ZMP
nrxn3a
Ensembl ID:
ZFIN IDs:
Description:
neurexin 3a [Source:RefSeq peptide;Acc:NP_001073478]
Human Orthologue:
NRXN3
Human Description:
neurexin 3 [Source:HGNC Symbol;Acc:8010]
Mouse Orthologue:
Nrxn3
Mouse Description:
neurexin III Gene [Source:MGI Symbol;Acc:MGI:1096389]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2921 | Nonsense | F2 line generated | Not yet available |
sa18056 | Nonsense | Available for shipment | Available now |
sa14031 | Nonsense | Available for shipment | Available now |
sa11330 | Nonsense | Available for shipment | Available now |
sa36373 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32142 | Essential Splice Site | Available for shipment | Available now |
sa9245 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa36372 | Essential Splice Site | Available for shipment | Available now |
sa36371 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa23034 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa2921
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064241 | None | None | 672 | None | 17 |
ENSDART00000088179 | Nonsense | 39 | 1697 | 1 | 33 |
ENSDART00000109034 | Nonsense | 39 | 261 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 17271478)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 17421489 |
GRCz11 | 17 | 17441325 |
KASP Assay ID:
554-3195.1 (used for ordering genotyping assays)
KASP Sequence:
GGCCTGGAGTTTACAGGGTTGCAAGGCCAGTGGGCACGCTATCTCCGCTG[G/A]GACGCCAGCACCAGAAGTGACCTCAGCTTCCAGTTCAAAACAGACGTGTC
Long Flanking Sequence:
CTGGATGATTGAGGTCTGAGGAGATACTAGAAGAAAACAACACCTCAGCAGACACACAGAACCTCATCTGCTAGTCTTCTCAAGTCGATTCATTCCAGGAAGCGAGCAAGAAGAACCTGATTGTCGCCTGAAAGAGATTGGATTGTTGTGCAATGTCATTGGCCTTATGACTGTTATTTAAGACTGTTCTCCTTATTAAGTCCCTCTCCTCTTTTAGGATACTTTTTTTTTCCGTTTCACGCTGCGTTGACGATCTCACCTCTTCTCTAGTATCTCTGGGCATATCGTGGGATGTACTTTGGATTTACTGACCTTTGAACCAAAGCGAATTCAATGATTTCCTTCTGTTCAGGATAATAACCCCAAATCTCCAGCACTTTTACAATGAATTTCTTCAGATTTCCAGTCCAGTTGCAGCTGCTGATCAGTACTGTGCTTGGGCCCTGCTTGGGCCTGGAGTTTACAGGGTTGCAAGGCCAGTGGGCACGCTATCTCCGCTG[G/A]GACGCCAGCACCAGAAGTGACCTCAGCTTCCAGTTCAAAACAGACGTGTCCACTGCCTTAATCCTGTACTTTGACGATGGCGGCTTCTGCGACTTCCTGCAACTCATGGTGGTTGAGGGGAAGCTCCAATTGCAGTTTAGCATTGACTGCGCCGAGACCACTGTTGTATCGGACAAGCGAGTCAATGACAGCAGCTGGCATTCTGCCACCCTGAGCAGGTACAACCTGAGAACTGTGCTGGGTCTGGATGGAGTGAGCAAATGGGCCGAAGTGCGGCCACTGAGGCAGTACATGAAGATCGTTAGTGACCTCTTCCTGGGCGGAGTCCCTCAAGATATTCGCATTTCTGTGCTCACTCTCCCGACAGTGAAGGATCTTCCGCCGTTTAAGGGAATTATCAGGGAACTGAAGTACAATAGCAAGGAACCTATTCTACTTAGCAGCCAGAGGGTCCGCATGGACATCGAGGGGATCTGCATGGAGAACCCATGCGAAAACGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18056
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 |
---|---|---|---|---|---|
ENSDART00000064241 | None | None | 672 | None | 17 |
ENSDART00000088179 | Nonsense | 150 | 1697 | 1 | 33 |
ENSDART00000109034 | Nonsense | 150 | 261 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 17271147)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 17421158 |
GRCz11 | 17 | 17440994 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAGGCAGTACATGAAGATCGTTAGTGACCTCTTCCTGGGCGGAGTCCCT[C/T]AAGATATTCGCATTTCTGTGCTCACTCTCCCGACAGTGAAGGATCTTCCG
Long Flanking Sequence:
CAATGATTTCCTTCTGTTCAGGATAATAACCCCAAATCTCCAGCACTTTTACAATGAATTTCTTCAGATTTCCAGTCCAGTTGCAGCTGCTGATCAGTACTGTGCTTGGGCCCTGCTTGGGCCTGGAGTTTACAGGGTTGCAAGGCCAGTGGGCACGCTATCTCCGCTGGGACGCCAGCACCAGAAGTGACCTCAGCTTCCAGTTCAAAACAGACGTGTCCACTGCCTTAATCCTGTACTTTGACGATGGCGGCTTCTGCGACTTCCTGCAACTCATGGTGGTTGAGGGGAAGCTCCAATTGCAGTTTAGCATTGACTGCGCCGAGACCACTGTTGTATCGGACAAGCGAGTCAATGACAGCAGCTGGCATTCTGCCACCCTGAGCAGGTACAACCTGAGAACTGTGCTGGGTCTGGATGGAGTGAGCAAATGGGCCGAAGTGCGGCCACTGAGGCAGTACATGAAGATCGTTAGTGACCTCTTCCTGGGCGGAGTCCCT[C/T]AAGATATTCGCATTTCTGTGCTCACTCTCCCGACAGTGAAGGATCTTCCGCCGTTTAAGGGAATTATCAGGGAACTGAAGTACAATAGCAAGGAACCTATTCTACTTAGCAGCCAGAGGGTCCGCATGGACATCGAGGGGATCTGCATGGAGAACCCATGCGAAAACGGAGGGACGTGCTCTGTTGTAGATGGGGAACCACTTTGTGATTGTTCTAAGACGGAATATGTTGGCCGATTCTGCAACGAAGGTAAATATATGGTTTATATATCAAAGCAGATACAGTGTAAAATCTTTAAATTTATTGGCAAAGGTCTAACTCTACTTGCTGAAATGTGAATAATGCTTACCAGAATCCTACATCCTCAGCTGCTCCATGCTACTGAAGTTTGATTCTGAGGTCCTGGTTAATGACATCTCTTAACTTGCCTACAGAAAGCTGCCCTGTTCTGTGCATTTGGCAGGTGTTATTGTGCAGGGAAATTCTTGATCTGCCACCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14031
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 |
---|---|---|---|---|---|
ENSDART00000064241 | None | None | 672 | None | 17 |
ENSDART00000088179 | None | None | 1697 | None | 33 |
ENSDART00000109034 | Nonsense | 238 | 261 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 17270881)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 17420892 |
GRCz11 | 17 | 17440728 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGACGGAATATGTTGGCCGATTCTGCAACGAAGGTAAATATATGGTTTA[T/A]ATATCAAAGCAGATACAGTGTAAAATCTTTAAATTTATTGGCAAAGGTCT
Long Flanking Sequence:
CTGCAACTCATGGTGGTTGAGGGGAAGCTCCAATTGCAGTTTAGCATTGACTGCGCCGAGACCACTGTTGTATCGGACAAGCGAGTCAATGACAGCAGCTGGCATTCTGCCACCCTGAGCAGGTACAACCTGAGAACTGTGCTGGGTCTGGATGGAGTGAGCAAATGGGCCGAAGTGCGGCCACTGAGGCAGTACATGAAGATCGTTAGTGACCTCTTCCTGGGCGGAGTCCCTCAAGATATTCGCATTTCTGTGCTCACTCTCCCGACAGTGAAGGATCTTCCGCCGTTTAAGGGAATTATCAGGGAACTGAAGTACAATAGCAAGGAACCTATTCTACTTAGCAGCCAGAGGGTCCGCATGGACATCGAGGGGATCTGCATGGAGAACCCATGCGAAAACGGAGGGACGTGCTCTGTTGTAGATGGGGAACCACTTTGTGATTGTTCTAAGACGGAATATGTTGGCCGATTCTGCAACGAAGGTAAATATATGGTTTA[T/A]ATATCAAAGCAGATACAGTGTAAAATCTTTAAATTTATTGGCAAAGGTCTAACTCTACTTGCTGAAATGTGAATAATGCTTACCAGAATCCTACATCCTCAGCTGCTCCATGCTACTGAAGTTTGATTCTGAGGTCCTGGTTAATGACATCTCTTAACTTGCCTACAGAAAGCTGCCCTGTTCTGTGCATTTGGCAGGTGTTATTGTGCAGGGAAATTCTTGATCTGCCACCTCTATTCCCCCATCGCTTCTTACGATCAATTGAAATCGAATGTCATTGAAATGCTCTACTAGCAAAGCCTACGTTTTTACCTCTGTAAAGCACTAAGCTGTTTGTTTCTGGCAAGCGTTTTGCGGTTATGTGTGTGTGTGTGTTAATCGCACCCTGCTGAGGAGGTGGGGTGTTACGAGGATGTTAAGGTGCCTTTTCAGATCCCTTGGTTGTTTTTCTGAAGTGGCCATTTTAGTTTCTCTGGGGATTTGAGGAGGCCATTTCACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11330
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 |
---|---|---|---|---|---|
ENSDART00000064241 | None | None | 672 | None | 17 |
ENSDART00000088179 | Nonsense | 455 | 1697 | 8 | 33 |
ENSDART00000109034 | None | None | 261 | None | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 17148445)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 17298456 |
GRCz11 | 17 | 17318292 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGCATTGTGGACCCCAAGATGAAGATMCAGGGCGATGTGGTGTTCAAGTG[T/A]GAAAACGTGGCAACGCTGGATCCRATTTCGTTCGAGACGCCTGAGGCCTA
Long Flanking Sequence:
ACGCAGCTGTAGTCTCAAATATGTAACAAAATGTAGCAACGTATTTCAAGTTTATATAATTAGGTCAAGCATGTATCTTAAATGAGCAATTTTTATAATCCATGTAATTTCTTTACATCTTTGTGTTTTCATTTAGTGTTTGTTTTTAATTTAAATTTTAGATGTGATATCATTAAATATGCATAAAACATGGATGGAAATGAAGAGGTAATAAAAAAAAAATCATTTTCTGCTTCTATCCAGTATGCCTTTTTTAAATTTCATTTATTCATGTAACATATGTTCACACAAAAAACTATATATAAAAAAAAGATTTATGAACATTTTAAATGAGTTGTCAGGTTTTGCAAATGAACTCTTTAAAAGGAGCAATTGAGTGATTCTTTGCTTGCATCCACGCAGGTTGTTTACAAAAACAATGACATCCGGCTGGAGCTGTCCCGGCTCGCCCGCATTGTGGACCCCAAGATGAAGATCCAGGGCGATGTGGTGTTCAAGTG[T/A]GAAAACGTGGCAACGCTGGATCCGATTTCGTTCGAGACGCCTGAGGCCTACATCAGCCTGCCTAAGTGGAACACCAAACGCATGGGCTCCATCTCTTTTGACTTCCGCACCACCGAACCCAACGGCCTTATTCTCTTCACCCACGGCAAGCCACAGGAGAGAAAGGACGCCCGCAGCCAGAAGAACACAAAAGTGGACTTCTTTGCCGTGGAGCTGCTGGATGGAAGTCTGTACTTGCTGCTGGATATGGGCTCTGGGACAATCAAAGTGAAAGCCACACAGAACAAGGTGAACGACGGGGCCTGGTACCATGTGGACATCCAGAGAGATGGAAGATCAGGTCAGTTACACACACTTAAAGGGGCTTTTTACAAGATGTTGAAATTATTAAATGGTTGTGACTTTTTTTATTAAACATTCAGATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATGTTTTTGTATTTTATAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36373
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064241 | None | None | 672 | None | 17 |
ENSDART00000088179 | Nonsense | 674 | 1697 | 9 | 33 |
ENSDART00000109034 | None | None | 261 | None | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 17143384)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 17293395 |
GRCz11 | 17 | 17313231 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCAGGCAAACAGTGCGACAGTTACCCATGCAAAAACAAAGGCTTGTGC[A/T]AAGAAGGCTGGAATCGGTTTATCTGTGACTGCACAGGCACTGGTTACTGG
Long Flanking Sequence:
TTAAAGTGAAAACAAGAAATCTAAAATTTTATTTAAACTAAATTTACATTAAAACATTTCTTCATCAGTTAACAGAAATAATCTTTTGTTTGATTTTTCAGTTAAAAAGTTCTTCAGTTCATGCGACAAAACTTCTTTTAAGTTTTATGATTGAAAGTTTAGTGCATTTTTGGTCTTTTTTTCCAGGCACCATATCAGTAAACAGCCGCCGCACTCCTTTCACTGCCAGTGGGGAAAATGAGATTCTGGACCTGGAGGGTGACATGTACTTAGGCGGCCTTCCTGACAGCCGGGGTAGTCTCATCCTGCCCACCGAACTGTGGACCGCCATGTTGAACTACGGCTATGTGGGCTGCATTCGGGACCTGTTCATTGATGGTCGCAGTAAAGACATCCGGCAGATCGCTGAGGCCCAGAACGGAGCAGGCATCAAACCATCCTGCAACAAGATGTCAGGCAAACAGTGCGACAGTTACCCATGCAAAAACAAAGGCTTGTGC[A/T]AAGAAGGCTGGAATCGGTTTATCTGTGACTGCACAGGCACTGGTTACTGGTCCCGCACCTGCGAGAGGGGTGAGTTCACTGATTTTACACTTACAAGCCTGGATTTATGGAGTTTGGGTGCAAGAATAAACCCAAGTGTTGGGGTTAATAGGGATAGTTCACCCAAAAATGAAAATTTTGTCATCATTTAGTTACTCTTGACTTGTTCAAAACCTATTTGAACTTCTCTCTTTTGTTAAACATAAAAGAAGATATTTTTAAAAAGGCTGGTTGTTGAGATCCATTGAAGTCCAATGTATTTTTTTTTACTACTGTGGAAATTAATGTTTTTTTCTTCTTCCTTTCTTCATGTTCAACAGAAGAAAGAAATTTATATAGGTTTAAAATCACATGAGGGAGAGTAGATGATGAGGTAATTAAAATTTTTGGGTCCTGATGGTTTTTAAAGATGGATTTGTTCATACATAATTTGTCTGATTTTACAAAACATTTTATTCCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32142
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064241 | None | None | 672 | None | 17 |
ENSDART00000088179 | Essential Splice Site | 696 | 1697 | 9 | 33 |
ENSDART00000109034 | None | None | 261 | None | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 17143314)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 17293325 |
GRCz11 | 17 | 17313161 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCTGTGACTGCACAGGCACTGGTTACTGGTCCCGCACCTGCGAGAGGG[G/A]TGAGTTCACTGATTTTACACTTACAAGCCTGGATTTATGGAGTTTGGGTG
Long Flanking Sequence:
AACAGAAATAATCTTTTGTTTGATTTTTCAGTTAAAAAGTTCTTCAGTTCATGCGACAAAACTTCTTTTAAGTTTTATGATTGAAAGTTTAGTGCATTTTTGGTCTTTTTTTCCAGGCACCATATCAGTAAACAGCCGCCGCACTCCTTTCACTGCCAGTGGGGAAAATGAGATTCTGGACCTGGAGGGTGACATGTACTTAGGCGGCCTTCCTGACAGCCGGGGTAGTCTCATCCTGCCCACCGAACTGTGGACCGCCATGTTGAACTACGGCTATGTGGGCTGCATTCGGGACCTGTTCATTGATGGTCGCAGTAAAGACATCCGGCAGATCGCTGAGGCCCAGAACGGAGCAGGCATCAAACCATCCTGCAACAAGATGTCAGGCAAACAGTGCGACAGTTACCCATGCAAAAACAAAGGCTTGTGCAAAGAAGGCTGGAATCGGTTTATCTGTGACTGCACAGGCACTGGTTACTGGTCCCGCACCTGCGAGAGGG[G/A]TGAGTTCACTGATTTTACACTTACAAGCCTGGATTTATGGAGTTTGGGTGCAAGAATAAACCCAAGTGTTGGGGTTAATAGGGATAGTTCACCCAAAAATGAAAATTTTGTCATCATTTAGTTACTCTTGACTTGTTCAAAACCTATTTGAACTTCTCTCTTTTGTTAAACATAAAAGAAGATATTTTTAAAAAGGCTGGTTGTTGAGATCCATTGAAGTCCAATGTATTTTTTTTTACTACTGTGGAAATTAATGTTTTTTTCTTCTTCCTTTCTTCATGTTCAACAGAAGAAAGAAATTTATATAGGTTTAAAATCACATGAGGGAGAGTAGATGATGAGGTAATTAAAATTTTTGGGTCCTGATGGTTTTTAAAGATGGATTTGTTCATACATAATTTGTCTGATTTTACAAAACATTTTATTCCACTCCAATTAGCTGTTCTCAGTATTTTCAGAATTATAGATGATAAAAAGATAACACCCCACTATGTTTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9245
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064241 | None | None | 672 | None | 17 |
ENSDART00000088179 | Essential Splice Site | 814 | 1697 | 12 | 33 |
ENSDART00000109034 | None | None | 261 | None | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 17103438)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 17253449 |
GRCz11 | 17 | 17273285 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGAGGGGCAAAAGCTACAAGCTAACGGTTGAYGATGAMGTAGCAGAAGG[T/C]ACTATCCTTGGTCCTCAATCTGAAAGACAAGCACAATTCTTGATGGGTTA
Long Flanking Sequence:
ATATTGTTTCAGTCAAACCAATAAGAATACTGTCTTTGAGTGGTATCCAGACCTTTTATGAGTTTAAGCTATTTAATCACAGGGTTTTGCTTTGATTTTTGTGGTAAAATGGTCACAAAATAAGCTTAACAATTTAGTTAATTTTTTTTTTGTTAAGGCTTATGTTTTGTTTTTAATGTAATATTCAATAAGATCTGCACCAAACCTCTGCTTTCTCTTTTCTTGTAATTGCTAGAATGAATTGAACTCTTACTTGGCATGCAGTAATTTTAGTATAAAATTCAATGTATCTGGGTTTTTTACCTTTTCACACTGAAAGCAAAGGTTTGGTCAGAGACCATTCAGGTTGGAATTAACATGTCCTGACCGTCATTCTCAGGCAAAGGACCAGAGACACTGTATGCCGGACAAAAACTCAATGATAATGAATGGCATACTGTGCGCGTGATCCGGAGGGGCAAAAGCTACAAGCTAACGGTTGACGATGACGTAGCAGAAGG[T/C]ACTATCCTTGGTCCTCAATCTGAAAGACAAGCACAATTCTTGATGGGTTATTAGATTCATATAATTGAAGCACTTGATGGAAGACAACTAAAGAAGTAACTGTGTGAAGGTTGCTAGTTTTTAAAGATTTTGTGGTTTTGATAAACTGTAGGCCATTTTTGGCAATTGCTTAGCCGAACTCAAGTGTTTCACAGCAATAAAAAACATAGTTTTAGTTCAGGTTCATTGCTGCGCTGGCTTAAGTAGGACTGACTTTGTGTAGCCAATAGTTGAAGTGTCTGACTCAGTGCTTGAATAAGGGTTTTGATGGTACAAACAGCATTTTTTCTGCCTGTACAGCAGTGCATTATTGTTTAAGGGTGTAGTATAGCAGCATTTTTTTCTTGTTTTCCTTTCCAACCTGCTGTGGTTTGTAGGTCAGATGGTGGGCGATCACACCCGGTTAGAGTTCCACAACATCGAGACTGGTGTGATGACTGAGCGCCGCTTCGTCTCCATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36372
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064241 | Essential Splice Site | 87 | 672 | 1 | 17 |
ENSDART00000088179 | None | None | 1697 | None | 33 |
ENSDART00000109034 | None | None | 261 | None | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 16960231)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 17110242 |
GRCz11 | 17 | 17130078 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACCCATTTCCATATACCGCTCTCCAGCGTTTCTTAGAAGCGGACATGG[T/C]GAGTTTGCATGGAGTTGTACCATTTGAGAAGACTTGCTTGCTGTTAATTG
Long Flanking Sequence:
TGTCGCCTCTTCAGGTCTTGCGAGTGACTGGTCGCAGACGCTCCTGCTATCCATCTATTCGCTCAGCAGCTGTAAAGGGCTCTCGTCCTTAAGTGAGTGCATTTTCAGAGGGGTCGGTTGTGAGGGTGCTGCTGGAACGAGGAGCTCGGGACTCCTAGCATGGGGTTTTCTGCATCATGAGAGAACTCTCCTCTTTCGGTACTTCGCGCCTAGTGTCTAAGTGTGAGTCGGGTGTGCGTTATGCGTCCCAGCAGAGTGGCGGCGCCGTTTCGGGGCGGTCGCCAGGGATTGAGCCCATGGATGTGGTCTCTGACTTTGGGATGTATTGTGGGTTCGGTGTGGAGTTCCTCACCTGGCTTGGATAATTCAGTGGTCGCCGCTGGACCTCCTGGGGTGGCAACTTCATACACCCATCCTGAACACCCGGTCCACAACCCTCGGCACCACGCTTCACCCATTTCCATATACCGCTCTCCAGCGTTTCTTAGAAGCGGACATGG[T/C]GAGTTTGCATGGAGTTGTACCATTTGAGAAGACTTGCTTGCTGTTAATTGCGATAGGGGAATAATAATTGGGATTTCGTTTATTGAGGGGAAGATTGTGTCAGATGTTCTCAATAGCGTTTATCCAGCTTGGTATCTGTGCTCGGAGTTTAATTAAAGACGGGAAGATAGCGCATCGGAGGGGCTATAATAAGTCTGGCTTTAGATTGGAATTTTGGAACAAGGGGGATCTGATAAGTGTTGAGCTATTTTGTGGTTACGGAGAGAGGAGTTCTGTCTCCCAAGGCACACAGGCAATTACCCTATTAAAGTCTAAAGCGAGCAGCCGAAACTGTGCTGTGGTGTGATTGCTCTTTTGCTGTGGCTCAGTGTCAACAAATCTAAGGTAGAGCTTGGATTGCAGTGGTTTTAAAAAACAAAATAAATCATTAGAAAAGTTGCCAGGTGTGTTTTATGTGCCCAATGAGAAGATGAACTTTGAGCGAAAACGTGTAGATGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36371
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064241 | Essential Splice Site | 336 | 672 | 15 | 17 |
ENSDART00000088179 | Essential Splice Site | 1361 | 1697 | 31 | 33 |
ENSDART00000109034 | None | None | 261 | None | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 16804161)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 16954989 |
GRCz11 | 17 | 16962922 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGTCTACCACCACCACCAGAAAACACCGCACCCCACCAACAATACAGG[T/C]AATGCACAACACACATGAAAAACACATGAGAGAAATGTGTGCTGAGATTA
Long Flanking Sequence:
GTAGTATAACCCCGAGCATTTCAGGAGAAAATTAAGCTGTAGTAATCCAGCACAGCCATCTAAGTCATTGTACCTTGGTCGGGTAGCTTAAATGCCCAAAACAACCATCAATCTTGTTGCTGAACGAGATATACTTTGCTCCGTTACCGACCCATTTAACCAAGAACTGTTCTGGATCTTTCTTGCATCCTCAGGGCGGCAGCTAACGATATTCAACACCCAGGCCACGATAACAATTGGTGGTTCAGACCGCAAGAGGCCATTTCAGGGCCAGCTCTCCGGACTCTACTACAATGGCCTCAAAGTGCTCAACATGGCTGCTCAGGGCAACCCTAACATCAAAATCAATGGCAGCGTCCGACTGGTGGGAGAGGTTCCTGCCGCTGGTTCAGCCAGAACTACGGCTCTCCCTCCAGAGATGTCCACCACCTTTATCGAGACCACCACCACCATGTCTACCACCACCACCAGAAAACACCGCACCCCACCAACAATACAGG[T/C]AATGCACAACACACATGAAAAACACATGAGAGAAATGTGTGCTGAGATTAGAATTAGAAGTTGATGCCTGCGTTTGGTCATTCTCTAGCAGTGGTGACTTTAACTCCAACCCTAATGCTAATAATACACAGGGCAACTTTTTGCTGTCATAAATGGGCAACCGGGTGAGAAACAGGGTAGCTAATTAGGGCAATTTGCTATAGATACAATACTGTTGCCCATTCTTAATAGAAAAACAACTAAGCAACAAAATTACACTGCAACATTGCCCAAATATTTGCCCTGTGTATCATCAGCATACTGTAATTGAACATAAATAAAGAAGCTAATCTTGGCCTGCAGACTAACTAGAAACTTCCAAACAAGTTTGTTTGTACTGTAGCTAAATCTTTGGCTCTCTGATTCACTGGGTGATAACTTAAAAGATTCATTCCAAATAACTGATTAATTTAAAAACACAGCAAATCATTAGGTGTGTTTAACCAATTGTCAAGTGCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23034
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064241 | Nonsense | 352 | 672 | 16 | 17 |
ENSDART00000088179 | Nonsense | 1377 | 1697 | 32 | 33 |
ENSDART00000109034 | None | None | 261 | None | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 16768421)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 16919249 |
GRCz11 | 17 | 16927182 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTAGACCACGGATGACATGGTTTCGTCGGCCGAGTGTTCCAGTGACGAC[G/T]AGGACTTTGCGGAGTGCGAAGGACATGCAGGTGGGCTAGGTCAGTTCACT
Long Flanking Sequence:
ACTAGATCGTATGCGACTGGCCGACCGGATATGATGTACTCCAGTCCAAGCAAGTCCGTGCACTCAAGATGAGAATTAGTAGTTTTTTTTTCTTGTTATTTTTTTGTCAAAAAATCTATATAAATAAAATTCTGTTCATAAATGAGTAATAAGGAGTTCTCTCTACAATCCCTCCAAAATATTTACTCTACAAACCTGTGCGACTGCCACAAGGGGGCGTATTTCATGTCGTGTTTGAATGTTGTTTGCAGTGGGAAGGTGGCTTATGTATGTATGCATATGTTTGGTCAGTGTTTTTAGTCACTTTAAAATTCCAATTTAGTTGGTTAAGTAACAAACAAAAATTGTTTTATCGTTCTCCAGTGTGCCTTACATTAAAGTCATTGTGCAATCTAGCACATTCAAGTCTCTCTTTTGTTTGTCTATTGTCCCGTTTTTCTGTCTGTGTGTTGTAGACCACGGATGACATGGTTTCGTCGGCCGAGTGTTCCAGTGACGAC[G/T]AGGACTTTGCGGAGTGCGAAGGACATGCAGGTGGGCTAGGTCAGTTCACTTTTGCTTGCCTCTATGTGGTGGCCTTTCATTTGCAACTGAGGATCAGATCCTCAAAGCATCGCCTTCCCCCCATGGATAGAAAAAGTGTAACTTACTGCCTAATCCAAGCCATGCAGATCAATATAGAGCACTGATATAGCAGGATATCACTTGAGAAATAACAGAAACTGTAAACTAATGCTAAGTCCATTCAGTATCCTTGAATCAGAGTTAATGTCAAATCATTCCACCAAACTTTGAATACGAGCTACACTTGGCCATGGGGTTTTCCGAAGTGGTTAACATGGTCACACTGATTACTAATTTTGTCCCCAGTGCCTATAATGAGAGCATACGCACAAAATTAGTACAGAAACGTGACATGTTCTCTGCATTGATGCTTCAAAATGTATCATCTTGAGGTTTTTCTGCCTTGTGATAGTGATAGTGGACTGCATTTTGCCACATGA
Associated Phenotype:
Not determined