ZMP
ITPR1 (2 of 2)
Ensembl ID:
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.
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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.
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