Busch Lab

ZMP

LOC100333724

Ensembl ID:
ENSDARG00000074149
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
sa10895 Nonsense Available for shipment Available now
sa31844 Essential Splice Site Available for shipment Available now
sa35136 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa21954 Essential Splice Site Available for shipment Available now
sa21953 Nonsense Available for shipment Available now
sa12719 Nonsense Available for shipment Available now
sa27817 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa21952 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa10895
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
ENSDART00000031993 Nonsense 235 2782 7 61
Genomic Location (Zv9):
Chromosome 11 (position 36810974)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 35708202
GRCz11 11 35970185
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAAGATTGTTTTATTTAWGAAGTGGAGCGACAACAAGGAGGCYATTCTT[A/T]AAGGGGTAGATGACCTATGAAATGTCATTTTTTTNYAAGATATGATGCTT
Long Flanking Sequence:
TTTTTACACAGTTTTTTTTAACTACCTCACACGTTTCTGTTAATATTATTAAAGCAATGGCTAATCAGAGATGTAGTTCTGTTGAGCTGCATACTTTCAAATTCTCTCACCATCAGCACCAGCAAACTCCTGAAACTATGAACTAAGGGAATCATTTTGCGGCGTCAGTGATTAAAACTGGAGTTTCAGCATAACTAATGCTTGACTAACGACACAGACGGACATGTTCTGACGAGACATTCCTTCAATTAAAATGATTTTATTTGTAATCAATTTATAAACAGATGTTGTCCACAAATCCTGAATCTGAACATCCTGACTCTTTATGCTCTGGTAACTCTCATTTCAGAGCCAGAATGACTCTGTAGTGTGAAATGTAGTTTGTATTAAGTGCTGTTTTTTCCCTCTGTGTTTCTCCTCAGGTGAACTCGGTGAACTGCAACACGAGCTGGAAGATTGTTTTATTTATGAAGTGGAGCGACAACAAGGAGGCTATTCTT[A/T]AAGGGGTAGATGACCTATGAAATGTCATTTTTTTTCAAGATATGATGCTTCTGTAGTAATTGCATCTCTGTGGTTGTTTAGGGGGACGTTGTTCGGCTGTTTCACGCGGAGCAGGAGAAGTTTCTGACCTGCGATGAGCACCGGAAGAAGCAGCACGTGTTTTTGAGAACCACCGGCCGTCAGTCCGCCACCTCTGCCACCAGCAGCAAAGCATTGTGGGAAATAGAGGTGAGTTTTAAAGTTGTATCTGTCGGGGTGATTGTCACAGATTAACACAACCTAAATGAGTTTGGCCTGAATATAATGTGAATCTGGCTGAATAGATTGAAGTAGTGGGAGTATAAACAGTGCTGTATAAGGAGTTGTAAAAAATAAAGCTGCAAGCAGCGATGAAAGGGACCTCGCACCTGGGTTTAAGCTGACATATATATATATATATACACCATTCTTCATATATAAATAGACTTCAACTATATATATATATATATATATATATATAT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa4430
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000031993 Nonsense 247 2782 8 61
Genomic Location (Zv9):
Chromosome 11 (position 36810862)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 35708090
GRCz11 11 35970073
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCATCTCTGTGGTTGTTTAGGGGGACGTTGTTCGGCTGTTTCACGCGGAG[C/T]AGGAGAAGTTTCTGACCTGCGATGAGCACCGGAAGAAGCAGCACGTGTTT
Long Flanking Sequence:
TCAGCACCAGCAAACTCCTGAAACTATGAACTAAGGGAATCATTTTGCGGCGTCAGTGATTAAAACTGGAGTTTCAGCATAACTAATGCTTGACTAACGACACAGACGGACATGTTCTGACGAGACATTCCTTCAATTAAAATGATTTTATTTGTAATCAATTTATAAACAGATGTTGTCCACAAATCCTGAATCTGAACATCCTGACTCTTTATGCTCTGGTAACTCTCATTTCAGAGCCAGAATGACTCTGTAGTGTGAAATGTAGTTTGTATTAAGTGCTGTTTTTTCCCTCTGTGTTTCTCCTCAGGTGAACTCGGTGAACTGCAACACGAGCTGGAAGATTGTTTTATTTATGAAGTGGAGCGACAACAAGGAGGCTATTCTTAAAGGGGTAGATGACCTATGAAATGTCATTTTTTTTCAAGATATGATGCTTCTGTAGTAATTGCATCTCTGTGGTTGTTTAGGGGGACGTTGTTCGGCTGTTTCACGCGGAG[C/T]AGGAGAAGTTTCTGACCTGCGATGAGCACCGGAAGAAGCAGCACGTGTTTTTGAGAACCACCGGCCGTCAGTCCGCCACCTCTGCCACCAGCAGCAAAGCATTGTGGGAAATAGAGGTGAGTTTTAAAGTTGTATCTGTCGGGGTGATTGTCACAGATTAACACAACCTAAATGAGTTTGGCCTGAATATAATGTGAATCTGGCTGAATAGATTGAAGTAGTGGGAGTATAAACAGTGCTGTATAAGGAGTTGTAAAAAATAAAGCTGCAAGCAGCGATGAAAGGGACCTCGCACCTGGGTTTAAGCTGACATATATATATATATATACACCATTCTTCATATATAAATAGACTTCAACTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACACACACAGTTGAAGTCAGAATTATTAGCGCCCTAGTTTATTTTTTTCCCCAATTTCTGTTTATTGGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31844
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
ENSDART00000031993 Essential Splice Site 342 2782 11 61
Genomic Location (Zv9):
Chromosome 11 (position 36806290)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 35703518
GRCz11 11 35965501
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTGTTTCCTGCTTCAGGTGGCAGATTTTTCACCCTTTAACTTCCAGG[T/C]ACAGTCAATCTCTCAAACGGCTCTCACTACTGTACCTTCATGTTCATCTC
Long Flanking Sequence:
ACTTGTCAGTGATTACTGGTCTTTAAAAATAGTTTCTGCTACAATCAAAAGCATTTTTAAGAGCGATGAACACCTGTTATTTACAATAGGACCAAAATTTTGCATTTAGTGCACTTGAAGCTTTTCAGAAGGGGAAATACTGTGTTAATGTCAAGTCTTCAAAAAAAAAAAAAAGATGAAAAAATCTTGCTATGCAGGTAAACCATGTTCAAAGATCAGGCCCTGACTATCTTGATTAGCTTGTGCCCACAAGTCTATCAGTTTCCTGCTGATTTCTCAGATTTCGTTGCACAATTTAAGGATGTTTTTGGTGTCTTTTTGCATTCACAGGTCAATCCTGACTATGAGGAAGAATCGCAGGAATCCCGTTCATCTGTAAGCAGTCAAATAGCTGTCGTTCTTGTGTTTGTGCTTTTGCTTTGTGTGAAGGCAAATAAACTGTTGGCTGTGTTTCTGTTTCCTGCTTCAGGTGGCAGATTTTTCACCCTTTAACTTCCAGG[T/C]ACAGTCAATCTCTCAAACGGCTCTCACTACTGTACCTTCATGTTCATCTCAGATGCCTAAATCAAAAGATGCCTCTTATCTTGAAGTTTTGTGCAGCATTGTGCTTTTGTCAAGTGTTTGTGCATTTTGTGCCATTTAAAAATTTCATTTGATTTTCTTTTTAGGCTTTGGTGGTTTTCTTTGGTTCTCATTTAACAAATGATTATAACTATTATTTAAATCTGTAGATACAGTGGGTTATAATTAAAGGGGTGGTCCAGAATTTATTTTAAGGCTTGGTTGTGTTTATAAGATGCAAAGCAATGTGTGCTCATGCTTCACTTTACTTTTTTTTCATCTTACTTTGATTATATACAGCTACTCCGCTATCATGAAAACGACATATTTCCTAGTAACGACATATTTCCTAGTTCCTCCAAAGGCCCGCCCTCAAGAGACTCTGATTAGTCAGAAATCATAATGTGCTGTGATTCGTGGATCGGTTCCATGTCACCAGGAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35136
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
ENSDART00000031993 Essential Splice Site 987 2782 23 61
Genomic Location (Zv9):
Chromosome 11 (position 36775444)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 35672672
GRCz11 11 35934655
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACATTCTGGTGATGGATACCAAGCTAAAAATCATAGAGATATTACAGG[T/C]GATTACAAACATTAAATAGTGGAACATGGAATAGCAATTAAATTTCAATA
Long Flanking Sequence:
CCTCATTTACTTCGGCTTTTACAACTTCAGCGACTTGTTACGTTTGACGAAGATCCTTTTGGCCATTTTGGACTGCGTTCATGTCAGCACCATTTATCCCATCAACAAGATGGAAAAAGGAGATGAGTCCAAAAGTAAATCTTCACACTCTTGATCTTTAATATTATAATAATTTAGGTTTATTTGGTAGATCAGCAGCTCAACTTTCAATATTGATATTGTGTATTATAATCAGACAATTGCTAATTGTTTGAAACAGATATGTTGCCTGAGAGGTGTTTAACAATTGGTTGGTTTTATTTCTGCAGGTAGTAATGTAATGAAGTCCATTCATGGTGTTGGTGAGCTGATGACTCAGGTGGTGCTGAGAGGAGGCGGATTCTTACCCACAACCCCTACAACACCTCCAGATGGAGATGTAGTGAAGACCCAGACAGAACCAGAGAAAGAAGACATTCTGGTGATGGATACCAAGCTAAAAATCATAGAGATATTACAGG[T/C]GATTACAAACATTAAATAGTGGAACATGGAATAGCAATTAAATTTCAATAAAAAATAAATAAATAAATAAACATTTTATTTTAAGCATTGCTATTCTGTGGTTTTATAGCGCTTAAAATATTTATTTATTTATTTATTTATATTTTAATCATTGCTACTCTATTGTTTTATAAGGCTTAAAATATTTATTTATTTATTTATTTATATTTTAATCATTGCTACTCTATTGTTTTATAGGGCTTAAAATATTTATTTATTTATATTTTAATCATTGCTATTATATGTTTTTTTAGGGCTTAAATGTTTTATTTTATTTTAATCATTGCTATTCAATGGTTTTATAGGGCTTAAAATATTTTATTTTATTTTACTTTATTTTAGACTTTTGGGACTTCAGCCTGAGGAACCCTAATTTCAGCAGTTAGTAAAAACAGAGTAGAAATCTGTTAACATTTTTTTTGTCATGTCTCTCTTGTTATTCAGTTCATTCTGAATGTTCG
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa27818
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000031993 Essential Splice Site 1166 2782 28 61
Genomic Location (Zv9):
Chromosome 11 (position 36771200)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 35668428
GRCz11 11 35930411
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACACTTCATCCACACACTTTATTTAGCCCTCGTGTTTATTCCTTTTCTA[G/A]AGGGACTCTGGCTCAGACAAAAAAAAGACGGACGGAAATGGCAGTGACAA
Long Flanking Sequence:
CAATGAAATTATACATGTTTTGAGGACAAAAAAAAATTGAAAGGTGAAATGAACATTATTGTTGCACTTTGACAATCCTTTAAAACATTTTTTTGTTTTATTTAATTTTAGAACTTCTTAAATAGAGCTTTAACTTACATTTGTTAATAATTATGTTATTATTAACATGATTATTAGTATTATATTTTAATAATTACAGTTAACTTAAAATCTAACAATATTGCATGATATAACATTTATAAATATTAAAATAATTCATAAAAAATATTTTATGTAATTAACTACCTGGCTGTAGCCTAATTTGATATAATTGGTAAAATACATTAATATATTTTGTATTTTGTAAGCTGTCTTATGTTCTGTTTTTGTAAGGTCTATTTTATTTTAAAACTTCTCTCACCTTTTCTTTGGGACCTTGAAACTGTTATTAATTAAATTCAATGCATCATTCACACTTCATCCACACACTTTATTTAGCCCTCGTGTTTATTCCTTTTCTA[G/A]AGGGACTCTGGCTCAGACAAAAAAAAGACGGACGGAAATGGCAGTGACAATTACAGAGACGTAAAAGAGGTAAAGTGTCTTTCACACGCACGCACATTTAGCTTTGTGTAGCAGTCAGCGGTTATATTGCCATTCACCATAAACACTGGCAAAGCTATTTATGTGGCCTCCTTTTCTAAAGTTGATCTAATTAGCCAGTGCTGAAGTGTTCATCTAGAGGAATTAACTCCACATGAACTGTCGAAGAGTGTTTGAGCTCTTCTTTTTCTCCTGTTTGAAATAAACCCAAATATACATAAAAGACACTTTTGAAATGTTGTTTTTAAGACCAGGCATTAACAGACTTAATATTCCAGATGCCGAATCGGTCACTTTTGGTTGACTCATTTGTACAGTGCTCAACATAAATAAGTAAACATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTTTCAGTGAATATAGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21954
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000031993 Essential Splice Site 1188 2782 28 61
Genomic Location (Zv9):
Chromosome 11 (position 36771129)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 35668357
GRCz11 11 35930340
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAAAGACGGACGGAAATGGCAGTGACAATTACAGAGACGTAAAAGAGG[T/A]AAAGTGTCTTTCACACGCACGCACATTTAGCTTTGTGTAGCAGTCAGCGG
Long Flanking Sequence:
ACAATCCTTTAAAACATTTTTTTGTTTTATTTAATTTTAGAACTTCTTAAATAGAGCTTTAACTTACATTTGTTAATAATTATGTTATTATTAACATGATTATTAGTATTATATTTTAATAATTACAGTTAACTTAAAATCTAACAATATTGCATGATATAACATTTATAAATATTAAAATAATTCATAAAAAATATTTTATGTAATTAACTACCTGGCTGTAGCCTAATTTGATATAATTGGTAAAATACATTAATATATTTTGTATTTTGTAAGCTGTCTTATGTTCTGTTTTTGTAAGGTCTATTTTATTTTAAAACTTCTCTCACCTTTTCTTTGGGACCTTGAAACTGTTATTAATTAAATTCAATGCATCATTCACACTTCATCCACACACTTTATTTAGCCCTCGTGTTTATTCCTTTTCTAGAGGGACTCTGGCTCAGACAAAAAAAAGACGGACGGAAATGGCAGTGACAATTACAGAGACGTAAAAGAGG[T/A]AAAGTGTCTTTCACACGCACGCACATTTAGCTTTGTGTAGCAGTCAGCGGTTATATTGCCATTCACCATAAACACTGGCAAAGCTATTTATGTGGCCTCCTTTTCTAAAGTTGATCTAATTAGCCAGTGCTGAAGTGTTCATCTAGAGGAATTAACTCCACATGAACTGTCGAAGAGTGTTTGAGCTCTTCTTTTTCTCCTGTTTGAAATAAACCCAAATATACATAAAAGACACTTTTGAAATGTTGTTTTTAAGACCAGGCATTAACAGACTTAATATTCCAGATGCCGAATCGGTCACTTTTGGTTGACTCATTTGTACAGTGCTCAACATAAATAAGTAAACATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTTTCAGTGAATATAGGTCATCTATTTTGTGCATTTGAACAAAGCAGATTTATCAAACAGATATATTTATTAACAATAGTGTTTTAGT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa4429
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000031993 Nonsense 1310 2782 31 61
Genomic Location (Zv9):
Chromosome 11 (position 36764548)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 35661776
GRCz11 11 35923759
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATGCAGTGAGATGAACGAACGTGTCGTGCAGCACTTTGTTCACTGCATC[G/T]AGACCCATGGCCGACACGTCCAGTACCTGAAGTTCCTGCAGACCATCGTC
Long Flanking Sequence:
ATTTTGTTGATGACGATGTTGATAATGTTGATAATGTTGATGTTAATGTTGTTGATGATGTTGATAATGTTAATGTTGTTGATGATGTTGATAATGTTAACATTGATTTTAAATTAATTAATTAATAGAATGTTAGTAAACTAAAAAGACTTTATTCATTTTTTATTCATAAATGCATCACAAAAAACTGAATATTCATTATTCAGTAGTCCTCTTAGATCACCATTTGGTGTTCATATTTATATATAGTTCATCATTAGGTCACATTTGTATTAGTGTTCATCACAAGATTTAGTTTGAAAGTCCACGTCCACTAAGTCACCTCAGATAGTTTGAATGCAATCCAGTTTTTTTTTTTCTTTGCTTAAAATTAGAAATCACTCTATGTGTTTGTTCTTCAGATCCTGGAGGCAATCACCATGCAGCACATATTCATGAACAACTTCCAGCTATGCAGTGAGATGAACGAACGTGTCGTGCAGCACTTTGTTCACTGCATC[G/T]AGACCCATGGCCGACACGTCCAGTACCTGAAGTTCCTGCAGACCATCGTCAAGGCAGAGAACAAATTCATCAAGAAGTGCCAGGACATTGTGATGGCCGAGGTGAGAAGCTGATGTGTGCTGGAAGATTATTCATTGTTAGTTGGATCGGGAACACTTTAAAGTAACAATTCACACCATTTAGTACTGGCTTATTACCTGCATATTGTTAATCTTTTATTAGCACTTGATCTTATTTTACATTCCTAATCCTACCCAATACCTTAACCAAACTACTAACTTCATAATAGCAGTTAGTAATAATAAGTAGTTATTAAGCCTTAGTTAGTAGGTTGTTAATAGAGTGAATTGTACATTAAAAAAATTGTGACAGTTTTGTCTAATGATGAAATTTCCCATAAATTCCAACTATTGATCATCACTTTGATTAATCAATAAAGATGCACTAAAAAGTTTTGTTTGCATGTTCCCCATATGTTTACTCCAGGTGCTCCGGTTTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21953
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
ENSDART00000031993 Nonsense 1468 2782 33 61
Genomic Location (Zv9):
Chromosome 11 (position 36757565)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 35654793
GRCz11 11 35916776
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAGCAATCACATGTGGAAGCTCTTTGAAAACTTTCTGGTCGACATATG[C/A]AGGGTAACGAAAGCTTATTCGGGGATTTTTAGCAACCCCAATTATTTGTT
Long Flanking Sequence:
GTATTTAAAAATGGAAATAACATACATATTTTGACCTGTACTTGAACTAAGTTCTACTTTTTGGATATAGATTGTTATTTCACTGATTAAACATGTATTACTAAAAAATAGGCTAAACTTAGTTATTTAAAACCTAGTGGCAAAAGTGGTACAGGTTTAAAATGGCATTAATTAGTACTGTGGGTATGCAGAGCAATGTTCTTGAACCCATATCAAATGTTTCTAGTTCTAAATATGCCTGACTATTTTTTATTTAATTTTTCTATGAAATTATCCTCACACTGAATGACATTTTAATTGGTGTCTTTTGTAAGTCATACTAAATATGTGTGATATAATCGTTTTCATACTTGAAAACTTCTTTACATCCCATCTTAGGTCAAAATAGCATACATCAACTTCCTGAACCATTGCTACGTGGACACAGAGGTGGAAATGAAGGAGATTTACACCAGCAATCACATGTGGAAGCTCTTTGAAAACTTTCTGGTCGACATATG[C/A]AGGGTAACGAAAGCTTATTCGGGGATTTTTAGCAACCCCAATTATTTGTTTAGCTGTGAAGTACAAAAAAAGTACCAATCTCTTGCTCGCTATCTTGAAACCAACATCAATTAAATGTTGCTGATTGCCTGTGTTTTTCAAAAAGACAAAAAGGAGTGATTCAATTTGTGTGGTATTATATGGGTTTGATGTATGATTTCTTATCATCTGAAACTGATGTGACATTTATTTTGGTGCAGGAAAGACGTGAATGAGTGTTTGTTCTGACTGTACAAATACCTCAATCTCTTAATTATTCTCCTTTCTATGGTTGTTTTCATCCAGGTCTGCAACAATACAAGTGACCGCAAACATGCTGACACGACACTAGAAAGCTACGTGACTGAAACCGTGATGAGTATTGTGACGACATTTTTCAGCTCCCCTTTCTCCGACCAGAGCACTAGTTTACAGGTAATGACCCCAATACAGCACAACATGTAAATATATATACTTGGTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12719
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
ENSDART00000031993 Nonsense 1883 2782 44 61
Genomic Location (Zv9):
Chromosome 11 (position 36685802)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 35583030
GRCz11 11 35845013
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTCAGAGAAGTTCTTYAAGGTGTTTTACGAGCGRATGAAACTCGCCCAG[C/T]AGGAGATCAAGGCCACAGTGACGGTGAACACCAGCGATCTAKSCAGCAAA
Long Flanking Sequence:
CATAAACTGTTATCAATTGTACAAAGATCTCACAAAGATAATATAATAATAGTTTATGTAATAATATAGATATATAATTATAGGTTTTATTGTATTTTGCTGTATATTATTGTAATATACAATAATATTGTTATTAAGGCATATATAATATTACAGTGCAACTAAACTTACAATTACATGTATTTATCTTGTTTATTTATCATGGTTTTGGAATTTAACTTGTTTATTAGTATAATTTGTGCTTAGATGTCAGTAATTGTTTGATTTTTATCTCATTCTAAAGGTCTAATATTATTATTATGATAAACTAAATGTTGACTATTATTTGTGCACAAAAATGTCCAGATTCAGGGGAAAAGACTTTTTTTTTTTTGTATACATCTATACACAGTATCTGTCTTCTTACCTTCCTACAGCGGTCGTTCTTCTGCCGCTTGACGGGTGATAATAAGTCAGAGAAGTTCTTTAAGGTGTTTTACGAGCGGATGAAACTCGCCCAG[C/T]AGGAGATCAAGGCCACAGTGACGGTGAACACCAGCGATCTAGGCAGCAAACGCAAAGATGAGGACACCAATGATAAGGATGTACAATCACGCAAGAAAGGTCAGGACTAATCGTAACAAGTAGTCGAAATCTAATGATCTAAAGTTTTGCAATTAGTTAATCGCCACGTCTATGCTATATTGAAAAAAAGTGATATGCTATAGCATGCTAAATAGTGTCATAATCAATATGTGGACTGATTTATTGACCTTAAAATTGTTTTTTTAAAAAATGAAAAACTGCTTGAGTGCATTATAAACTACAGACAAATGCACATCATGCTACACAAACATAATCCTCTCTATCTCTCAGTCAAAGATGTGGCTGTTATAACCGAAGAAGTGCGAGAGCAGCTACTAGAAGCCTCTACGGTCACTAAGAAGGCCTTCAGCACTTACAGAAGAGAAGCGGACGCGGATGAGCATCTGAATGCTACGGAGGGACCAAGCAGCACAGCTGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27817
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
ENSDART00000031993 Essential Splice Site 2337 2782 52 61
Genomic Location (Zv9):
Chromosome 11 (position 36670273)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 35567501
GRCz11 11 35829484
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTTGGTAGCATTCTTCTATCCACTGGAAGGTGGAGGTGTCCGTGGAGG[T/C]GAGACAAATTTTTTTTTTTATGTTTGACGTGAAGTTTTATGTGTAATATT
Long Flanking Sequence:
TGGTCATCTGGATACTTGAAGTATTAATTAACATTTCTTAGATAGTATTGTGAGGGATGCAGCCATCAAAACTCAAATGTATTGCAATTTGGATTTCCTCCACTAGGTGCATGAATGTTCACACTAGAGTATTCGCAACTGAATTTGAACATTAACAGAAAGTTCCAATAAAACTCTATAACTGTCGGTTTATGCCAGAACCACTTGTGTGAAGCTCTGACATGGTGTGCATCAGGGCTTTAGTGTTAGACCCTTTTATTTTTGTGATAGTATCCAAATGAACATTGTGGGATGATGTGTTTTGTGTTGTGTTGGTGTGCATTGTCTTTTAACACTTGGAATTGAATTTTTAACTTGCTGCCTCCTCCAGCTCAGCCCATCCTGTACTGGTGTTCCCGTAACATGTCCTTTTGGAGCAGCATTTCCTTTAACCTCGCCGTCCTCATGAACCTCTTGGTAGCATTCTTCTATCCACTGGAAGGTGGAGGTGTCCGTGGAGG[T/C]GAGACAAATTTTTTTTTTTATGTTTGACGTGAAGTTTTATGTGTAATATTAAACTGATTTTTACAGTGGTGGAAAAATATTGAACACGTCACCATTATTCTCAGAAAACATTTTTAAAGGTGCTGTTGACTTGAAATTTTTACTGGATGTTGGTAACAACTAAATAAATCCATGTATGCAAAAAACCCATTTCAAATTAGTTTACAAATGAAGTTATATTTAATAAAAAAGTATTGAACACATGAAGAAAGGGAGGTGTAGAAAGGCAGGGAAAACCCAGACAGAAGTTGAAATTTCTCTGTAGTTCTTTAGCAGCCCTCTGCCCTTCGTCATTGTAAATTAGCTGCTTCAGTCCAACATCTACATTAGCAGGATGATAAGGATGAAACCAGAGTGGACATTTCAGCAAGACAATGATCCCAAACACAGCCAAGGAAACTCTCAAATGGTTTCAGGGAAAGAATGTTGAATTTTTATGTGTGTATTGTTTGGGCTTTTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21952
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
ENSDART00000031993 Essential Splice Site 2450 2782 54 61
Genomic Location (Zv9):
Chromosome 11 (position 36655247)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 35552475
GRCz11 11 35814458
KASP Assay ID:
2260-4544.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATATGCAGCCTTGGGGTCTTCGTTCACGTCTTCTTCTATAGTTTACTT[G/T]TGAGTACAAACACAAGCGCTCATTCACTCCAGCTCATCTTTCACACATCG
Long Flanking Sequence:
CCTCCTTGCTGAAGGAATGATTTAAGTTTCCAAAATAAAAGAGATTGTATTTTTTCCTGCAAAACTCAAAATGAGCTTACATCTTTTTATTATATTCAAAACATTTGAAGTTTATTTTTTTCTTTTGCTTTAGAAAAATCAGCAGAAAGCTTATGTTCAAATAATGACATCTCATTAACTTTATGGAAACATCTTATAACTGTCACATTAAAAAACACTTCAATCTCAGGTTGCATTCAATTGTAGGCTACTAAAATAACTGTTCTCATTGTTGCTTATCATTACACAAGAGAGAGAGCTAAAAATCTGTGGTCAAACTTTGCTGTTGTTTTCAGGTGGGCAATAAAGTGATCTTCCTAATGAGTTTTGTGGGCAATCGGGGCACGTTCACGAGAGGATACAAGGCCATGATCATGGACGTGGAGTTCCTGTATCATCTGCTGTACCTCATCATATGCAGCCTTGGGGTCTTCGTTCACGTCTTCTTCTATAGTTTACTT[G/T]TGAGTACAAACACAAGCGCTCATTCACTCCAGCTCATCTTTCACACATCGACCTCTGACCTCTCACACTTTCACTGACACTGTTTCCCAGTTCTGGGTTGGGGCTGGAAGGGCATCCGCTGCGTAAAACATATGCCGGATTAGTTGCTGATTCATTCCTCTGTGGTGACCCCTAATAAATAAGACACTAAGCCAAAGGAGAGTGAATGAATGAACTATTCTGTTTAGAAATCTTCTTACTATTAAACAAAACTATACTGGAGGGCTAATAATTTTGAACGGCTAATAATTCTGACTTCAACTGTATTTTTAGAATGGGCGTCTCTTCTAACACACACACACACACACACACATACACACAAGCACACACACACACACACACGCGCTTTCATTCACCCCATCCCAGCTTTAACATATGGACGTCTCTTCTAACTCTGACCTCTGACCTCTCGCACTTTCACCGACACTGTATACACACACACACACACACACACACACACA
Associated Phenotype:
Not determined