ZMP
vcanb
Ensembl ID:
ZFIN ID:
Description:
versican b [Source:RefSeq peptide;Acc:NP_999853]
Human Orthologue:
VCAN
Human Description:
versican [Source:HGNC Symbol;Acc:2464]
Mouse Orthologue:
Vcan
Mouse Description:
versican Gene [Source:MGI Symbol;Acc:MGI:102889]
Alleles
There are 12 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2565 | Nonsense | F2 line generated | Not yet available |
sa27680 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31805 | Nonsense | Available for shipment | Available now |
sa34986 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17214 | Nonsense | Available for shipment | Available now |
sa41736 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa41737 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa923 | Nonsense | Available for shipment | Available now |
sa8831 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa847 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa2565
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000012522 | Nonsense | 96 | 1570 | 2 | 14 |
ENSDART00000134304 | Nonsense | 95 | 1569 | 3 | 15 |
ENSDART00000012522 | Nonsense | 96 | 1570 | 2 | 14 |
ENSDART00000134304 | Nonsense | 95 | 1569 | 3 | 15 |
Genomic Location (Zv9):
Chromosome 10 (position 44672958)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 43366608 |
GRCz11 | 10 | 43194988 |
KASP Assay ID:
554-3258.1 (used for ordering genotyping assays)
KASP Sequence:
ATGGGGAAGCCGTCGCTGTGGTGGCCCAGAACGGCATCATCAAAATGGGC[C/T]AAGAGTATATGGGCCGGGTGTCAGTGCCCAGCCGACCGGAAGACCAAGGG
Long Flanking Sequence:
CCATGAAACTCCAGTTCATTTAATTATTAGAAAATAATACACCAACTACAATTCTAATAATTCCTAAAATACTTTTAGGTAAACAAACAAAAAAAAAAAATACTGGGTTGTTTTAACCAAACATTGGGTCAAAAATGAACAAATCCAACATTTGATTAAAAATTGTACTTTAAATTAAATATATTTTTTAATCAGATTTTACAGTGTAGCTACGTTTTTAGGAGGGTACCTGTTGACTAGCTTGTGCACTCTTGTTAAAACTCCCCCTCTGTCCCCCATCAGACTCTGTTCGCCGGATGCGGGTGGTTCGGAGCTCTTCCCGGGTCCACGGCGCTCTAGCGCAGTCTGTTGTTTTACCGTGTCGTTTTCTGGTGCTGCCGCCGCTACCGGGCTCCTCCGTCATAACTCACTCTGATCACCTGCGCATCAAGTGGACCAAACTCCAGAGCCATGGGGAAGCCGTCGCTGTGGTGGCCCAGAACGGCATCATCAAAATGGGC[C/T]AAGAGTATATGGGCCGGGTGTCAGTGCCCAGCCGACCGGAAGACCAAGGGGACGCTTCTCTGACCATCTCCAGACTCAGGGCCAGTGACGCCGGGGTGTATCGCTGCGAGGTCATGCACGGCATTGAGGACACTCAGGACTCCATTACTCTGGATGTCAGTGGTCAGTGATACTCTTTGACTATTATTAAGATTATGCAAGCTCTGATCACTGCAATGAGCTGTTAAACACTAGCCTAGAGCGCCATCTACTATTAAACACTAGTCTAGAGCGCCATCTGCTGTTAAACACTAGCCTAGAGCGACATCTACTATTAAACACTAGTCTAGAGCGCCATCTACTGTTAAACACTAGCCTAGAGCGCCATCTGCTGTTAAACACTAGCCTAGAGCGCCATCTACTGTTAAACACTAGAGCGCCATCTGCCGTTAAACATTAGCCTAGAGCGCCATCTGCTGTTAAACACTAGCCTAGAGCGCCATCTACTGTTATACACTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27680
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 |
---|---|---|---|---|---|
ENSDART00000012522 | Essential Splice Site | 208 | 1570 | 3 | 14 |
ENSDART00000134304 | Essential Splice Site | 207 | 1569 | 4 | 15 |
Genomic Location (Zv9):
Chromosome 10 (position 44682405)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 43376093 |
GRCz11 | 10 | 43204473 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGGATTCGAGCAGTGTGACGCCGGATGGATGGCCGACCAAACCGTCAGG[T/C]GATAAAACTGTACAATACATACAGTTGAAGACTGTATTATTTTTTCCCCC
Long Flanking Sequence:
TAATTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTACAGAAATTGCCAACTGGCCCAGATGAGGCTCGAACCAGCAACCTTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTAACAATTTTTTCCTACATCAAATTTGATCAAATGGTTATAGTTTTTGCTGGTGTCTGCAGAACCTGACGTGTGTTTTCTGTGTTCAGGTGTTGTGTTTCATTACCGGGCGAACACCAGCCGCTACAGTCTGAACTTCACACGAGCTCAGCAGGCGTGTGCAGATGTGGACTCCAGCATCGCCACCCCTGAACAGCTTTATTCAGCATACGAGGACGGATTCGAGCAGTGTGACGCCGGATGGATGGCCGACCAAACCGTCAGG[T/C]GATAAAACTGTACAATACATACAGTTGAAGACTGTATTATTTTTTCCCCCAATTTCTGTTTAAAGGAGAGCAGATTGTTTCAGCACATTTCTAATCATAATAGTTTTAATAACTCATCTCTAATAACTGATTTATTTTATCTTTGTCATGATGACAGTAACTAATATTTGACTAGATATTCTTCACTTCTATAAAGTGAAAGTGACATTTAAAGGCTTAACTAGGTTAATTAGGTTAACCAGGCATGGTTAGGGTAATTAGGCAAGGGGCCATCTAAACTAGAACCGCCACTTCAATTGATAAAAGACAAAGTCTGCCATTCTCTAATTCTCATACGGCTCTCCCGACAAAAATGCTTGCTTTAAGCCAACAGTTTGCAGTATCGGCCCTGACAACATATTGGGAAAATAACATGCAACAAACCTGGTGGATCATGACCCGTGATGTGCCCGGACACGATCTCACCCAGTCATTGGGTCTCATAGCTTGGCAGATCTGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31805
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 |
---|---|---|---|---|---|
ENSDART00000012522 | Nonsense | 826 | 1570 | 7 | 14 |
ENSDART00000134304 | Nonsense | 825 | 1569 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 10 (position 44709219)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 43402807 |
GRCz11 | 10 | 43231187 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCAACCATGAGTGAATTGCCCATATTTTCAACCAAATCTCCAAGCCAG[G/T]AGATAACCCCACAAGCCATATCATTTAGCACATCAATCAATGAAGAAAGT
Long Flanking Sequence:
TGACCCCTCCAATTGAAGAAATCATCCCTGACGATGAGATAGTAATTCTTATGTCAGAATTTGAAGGTGTTGTATCTTCCCCTAAAACAGATGAATCTGGCTTGACTACGAGAAGTCCAGTTGAGCCCCATTTCACAACAAAAATCTCAAAGCCAGACTTGGGCAGTGGAGATCTTGAAATATATTCTTCAGCTTCTGTTACCGTCACCCCAGAAGTGAGTTTCATTAATGGAAAGCATGAGTTGACCCTGAAACCAGACGTTGAACATGAGGCTAGAGGAGATCAGTTTGACACTGCGACCCCTCCAATGGAAGAAATTATTCCTGATGATGAGGTTGTAATAGTTCTGGCCGAAGCTGAAGGTCTTACATCTTCCTACAAAACGGATGAATCTGGCTTGACTACAAGAAGCCCAGTTGAGCCCTATTTCACAACAAAGATCTCAGAAAGTGCAACCATGAGTGAATTGCCCATATTTTCAACCAAATCTCCAAGCCAG[G/T]AGATAACCCCACAAGCCATATCATTTAGCACATCAATCAATGAAGAAAGTTCAGGGATGCGCCCAACAGATGATGAAGAGGAGCTGACTACATTGGAAGGCTCTGCGGATGACCTGCAGTCAGCTACAGCTTCTACTGACCCAGATATGGTGGCTACTGACGAGACTGAAATAGGTGGAACAGAGAAGCCTACACAGGCATATGGGGTGCATTGCTCCACCCAAGGACCAATTACAACTCCAGAAACATCTCAAACTACAGCATCCAGCCCTGTAGAAAAAGAAATAAAGCCGGAAAGAGATGATTTTGAGGGTTCCACCTCAGCAGAAGAAGAGAGCTCTGGACAAGATATGTATTCTCGAGAGGAACCAAAACAACCGATTTTATCTCCAACTCTCTCTGTTCCTTCTCACTCCTTTACAACTTCCTCAACAAGTACTCATCCCAAAGACCCAAGGGAACCTGCTAGTTTACTCTTGCCTAGTGCAGAGCCTGCAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34986
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 |
---|---|---|---|---|---|
ENSDART00000012522 | Nonsense | 946 | 1570 | 7 | 14 |
ENSDART00000134304 | Nonsense | 945 | 1569 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 10 (position 44709579)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 43403167 |
GRCz11 | 10 | 43231547 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGTTCCACCTCAGCAGAAGAAGAGAGCTCTGGACAAGATATGTATTCT[C/T]GAGAGGAACCAAAACAACCGATTTTATCTCCAACTCTCTCTGTTCCTTCT
Long Flanking Sequence:
AAGGTCTTACATCTTCCTACAAAACGGATGAATCTGGCTTGACTACAAGAAGCCCAGTTGAGCCCTATTTCACAACAAAGATCTCAGAAAGTGCAACCATGAGTGAATTGCCCATATTTTCAACCAAATCTCCAAGCCAGGAGATAACCCCACAAGCCATATCATTTAGCACATCAATCAATGAAGAAAGTTCAGGGATGCGCCCAACAGATGATGAAGAGGAGCTGACTACATTGGAAGGCTCTGCGGATGACCTGCAGTCAGCTACAGCTTCTACTGACCCAGATATGGTGGCTACTGACGAGACTGAAATAGGTGGAACAGAGAAGCCTACACAGGCATATGGGGTGCATTGCTCCACCCAAGGACCAATTACAACTCCAGAAACATCTCAAACTACAGCATCCAGCCCTGTAGAAAAAGAAATAAAGCCGGAAAGAGATGATTTTGAGGGTTCCACCTCAGCAGAAGAAGAGAGCTCTGGACAAGATATGTATTCT[C/T]GAGAGGAACCAAAACAACCGATTTTATCTCCAACTCTCTCTGTTCCTTCTCACTCCTTTACAACTTCCTCAACAAGTACTCATCCCAAAGACCCAAGGGAACCTGCTAGTTTACTCTTGCCTAGTGCAGAGCCTGCAGTAAATGTGGTTTCAACTTTACAAACAAGAGTAATCCCAGAGGAGAAAGACCAAAGCAGGAGTACCACTAAGAGTCCTTTATTGGTGCCTGAGTTTGAAAAAGATGTAAGCACAGTCTTCGCCATCTCTGGGGACAGTGGCTCTGGTGATCATCCAACAGAAGCATTAACAAAACAACCTTTCATTGTGACTACCGTTCCTTCTCTTTTCATTCAACAAACTGTTGAAACTAGTGTTGATGCAAATGAACCAACTAAAGCATTTGAAGGTTCTGCTGAAGACACAACGCCATTGTCTTTCACCACTGCCCGAACTGAAACTAAATTCACAACACAAAGATCAGATGCTAGAATTCTGCCCACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17214
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 |
---|---|---|---|---|---|
ENSDART00000012522 | Nonsense | 1231 | 1570 | 7 | 14 |
ENSDART00000134304 | Nonsense | 1230 | 1569 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 10 (position 44710434)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 43404022 |
GRCz11 | 10 | 43232402 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACTGTTGTAGATTATGAAGATRTGCAGGGTGCCTCAGTTGTTGAAAGA[C/T]AAYCACCAATCAGGGAAGAGTTCACCACAAAWAAGCCAGAGGTCTGGACY
Long Flanking Sequence:
AAACTGTTGAAACTAGTGTTGATGCAAATGAACCAACTAAAGCATTTGAAGGTTCTGCTGAAGACACAACGCCATTGTCTTTCACCACTGCCCGAACTGAAACTAAATTCACAACACAAAGATCAGATGCTAGAATTCTGCCCACGGATAGTCTAAGAGCAATAATGTCTTCCTCCCAAGAAACTGTTCTAATCCAAAAAACTCATTCGGAAGAGACAACCACTTTAGTGGTGCCATCAGAGACTACAGAAGAGACGATGTTACCTTCTAAATTTGGATTCTCAACAGAGGAGCCTCTCATCTCAACGTCTGTACATTCCAGTGGCCCCATCACTATTGCTGATACAAATTTAAGCATTTCAGAGTCAGTCCAGGATATTACAAGTACTTCTTCTACAACAGAAGACATGATCACCACCCCTAAAGCCACAAGTACTTCGTCATTTGAAGAGACTGTTGTAGATTATGAAGATATGCAGGGTGCCTCAGTTGTTGAAAGA[C/T]AACCACCAATCAGGGAAGAGTTCACCACAAAAAAGCCAGAGGTCTGGACTGATTCCAGCTACACTGTGGAGAGCCATGTGGTGGATTTGCAAGGTAGAGTTTTGAGCTGTATTTTTGCAAAGCATACAGAATTTCCACAGTGCTGATTTGTCCATAGTGGATTTGTCCTTTCACTGAAAGTTATGACTTTGTTGTTTTAGATCACGCACTTTGCTCGGTCAGTGTGTGTGAAAACGGCGGAACATGCTTCTCCAGCAGAAAAGGAAATGTTTGTGTCTGCATGCCTGGATTTAGTGGGGAACGCTGTGAAAACGGTTTGTAGCTTTTAGCATTTTAAGTTTTATTCACTCTTGATGAACGCGTTTCTTGGTATAGTGGGACATTTTCATTTCCTATTTCCTGCAGATGTCGATGAATGCCAGTCGAATCCTTGCCGCAATGGTGCTACATGCATTGATGGAATGAACTCTTTCAAATGTGTCTGTCTGCCCAGCTATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41736
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000012522 | Essential Splice Site | 1338 | 1570 | 10 | 14 |
ENSDART00000134304 | Essential Splice Site | 1337 | 1569 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 10 (position 44726467)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 43420055 |
GRCz11 | 10 | 43248435 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATTCAAATGTTAGTTTCTTATATCTCGATGTCTCTCATTTGAACTTTC[A/T]GATACGGAGGTGTGCGACTTTGGTTGGCAGAAGTTTCAGAGCCACTGCTA
Long Flanking Sequence:
ATTGAGAAACAGCCATAACCAAGGGAACTTTGCTGCTGTACCATGGCTGAAGCAGCGCAATGATATTACACAGCGGCTGAATATACTCCCCAGCTAGGTGACCTCTAATGAGACCACCTGCTTCATTATATATCATTATGCTATTACTACAGCCACGGTCAAGCTTTAAATAGAAAAATGATCTAATTTCAAGATGCTAATGGTCTAATCTGATTCAATGATTTATGCTAAGCTAAGCTATAAGTGTTCTTATCAGACCCGAAAATCGACTGAATGTACGCAAACATGGTAAAACCTAACTATTTAACTCTAGGAGAGCTTTAAATGAGCCTGTTTTTAAAAATAAAAGTGTTTTTCTTTATTTTACATTACAGCAGCTTATGCCGTTTGAATAGGAGTGCACAGGCTGATAGTGCTTGTGTTAGGGAAGCTACACGTCGGCTTTTATTCTCATTCAAATGTTAGTTTCTTATATCTCGATGTCTCTCATTTGAACTTTC[A/T]GATACGGAGGTGTGCGACTTTGGTTGGCAGAAGTTTCAGAGCCACTGCTATAAGTACTTCACCCACCGGCGGACATGGGAGGCAGCAGAAAGAGAGTGTCGTCTGCAGGGCGGACACCTGACCAGCGTCCTGTCCCACGAGGAGCAGCTCTTCGTAAATCGTAAGTTCTTCTTTATGAAATGTTTTATAGTGATTGTAAAGCTTATAGTATTCGACAAATTCTCCTCTCCGTATGCACCAGACACTTTCTTATCAACACTCCATACTTTTGGAAAATCCTGTCTTATAAGTTACAGATAAAAGTGTCTGCTATATAAATGGAGGGGGGGGGGGGGGTAGAAAGGGAAGAAGAAAGTTGCAGCCAATCTGCAGTAGGGGGTGTGTCCTCTAATGGTCACGGAGGAGGAAGTTGTATTCGATCAGCAGTAGGGGGTGTGTCCTAATTTTGGGGGAGAAAATTGTGGTCAAATCTGCAGTAGGGGGTGTGTCCTCTAATGGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41737
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000012522 | Nonsense | 1346 | 1570 | 10 | 14 |
ENSDART00000134304 | Nonsense | 1345 | 1569 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 10 (position 44726494)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 43420082 |
GRCz11 | 10 | 43248462 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGATGTCTCTCATTTGAACTTTCAGATACGGAGGTGTGCGACTTTGGTTG[G/A]CAGAAGTTTCAGAGCCACTGCTATAAGTACTTCACCCACCGGCGGACATG
Long Flanking Sequence:
CTTTGCTGCTGTACCATGGCTGAAGCAGCGCAATGATATTACACAGCGGCTGAATATACTCCCCAGCTAGGTGACCTCTAATGAGACCACCTGCTTCATTATATATCATTATGCTATTACTACAGCCACGGTCAAGCTTTAAATAGAAAAATGATCTAATTTCAAGATGCTAATGGTCTAATCTGATTCAATGATTTATGCTAAGCTAAGCTATAAGTGTTCTTATCAGACCCGAAAATCGACTGAATGTACGCAAACATGGTAAAACCTAACTATTTAACTCTAGGAGAGCTTTAAATGAGCCTGTTTTTAAAAATAAAAGTGTTTTTCTTTATTTTACATTACAGCAGCTTATGCCGTTTGAATAGGAGTGCACAGGCTGATAGTGCTTGTGTTAGGGAAGCTACACGTCGGCTTTTATTCTCATTCAAATGTTAGTTTCTTATATCTCGATGTCTCTCATTTGAACTTTCAGATACGGAGGTGTGCGACTTTGGTTG[G/A]CAGAAGTTTCAGAGCCACTGCTATAAGTACTTCACCCACCGGCGGACATGGGAGGCAGCAGAAAGAGAGTGTCGTCTGCAGGGCGGACACCTGACCAGCGTCCTGTCCCACGAGGAGCAGCTCTTCGTAAATCGTAAGTTCTTCTTTATGAAATGTTTTATAGTGATTGTAAAGCTTATAGTATTCGACAAATTCTCCTCTCCGTATGCACCAGACACTTTCTTATCAACACTCCATACTTTTGGAAAATCCTGTCTTATAAGTTACAGATAAAAGTGTCTGCTATATAAATGGAGGGGGGGGGGGGGGTAGAAAGGGAAGAAGAAAGTTGCAGCCAATCTGCAGTAGGGGGTGTGTCCTCTAATGGTCACGGAGGAGGAAGTTGTATTCGATCAGCAGTAGGGGGTGTGTCCTAATTTTGGGGGAGAAAATTGTGGTCAAATCTGCAGTAGGGGGTGTGTCCTCTAATGGTCACGGAGGAGGAAGTTTTATTCGATTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa923
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 |
---|---|---|---|---|---|
ENSDART00000012522 | Nonsense | 1375 | 1570 | 10 | 14 |
ENSDART00000134304 | Nonsense | 1374 | 1569 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 10 (position 44726579)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 43420167 |
GRCz11 | 10 | 43248547 |
KASP Assay ID:
554-0829.1 (used for ordering genotyping assays)
KASP Sequence:
CCCACCGGCGGACRTGGGAGGCAGCAGAAAGAGAGTGTCGTCTGCAGGGC[G/T]GACACCTGACCAGCGTCCTGTCCCACGAGGAGCAGCTCTTCGTAAATCGT
Long Flanking Sequence:
ACCACCTGCTTCATTATATATCATTATGCTATTACTACAGCCACGGTCAAGCTTTAAATAGAAAAATGATCTAATTTCAAGATGCTAATGGTCTAATCTGATTCAATGATTTATGCTAAGCTAAGCTATAAGTGTTCTTATCAGACCCGAAAATCGACTGAATGTACGCAAACATGGTAAAACCTAACTATTTAACTCTAGGAGAGCTTTAAATGAGCCTGTTTTTAAAAATAAAAGTGTTTTTCTTTATTTTACATTACAGCAGCTTATGCCGTTTGAATAGGAGTGCACAGGCTGATAGTGCTTGTGTTAGGGAAGCTACACGTCGGCTTTTATTCTCATTCAAATGTTAGTTTCTTATATCTCGATGTCTCTCATTTGAACTTTCAGATACGGAGGTGTGCGACTTTGGTTGGCAGAAGTTTCAGAGCCACTGCTATAAGTACTTCACCCACCGGCGGACATGGGAGGCAGCAGAAAGAGAGTGTCGTCTGCAGGGC[G/T]GACACCTGACCAGCGTCCTGTCCCACGAGGAGCAGCTCTTCGTAAATCGTAAGTTCTTCTTTATGAAATGTTTTATAGTGATTGTAAAGCTTATAGTATTCGACAAATTCTCCTCTCCGTATGCACCAGACACTTTCTTATCAACACTCCATACTTTTGGAAAATCCTGTCTTATAAGTTACAGATAAAAGTGTCTGCTATATAAATGGAGGGGGGGGGGGGGGTAGAAAGGGAAGAAGAAAGTTGCAGCCAATCTGCAGTAGGGGGTGTGTCCTCTAATGGTCACGGAGGAGGAAGTTGTATTCGATCAGCAGTAGGGGGTGTGTCCTAATTTTGGGGGAGAAAATTGTGGTCAAATCTGCAGTAGGGGGTGTGTCCTCTAATGGTCACGGAGGAGGAAGTTTTATTCGATTAGCTGTAGGGGGTGTGTCCTAATTTTGGGGGAGAAAATTGTGGTCAAATCTGCAGTAGGGGGTGTGTCCTTTTATGGTCACGAAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8831
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000012522 | Nonsense | 1443 | 1570 | 12 | 14 |
ENSDART00000134304 | Nonsense | 1442 | 1569 | 13 | 15 |
Genomic Location (Zv9):
Chromosome 10 (position 44736034)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 43429622 |
GRCz10 | KN150172.1 | 5782 |
GRCz11 | 10 | 43258002 |
GRCz11 | KN150172.1 | 5782 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCCGGACAGCTTCTTCTCCACCGGTGAGGACTGTGTGGTCATGATCTG[G/A]CATGAGAGCGGACAGTGGAAMGATGTGCCCTGCAACTACCACCTGACCTT
Long Flanking Sequence:
GTCTTACCGCTGATTTATATCTGGTGACGATGTCTGTGGGTGTCACCATTCAAAATGAAAGTGCAGCTTTCCACTTATAATGTCTTATTGCCCATCGCCATGAATTAAAATAAGGACGCATGACAGCTGAGCGGGACTCTGCAAAATAAACCATGAAACTCTGACCAATGTAAGGAGAGTTAACTCACATGTGACTTGTACAGTAGCTCTTTTGGTCCGTTTAGAAACTTTGCAGTGTGAAAGCGAACCGCACCAAGAGCAAAGAGTATTAATGTAACTATTTTAATCCCTGTTTCGGAACACATGAATCGATTCACAGGTGTGAATGCACACAAAGTCTCATTTTTCTTTGTTGTTGTAATTTATATATTTTTTTGTGTTCAAATCAAGAAAAAAGAAATTCACAAGTGTGCTCTGGTTCTCCAGCAATTCGAGAACTGGCGTGATGGTCAGCCGGACAGCTTCTTCTCCACCGGTGAGGACTGTGTGGTCATGATCTG[G/A]CATGAGAGCGGACAGTGGAACGATGTGCCCTGCAACTACCACCTGACCTTCACCTGTAAGAAGGGCACAGGTGAGACAGCGCTTTATTTATTTCATTTCTTTATTGTTTTTGACTATAGGTGTGTTCCAAATTGCATACTTATACGCACTATTCCACACCATTTTGAAGTATAAGTAGTGCATTCAGACTGAAAACTTAAACAAAAACAAAAAAGAATAAGTACCCTTTAAATACCTGGATGATGCACTTATTCAACTAATAAATAGAAGTGAGCTTTGCAGAAGTGGAGGAGGTTTCAGCCGCTAAGCTGAAGGGAAGGAGCTATAGGCCACTAAACTAAATAAACTAAACTGAACATATCCTGAACATTGCCAGAACATAACCTGAAGATAATTGAATTGAACACAACCAGAAAGTAAGCAGAACATAACCTAACAATATTATGAACATAAACTGAACATAACCAGAACATAACCTGAACATAACCAGAACATAAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa847
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 |
---|---|---|---|---|---|
ENSDART00000012522 | Essential Splice Site | 1527 | 1570 | 13 | 14 |
ENSDART00000134304 | Essential Splice Site | 1526 | 1569 | 14 | 15 |
Genomic Location (Zv9):
Chromosome 10 (position 44737974)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 43431562 |
GRCz11 | 10 | 43259942 |
KASP Assay ID:
554-0750.1 (used for ordering genotyping assays)
KASP Sequence:
ATGCAGAGAAGACGGACAGTGGGACAAGCCCAAAATCACATGCTTGAATC[G/A]TAAGTTGTATGAGTTATTCTGTATAAYAAAACTAAAGCCATGAAAACAAT
Long Flanking Sequence:
CATAACCTGAACATCATCTGAAAGTAACCTGAACATAACCAGAACATTACCAGAACAAAATTTAAATATAACCTGAAAATAAACTGATCCTATTTAACCTGAAAATAACTTAATTTAACATAACCTGAACAAAACCAGAACATAACCTGAACATATCCTGCAAATATCCTGAACATTACCAGAACATAACCTTAAAATAACCAGAACATAACCTAAACAAAACCAAAACATAACCCGAAAATAACCTTAACATTACTGTAATGTATCCACAACATAACCTGACCATAATATGAAAATATCTTTATCCTGTTTCCCAGTGTCCTGCGGTCAGCCTCCTCTCATAAAGGACGCTCAAGTCTATGGCAGCATGAAGCCGCGATACGAGATCAACTCTCTGGTTCGATATCACTGTAAAGAAGGCTTCATCCAGAGACATGTCCCTACTATCAGATGCAGAGAAGACGGACAGTGGGACAAGCCCAAAATCACATGCTTGAATC[G/A]TAAGTTGTATGAGTTATTCTGTATAATAAAACTAAAGCCATGAAAACAATTTAATATGTAACTTAATATTAATCTTTTTAAAAACATTTTTTATTTATTTTCTTGCAAACGTTTTATTATTTTAATTTTTTCATTTCTTCAATCAGATTTAAAATGTTATTTATTTATTTTTAGCTTTTAGTTCAAAATAAAAATTCACGCTAGACAAAAGAAGATATATATTGTAATAAAATACTCTTTAACATTTTATTTTACAAAAAAAGGTATAGATATTAATGAAATTTACTAAAAGATTAAAGACATTAGTGAATTATAGAGGACGAAACCTATTTAATTTTTATTTATTTATATATTTATTTATGCGGGAATTTGTGTATTTTATATATATATTCTTGTGTTTATTTGCATTTTTATTTATTGTTTTATTCATGCAAGAATTTGTGTTTTTATATATATTTATTTATTGATTTATTTATGCAGGCATTTTAGAATTTATTATT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |