ZMP
plxnb1b
Ensembl ID:
ZFIN ID:
Description:
Plexin B1b [Source:UniProtKB/TrEMBL;Acc:B6E523]
Human Orthologue:
PLXNB1
Human Description:
plexin B1 [Source:HGNC Symbol;Acc:9103]
Mouse Orthologue:
Plxnb1
Mouse Description:
plexin B1 Gene [Source:MGI Symbol;Acc:MGI:2154238]
Alleles
There are 14 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9253 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33867 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45252 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12455 | Nonsense | Available for shipment | Available now |
sa20697 | Nonsense | Available for shipment | Available now |
sa17905 | Nonsense | Available for shipment | Available now |
sa31510 | Nonsense | Available for shipment | Available now |
sa16675 | Essential Splice Site | Available for shipment | Available now |
sa40688 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33866 | Nonsense | Available for shipment | Available now |
sa20696 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9253
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 |
---|---|---|---|---|---|
ENSDART00000042248 | Nonsense | 116 | 2220 | 1 | 36 |
Genomic Location (Zv9):
Chromosome 6 (position 23630836)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19886282 |
GRCz11 | 6 | 21946504 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTGACCAATAACCACAACAAGCTACTACTTGTGGATCCTTACAGTCAG[C/T]AACTCATCAGCTGTGGAAGTGTTCATCAAGGAATATGTCAGAAACGAAGT
Long Flanking Sequence:
AAACTTACATACCACACCTTTATATATATAATAATAATAATAATAATAATAATAATAATGGAAGATTCATTAGCAAAATGAAATTTCCACTTGTTTAATCGATTTTTTCCCCTCTCTTTTATTTTTTGTCCTTCTTTGTTGTCAGAATAGTTGACATGCCACCTGGGATGGTGTGTGTGACTTCTCTTTTCACCATACTGTGTTGCTGCGCGGTCACCCAGAGTTCAGCTTCTTCCAGACAACATCCCACTTTTTTACGCAATGACACCTACTTTGAGCACCTGGCTCTGCATCCTGACCCTTCAGTGGGTCGAGTGTATTTAGGTGGCCGTGATCGACTTTACCAGCTTTCTTCAGATCTTCAGCTTGAGGCAGAGGAAGAGACGGGGCCTGTGATAGACAGTCGTGAATGCCTTCCCCCCATCAGTGAAGCAAACTGCCCACAAGCACAGCTGACCAATAACCACAACAAGCTACTACTTGTGGATCCTTACAGTCAG[C/T]AACTCATCAGCTGTGGAAGTGTTCATCAAGGAATATGTCAGAAACGAAGTTTGGATGCAGTAGGGAAAGTGATTTTCACTGCAGAAAGGCCTGTGGATACACAATATGTGGCTGCTAATGACCCCAGCGTGTCTACAGTAGGACTTGTGGCACTCACAAGAGGACGTGGGGTACAGCAGCCAATGTTATTCGTTGGACGTGGTTACACCAACAGTCAACCTCCAATATCTACTCGAAACTTAGTTACAGAACCCGTTTTCTCGTATGAAGAAACTTCAAAGTTAGCAGTAGCTGGAAGGCTTTCGGAGTACGACCATCATTTCGTGACCTCATTTACACATCGTTCTTATGTCTACTTTATGTTCTATCGAAGGGACTTAAAGTCACAATCGAGGGAATATCGCACATATGTTTCCCGTATGTGTTTGGATGACACTGCGTATTATTCTTATGTTGAAGTTCCATTAAGTTGCCGTTCATCCAGAGGAAAGAATTATAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33867
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 |
---|---|---|---|---|---|
ENSDART00000042248 | Nonsense | 258 | 2220 | 1 | 36 |
Genomic Location (Zv9):
Chromosome 6 (position 23630409)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19885855 |
GRCz11 | 6 | 21946077 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTAAAGTCACAATCGAGGGAATATCGCACATATGTTTCCCGTATGTGTT[T/A]GGATGACACTGCGTATTATTCTTATGTTGAAGTTCCATTAAGTTGCCGTT
Long Flanking Sequence:
TGAAGCAAACTGCCCACAAGCACAGCTGACCAATAACCACAACAAGCTACTACTTGTGGATCCTTACAGTCAGCAACTCATCAGCTGTGGAAGTGTTCATCAAGGAATATGTCAGAAACGAAGTTTGGATGCAGTAGGGAAAGTGATTTTCACTGCAGAAAGGCCTGTGGATACACAATATGTGGCTGCTAATGACCCCAGCGTGTCTACAGTAGGACTTGTGGCACTCACAAGAGGACGTGGGGTACAGCAGCCAATGTTATTCGTTGGACGTGGTTACACCAACAGTCAACCTCCAATATCTACTCGAAACTTAGTTACAGAACCCGTTTTCTCGTATGAAGAAACTTCAAAGTTAGCAGTAGCTGGAAGGCTTTCGGAGTACGACCATCATTTCGTGACCTCATTTACACATCGTTCTTATGTCTACTTTATGTTCTATCGAAGGGACTTAAAGTCACAATCGAGGGAATATCGCACATATGTTTCCCGTATGTGTT[T/A]GGATGACACTGCGTATTATTCTTATGTTGAAGTTCCATTAAGTTGCCGTTCATCCAGAGGAAAGAATTATAACCTCCTGCAAGCTCTACATGTTGGCCTGCCAAAGTTTGGCAAAGTTTGGGGAAGGGAAAATGCAGCTACTTCAGAACAAGAGGTCCTGTTGGGAGTGTTTTCAAGTCATTTCGCTTCCTCAAGCCGGCCCAACGAAGAGTCTGCAGTATGCGTGTTTTCACTCGAAGAAGTGGATAAACGTATCAATTCCACAAGAGATCTGTGCTACACTGAAATGGGTCGTGCAGATGGACAGGAGGCTGCATACATTGAGTATGAAGTCAAATCAAACTGTGCCAATCTTCCAGCGGTAAGTTTGAAAACTAGTAAGTTTACTGCTTCACTGTGAACAGCTTCCAAGTACCACTATTATATCAAATAATTTCTAGAGCTCTATATTTAATGACAGATAAACCTGTAACCTTAGTTTGACAAGTCTAACATTGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45252
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 |
---|---|---|---|---|---|
ENSDART00000042248 | Nonsense | 541 | 2220 | 5 | 36 |
Genomic Location (Zv9):
Chromosome 6 (position 23623843)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19879289 |
GRCz11 | 6 | 21939511 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAATGGGAATCAGAAAGATCAGTGGCTGTGGAGCTTTGACATTGAACAA[C/T]AATGCCTGAGTGTGACGTTTCTCAATCCATCCAACATCAGCCGAGAAGAG
Long Flanking Sequence:
TGTTGGAGAACCCAAAATCAAAATATAACCCTTTATAATTTATAATAGGGACTTTTTTTATTCTGCTTGAGCTATCGAAATGTGCAGAGGAAATGATGTTAATTTTGACTTCCTGGAAACTAAATGTTCATTAAAATATATTAACATTTTTATTTGTATTCCTCTTTTTTATTAATGATAATTAGTAAATTATGTGTATTATTATTATTAATGATTGTTTTCTTACTGTGCTCTCGCAGCTAGAGAAGAGGCCTGTAGCAGAGTGTGAAAAGCAGTTGGATTGTCAGTCCTGTCTGATGGCTCATGATCCATATTGTGGCTGGTGTGTTCTTGAGGGAAAGTAAGTTCAAGTTTGAGAAGAACCACATATCCATAATGCTTTGTTTTGGGAAGTTGGTTTCTTGAACATTGTGTCTTTGTACACCAGGTGTGGCCTGCGTAGCGAGTGTAGTAATGGGAATCAGAAAGATCAGTGGCTGTGGAGCTTTGACATTGAACAA[C/T]AATGCCTGAGTGTGACGTTTCTCAATCCATCCAACATCAGCCGAGAAGAGAGGAGAAATGTACGCTTTATGATTTAACACATTGTAACTGAGCACTCAAATAACCAAAAACATTTCACTCTGACAGATCGCTTTCATTGTTTTATTTTTACTTTCAGATCTCTTTAGCAATACCGGGTCTTCCCAGACTGGATCAAGGACACAATTATTCATGTGTCTTCCTGGGCAAGCCAAGTTTGGCTATTGTAACAGAGACCGGTGTCATCTGCTCCTCTCCACACATAAATACATTGCCATCTGTGCCACCTGGACAAGGTGAGGGAATTTCTTTATATATATCACATCTTTATATATATATTACATGTACATAAGTATTTACAGCACCTGCCATGAAGCTCTAAATTGAGCTCAAGTACATTCTATTTCCACTGATCATTCTTGAGATGTTTCAGCAGCTTAATTGGAGTTCACCTGTGGTGAATTGAGTTGATTGGACATGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12455
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 |
---|---|---|---|---|---|
ENSDART00000042248 | Nonsense | 1028 | 2220 | 10 | 36 |
Genomic Location (Zv9):
Chromosome 6 (position 23610795)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19866241 |
GRCz11 | 6 | 21926463 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCAAACTCAGAGAAAAATCTCTCTGCTGGCTCGCAACTTGCAGCTCTAT[C/T]AGGTAACAACAAAAAAACACCCACTTCTCTCTGATATAAAAAAAANTNNC
Long Flanking Sequence:
ATACAAAAACACTTGTGTATGATTTACGCAATGAATATAACAAAATAAAAAATAAAGAAATAAAAAACAAAACCGCAAATAAGAACAAAAACACTTTATAGCATTTTAAGCGTTTAAATTTAAACCTCTTTTATTAAATTAAAAAAAAATATTCTTTTAAAACTTTACTCTCCACGTCTGACCTGCTGATCTTTTCTGTTTTTGTCATGTTATTTAACAAGAAGTTGAAAGTTTGAATTAAATGTTACACGGTAAAATACATAAAATTAAGATGTCATATGTATATAACCCCTGTATGTTTTTACAGTGTGATCAAATAAATTTTATCATGCATGCTTGTAAAATTGTCCTTTTTAAAAATAAATCAGGCTGACGAAGGCGCATTTGTCAATTGGGGAGCATCTGCATGTCCGTGTGTGGAGAAGATTCAAGGATCCTCTCTGCTCCCTGTCCAAACTCAGAGAAAAATCTCTCTGCTGGCTCGCAACTTGCAGCTCTAT[C/T]AGGTAACAACAAAAAAACACCCACTTCTCTCTGATATAAAAAAAAATATCTAGATTTAATAAAAAAAAAACTGTTTCTTCCTAGGACCAGGAGCTGGCATATGAGTGTGTATTGGTGATCGAGGGCCAAACTGTGGTGGTTGATGCAGATGTTGCACAGAATGAGGCGAATCCTTTGCTGTTTGACATCACTTGTCTTGCTCATCAGGTACCACAAAACAAAATGGACTCCAGTGGCTACCTGTAATGTTCACTTGCCCTAATATAATAGTACATAATGGACAAGCACTGACATGTGCCACTGCTGATCTCATCTCCCGATATTTTACTGGAATTTCCTGTCACTTCTCTGTAACGCCAAAACAATCATTTTAGACACAACAACTCCTGAATAATTTTAAATGCTTGTGTGTTCTGTGTGAAAAGACTGAAGTTTGCTGATTGTGTGAGTGTTGACTGAAATCATTCTACCCATGTCTTCTACAGTATGCATATGCAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20697
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 |
---|---|---|---|---|---|
ENSDART00000042248 | Nonsense | 1034 | 2220 | 11 | 36 |
Genomic Location (Zv9):
Chromosome 6 (position 23610693)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19866139 |
GRCz11 | 6 | 21926361 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATTTAATAAAAAAAAAACTGTTTCTTCCTAGGACCAGGAGCTGGCATA[T/G]GAGTGTGTATTGGTGATCGAGGGCCAAACTGTGGTGGTTGATGCAGATGT
Long Flanking Sequence:
ATTTTAAGCGTTTAAATTTAAACCTCTTTTATTAAATTAAAAAAAAATATTCTTTTAAAACTTTACTCTCCACGTCTGACCTGCTGATCTTTTCTGTTTTTGTCATGTTATTTAACAAGAAGTTGAAAGTTTGAATTAAATGTTACACGGTAAAATACATAAAATTAAGATGTCATATGTATATAACCCCTGTATGTTTTTACAGTGTGATCAAATAAATTTTATCATGCATGCTTGTAAAATTGTCCTTTTTAAAAATAAATCAGGCTGACGAAGGCGCATTTGTCAATTGGGGAGCATCTGCATGTCCGTGTGTGGAGAAGATTCAAGGATCCTCTCTGCTCCCTGTCCAAACTCAGAGAAAAATCTCTCTGCTGGCTCGCAACTTGCAGCTCTATCAGGTAACAACAAAAAAACACCCACTTCTCTCTGATATAAAAAAAAATATCTAGATTTAATAAAAAAAAAACTGTTTCTTCCTAGGACCAGGAGCTGGCATA[T/G]GAGTGTGTATTGGTGATCGAGGGCCAAACTGTGGTGGTTGATGCAGATGTTGCACAGAATGAGGCGAATCCTTTGCTGTTTGACATCACTTGTCTTGCTCATCAGGTACCACAAAACAAAATGGACTCCAGTGGCTACCTGTAATGTTCACTTGCCCTAATATAATAGTACATAATGGACAAGCACTGACATGTGCCACTGCTGATCTCATCTCCCGATATTTTACTGGAATTTCCTGTCACTTCTCTGTAACGCCAAAACAATCATTTTAGACACAACAACTCCTGAATAATTTTAAATGCTTGTGTGTTCTGTGTGAAAAGACTGAAGTTTGCTGATTGTGTGAGTGTTGACTGAAATCATTCTACCCATGTCTTCTACAGTATGCATATGCAGAGCCTGTTAGGGAGTATAATGCCATGGTGTATGTGAAGAGAAAAGACACTTTTCATATCGACAGCTCTGATCTTTATGGTAAGTATGAGTGTTTTGATGCTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17905
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 |
---|---|---|---|---|---|
ENSDART00000042248 | Nonsense | 1222 | 2220 | 15 | 36 |
Genomic Location (Zv9):
Chromosome 6 (position 23604635)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19860081 |
GRCz11 | 6 | 21920303 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATGTACAACTACAGCAAGTGGCAAGGAGAAGTCTGGTCACATCTCGGTG[A/T]GAGTTTCTGGTGGAGGTTTCGGCTTGTCAAGTCAGATATTCAGCTACCAG
Long Flanking Sequence:
AAATAGATTGAAACTGAGTTCCATATAAAAACTAAGTTGTTCTTTTCTTTTCATTTGTTTAACTACTACAATGTCACATTTGTTTTTTATAGGAAGCTTTTTGGTTTGAAGTAAAAAGAAGGATTTGTTTAATTTGCTGTTAAGCAGAAACCCCAGTATAGCTCTATCACTCTTTAAAGTAAAATAAAACTTTAATGATGTTATTTTAACACATAAAAAATTAAAATGAGAGTAATCTTCTGGCTTTTTTCTTTTTTTTGCTGTATCGAAAACATACCGAACCGTGACACCACTGTGTCGTATCGAACCGAACCGTGTTATATATAGTATTTATGTTAATACATAACATTATAAAGAATTTTCTTATTGCATGGTTTCTGTTCATTTGCTGTGTTTTATGCCTCTTTTGTGTTTGTGCTTATACATTTGTCTTCATGTTTTTTAGAATTATATGTACAACTACAGCAAGTGGCAAGGAGAAGTCTGGTCACATCTCGGTG[A/T]GAGTTTCTGGTGGAGGTTTCGGCTTGTCAAGTCAGATATTCAGCTACCAGGTTAACTTTTATTTACTACCAATAAGCAAATTTTTTTTTGTCCATGGCTAACACCCGATTTATGTAACAGTTCATCATTTTTGTACACTTTTAAATACGGATTTAGAACTGCAATACACACCGATTTGTACCCTAAGCATCTGATTTTTTTTGATGAGCAGTGACTAATTTTAGAATTAAGGCCAAAAAGTTCTATCTTGGTCTCATCTGACCAGAGAATCTTATTTCTTATTAGCTTGGAGTTCTTCTGGCGGGCTTTCATGTGTTTTGCACTGAGGAGAGGCTTCCTGCTGTAAAGCCACTATTGGTGGAGGGCGGGCTGCAGTGATGGTTGACTTTCTACAACTTTCTACCATCTCCCGACTGCATGTTTAGAGCTCAGCCACAGTGATCTTTGGGTTCTTCTTTACCTCTCTCACCAAGGCTCCTCTCCTCCGATAGCTCAGTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31510
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 |
---|---|---|---|---|---|
ENSDART00000042248 | Nonsense | 1381 | 2220 | 18 | 36 |
ENSDART00000042248 | Nonsense | 1381 | 2220 | 18 | 36 |
Genomic Location (Zv9):
Chromosome 6 (position 23594519)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19849965 |
GRCz11 | 6 | 21910187 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTGACGGTGTTCCCAACAGACTCCATTTCCACCTGGAAAAAACAAAGA[C/T]GAAGGAGAAAAACTAGAAGTACAACAGATGTGGAAGTGCTGGAAACTGAC
Long Flanking Sequence:
AAAAGCTTTATTCAGATTAAGGCAAATAATTTGATGTCCATGTAAACGTAGTCAATGAACAGCATATATTTTATAGCATTTGTTGAAATTCACCATAGTTAAAGTTAATAGTACATCAGTACAATAATGGATGTAAAAAAATACAACTCTGCATTTTAATGATGTGTTAGTAAATGTTGAAACATACTTTAGTTAAAGCTATATTTTTACAAAAATAATAATAAAAAAAAATTATTATTCAAATAACATGGGTAGCTAATAACTCCTATCCTAAATGAAACCTTATTGTAAAGTGATAATCTACAAACTTTGTTTAAGCTTTCACATTCCTAAGACCTCTTTTCTGTGCTCTTGGAAATAATATTTCTTCTTTTATACATTTATACAGTGGAGGTCGTGTAATTAAAGTCTCAGGCCATAACTTGGATGTGGTACAAAAACCTCGGATGCGAGTGACGGTGTTCCCAACAGACTCCATTTCCACCTGGAAAAAACAAAGA[C/T]GAAGGAGAAAAACTAGAAGTACAACAGATGTGGAAGTGCTGGAAACTGACTGTACAGGAAACACACACTGTTCTGTCAAACAGGTGATTTTTTTATTCACTTCAATTAAACCCACACATATAATTAATTCTCAAAATATTATTATCATTATTTATTTTTTTTAGAAAACTGCATGAACTCAGATAAACTGTTTGTTATTAGATTATTCAGAGATACTTTATGAGCTATTCATTTTTATTTTATAAACTGTTTAGATTCCATCATGAAAATAGTGAGTTGGTATTGTTTTGTTGTTACTTTATTGTCTGTTGAACATTTAATAATTTAGCAGTTAAAAATTCTGAAATACTTCCCTATATAAAAAACAGGTTTAAGATTAATCAAATGAGTGTTATTTTGTTGACTCTCTACACACAGTCTTTTTCTAATGTTTTCATTTTTTCTGTAGTTTGAAGAGCACTGTGAGGTGCAGACCTCCTCTCTGTTATTGTGCTGGACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16675
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042248 | Essential Splice Site | 1893 | 2220 | 28 | 36 |
Genomic Location (Zv9):
Chromosome 6 (position 23576133)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19831579 |
GRCz11 | 6 | 21891801 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
MTGTATCCTGCTTTTTTCTTTTTTTNCATTGTTTCTTTTCAYATTTTTCA[G/T]AATGGCGCTCTGGCGTAGCTGGTCATCTAATCCTGTCAGATGAAGATCTA
Long Flanking Sequence:
AAGGCGGGGCTTTATTTACCATATTGACCATTACACTTTTCAAAACTTTACAAGTGACATGTCTTGTGTCTTCTCTCGTATTTGGGTTTACTTAACAGAGTAGATCAATTAAAGATCTTCTGGAATCCAGTTTTGACCGGAATCAATTGATCGACCGGAATTGTCAAATAAACAGGGCACATACAAGTTTGCTTGTATTAAAAAAACAAATCTCAGTGTTTTTCATTCTTTCTCTCTTTAGACGGTGAACGTCTTGATGCAGGGAATAGGCATGAATGAGGCTCAGCCGGTTGCTGCTAAAGTTTTAGATTGTGACACTATAACCCAAGTGAAGGAGAAGATTCTAGACCAGGTGTACAAGGGCACCTCATTCTCTCATCGACCACATACTGACTCTGTAGACTTGGGTGAGAACAACCCTACATGTCTGCTCTTGCTTTCACATATCAGCTGTATCCTGCTTTTTTCTTTTTTTTCATTGTTTCTTTTCACATTTTTCA[G/T]AATGGCGCTCTGGCGTAGCTGGTCATCTAATCCTGTCAGATGAAGATCTAACATCTGTGGTTCAGGGCAACTGGAAACGTCTCAACACGCTCCAGCATTATAAGGTACAACACAATCTTTAAAACACACTATGCTGTTCAACACTCATGCTATTTTTTTTTCCATTTACAAAGCACTGTTTACTATGTATATTGTTACATACAAATAAGTATGCAAATAAACTTAAAGGAACACCCCACCTTCCTTTTGAAAAGGAATTATTTTACAAATTTCTTAGAGTTAAACCACTGACTGTTTTTGAATCAATTCAGCTGATTTCTTGTTCTGGTTGGGTCACTTTTAGCTTAGCTTAGCATAATGAATTGAATCAGATTTGATTATTAGCATTTTGTTCAACAAATAAAAAAAAAGATTTTTAATTATTTTCGTTATTTTCATAGTTACACTGAATAATAAATAAAAAAATAAAATTTTCTAGGACAATATTGCTAGGAACTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40688
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 |
---|---|---|---|---|---|
ENSDART00000042248 | Nonsense | 1936 | 2220 | 29 | 36 |
Genomic Location (Zv9):
Chromosome 6 (position 23572897)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19828343 |
GRCz11 | 6 | 21888565 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTTACTTTTCACTGGATTTTAGGTTCCAGATGGAGCAACTGTTGCTT[T/A]GGTGCCACGCCATAGCAAACACATTCACCATGATACCCACGATTACATCG
Long Flanking Sequence:
TATATATTTATAGCTATCGTCCTGTTAATTAATCAATCTTTAACATTTTTGTGAAATTCATTACATTTATTTATAGATCAAAATCACAATTCAAACCCACTATATTTTTAATGGACTTGAGCCAGACAATATAATAACTGACCAAGTCGTCTTGGTGTATGGACAAATCAGGAGCGGTAATGTGTTCATGCCACTTCCCACTCCAAAGTTGTGATCTGTATGCGCAACATTAAACGTTCATATAATCTTCATTGAACCACTTTAAATCTTCGTTTGAGCCATTATCATTAATAAATAACTTCTAATTTGTTTTGGTGTAGAATTCACTTTTGGAAGGTTTCATTGCTTATTGTATAAATCAAACCCCAGTTGTATTTTGTATTGGTGTGAACAAAGATAAATAAAAACTAATGCTTGTTAATTAATGTTGTGAAGTGTTAGTAAGTATAGTCTTTTACTTTTCACTGGATTTTAGGTTCCAGATGGAGCAACTGTTGCTT[T/A]GGTGCCACGCCATAGCAAACACATTCACCATGATACCCACGATTACATCGCTGGCGAGAGTGAGTAAAATGGTTATGCACTGTGTTTATGTTCACACATACAGCACTTGATTTTTCGATTAATTTTGAAACTGTACAGTTATGTTAAAAAAGAAAGGCTCTGGTGATAAGTACACTATAGCAATAATCTGAATGCACATGTTCATGTCTGAAGTAAATATACTCAAAAAACAAACAAAAAAGATATGCATGAAACCACTTTAATGTAAAAGTGTCTTTTACAATTAATATAGTATCTAACATTTAGTTTAACAGACTGTCAGTGTGCTTAAACATTACAGTGCTAAGCATATATAAATACAATATATATAAATGAATCTTTTAAATTCATATTTTTAATATGAAGCTATACAATATTATATTCGTGCATATACATTAGATCAGTCAGTACTGAAGCCAAATCTGGAGCTTATCTAACAAAATAACTTACAAAAACAATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33866
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 |
---|---|---|---|---|---|
ENSDART00000042248 | Nonsense | 1987 | 2220 | 30 | 36 |
Genomic Location (Zv9):
Chromosome 6 (position 23569698)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19825144 |
GRCz11 | 6 | 21885366 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGGCATCTGGTGAAGGCCAGCGAGGAGCCAGAGTTACCCAAACACAGA[C/T]GAGGCAGTTTAAAAGAACGAGAACGAGCCAAGACCATTCCAGAGATTTAT
Long Flanking Sequence:
TGAAATCTCCAGTGAGCCCATGCTTGGGATCCCTTTGCTCACAGAGGCTGCCTGTGTGTAAACAGATCCTTCTCCAGAGAATTAAAGCAATTAAAAGACAAACTTTGCCTAACTTTATTCAGTTTTGGTCTTCACATTAAAATATATGCCTTGTGAACAGGAAGAAAATAATTTGCCATTACAGTGCAAAATTAAACCACCCTCTATTTAATATTCCATTTCAGATGGAAACCTGTGTAACTGTAAAGCTGCTATTACTTAAGATACTTTCTACATTTTTTAAAACCCACTATATGTAAATAGAGATTACATTTTAAAATAAATAATTGAAGTGTGCTTTTTATATTTGTAGCTAGCCATTTTTTTGTGTTGTGTGTTGTTTAAACTGCTTGAATTTTGACTACGCAGAGACGCCCATGCTGGAGGATGCAGATGAAGGAGGAGTGAGGCTGTGGCATCTGGTGAAGGCCAGCGAGGAGCCAGAGTTACCCAAACACAGA[C/T]GAGGCAGTTTAAAAGAACGAGAACGAGCCAAGACCATTCCAGAGATTTATCTCACGCGGCTCCTGTCAATGAAGGTGTCCTGACAAATACACAATCACAAAGCTTGTAGATACAGACATACGAAGAAACCAAACTCATATCAGTCATGTTCATTTTTGTTTCCTATTTCTAATTCTAAGTAGCTAATTTGCTAAAACAAATGAATACATATATAGCAGGGTATAAATTGAACATTTGCCAAACATAAGTATTTAATAAAACAGCTCGAGAAATGATGTAGGAGTCTCACATCGTTGTCACCTCTTTCACCCCTGATGAGTTTGCATCCCTGCAAGTAATTGTAATTAAACAAGTGTGTAACCTGAAATTTTGGGGAGTCACTTTAAATGTGAAGCAATATAGATTTCTACAACTATTGTTGTAAAAAAAAATATATATATATATATTTTGAGGTGATTTTGAGTCTTAATTTGGCCATAAGCTTTTCTGTGTTTTGGTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20696
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 |
---|---|---|---|---|---|
ENSDART00000042248 | Nonsense | 2003 | 2220 | 30 | 36 |
Genomic Location (Zv9):
Chromosome 6 (position 23569648)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19825094 |
GRCz11 | 6 | 21885316 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGAGGCAGTTTAAAAGAACGAGAACGAGCCAAGACCATTCCAGAGATTTA[T/A]CTCACGCGGCTCCTGTCAATGAAGGTGTCCTGACAAATACACAATCACAA
Long Flanking Sequence:
CCTGTGTGTAAACAGATCCTTCTCCAGAGAATTAAAGCAATTAAAAGACAAACTTTGCCTAACTTTATTCAGTTTTGGTCTTCACATTAAAATATATGCCTTGTGAACAGGAAGAAAATAATTTGCCATTACAGTGCAAAATTAAACCACCCTCTATTTAATATTCCATTTCAGATGGAAACCTGTGTAACTGTAAAGCTGCTATTACTTAAGATACTTTCTACATTTTTTAAAACCCACTATATGTAAATAGAGATTACATTTTAAAATAAATAATTGAAGTGTGCTTTTTATATTTGTAGCTAGCCATTTTTTTGTGTTGTGTGTTGTTTAAACTGCTTGAATTTTGACTACGCAGAGACGCCCATGCTGGAGGATGCAGATGAAGGAGGAGTGAGGCTGTGGCATCTGGTGAAGGCCAGCGAGGAGCCAGAGTTACCCAAACACAGACGAGGCAGTTTAAAAGAACGAGAACGAGCCAAGACCATTCCAGAGATTTA[T/A]CTCACGCGGCTCCTGTCAATGAAGGTGTCCTGACAAATACACAATCACAAAGCTTGTAGATACAGACATACGAAGAAACCAAACTCATATCAGTCATGTTCATTTTTGTTTCCTATTTCTAATTCTAAGTAGCTAATTTGCTAAAACAAATGAATACATATATAGCAGGGTATAAATTGAACATTTGCCAAACATAAGTATTTAATAAAACAGCTCGAGAAATGATGTAGGAGTCTCACATCGTTGTCACCTCTTTCACCCCTGATGAGTTTGCATCCCTGCAAGTAATTGTAATTAAACAAGTGTGTAACCTGAAATTTTGGGGAGTCACTTTAAATGTGAAGCAATATAGATTTCTACAACTATTGTTGTAAAAAAAAATATATATATATATATTTTGAGGTGATTTTGAGTCTTAATTTGGCCATAAGCTTTTCTGTGTTTTGGTAGCTGAATGATTTTTGGTGGCAAATCTTATTTGGACACATATTTTGAGAAAA
Associated Phenotype:
Not determined