ZMP
mxra5
Ensembl ID:
ZFIN ID:
Human Orthologue:
MXRA5
Human Description:
matrix-remodelling associated 5 [Source:HGNC Symbol;Acc:7539]
Alleles
There are 11 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa45076 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa12853 | Nonsense | Available for shipment | Available now |
| sa39635 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa10494 | Essential Splice Site | Available for shipment | Available now |
| sa32705 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa16998 | Essential Splice Site | Available for shipment | Available now |
| sa39636 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa14854 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa16209 | Nonsense | Available for shipment | Available now |
| sa31212 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45076
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 |
|---|---|---|---|---|---|
| ENSDART00000113486 | Nonsense | 261 | 2480 | 4 | 9 |
| ENSDART00000137151 | None | None | 943 | None | 2 |
| ENSDART00000140435 | None | None | 206 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 32990050)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 32592230 |
| GRCz11 | 1 | 33324798 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAAGCCTATCCAAGTGGTCAACTATGCCCTTTGTGTTTCTCCCCAAAA[C/T]AACTAAAGAAGAAACAGCTCCAAGAATTGGAGAAACCCACGTGCAATAGT
Long Flanking Sequence:
CCACTTTCTCTGTTCTTGGACACTTCCCAGTGTCAACCCTAAAACACTTGTACCTGTCAGATAATATACTGACCACACTGTCACAGAAGATGCTAGCAAGCATGCCCTACCTGGAGAGCCTCTCCCTGCATGGGAACCCCTGGACCTGTGACTGTCGCATGAGATGGTTCAACGAATGGAATAAAAATTCACAAGGTCATTATTATCATAATTGACAATATTACTGATGTTCAATGAGGATATTCTAATTAGGGGAAAGTGATATTGTGTGATCAGTATTACATATTATTATTATTATTATTATTATTATTATTATTGTTGTTGTTATTATTAATATTGTTGTTGTTATTACAGAGCATTTCATTAAGTAATTTCCTTTCACTGAATGTTCACTTTTTTCTAACCTTTACTTTTTTTTTTTTTTTCCAGGAGTGCTAAAATGTAAGAAAGACAAAGCCTATCCAAGTGGTCAACTATGCCCTTTGTGTTTCTCCCCAAAA[C/T]AACTAAAGAAGAAACAGCTCCAAGAATTGGAGAAACCCACGTGCAATAGTCCCATCATCAGCATTTCTAATAGAGCCATTTCTTCAGAGGACACAGAAAGTGACCTCTTGACAATGGATGAATTTCGTCAACCCCTTGGCAATATTTCTCTTGGTCTGTCAGATGAACATGGACATCAAGTAGATTTGGAATGCCTTGTAATTGAGCCAAGAGAGCTTACTAGCATAGGCTGGGACTATGTTAACCAGTACCAAATATCAGTAAATTTGACTCTTACATTAGATTTGATATGTGGTATAGACAGGTCTAGTTATGAGAGGCTGTGGCGATTAATTGCTTATTACAGTGATGTTCCAGCTCACCTTCGAAGGGAAATAATGCTAAGCAAGGACCCTTATTTGAGCTACAGATATCGACAAGATATTGAAAGGGATGCTCTTTACTTCACAGGAGTAAAAGCCAATATTGCAGCTAACCCACCCTGGTTAATGCAGTCATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12853
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 |
|---|---|---|---|---|---|
| ENSDART00000113486 | Nonsense | 340 | 2480 | 4 | 9 |
| ENSDART00000137151 | None | None | 943 | None | 2 |
| ENSDART00000140435 | None | None | 206 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 32990289)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 32592469 |
| GRCz11 | 1 | 33325037 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAATGCCTTGTAATTGAGCMAAGAGAGCTTACYAGCATAGGCTGGGACTA[T/A]GTTMACCAGTACCAAATAWCAGTAAATTTGACTCTTACATTAGATTTGAT
Long Flanking Sequence:
ATATTCTAATTAGGGGAAAGTGATATTGTGTGATCAGTATTACATATTATTATTATTATTATTATTATTATTATTATTGTTGTTGTTATTATTAATATTGTTGTTGTTATTACAGAGCATTTCATTAAGTAATTTCCTTTCACTGAATGTTCACTTTTTTCTAACCTTTACTTTTTTTTTTTTTTTCCAGGAGTGCTAAAATGTAAGAAAGACAAAGCCTATCCAAGTGGTCAACTATGCCCTTTGTGTTTCTCCCCAAAACAACTAAAGAAGAAACAGCTCCAAGAATTGGAGAAACCCACGTGCAATAGTCCCATCATCAGCATTTCTAATAGAGCCATTTCTTCAGAGGACACAGAAAGTGACCTCTTGACAATGGATGAATTTCGTCAACCCCTTGGCAATATTTCTCTTGGTCTGTCAGATGAACATGGACATCAAGTAGATTTGGAATGCCTTGTAATTGAGCCAAGAGAGCTTACTAGCATAGGCTGGGACTA[T/A]GTTAACCAGTACCAAATATCAGTAAATTTGACTCTTACATTAGATTTGATATGTGGTATAGACAGGTCTAGTTATGAGAGGCTGTGGCGATTAATTGCTTATTACAGTGATGTTCCAGCTCACCTTCGAAGGGAAATAATGCTAAGCAAGGACCCTTATTTGAGCTACAGATATCGACAAGATATTGAAAGGGATGCTCTTTACTTCACAGGAGTAAAAGCCAATATTGCAGCTAACCCACCCTGGTTAATGCAGTCATCAATGGACCTCCAACTAAACAGACTTCAGTCAACAAGTAAAAATGTTCGGCTAATTCTCAGCACCTATATGACTGATGTAATGGAAAGAGAAACCATAAGAAAGCAGAGTCAAGGCTGGGTCTTAATTGAGTCCAAGAATGACACCAGAACAATGCAAGCTGCTGTCGTGGGAAGTCCTACTAAAATAAACTGTACCGTTCATAGCTCAGGGAATGAGTCAGTAAAATGGATGCTTCCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39635
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 |
|---|---|---|---|---|---|
| ENSDART00000113486 | Nonsense | 462 | 2480 | 4 | 9 |
| ENSDART00000137151 | None | None | 943 | None | 2 |
| ENSDART00000140435 | None | None | 206 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 32990653)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 32592833 |
| GRCz11 | 1 | 33325401 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTCAGCACCTATATGACTGATGTAATGGAAAGAGAAACCATAAGAAAG[C/T]AGAGTCAAGGCTGGGTCTTAATTGAGTCCAAGAATGACACCAGAACAATG
Long Flanking Sequence:
ACCTCTTGACAATGGATGAATTTCGTCAACCCCTTGGCAATATTTCTCTTGGTCTGTCAGATGAACATGGACATCAAGTAGATTTGGAATGCCTTGTAATTGAGCCAAGAGAGCTTACTAGCATAGGCTGGGACTATGTTAACCAGTACCAAATATCAGTAAATTTGACTCTTACATTAGATTTGATATGTGGTATAGACAGGTCTAGTTATGAGAGGCTGTGGCGATTAATTGCTTATTACAGTGATGTTCCAGCTCACCTTCGAAGGGAAATAATGCTAAGCAAGGACCCTTATTTGAGCTACAGATATCGACAAGATATTGAAAGGGATGCTCTTTACTTCACAGGAGTAAAAGCCAATATTGCAGCTAACCCACCCTGGTTAATGCAGTCATCAATGGACCTCCAACTAAACAGACTTCAGTCAACAAGTAAAAATGTTCGGCTAATTCTCAGCACCTATATGACTGATGTAATGGAAAGAGAAACCATAAGAAAG[C/T]AGAGTCAAGGCTGGGTCTTAATTGAGTCCAAGAATGACACCAGAACAATGCAAGCTGCTGTCGTGGGAAGTCCTACTAAAATAAACTGTACCGTTCATAGCTCAGGGAATGAGTCAGTAAAATGGATGCTTCCTGATGGCTCTACTATAGAAACACCTTATCGCAATAGCGAAAATAGGCTTTCAGCATCAAGTTCTGGTCTTCTTGAAATCAAGTCTCTTGATCATTCTGACTCAGGAGTCTACTACTGTATTGCACAGGTTTCAGACGACCTTACTGTCTTCCCTTTCCGCTTGACAGTGGAGGAATCCTCCAGCCCACCTCCTGGAGGTGAAGGAATAAGTGAGCCAGTTACACGATTTGCAGGTGAACCTTTCTCTCTTCCATGTGCTGCCACTGGATCACCTGATGCTGATATACACTGGATTCTCCCTAATGGCAGCATTGTTAACAAGTGGCTGAACATTTCCAGGATATCTGTGGCTTCAAATGGATCTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10494
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113486 | Essential Splice Site | 761 | 2480 | 6 | 9 |
| ENSDART00000137151 | None | None | 943 | None | 2 |
| ENSDART00000140435 | None | None | 206 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 32991665)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 32593845 |
| GRCz11 | 1 | 33326413 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTTCGTAGTGGAGGAAATGATACAAAAGCAACTACTCCAARCTATGCTC[A/T]GACCAGTACAAACAAAATACAGGAGTCAGAGMAAAACACAAAGCAGTCAG
Long Flanking Sequence:
CAGTCAGCTTTCAGACAACGGATACTATAAATGTGTAGCAGGAAACCAGCATGGGATGGATACTTTGGCAACAAAACTCATAATATCAAGGCCACCAGGGATACTGGCCTTACGGAAGTACTCCAGTAGCCCTCAACCTGCAGAGGGAGTTTCAACCAAAATAAATATCCTTATGACAAACGATATGGAATCGTCTGGGGATAATGAACCTGAAGATTTTTTGGCGAAAGCACTTGCAAAGAAAGTAGAAATACCAAATCGACGAAGGATCCCAAATATGGGAATAAGAGGAGGTCATCCATCTAGAAATTCCTGGAGACACGCTTCTACACCAAGAAGGAGAGTAGGTACCCAAGTGATAGACAGAGCTAACACTGTAGATTCAAGAAGAAGAATTAGCATGTTAAAGAACCAAATAGACCCAAAACACTGGGCAAGCATTTTGTCAAAGGTTCGTAGTGGAGGAAATGATACAAAAGCAACTACTCCAAACTATGCTC[A/T]GACCAGTACAAACAAAATACAGGAGTCAGAGCAAAACACAAAGCAGTCAGAAATTGTTAACAAGATTGAAGGATCATCTTCAGAATTTACAACAACAAGACCACCAGTAAAGGATGCCACAGTGTCACAGATGCCCGATGGGGCTACTGAGTTCAACTTGGATATTAGGGCTCTGGATTATGACAATACAAGACATGTTATATACCAGATAGCCACTCCTGAAACTGTTCCAAATTCAGATTTGTTTACAGACATCACGCAACCCACAGTTGGACCACAGATGACCCGATTTACTGTGGGAGATTCGGGGATTTCAAAAAGAGTAGCAATGAGCACTGTGTGGAGCACAACGTCATATGGAACCCATTTACAGGAAAACCAAAGCCACACAATGGATAGTGGCAGAGTAACTGAAGCAATTCAACAGTTTGATGGCAAATATGACGTAGAAAACAGAGTTGTGCAAAACCAAGAGCATGTGGGACAGGTTTATCAGAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32705
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 |
|---|---|---|---|---|---|
| ENSDART00000113486 | Nonsense | 1517 | 2480 | 6 | 9 |
| ENSDART00000137151 | None | None | 943 | None | 2 |
| ENSDART00000140435 | None | None | 206 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 32993937)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 32596117 |
| GRCz11 | 1 | 33328685 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAGCACAAACATAAGATCAGTAACAGCACATGCCGAGACTAATGCCTA[T/A]TTACCATGTATGGCTGTGGGAAAACCCCATCCCTTCCTTACCTGGACTAA
Long Flanking Sequence:
AAGCCTCCTACAGTACATACATATATGCTTTACCCTACTACACCTACTTCTGAACCCATTTTAGGTGAATCATACAATGAAAATCACATTCCTTATGATGACAAAAACAGATTTGTAACAACAGGCCAGGAAAACATTAGTAAGGCAGAACTTAGCAAAACATACATAAGGGCAAGGCCTCCAGTCACACAATTTCCTTATCAATTAACCAGTGCCTCCAAGGAGACAGGATCTCAAGAATTAGGGAAAAGCATCCGCAAAAAGACAACAACAAAAAGACCCACAACTACACCACTTAACTTAACTTTAATAGCATCTGTACCCCTGCAAAAACTTCCTGGCAGGCTGGGTGTTCAGGGCAGAGGAATCTCTTCTGAGCATTACACAACATCAGAAGGACTTCAACAAAGACCAACAGCATTGCCTGAGGGCAGAGGCCGACCTCAGATTACCAGCACAAACATAAGATCAGTAACAGCACATGCCGAGACTAATGCCTA[T/A]TTACCATGTATGGCTGTGGGAAAACCCCATCCCTTCCTTACCTGGACTAAAGTATCTACAGGTAAGTCTTATACTTTTGAAATAACTTATGATGACATTTCAATACACAATATTCATGCATAGATTGAGGCATTGATAATGTAGCTCTGAAATAATTCTGTTTTCCTGCAGGAGCTAGTATCTCACAGAACACCAGGTTTCAGAGATTTGAGGTCTCCTCTAATGGTACGCTTATAATCCACAAGGTAATTCCTCTGGACCAAGGCCAATACCTCTGCAGTGTTCAAAACCAATTTGGAGAGGACAGGATTGTAGTTAATTTAATAGTTCTGGCTGAGCATCCTAGAGTGCTACAGCCTCGTTATAGAGAAGCCACGGCATACCTTGGACAAACGATTGAGTTTGAATGTCAGTCAAAAGGGCATCCGCAGCCTCGAATTACCTGGGTCTTACCTAATAAGGAAGTTGTACATTCAAGTGTACCTACACATGGCACTCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16998
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113486 | Essential Splice Site | 1845 | 2480 | None | 9 |
| ENSDART00000137151 | Essential Splice Site | 308 | 943 | None | 2 |
| ENSDART00000140435 | None | None | 206 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 32995032)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 32597212 |
| GRCz11 | 1 | 33329780 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGATMATCTGGAGGACTCCATCTRAAAAGCTTGTGGATGCTCACTACAGG[T/A]AATATAAACACTTCACTGAAGCACATCTCCTTTGCAGGAAAGCACATTCT
Long Flanking Sequence:
CTGCAGGTGCTGATGCCATATCTGTTCGGCTGACTGTTGCTACTTTGGCACCCATCATTCAGCAGCTAAGCCTTGAGAATGTCACTTTTCCAGAGGGAAGCACAGTCTACTTTAATTGCTCAGCCAGGGGTGCCCCTCCACCTTCTATTAACTGGATCACACCTGATGGCATGCAGCTTCATCCCTCACAATTTATTAATGGACGTAACTTGTTTGTTTTTCCCAATGGGACACTCCATCTTCATAGTCTCTCTCTAACAGATGCAGGGAGGTATGAATGCTCAGTTACTAATGTCATCGGCAATGCACGAAGGGCCATTATTTTGACTGTAAGGAAGTCCATGAAGTACTCAAGAGCCAAGATTACATTCTCATCTCCTCAAAAAACAGATGTAGTCTACGGAGGCAGGTTGCACCTGGACTGTATTACATCAGGGAATCCAGAACCCAGGATCATCTGGAGGACTCCATCTAAAAAGCTTGTGGATGCTCACTACAGG[T/A]AATATAAACACTTCACTGAAGCACATCTCCTTTGCAGGAAAGCACATTCTGGGTTTATATAAAAAGGTGCACATGTCTTCTGTATTCCTTTCTTTTTCCTCTCCCTTTGCATTTCTTTTGATTCATGAGGCTTGCACTTAGACACAGAGTTTCATAAGTTTGCATCTTGTTTTGACTGATCAGACATTTTAAACTTTGCATGCAAATTTAACACTCTAATTGTTCCTCTAACAGAAGGATTGTTTTGATAAAAAAAAAAATGTCCTCAGAAGTGCAACAGTAAATAAAAAAGTAACATTTTACATTACATTGATCAAATTGCAGTTACTCGGAAATAATAATAATGCATCTGTATGTTTTTCTATATTTCAGTTATGATTCAAGGATCAAAGTGTCTGCTAATGGTACATTATCCATAATATCTGTGACAGAAAAAGAAGATGGGGAATACCTCTGCGTTGCTCGCAACAAAATTGGGGATGATTTTGTACCCTTTAAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39636
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 |
|---|---|---|---|---|---|
| ENSDART00000113486 | Nonsense | 2099 | 2480 | 9 | 9 |
| ENSDART00000137151 | Nonsense | 562 | 943 | 2 | 2 |
| ENSDART00000140435 | None | None | 206 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 32996165)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 32598345 |
| GRCz11 | 1 | 33330913 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTGACCAGGGTAGAAATCCTTGTCTCTCCACCTGCAATTAATGGCTTC[A/T]AAGGCACCACAAACTCACTGAGAGTGTCTAGTGTTAGAGATCAGAGGAAA
Long Flanking Sequence:
CTGATGGTACTATGATTAACAGTGTCATTAAGTCTGAGCGCAATGTTGGCAGTCGAACTCGCAGGTATGTTGTCTTTGACAATGGAACTCTCCTCTTGAATGAAGTAGGGATGCATGAAGAGGGTAACTATACTTGCTATGCTGAGAACCAAGTTGGAAAAGATGAGATGAACGTGCATGTTAAAGTGGTTGCAGATGTTCCTGTGATTGTGAATAAGACACAAGATGTCATCAGGGTGCTCTATGGAGAATCTGTCTCTTTGCAGTGCAGTGCCAAAGGTGAGCCAACACCCCTTGTATTGTGGTTCTCACCCACTAATAGAGCCATCACTTCATCTTCAGACAAGTATTTTATACACAACAATGGGACTCTAATTATTAAGAAAGTTCAGAGATTTGATGGTGGGAACTACATATGTCTTGCCAGGAACAGTGCAGGGCAAGATCGCAAAGTGACCAGGGTAGAAATCCTTGTCTCTCCACCTGCAATTAATGGCTTC[A/T]AAGGCACCACAAACTCACTGAGAGTGTCTAGTGTTAGAGATCAGAGGAAACTGATCGATTGTGACGCTACTGGTACCCCTGCCCCACGAGTCATGTGGGTTCTTCCAGAGAATGTTGTACTTCCTGCACCATATTATGGCAGTCGAATGACTGTATATCGCAATGGCACTTTGGATATCCGTTCAGTGAGAATGACAGATTCAGGTCAGTTAGCCTGCATTGCTCGTAATGAGGGAGGCGAAACAAAGTTCATTGTTCAGCTCCATGTAACAGATATTTTAGACAAGCCAAAACTTAAGAGTCCTAAAATGGAGACATTTTTACTGACTGTGGGCAGGACTATAAACCTGAACTGTTCATTTGAGATTTCACCAACCCTACAGCTAACCTGGATCCTTCAAAATGGCTCCCCGCTTCAAAGTGGTGCACAGTTCAATAAATTCCTACACAGAGCTGATGGGACTTTGGTCATCAGTAATCCTGCTCTTTCAGAGTCAGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14854
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 |
|---|---|---|---|---|---|
| ENSDART00000113486 | Nonsense | 2128 | 2480 | 9 | 9 |
| ENSDART00000137151 | Nonsense | 591 | 943 | 2 | 2 |
| ENSDART00000140435 | None | None | 206 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 32996252)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 32598432 |
| GRCz11 | 1 | 33331000 |
KASP Assay ID:
1641-0476.1 (used for ordering genotyping assays)
KASP Sequence:
GAGATCAGAGGAAACTGATYGATTGTGACGCTACTGGTACCCCTGCYCCA[C/T]GAGTCATGTGGGTTCTTCCAGAGAATGTTGTACTTCCTGCACCATATTAT
Long Flanking Sequence:
CTCTCCTCTTGAATGAAGTAGGGATGCATGAAGAGGGTAACTATACTTGCTATGCTGAGAACCAAGTTGGAAAAGATGAGATGAACGTGCATGTTAAAGTGGTTGCAGATGTTCCTGTGATTGTGAATAAGACACAAGATGTCATCAGGGTGCTCTATGGAGAATCTGTCTCTTTGCAGTGCAGTGCCAAAGGTGAGCCAACACCCCTTGTATTGTGGTTCTCACCCACTAATAGAGCCATCACTTCATCTTCAGACAAGTATTTTATACACAACAATGGGACTCTAATTATTAAGAAAGTTCAGAGATTTGATGGTGGGAACTACATATGTCTTGCCAGGAACAGTGCAGGGCAAGATCGCAAAGTGACCAGGGTAGAAATCCTTGTCTCTCCACCTGCAATTAATGGCTTCAAAGGCACCACAAACTCACTGAGAGTGTCTAGTGTTAGAGATCAGAGGAAACTGATCGATTGTGACGCTACTGGTACCCCTGCCCCA[C/T]GAGTCATGTGGGTTCTTCCAGAGAATGTTGTACTTCCTGCACCATATTATGGCAGTCGAATGACTGTATATCGCAATGGCACTTTGGATATCCGTTCAGTGAGAATGACAGATTCAGGTCAGTTAGCCTGCATTGCTCGTAATGAGGGAGGCGAAACAAAGTTCATTGTTCAGCTCCATGTAACAGATATTTTAGACAAGCCAAAACTTAAGAGTCCTAAAATGGAGACATTTTTACTGACTGTGGGCAGGACTATAAACCTGAACTGTTCATTTGAGATTTCACCAACCCTACAGCTAACCTGGATCCTTCAAAATGGCTCCCCGCTTCAAAGTGGTGCACAGTTCAATAAATTCCTACACAGAGCTGATGGGACTTTGGTCATCAGTAATCCTGCTCTTTCAGAGTCAGGCACATATCGTTGTTTGGGACGCAATGCTGCTGGGATGGTTGAAAGAACTGTCACGTTAATTCCAGGGCACAAGCCAGAGATCAGTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16209
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 |
|---|---|---|---|---|---|
| ENSDART00000113486 | Nonsense | 2396 | 2480 | 9 | 9 |
| ENSDART00000137151 | Nonsense | 859 | 943 | 2 | 2 |
| ENSDART00000140435 | None | None | 206 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 32997058)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 32599238 |
| GRCz11 | 1 | 33331806 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
RTTATTGCATWTCCACCACGTATCACTAGYGRTCCGGCTCCTGCTACCTA[T/A]GCCAAAAGAGGAGTWGCAGTTCAACTTAATTGCTTGGCCATAGGTATCCC
Long Flanking Sequence:
ATCCTTCAAAATGGCTCCCCGCTTCAAAGTGGTGCACAGTTCAATAAATTCCTACACAGAGCTGATGGGACTTTGGTCATCAGTAATCCTGCTCTTTCAGAGTCAGGCACATATCGTTGTTTGGGACGCAATGCTGCTGGGATGGTTGAAAGAACTGTCACGTTAATTCCAGGGCACAAGCCAGAGATCAGTAACAGGTATAACTCACCTGTTAGTATCATTAATGGGCAGAGTTTAAATCTGCACTGCATGTCAAACACTGATTCTGTCCACCTTACCTGGACCCTGCCAAGCGGAATGATCTTAAACCGACCTCAGAGAGCAGGTCGTTATGCTGTTCTTCCCAACGGAACCCTTTCTATCCAACAGGCCTCTGTCCATGACAGGGGCTCATACACATGTAGGGCCTCAAATGAATATGGCAGCTCCCTCTTATCTGTCCCAGTCATCATTATTGCATATCCACCACGTATCACTAGTGGTCCGGCTCCTGCTACCTA[T/A]GCCAAAAGAGGAGTTGCAGTTCAACTTAATTGCTTGGCCATAGGTATCCCCAAAGCAGAAGTAGCATGGGAGACCCCCGATCGAACACGGCTTATTGTCAGCCCCCAACCACGGCTTATTGGAAACAAGTATCTCCATCCTCAGGGTTCCTTAATCATCCAGAATCCGACAACAAAAGATGCAGGATTGTATAGATGCACAGCCAGAAATGTAGTTGGGGTTGACACAAAGGGTACTTACCTTTATGTGTACTGAAAAAATATAACCATCTACAGGTCATATGCCCAAGGAACTGCGACGTTAAGCTGAAACACAGCTTGATAGTAATAGCATTTGTCAATGTGAAATATAGAATGAAATCAGATCCATCAAAAATATATACAGTTGCATGGTCAGAATTATTAGACCCCCCTTTGAAATTTTCTTTCCTTTTTAAATATTTAGCAAATTATGTTTAACAGAGCAAGGACATTTTCACAGTATGCCTGATAATATTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31212
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 |
|---|---|---|---|---|---|
| ENSDART00000113486 | Nonsense | 2414 | 2480 | 9 | 9 |
| ENSDART00000137151 | Nonsense | 877 | 943 | 2 | 2 |
| ENSDART00000140435 | None | None | 206 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 32997110)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 32599290 |
| GRCz11 | 1 | 33331858 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAAAGAGGAGTTGCAGTTCAACTTAATTGCTTGGCCATAGGTATCCCC[A/T]AAGCAGAAGTAGCATGGGAGACCCCCGATCGAACACGGCTTATTGTCAGC
Long Flanking Sequence:
TACACAGAGCTGATGGGACTTTGGTCATCAGTAATCCTGCTCTTTCAGAGTCAGGCACATATCGTTGTTTGGGACGCAATGCTGCTGGGATGGTTGAAAGAACTGTCACGTTAATTCCAGGGCACAAGCCAGAGATCAGTAACAGGTATAACTCACCTGTTAGTATCATTAATGGGCAGAGTTTAAATCTGCACTGCATGTCAAACACTGATTCTGTCCACCTTACCTGGACCCTGCCAAGCGGAATGATCTTAAACCGACCTCAGAGAGCAGGTCGTTATGCTGTTCTTCCCAACGGAACCCTTTCTATCCAACAGGCCTCTGTCCATGACAGGGGCTCATACACATGTAGGGCCTCAAATGAATATGGCAGCTCCCTCTTATCTGTCCCAGTCATCATTATTGCATATCCACCACGTATCACTAGTGGTCCGGCTCCTGCTACCTATGCCAAAAGAGGAGTTGCAGTTCAACTTAATTGCTTGGCCATAGGTATCCCC[A/T]AAGCAGAAGTAGCATGGGAGACCCCCGATCGAACACGGCTTATTGTCAGCCCCCAACCACGGCTTATTGGAAACAAGTATCTCCATCCTCAGGGTTCCTTAATCATCCAGAATCCGACAACAAAAGATGCAGGATTGTATAGATGCACAGCCAGAAATGTAGTTGGGGTTGACACAAAGGGTACTTACCTTTATGTGTACTGAAAAAATATAACCATCTACAGGTCATATGCCCAAGGAACTGCGACGTTAAGCTGAAACACAGCTTGATAGTAATAGCATTTGTCAATGTGAAATATAGAATGAAATCAGATCCATCAAAAATATATACAGTTGCATGGTCAGAATTATTAGACCCCCCTTTGAAATTTTCTTTCCTTTTTAAATATTTAGCAAATTATGTTTAACAGAGCAAGGACATTTTCACAGTATGCCTGATAATATTTTTTCTTTCTTTTTTAAAAACATTTTAAGATCAAAAATAGCCCCTTTAAGCTATAT
Associated Phenotype:
Not determined