGAGTTGCAGCTTATTTGCATATAAAAAGCGTGCATGAAAACTTTTTTTTTTTCGCACACTTTCTGGGGACACCATAGATTGTTGTAAAAATGGACACAATAACATACTGTTAATTTGCTTTTTTTAATTTTTGTCATTCGGCAAGTTTTTGTTTTGGTCTCTATGTAGGAAGATTTTAAATAGACTTTTAAGTAAACCCTGATACCCAGGCACATCTCTTAATCTAAGAGCTATAATAGATCATAGAGTGATCTGATTTAACCTGTTGTTTTCCAGCTGTCGCGTCACAATAAGGAATTGCAAATACTACTGAAACCAGGTGGAGAGGACCAGGCCCTGGAGTATTACACAAAACACACCTCACAGATAGAGG[T/C]AGCACAAACACCTTTAACTGATCAAACTTTTAAAGTCCACTCTTTACATTTGATCTTATATATGTGTCTGTTTGAATACACAGATAGTTCGACAGGATCGCACTATGGAACAGATTGTGTTTCCTGTACCAAATATCTGCTCTTTTCTGACAAATGAGTCCAAGCTGCGTGTGTACTATGGTACAGAGAGAGACGAGCAAGGCAGTAAAATAAATGACTTCTTCTTGCATGCAGACGACCTCTTTAATGAAATGAGGTGGCAGAAAAAACTAAGAGGTAAATGTGTATTTGTGTGTATGTTCATCTCCAGGTGTTTGGTTTTCAGTTGTTTCTCCAGTTTGTTTAGCTGAATCAGTGGTTCTTGGTCAGTATTGACCTAAACAGTATCCTGCAGGACGTATACAGAGAATCCTACAGGAAACATGCAGGAAAAAAATGCTATCTTCAGTGTTGTGCAGTAGTGTCGCTACAAGTAGTGACGCTACTAGCTTAACTACATT
Associated Phenotype:
Not determined