ZMP
JAG2 (2 of 2)
Ensembl ID:
Description:
jagged 2 [Source:HGNC Symbol;Acc:6189]
Human Orthologue:
JAG2
Human Description:
jagged 2 [Source:HGNC Symbol;Acc:6189]
Mouse Orthologue:
Jag2
Mouse Description:
jagged 2 Gene [Source:MGI Symbol;Acc:MGI:1098270]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35540 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22342 | Essential Splice Site | Available for shipment | Available now |
sa11543 | Essential Splice Site | Available for shipment | Available now |
sa6320 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10076 | Nonsense | Available for shipment | Available now |
sa28157 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35541 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35542 | Nonsense | Available for shipment | Available now |
sa13426 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35540
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025007 | Nonsense | 67 | 1136 | 1 | 29 |
Genomic Location (Zv9):
Chromosome 13 (position 33713239)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 33379219 |
GRCz11 | 13 | 33488764 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAATACCAGGTGGAGGTCACCACATCTGGCTTTTGTACGTACGGCACT[G/T]GAAGCTCGAGCGTGGTCGGGGGGAATACGTTTCAGTTGAAAGGATTCAAT
Long Flanking Sequence:
GATCCTTAAAGTTTAAAGGCTTTTAAAACCAATCCCCGTGCGCCCTAATAGATCTACTTTGAAACGTAAAGCATTGCATAAATTGCTAATACAGTACATACTTTTAAGTTAATATTACATTATGACACGAGCCTGTTTATTAACATTTGTCTGCAATACCGTTATGTCCATAAAACACTTCTTAAAAGCTTCTCCGGTATAACCTACTTTTTAAAAATGACCGGAAAATTATTCTGTGCAATCTTACAAAGCCACATTCTCTTTCCAACTCATATTTTAACTGCTGTTTATGTTATTTTTAGGTGTGCCAGTCGTCGGGTTATTTGGAGCTGCAGTTGATCAGCGTGGAGAATGACAGGGCTGAGCTCGCGAATGGAAACTGCTGTGACGGCGCACGAGACGGGCTGTGCGACCAGGACCAATGCGACACCTACTTGAAAGTGTGTCTAAAGGAATACCAGGTGGAGGTCACCACATCTGGCTTTTGTACGTACGGCACT[G/T]GAAGCTCGAGCGTGGTCGGGGGGAATACGTTTCAGTTGAAAGGATTCAATGGAAACCCAAACAAGGCCAATGACCTCGGGACCGTTATCATACCGTTTCAATTCGCCTGGCCGGTAGGTGTTCATATGCTCTTTCAACACAAACAGACCCTTTTGTATACATTTTCTTGCTGTGTATATTGTAACTATATATTGAGTGAGTCTTATAAGTATTAACGTTTTTTCCAGAAGCGTTATTACATAAAAAGGTGTTGGAAAGTGCAATTTTTTTATGTAACATTATTGCTTCCGTACTGATTATAGCTATTCTATTTAATGTAAAACGTTGCTTCCACTAAATGACAGCAGTTTTAAGATGATTATTAGATATAGTCCAATGTAGATAATGTTTAGCTTGACCACCTTGGTACCAGTTTAGATCAGCTAGAAACCAAAGCTGTTGTTTCCAACAGATGGCCAGAACGCACGAGTGAAACACGCATAGCTGGTCTTAACAACACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22342
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025007 | Essential Splice Site | 232 | 1136 | 6 | 29 |
Genomic Location (Zv9):
Chromosome 13 (position 33745537)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 33411517 |
GRCz11 | 13 | 33521062 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGAGTCTGTTCGTTAGAGTAAAATTGTTCCACACACACATCACACACA[T/G]TTGACGGCATGCATGTCAGCTTTAAATAGTAGTGAATGAGCTGAGCAAAC
Long Flanking Sequence:
TCAGTTCAAATGAAACAGAAAACAACAATAAATTAAAACAAAAATACCAATACCAATTAAAACTATAATAAAACTACAAAAGGAACTCATTGATACTAACAAAAATACTAATATGAAATTAGTTTTTCTTTTACTATTAATACATTCAGTTTTTGATACAATTTTGATACCTAAATGTCCAGTCTAATCAACAATACAACAGCTCTGTCATGTCAATAAATTGGTGATCACAATCAAAATAACCATGTCTAAATGAATGGAGAGCATCAGAATGTAATAAAGCTCATTCATATTTCATTCATGTCTTTCAGCTATCTGTAAGCAAGGCTGCAGTGAGCTTCATGGAAGCTGTGAAACACCAGGAGACTGTGTGTAAGTGCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTTTAATCTCAGGTTATGGATCCTGAAGAGATGAATGAGTCTGTTCGTTAGAGTAAAATTGTTCCACACACACATCACACACA[T/G]TTGACGGCATGCATGTCAGCTTTAAATAGTAGTGAATGAGCTGAGCAAACAACTGAAGGATAATATGATAATATTAGCTCCACTGCCCTCATGAATGGCTGGCTATATTCAGAATTCAATTCTAGGTTTATTACATACTACAGAGAAAATCAATGCATCAAACATTTCAAAGAATCCATGCTACTGTTAGTCCTTCACGTTAGCAAGTTCACTAAGCTGTCTTGTTTTGTTGAGCGATGATTCTTTTCCTTTGCTGTAATTCAGCCATCTTTTAAAGTATGCGAGGTGGAAATGACCTTTGACCTGCTGTCTGACTGGAATTCTTTGCAGTCAAAGATTAGGAAACAGACAGAGGTCATGACCTGTGTCTGCTACTGGAAATAAGTTTACACTCTTGTATCCATTAGAGTTACCGGTGTAGTGAACATATGCAATGGGAGACACTACCAGAAGCGCAGAAAAACATTTTATGTTGATAGATGAACAGATAGATACATATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11543
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 |
---|---|---|---|---|---|
ENSDART00000025007 | Essential Splice Site | 273 | 1136 | 7 | 29 |
Genomic Location (Zv9):
Chromosome 13 (position 33746802)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 33412782 |
GRCz11 | 13 | 33522327 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGACGTGCACCTRTGAGAAAAATTGGGGTGGACTTCTGTGTGACAAAG[G/A]TARGTGATACTTTTAAGTAACYACAGATGCAATTAACTGRATAAATRAAA
Long Flanking Sequence:
TTAGGGTAATTAGGCAAGTCATTGTATAATGATGGTTTGTTCTGTAGACTATCAGAAAAAAATAGCTTAAATTAACTAATAATTTTGACTTTAAAATGTTTTTATTCTAGCTGAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAAATATTGTCAGACATACTGTGAAAGTTTCCTTGCTTTGTTAAACATCATTTGGGAAATATTTAAAAAATAAAATAAAATCTCTTTAACTGTACGTAGGTATAGATTTAGCTTAGAGAAGCTTTTGTATAAACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACTTACTTATGCTCTGTTTGTATTACAGGTGTAAGTATGGATGGCAGGGCCCATTATGTGATGAGTGTTTGCCGTATCCAGGTTGTAAACATGGGACCTGTGTGAAACCCTGGACGTGCACCTGTGAGAAAAATTGGGGTGGACTTCTGTGTGACAAAG[G/A]TAAGTGATACTTTTAAGTAACTACAGATGCAATTAACTGAATAAATGAAAATAAAAAATGTGTACAAATATTTTAAGTCTATATAGAAAATGTAATTATGAATAAAATAAAAAAAGGCATTGCTATTTAAAAGACTGGGGGATGATAAGAACATTAGGTCACGCTTCATTTTGATGGTCCGTTTTCTTAAATTTAAGTTATATTACATCTACATGTCTACTAATTCTCATTAGATTATAAGTATAAGACTGTTAGGTTGAGGTTAGAGTTGTGTAAGTTGACTTGCAAAGTTTTTTATAGGCAGTTAAATGTTTGTTTAGCAGCAGTATCAACAGATATTAAGCAGACAGTCTACTAATACTTAAATGGACCGTTAAAATAAAATGTTACCGTAGACTAATAATTTATACAGCAAGGATGCAATAAACTAACCGTAACTGAAGGTAAATATATTTATGTCGCAGAAGATTTCTGTCTCAAATAAATTGACCTTTATATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6320
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 |
---|---|---|---|---|---|
ENSDART00000025007 | Nonsense | 301 | 1136 | 8 | 29 |
Genomic Location (Zv9):
Chromosome 13 (position 33748865)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 33414845 |
GRCz11 | 13 | 33524390 |
KASP Assay ID:
554-5422.1 (used for ordering genotyping assays)
KASP Sequence:
TGTAAATGGAGGCACGTGTTTGAATACAGAGCCGGATGAATATTTCTGCT[T/A]GTGCCCTGAGGGMTATTCTGGTGAAAACTGCCATATCTGTAAGAAAGCTT
Long Flanking Sequence:
AGTCTACTTATGATGTAATGAGAATTATTTGGCACATAGATGCAATGTAACTTACAGTAATTCAACAAAACCATCAAAATCGTGACCTACTATTTTTCTATAGCCCAACAAATATTACTATTACAACAGCAATATTAGTATTTCACCAGACCCCAAACTAATGTTATTTTAACATAACCAGATGCAACCTTTCACAAAATAAAAAGTAAATAACTTGTATGTGAGATTGCTAGTGACCTGAAACATATTACTTAACTAAAAAATGTTTAGCTAAGATAGTAAATGAATGCAGCTGAGGTCTGTTCCCTCTCACTTCAAACATTCACTGACATCCACGCACATTTTTCTGCTCTGAATGGACTTGTTCTGCTATATTCTTTCCTGCTGCAAAAGAAAGATCATGTTTTGTTTCTCCACAGATCTGAATTACTGTGGCACACACAGTCCATGTGTAAATGGAGGCACGTGTTTGAATACAGAGCCGGATGAATATTTCTGCT[T/A]GTGCCCTGAGGGCTATTCTGGTGAAAACTGCCATATCTGTAAGAAAGCTTTCTGATACTGCTGTTATATAAGTATGTTATAAATGATTATAAATGACTTCATATTCCAACATAGATTTATTTACATGCACATATACAGCATATTTGTTATTTTACTGTATACCAATATATGTGTGTTTGTATCATACAGCCAAGCATGCGTGCATGTCAAACCCTTGTGCAAATGGTGGGACGTGTCATGAGCTGGCATCAGGATTTGAGTGCCTGTGTCCCCCAGGGTGGGACGGCCCAACTTGTGCTAAAGGTCAGAAGTCACTCACATTACTCTCCACGAAGCAGACTGTAGAGTGTTGCAGCAGTGACATTAAACCTGGAAGATTAATTTACAATCCTAGTTTCTTGGATTTTTCTATGCTGTAATTTTGTTTTCAGTTAAAGAGTAAAAAAAAGCAGGGGTTCCCAAACTTTTCAGCTTACGACCCCCAAAATAACAATTCCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10076
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 |
---|---|---|---|---|---|
ENSDART00000025007 | Nonsense | 538 | 1136 | 15 | 29 |
Genomic Location (Zv9):
Chromosome 13 (position 33757995)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 33423975 |
GRCz11 | 13 | 33533520 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTACTGYGCCTGTGCTGATGAATRCGAGGGGAAGACATGCAGTCAGCTA[C/T]GAGACCACTGCAAGACCAGCACGTGCCATGGTAGACTACTTCCTATATAT
Long Flanking Sequence:
TTTAAGGAAATGCCAGGAAATATAATTTATTATCAGAGTAGATCTTAACTTCTTTACAAGTTTACCTGGGCCTCTGCCCTGCACACCTGCGAATCATCTCCACCTTTGTGTGTTTTTATTAGGATGGTCGTCATGGTTACGTGTGCCAGTGCCAGCCGGGCTTCATGGGAAGACACTGTGAAGTGCAGCAGAGCAGGTGTGCCAGCTCCCCATGCCAAAATGGTGGACGGTGCCGTTCACTAGCCACGGGCTATGAGTGCGAGTGCCTGTATGGATACACCGGAAACAACTGTGAGGTAAAGTCAGTAATTACACAGGTACATTAAGAACTTTCTCTTTTCAACCCCTCATATACAATCATTCTCCGACTCTCCCTGTAGGTGCAGGTAGATTTATGCAATCCAAACCCATGTCAAAAAAAAGCGCAGTGTCACTCTCTACAGGGAGATTTTTACTGTGCCTGTGCTGATGAATACGAGGGGAAGACATGCAGTCAGCTA[C/T]GAGACCACTGCAAGACCAGCACGTGCCATGGTAGACTACTTCCTATATATGCCCTTTGCATATAATGCTTTGCACCCAAAAATAACATCAATTATTTTCTGTGGTGTTCTCTTTTCCTCATAAGTGATCGACAGCTGTACTACTGCTATTACAACCAATGGCACAGAGAAGGCAGTGAGGTACATCTTATCAAATGTGTGTGGTCCTCACGGCCGCTGCATCAGCCAGTCTGGAGGAAACTTCACCTGCGCCTGCCAACCCGGATTCTCTGGGACGTACTGTCATGAGAGTGAGTGATGTTGTACACATCCACACACAATATTAATAAAGTCTGGGTGATCTGGAAGTTTCTGAGAATTTTATTTCAGTATTTTGATGTACCTCGAAATGAAACAGAATATTGAGTAGGTGGCAAGGATTTCTTTTGGACATCATTTCCTCATGACAAACTAACGGTAAGAGGGGCGAGGTTTAGAATATTGGTATGCAGTTGCTATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28157
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 |
---|---|---|---|---|---|
ENSDART00000025007 | Nonsense | 742 | 1136 | 20 | 29 |
Genomic Location (Zv9):
Chromosome 13 (position 33762112)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 33428092 |
GRCz11 | 13 | 33537637 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGCCCGTGTCTAAATGGGGGCACTTGCATAGGCTCGGGCAGCGTCTTC[A/T]AGTGCATCTGTAAGGATGGATGGGAGGGGCCTACTTGTGCTCAGAGTAAG
Long Flanking Sequence:
GTTTACTGTAGTAAAAAACAAAATTATACTACAGTATTTTTTACAATTTATCAATTTACCAGTTAATACTATAGTATTTTTCAAAGTATGCAAATATTATAATATACACAGTATAGTCCACTTTACTATGTTATGGTTTAAAAATAGTTTAGTATTTATTATAAATTACCCTGGTATTTGTTCATGTTACACCAAGTGAAAAATAAACCGTAAAAAGCTCAATTTAGAGCTAATTGAACACCCATTTTCACCAATGATGATACAGCTCTAAATTTAAATCCACACCACAACTACAATGAAAATAGTTCAGACTTATGTCATTGTTTGAATCACTTTCAGATTTTTTTTCAGCTAATGAACAATAAAATCCTTGACTGCCAGTCTGTTTACAATGAATCTTACTCACTACCTCCGTCTCCCTCTGTCTAGCCATGAACAGCTCATGTGAGTCTGGCCCGTGTCTAAATGGGGGCACTTGCATAGGCTCGGGCAGCGTCTTC[A/T]AGTGCATCTGTAAGGATGGATGGGAGGGGCCTACTTGTGCTCAGAGTAAGATCACGCCCACTTTTCTGTGTTCCTCTCAAAAATATGCGAATGTGCTTTACTCCCACGTGTATGCATGCGATTGGGCCTCAGATGTGCTGGCAGGCTGTGTGTTGCCCTGACAGGTCTAGTTCTGATATATCCTCTGGTAGTTCTGCTTTCATGAGATCTGTTTTGATTCTGTTTTCAGATGTTGACGACTGCAACCCTCATCCATGGTGAGTGATGCAAAAGATTAAATAAGTGAAGAAAAGCACATAATAGAGAATCAAACAAAACATCAAACTCTTCAACAATTGGGCTTGTCACTCATAAAAGTTGGAATAATTTGAATATAAAGGTTTACATCTACTCTCTGTGCATGTAGCAGTTGAGATGGAGTGTGCATTATTGAGACCTTCTATCTGTTTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35541
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 |
---|---|---|---|---|---|
ENSDART00000025007 | Nonsense | 745 | 1136 | 20 | 29 |
Genomic Location (Zv9):
Chromosome 13 (position 33762123)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 33428103 |
GRCz11 | 13 | 33537648 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAAATGGGGGCACTTGCATAGGCTCGGGCAGCGTCTTCAAGTGCATCTG[T/A]AAGGATGGATGGGAGGGGCCTACTTGTGCTCAGAGTAAGATCACGCCCAC
Long Flanking Sequence:
TAAAAAACAAAATTATACTACAGTATTTTTTACAATTTATCAATTTACCAGTTAATACTATAGTATTTTTCAAAGTATGCAAATATTATAATATACACAGTATAGTCCACTTTACTATGTTATGGTTTAAAAATAGTTTAGTATTTATTATAAATTACCCTGGTATTTGTTCATGTTACACCAAGTGAAAAATAAACCGTAAAAAGCTCAATTTAGAGCTAATTGAACACCCATTTTCACCAATGATGATACAGCTCTAAATTTAAATCCACACCACAACTACAATGAAAATAGTTCAGACTTATGTCATTGTTTGAATCACTTTCAGATTTTTTTTCAGCTAATGAACAATAAAATCCTTGACTGCCAGTCTGTTTACAATGAATCTTACTCACTACCTCCGTCTCCCTCTGTCTAGCCATGAACAGCTCATGTGAGTCTGGCCCGTGTCTAAATGGGGGCACTTGCATAGGCTCGGGCAGCGTCTTCAAGTGCATCTG[T/A]AAGGATGGATGGGAGGGGCCTACTTGTGCTCAGAGTAAGATCACGCCCACTTTTCTGTGTTCCTCTCAAAAATATGCGAATGTGCTTTACTCCCACGTGTATGCATGCGATTGGGCCTCAGATGTGCTGGCAGGCTGTGTGTTGCCCTGACAGGTCTAGTTCTGATATATCCTCTGGTAGTTCTGCTTTCATGAGATCTGTTTTGATTCTGTTTTCAGATGTTGACGACTGCAACCCTCATCCATGGTGAGTGATGCAAAAGATTAAATAAGTGAAGAAAAGCACATAATAGAGAATCAAACAAAACATCAAACTCTTCAACAATTGGGCTTGTCACTCATAAAAGTTGGAATAATTTGAATATAAAGGTTTACATCTACTCTCTGTGCATGTAGCAGTTGAGATGGAGTGTGCATTATTGAGACCTTCTATCTGTTTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35542
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 |
---|---|---|---|---|---|
ENSDART00000025007 | Nonsense | 821 | 1136 | 23 | 29 |
Genomic Location (Zv9):
Chromosome 13 (position 33764387)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 33430367 |
GRCz11 | 13 | 33539912 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTATGGAGCCACATGTGTAGATGAGATTAATGGATATCGCTGTCTGTG[C/A]CCCATGGGACGAGCTGGACCACGCTGCCAGGACTGTGAGTTCCCACTGAC
Long Flanking Sequence:
GAAGTTATTATTTGTTGTTACTATGAATTGGGTAGGTGACAAGACTTTATTCAGTTATTGTACATAATAAATGCAGGTTTTTGATAATTTATTTTTTTTTAATGAGACTTTTTAAAAACTAAAATAGAGATTTGTATGTGCTTTTCATGTCTGTTTTATGTATGATAAACTTCTACAAATTGACGTAAACCTTTTTATTAAAAAAAATCAACTGCAGACTTGCATACAGATATGAATTCAAACCAATAGATCAGTGATAAACTAAAAGCCCCTGCCCTACATTTTTTCTCCTTTTTTGGTGATTTTTTTCACTCATTCGATGCATGCCATGTCACAATACACCTTAGAAGTAAAGATCTATTGCTGTTATAACTGTCTCTTGCTCACACACACTCTGTTGTGTCTTTCTCCTCAATCCCAGACATAGATGAATGTCAGTCGTCTCCCTGTTCTTATGGAGCCACATGTGTAGATGAGATTAATGGATATCGCTGTCTGTG[C/A]CCCATGGGACGAGCTGGACCACGCTGCCAGGACTGTGAGTTCCCACTGACAGACCACCCTACTTGTTTGCATTATGAGAAATGAAGTGTTGAATGTCTTTCCACCCTACTCATGTTGTGTGAACACACCTTATCTTGAGCCAAAGAAAACGCAATAAATTGCCTTTTCAAAAGCAATCAGCAGGGTTTGTAATGCAGGGTTTCCGAACAGAAAATATGTGTTAAACGTGAATGCAGATTCAGCTTAATATTTCATTGTCCTTCCCACATTAAAATTCGGATGACAGGGATAGTTATACCTCATGTGGTTTTAAACCGTGTTGAACACAAAACAAATCATTCTGAAGAATGGTGGTTGCTGCCACCAATCAACTTCCATAGTTGGAAAAGCTATTACTATGAAAGTCAATGGGTGGCAGCTATCAGCATTTATTTCAAATGATCTTCTTTTATGCTCAACAGATGTAAATTGGTTCAAGCATGAGTAAATAATGACAGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13426
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 |
---|---|---|---|---|---|
ENSDART00000025007 | Essential Splice Site | 956 | 1136 | 25 | 29 |
Genomic Location (Zv9):
Chromosome 13 (position 33767490)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 33433470 |
GRCz11 | 13 | 33543015 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAACTGTGCTCKTGTTACACTTGTATTTGACTCWGACACTGTACCGCAG[G/A]TAAGAGGTTTTCATTTAATTTGTTTTATGCATTTAAAAGAGGTGAAGCTT
Long Flanking Sequence:
CATATATACTGTTTCTATATTATTTATCATACAAAATATTGTTTTATACTACCACAATTTCAATTAAAAAAGTGGAATTTTTAACATCAAAAATGCAGAGGAGAGATTAATGTCCCATAATGCAATCAATAAACATAAGTAAATGGAAAACAAAAAACATATCCCTTTAATTAATGGATATTTTTACAGTATATGTAAAAAAAAAAAACTCAATCTTCATGAAGTTTTATTTAATGTGACCACAGGTGAATTGTGGTCATCAGTCCTGCTTGTTGCAGTCAGATTCTGAAGTGGCACAGCGCCCCCTGTGTCCACTAGGACAGGAGTGCGTCGAGCATCATTTCCTCTCTTGTCTTCGTCCACCCTGTGATCAGCTGGGAATGTGCTCCACTCGCGGGCGTCTACAACCTATCAACACTCGCTGTCTGCCCAACAACGGCTACCTAGATGTCAACTGTGCTCGTGTTACACTTGTATTTGACTCTGACACTGTACCGCAG[G/A]TAAGAGGTTTTCATTTAATTTGTTTTATGCATTTAAAAGAGGTGAAGCTTATTGCTTTTATCTCAGATTAACAGGATTTCTGATCAAAACACTAAGTATTGTTGATTTGTTTGACAGGGTACTACTGCTGAAGGAGTCTGCACAGAGCTAACTTATCTTCCAATCACACGAACCCTGGCCAAAGACCACGCCCTTTTCCTTCTTTGCGACCAATCACCCTCAGGCCACAATGCTGTGGAGGTTGCTATGGTAATTTCTTCAATGACCATATGAAATTTGCACAATATTTAGAAACAAAATTTGTGTCTGGTGCTAATGTTTAATCTTGGAGCTGCTAAGAAAAAACAAACATCTTGACACCAAACAATTGAATGATTTCGTAATTTTTTTTTCAATATATTGTGTAGAGCTGCAGTCTTTTCCCCTAAATATACGCATTGTCTTGTGATGTTAATCGGACAGCTAAACAAATTAATGAAATTTACAGGAGGTTCTGGGGA
Associated Phenotype:
Not determined