ZMP
fstl5
Ensembl ID:
ZFIN ID:
Description:
follistatin-related protein 5 [Source:RefSeq peptide;Acc:NP_001027012]
Human Orthologue:
FSTL5
Human Description:
follistatin-like 5 [Source:HGNC Symbol;Acc:21386]
Mouse Orthologue:
Fstl5
Mouse Description:
follistatin-like 5 Gene [Source:MGI Symbol;Acc:MGI:2442179]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7399 | Missense | Mutation detected in F1 DNA | Not yet available |
sa12250 | Nonsense | Available for shipment | Available now |
sa35762 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35761 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22551 | Nonsense | Available for shipment | Available now |
sa1377 | Nonsense | Available for shipment | Available now |
sa19099 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11024 | Nonsense | Available for shipment | Available now |
sa22550 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa7399
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058796 | Missense | 147 | 854 | 5 | 16 |
ENSDART00000135479 | None | None | 234 | None | 1 |
Genomic Location (Zv9):
Chromosome 14 (position 50077721)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 48154959 |
GRCz11 | 14 | 47142040 |
KASP Assay ID:
554-4176.1 (used for ordering genotyping assays)
KASP Sequence:
CATACACAGAACTGACYAGCGTTTCTCTTCCACTCTTCACAGATGATAAC[T/C]GCCGYCTGGGAGATTAYAAAAAATTGAAGAGCAAGATGTTGGACATACAT
Long Flanking Sequence:
CCTTTGCTCCTGTTCAGTCCAAACTTCCCAAGGTAACATAAATAGTAAATTGTTTGTGTTGTGAGAAAATGCAACACGTTTTATGAATTTGTTTGGGTTGTGTGAAAATGCAGTGTGTTTTTTAAAGATGTGTTGTGAGTATTTGCAGCACATGTTCTGTCAAACAGATGAAGATATTTTCTTCATTTGCTGGTGTTTTTCGTAATTGCATGTTTTTTCTTAAAATGCAGGACGTTACACCCTTCTGGCCACCGTATTTTGCCTACCAAAAATCCTCAAATTTTTCTGATTCTCAATGTGAGATCCGCAAAAAAAATTACAAATTCTCATCATTTATTTACATAGCAGACCTTTCTAGTTCCTCACACCACCATTAGTGAAAAAGACTTCATATCGGCACAGTATTGATGCATTAGTAATGTTGCAGACCAGTGAATTCATCTCCATTAACATACACAGAACTGACCAGCGTTTCTCTTCCACTCTTCACAGATGATAAC[T/C]GCCGTCTGGGAGATTATAAAAAATTGAAGAGCAAGATGTTGGACATACATGCTCAGAGGTACTTGACCGCCGCTAACCATGGCAGCCACGAGAAGGATATGGCCGCTAGGAAGCATCTGGTGGACATGATGTTTAAGCGATTTGACGCAGACGGCAATGGAAAAGTTGACAGCAGCGAGCTTTCACAGGTAACACTGAACTATAGCCATCAAATCAAACTCATTTAAAAGGCATTAATCTAACATTGACAACAAAAATGTATTATATGACTGCCCCTTAATCAATTTTTGATGTGTTTTTGATACCAATGTTAGATGTTAATTGATTTGTATATTTAAAGTGATTTTTACGACTTTTTATATCATTTGACTGGGTAGTTTCACTAAAAGGTGGCACAAGTAGCATTATTTGAACTGATTTGTTTACTTCCTTATTACCAAAGAGCTTAGAATGACCATGAGGCGACACTCAATAGAACGTTCCACTGCAACAGCAGCGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12250
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 |
---|---|---|---|---|---|
ENSDART00000058796 | Nonsense | 192 | 854 | 5 | 16 |
ENSDART00000135479 | None | None | 234 | None | 1 |
Genomic Location (Zv9):
Chromosome 14 (position 50077586)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 48154824 |
GRCz11 | 14 | 47141905 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCACGAGAAGGATATGGCCGCTAGGAAGCATCTGGTGGACATGATGTTT[A/T]AGCGATTTGACGCAGACGGCAATGGAAAAGTTGACAGCAGCGAGCTTTCA
Long Flanking Sequence:
TGAGTATTTGCAGCACATGTTCTGTCAAACAGATGAAGATATTTTCTTCATTTGCTGGTGTTTTTCGTAATTGCATGTTTTTTCTTAAAATGCAGGACGTTACACCCTTCTGGCCACCGTATTTTGCCTACCAAAAATCCTCAAATTTTTCTGATTCTCAATGTGAGATCCGCAAAAAAAATTACAAATTCTCATCATTTATTTACATAGCAGACCTTTCTAGTTCCTCACACCACCATTAGTGAAAAAGACTTCATATCGGCACAGTATTGATGCATTAGTAATGTTGCAGACCAGTGAATTCATCTCCATTAACATACACAGAACTGACCAGCGTTTCTCTTCCACTCTTCACAGATGATAACTGCCGTCTGGGAGATTATAAAAAATTGAAGAGCAAGATGTTGGACATACATGCTCAGAGGTACTTGACCGCCGCTAACCATGGCAGCCACGAGAAGGATATGGCCGCTAGGAAGCATCTGGTGGACATGATGTTT[A/T]AGCGATTTGACGCAGACGGCAATGGAAAAGTTGACAGCAGCGAGCTTTCACAGGTAACACTGAACTATAGCCATCAAATCAAACTCATTTAAAAGGCATTAATCTAACATTGACAACAAAAATGTATTATATGACTGCCCCTTAATCAATTTTTGATGTGTTTTTGATACCAATGTTAGATGTTAATTGATTTGTATATTTAAAGTGATTTTTACGACTTTTTATATCATTTGACTGGGTAGTTTCACTAAAAGGTGGCACAAGTAGCATTATTTGAACTGATTTGTTTACTTCCTTATTACCAAAGAGCTTAGAATGACCATGAGGCGACACTCAATAGAACGTTCCACTGCAACAGCAGCGCCCAGCAACAGCCCTGGATTCCGCCATTTTGAAGTGAAAGCGATCGGCTGTCCGTAGGATCTCATTACTGTCGCGATGGCAAGCAGCTGCTTTGTTTTTGATTTATTTATTTAAAAAGCACATTAAGACTTAGATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35762
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 |
---|---|---|---|---|---|
ENSDART00000058796 | Essential Splice Site | 250 | 854 | 7 | 16 |
ENSDART00000135479 | None | None | 234 | None | 1 |
Genomic Location (Zv9):
Chromosome 14 (position 50031947)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 48109185 |
GRCz11 | 14 | 47096266 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCCTCAAGAGAAAGCTAATCATCAAGCCTTGTGTGTTTTGTTGTCCTC[A/T]GAGGTGTACCAGCTCAGCCTTCCAGAAGAGCAGAAGCTGAGCGTCACCAC
Long Flanking Sequence:
CTTTTAAATTCAGTTCAGCTCTTTCTTTCTCTCCATTCAGTTTTGCTCAACATTTTCAGTGTATTTCATTTGCGTTTAAAACAACATGCTAGCAACACTCAGCAACTTGGAAATTCATGCTATAAACATGCTAGCATCATGCTATTTCATGCTAGAAACATGTTAATTCATGCTAGAAAGCATGCTTCATGTTAGAAATGTTAATTTATGGCAACATTCTTATTCACTAGAAATCATAAATTCTAAACAAGATGCTAATTCTTACTAGAAACATGCTAATTTATTGTTATGAACATGTAAGCGACATGTTAATTTATAGAAGAAACATGTTAGCAATGAGGTAATTATTGTTAGTCATGTTTCTGCATCATTCTGGCTTGATATATTGTGATAGTATTGTAAGTTCAGTAGAGATATGAGTGTTTGGAAGTCTATATTTTTCATCATAGTGCTCCTCAAGAGAAAGCTAATCATCAAGCCTTGTGTGTTTTGTTGTCCTC[A/T]GAGGTGTACCAGCTCAGCCTTCCAGAAGAGCAGAAGCTGAGCGTCACCACGGTAACAGTGGGTCAGAGCGCTGTCCTCACGTGTGCCATCATGGGGGACCAGCGGCCTCCCATCATCTGGAGACGCAACGGCCACGATCTCAACATGATGGAGCTGGAGGACATCAACGTGAGTGATGCTTTTACCATATAGTGTATTTTTGTGTGTGTATGTGTGAGTGTTTCAGCCATCTGTAAAGCACACTCAGGGGCCGATCATGTAGAACATGCTTTTTCATTCTGAGGTCTACTGCACTGAGTTTTTTGTTGGGCTTTTTATGTAATTGTATTTATTTATCTTTTTTTTTTTTTTTTTTTTTTGTAGATTTTTTTTCTCTGCCTGTTCTGTAGTATTCACTAAACTTTGGAGTGATTTCCAAAGTTCTATAATATTTATTCATTCATTCATTTTATTTTCGACTTAGTCCCTTTATTAATCAGGGGTCGCAACCCAACACTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35761
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 |
---|---|---|---|---|---|
ENSDART00000058796 | Nonsense | 394 | 854 | 9 | 16 |
ENSDART00000135479 | None | None | 234 | None | 1 |
Genomic Location (Zv9):
Chromosome 14 (position 50009845)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 48087083 |
GRCz11 | 14 | 47074164 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAGCTGTCCTGGCTGAAGAACGGCATGGACATCACCACTAAACTCTCC[A/T]AACAGCTCACACTTCAAGGTACAAACACATCACCTGACGACACTATATAT
Long Flanking Sequence:
CTTCCTCCAGTAGAAAAAAATGTTATAGGAAATATTGTAAAAAAAAAAAAATAAAAATCCTTGCTCTGTTAAACATCATTTGAGAATTATTTGAAGAAGAAAAAAATCACTGGAGTGTGAATAATTTCAACTTTTTATCTGTTATTAAAGGTAGAAATGCTCATAGCTCTTTTCTGTTTTGTAATTTGAATAAAAACTATGTTAGAAAGAAATATACACATATATAGGGGGGGAAAATGTTATTTTAGATGTCGGTTTTATTTCAACAAAGTTAATGAATTACAAAAGAAAATAAAAAATGACCAACTCTGGAGTTCAAGTGTTCATTCACCCTTTTTTTCTCTGTTGTTCTGACAGTCCCTCCTGTTATCCGAGTGTACCCAGAGAGCCAGGCACGTGAGCCGGGCGTCACAGCCAGTCTGCGGTGCTATGCAGAGGGCATCCCTGACCCACAGCTGTCCTGGCTGAAGAACGGCATGGACATCACCACTAAACTCTCC[A/T]AACAGCTCACACTTCAAGGTACAAACACATCACCTGACGACACTATATATAAAAATACACTTCATTGAACATGTACACATATACATCAACTACAGTATATACGATATAACTGCAGGTTTAACTATGTTTATATTAGGGCTGAACGATACTGGAAAAACTGATATTACAATATTTTTTTTCTGTGATACATTTTGCGATTTGAATATAATGTCACAAGATGACATGAGTAACTCTATTTGGAAAGTCTTCCTAATTTTAGAGAAGTGCATCTGCATAAAATATACACAATTATACAAAACTATACCAAATAAAATAAAGCACACATGAAAACAATAAAGCAAAATATAACAACATCAGTTTCCGATGGAGTCTAACAGCATTGAGGTTCAGAAATGCAATATTCAAATATGAATTACCACTGTATATTCTTTATTGTATAAATATTAAACAATAATTTTGTCTTGTGCCCAAATGGTTTGACTTTGCTTGAAATCTTACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22551
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 |
---|---|---|---|---|---|
ENSDART00000058796 | Nonsense | 399 | 854 | 9 | 16 |
ENSDART00000135479 | None | None | 234 | None | 1 |
Genomic Location (Zv9):
Chromosome 14 (position 50009830)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 48087068 |
GRCz11 | 14 | 47074149 |
KASP Assay ID:
2260-7926.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGAACGGCATGGACATCACCACTAAACTCTCCAAACAGCTCACACTT[C/T]AAGGTACAAACACATCACCTGACGACACTATATATAAAAATACACTTCAT
Long Flanking Sequence:
AAAAATGTTATAGGAAATATTGTAAAAAAAAAAAAATAAAAATCCTTGCTCTGTTAAACATCATTTGAGAATTATTTGAAGAAGAAAAAAATCACTGGAGTGTGAATAATTTCAACTTTTTATCTGTTATTAAAGGTAGAAATGCTCATAGCTCTTTTCTGTTTTGTAATTTGAATAAAAACTATGTTAGAAAGAAATATACACATATATAGGGGGGGAAAATGTTATTTTAGATGTCGGTTTTATTTCAACAAAGTTAATGAATTACAAAAGAAAATAAAAAATGACCAACTCTGGAGTTCAAGTGTTCATTCACCCTTTTTTTCTCTGTTGTTCTGACAGTCCCTCCTGTTATCCGAGTGTACCCAGAGAGCCAGGCACGTGAGCCGGGCGTCACAGCCAGTCTGCGGTGCTATGCAGAGGGCATCCCTGACCCACAGCTGTCCTGGCTGAAGAACGGCATGGACATCACCACTAAACTCTCCAAACAGCTCACACTT[C/T]AAGGTACAAACACATCACCTGACGACACTATATATAAAAATACACTTCATTGAACATGTACACATATACATCAACTACAGTATATACGATATAACTGCAGGTTTAACTATGTTTATATTAGGGCTGAACGATACTGGAAAAACTGATATTACAATATTTTTTTTCTGTGATACATTTTGCGATTTGAATATAATGTCACAAGATGACATGAGTAACTCTATTTGGAAAGTCTTCCTAATTTTAGAGAAGTGCATCTGCATAAAATATACACAATTATACAAAACTATACCAAATAAAATAAAGCACACATGAAAACAATAAAGCAAAATATAACAACATCAGTTTCCGATGGAGTCTAACAGCATTGAGGTTCAGAAATGCAATATTCAAATATGAATTACCACTGTATATTCTTTATTGTATAAATATTAAACAATAATTTTGTCTTGTGCCCAAATGGTTTGACTTTGCTTGAAATCTTACATTTACAGGGCTTAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1377
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 |
---|---|---|---|---|---|
ENSDART00000058796 | Nonsense | 784 | 854 | 16 | 16 |
ENSDART00000135479 | Nonsense | 164 | 234 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 14 (position 49940216)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 48017454 |
GRCz11 | 14 | 47004535 |
KASP Assay ID:
554-1289.1 (used for ordering genotyping assays)
KASP Sequence:
CCGGCAGGCAGACGGATGCTCTTTTTGTGGAGCTCAGTTCTGGCAGTGTC[A/T]AAATGATCAAGAGCTTGAAGCAGCCCACGGCGTCGGCGCAGTGGCCCTGG
Long Flanking Sequence:
GCTCTCTCTTCAGGTTTGGTATCGTCCTCCATAAGAATGAACCAGCTCTTCACAAGATCGACTTGGAAACCACGTCATATGTTAAAAACATCAGCCTGCAGCAGTACGACTGTATCCCACAATCCCTGGCTTACACACACCTGGGCGGATATTATCTGGTCAACTGTCGACCGGACTCAACAGGTGCGGCGCGGCCACAATTAATCATCGACAGCATAACAGACAACGTCATGGGCCCTAATGGCGACGTGAGCGGCACACCTTATGTCTCTCCTGATGGCCACTATTTAGTGAGTGTGGACGACCGTGACGGGCTAATGCGCTTACAGCATGTGTCCGTACGGGGAGAGATCGGCCAACCCTTTGACATTCACACCAACCTGCACCTGTCCGATCTGGCCTTCATGCCCTCGTTCACTGAGGCCAACCAGTATAATGTGTTCGGAAGCTCCGGCAGGCAGACGGATGCTCTTTTTGTGGAGCTCAGTTCTGGCAGTGTC[A/T]AAATGATCAAGAGCTTGAAGCAGCCCACGGCGTCGGCGCAGTGGCCCTGGAACCGTCAGAACCGAGTTATGACCGGAAGCGGGCTGTTCGGACAGTATCTCATGACCCCGTCACAAAGCTCCCTGTTTATACTGGATGGGCGTCTGGATAAACTCAACTGTGAGATCACCGACGTTCCCTTGGGAAATACTGTGGTGTGGGTGGGAGAGGCGTAAGACGTCTTAAAAAGGGGGCTTGAGAGGGAAACAACAAACAGGTTGCACTGAATTCGGTCTCTGTTTAATTTATCGAGCAGTTTGGAACTAAATCTAATTTGACTCTGCATTGGAAATGAGAATTGTGGGAAAGGCTTGGCAAGGCTTTCGAGTCAAATAGCTAATAAGTAGTACCAAAAAAAAGTAAAAATGTAAAATTAGATGGTGTCGAACTAGCTTTGATTGAAGGAGATCGAATGAATCGATTTGAGTGATGCGAACGCAGAAATAAATCATCATTCGTCC
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa19099
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 |
---|---|---|---|---|---|
ENSDART00000058796 | Nonsense | 822 | 854 | 16 | 16 |
ENSDART00000135479 | Nonsense | 202 | 234 | 1 | 1 |
ENSDART00000058796 | Nonsense | 822 | 854 | 16 | 16 |
ENSDART00000135479 | Nonsense | 202 | 234 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 14 (position 49940102)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 48017340 |
GRCz11 | 14 | 47004421 |
KASP Assay ID:
2260-7925.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTTATGACCGGAAGCGGGCTGTTCGGACAGTATCTCATGACCCCGTCA[C/T]AAAGCTCCCTGTTTATACTGGATGGGCGTCTGGATAAACTCAACTGTGAG
Long Flanking Sequence:
TCCCACAATCCCTGGCTTACACACACCTGGGCGGATATTATCTGGTCAACTGTCGACCGGACTCAACAGGTGCGGCGCGGCCACAATTAATCATCGACAGCATAACAGACAACGTCATGGGCCCTAATGGCGACGTGAGCGGCACACCTTATGTCTCTCCTGATGGCCACTATTTAGTGAGTGTGGACGACCGTGACGGGCTAATGCGCTTACAGCATGTGTCCGTACGGGGAGAGATCGGCCAACCCTTTGACATTCACACCAACCTGCACCTGTCCGATCTGGCCTTCATGCCCTCGTTCACTGAGGCCAACCAGTATAATGTGTTCGGAAGCTCCGGCAGGCAGACGGATGCTCTTTTTGTGGAGCTCAGTTCTGGCAGTGTCAAAATGATCAAGAGCTTGAAGCAGCCCACGGCGTCGGCGCAGTGGCCCTGGAACCGTCAGAACCGAGTTATGACCGGAAGCGGGCTGTTCGGACAGTATCTCATGACCCCGTCA[C/T]AAAGCTCCCTGTTTATACTGGATGGGCGTCTGGATAAACTCAACTGTGAGATCACCGACGTTCCCTTGGGAAATACTGTGGTGTGGGTGGGAGAGGCGTAAGACGTCTTAAAAAGGGGGCTTGAGAGGGAAACAACAAACAGGTTGCACTGAATTCGGTCTCTGTTTAATTTATCGAGCAGTTTGGAACTAAATCTAATTTGACTCTGCATTGGAAATGAGAATTGTGGGAAAGGCTTGGCAAGGCTTTCGAGTCAAATAGCTAATAAGTAGTACCAAAAAAAAGTAAAAATGTAAAATTAGATGGTGTCGAACTAGCTTTGATTGAAGGAGATCGAATGAATCGATTTGAGTGATGCGAACGCAGAAATAAATCATCATTCGTCCTCATTTTCCCACTTGAAAAGACCTCCAAAATGCATTCGGCCCATTTTTTTCCAGTGCCTTGAAGGAACGCTCGCTTAAAAAAGAAAGTAAACATAATTATTCCCTGCGAGCCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11024
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 |
---|---|---|---|---|---|
ENSDART00000058796 | Nonsense | 822 | 854 | 16 | 16 |
ENSDART00000135479 | Nonsense | 202 | 234 | 1 | 1 |
ENSDART00000058796 | Nonsense | 822 | 854 | 16 | 16 |
ENSDART00000135479 | Nonsense | 202 | 234 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 14 (position 49940102)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 48017340 |
GRCz11 | 14 | 47004421 |
KASP Assay ID:
2260-7925.1 (used for ordering genotyping assays)
KASP Sequence:
GAGTTATGACCGGAAGCGGGCTGTTCGGACAGTATCTCATGACCCCGTCA[C/T]AAAGCTCCCTGTTTATACTGGATGGGCGTCTGGAWAAACTCAACTGTGAG
Long Flanking Sequence:
TCCCACAATCCCTGGCTTACACACACCTGGGCGGATATTATCTGGTCAACTGTCGACCGGACTCAACAGGTGCGGCGCGGCCACAATTAATCATCGACAGCATAACAGACAACGTCATGGGCCCTAATGGCGACGTGAGCGGCACACCTTATGTCTCTCCTGATGGCCACTATTTAGTGAGTGTGGACGACCGTGACGGGCTAATGCGCTTACAGCATGTGTCCGTACGGGGAGAGATCGGCCAACCCTTTGACATTCACACCAACCTGCACCTGTCCGATCTGGCCTTCATGCCCTCGTTCACTGAGGCCAACCAGTATAATGTGTTCGGAAGCTCCGGCAGGCAGACGGATGCTCTTTTTGTGGAGCTCAGTTCTGGCAGTGTCAAAATGATCAAGAGCTTGAAGCAGCCCACGGCGTCGGCGCAGTGGCCCTGGAACCGTCAGAACCGAGTTATGACCGGAAGCGGGCTGTTCGGACAGTATCTCATGACCCCGTCA[C/T]AAAGCTCCCTGTTTATACTGGATGGGCGTCTGGATAAACTCAACTGTGAGATCACCGACGTTCCCTTGGGAAATACTGTGGTGTGGGTGGGAGAGGCGTAAGACGTCTTAAAAAGGGGGCTTGAGAGGGAAACAACAAACAGGTTGCACTGAATTCGGTCTCTGTTTAATTTATCGAGCAGTTTGGAACTAAATCTAATTTGACTCTGCATTGGAAATGAGAATTGTGGGAAAGGCTTGGCAAGGCTTTCGAGTCAAATAGCTAATAAGTAGTACCAAAAAAAAGTAAAAATGTAAAATTAGATGGTGTCGAACTAGCTTTGATTGAAGGAGATCGAATGAATCGATTTGAGTGATGCGAACGCAGAAATAAATCATCATTCGTCCTCATTTTCCCACTTGAAAAGACCTCCAAAATGCATTCGGCCCATTTTTTTCCAGTGCCTTGAAGGAACGCTCGCTTAAAAAAGAAAGTAAACATAATTATTCCCTGCGAGCCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22550
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 |
---|---|---|---|---|---|
ENSDART00000058796 | Nonsense | 844 | 854 | 16 | 16 |
ENSDART00000135479 | Nonsense | 224 | 234 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 14 (position 49940035)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 48017273 |
GRCz11 | 14 | 47004354 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGGATGGGCGTCTGGATAAACTCAACTGTGAGATCACCGACGTTCCCT[T/A]GGGAAATACTGTGGTGTGGGTGGGAGAGGCGTAAGACGTCTTAAAAAGGG
Long Flanking Sequence:
AGGTGCGGCGCGGCCACAATTAATCATCGACAGCATAACAGACAACGTCATGGGCCCTAATGGCGACGTGAGCGGCACACCTTATGTCTCTCCTGATGGCCACTATTTAGTGAGTGTGGACGACCGTGACGGGCTAATGCGCTTACAGCATGTGTCCGTACGGGGAGAGATCGGCCAACCCTTTGACATTCACACCAACCTGCACCTGTCCGATCTGGCCTTCATGCCCTCGTTCACTGAGGCCAACCAGTATAATGTGTTCGGAAGCTCCGGCAGGCAGACGGATGCTCTTTTTGTGGAGCTCAGTTCTGGCAGTGTCAAAATGATCAAGAGCTTGAAGCAGCCCACGGCGTCGGCGCAGTGGCCCTGGAACCGTCAGAACCGAGTTATGACCGGAAGCGGGCTGTTCGGACAGTATCTCATGACCCCGTCACAAAGCTCCCTGTTTATACTGGATGGGCGTCTGGATAAACTCAACTGTGAGATCACCGACGTTCCCT[T/A]GGGAAATACTGTGGTGTGGGTGGGAGAGGCGTAAGACGTCTTAAAAAGGGGGCTTGAGAGGGAAACAACAAACAGGTTGCACTGAATTCGGTCTCTGTTTAATTTATCGAGCAGTTTGGAACTAAATCTAATTTGACTCTGCATTGGAAATGAGAATTGTGGGAAAGGCTTGGCAAGGCTTTCGAGTCAAATAGCTAATAAGTAGTACCAAAAAAAAGTAAAAATGTAAAATTAGATGGTGTCGAACTAGCTTTGATTGAAGGAGATCGAATGAATCGATTTGAGTGATGCGAACGCAGAAATAAATCATCATTCGTCCTCATTTTCCCACTTGAAAAGACCTCCAAAATGCATTCGGCCCATTTTTTTCCAGTGCCTTGAAGGAACGCTCGCTTAAAAAAGAAAGTAAACATAATTATTCCCTGCGAGCCTGTGGATAAAACGCGGAGAGAATGCGAGAGCTACACTTTAAATTTCACCTGTTTATAACTCCCACAGAC
Associated Phenotype:
Not determined