ZMP
LOC557250
Ensembl ID:
Human Orthologue:
MTUS1
Human Description:
microtubule associated tumor suppressor 1 [Source:HGNC Symbol;Acc:29789]
Mouse Orthologue:
Mtus1
Mouse Description:
mitochondrial tumor suppressor 1 Gene [Source:MGI Symbol;Acc:MGI:2142572]
Alleles
There are 12 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa32636 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa44504 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa30582 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa12425 | Nonsense | Available for shipment | Available now |
| sa25552 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa6577 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa1312 | Essential Splice Site | Available for shipment | Available now |
| sa1993 | Essential Splice Site | F2 line generated | Not yet available |
| sa19459 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32636
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000048855 | Nonsense | 36 | 1416 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 1 (position 15282671)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 15847839 |
| GRCz11 | 1 | 16540776 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCACCTCCTGCGCTTCCCAACAGACCTCAGCATGAATTGTGTCTCCCGT[T/G]ACGCAGTAATGAGCACAATAACATTGCGTTCAACTCTGAGTCTTCCTCCC
Long Flanking Sequence:
TTGGGTTGCAGCTGGAAGGGCATCCGCTGTGTAAAACATATGCTGGATAAGTTGCCAGTTCATTCCGCTGTGGCGAGCACTGATGAACAAAGCGACTAATCCGAAGGAAAATTAATACGTTTTTACATTTATTTTCTCCAAACATTTACGCAGACCCCATAGCCTTCAATAGGATTAGGTTTAAAGTTAAACCCATTAAACACAATTGACATGTGCTGTCTTTTCTTAATTCACAGAGCCATTAAAGAGTGTCAGCAAAGCCATGGGTGCCATCGTCTGAACGATCAAAGAAGTAGCCTTTCTATGATGAGAAACACCTTAATCCCTTCTTCTACAAAGTGGAGTAGTTCCGGTCCATCAGCAAATTGGATCTAGCTATGGAGGTTTGGGCTGTATGATTAAATCTCAATCCTCGTACCTCATGGAACCACCAACAAACATATCTGAGCTTCCACCTCCTGCGCTTCCCAACAGACCTCAGCATGAATTGTGTCTCCCGT[T/G]ACGCAGTAATGAGCACAATAACATTGCGTTCAACTCTGAGTCTTCCTCCCTGTCCTCGTCATCGATTTCTCTCCTGTATGACCGAGGTGAGACGTCACCTGACTCCGTGCGCAGCTTGAGTAGTCTGAGCAGTGTCAGAACCGATAGTCCTCTGGATGTGGACATGCCTGAGGCGGAGATGGGAAAAGTAATGGCCAACAGTGATGATTCAGGCATACAGAGCCCAGACTGCAGACCAGACTATGCAGAGGACGACAACTCTGTGTCAGTCTATCTGGATGCTAATGAGGACTGCTGGAGTGACAACGACAACCATAATGTAACTTCGGTGGTATCGCAGAAGGTCAGTCAAACTGATGGCGATGATACATCCTTGTGCTCTTCAGAAAACGGTGACGATGACACCAAAGATGAGGAGGAAGAAGAAGACTCTTTTCTTTCTTTAGTTTCGGTAGAAGTGATGATGAAGAGCCAAGCTGGAGTCTCAGGTCTGGAGGGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44504
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 |
|---|---|---|---|---|---|
| ENSDART00000048855 | Nonsense | 117 | 1416 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 1 (position 15282915)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 15848083 |
| GRCz11 | 1 | 16541020 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCAACAGTGATGATTCAGGCATACAGAGCCCAGACTGCAGACCAGACTA[T/A]GCAGAGGACGACAACTCTGTGTCAGTCTATCTGGATGCTAATGAGGACTG
Long Flanking Sequence:
AAGAGTGTCAGCAAAGCCATGGGTGCCATCGTCTGAACGATCAAAGAAGTAGCCTTTCTATGATGAGAAACACCTTAATCCCTTCTTCTACAAAGTGGAGTAGTTCCGGTCCATCAGCAAATTGGATCTAGCTATGGAGGTTTGGGCTGTATGATTAAATCTCAATCCTCGTACCTCATGGAACCACCAACAAACATATCTGAGCTTCCACCTCCTGCGCTTCCCAACAGACCTCAGCATGAATTGTGTCTCCCGTTACGCAGTAATGAGCACAATAACATTGCGTTCAACTCTGAGTCTTCCTCCCTGTCCTCGTCATCGATTTCTCTCCTGTATGACCGAGGTGAGACGTCACCTGACTCCGTGCGCAGCTTGAGTAGTCTGAGCAGTGTCAGAACCGATAGTCCTCTGGATGTGGACATGCCTGAGGCGGAGATGGGAAAAGTAATGGCCAACAGTGATGATTCAGGCATACAGAGCCCAGACTGCAGACCAGACTA[T/A]GCAGAGGACGACAACTCTGTGTCAGTCTATCTGGATGCTAATGAGGACTGCTGGAGTGACAACGACAACCATAATGTAACTTCGGTGGTATCGCAGAAGGTCAGTCAAACTGATGGCGATGATACATCCTTGTGCTCTTCAGAAAACGGTGACGATGACACCAAAGATGAGGAGGAAGAAGAAGACTCTTTTCTTTCTTTAGTTTCGGTAGAAGTGATGATGAAGAGCCAAGCTGGAGTCTCAGGTCTGGAGGGCTCTACTGTATCTCAAGTGGCAATACCAAAAGCTGGTTTACAAGACACATCTGAGGACCTACAATCGGATGTGTCTAAAGGGTGTTTGTTGAATGAAACCAACAGGGAAGTTGTCAACGAAAAAGGGGAAGTCTCTTTAGCCATTCAAGAAACTGATGTTGTGAATGAGACATTTGCGTCACCTGAAAGTTCTGAGGATATTAACGTCTCCAGTTTCATAATAGGTACCAGATCCATCTTAAAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30582
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 |
|---|---|---|---|---|---|
| ENSDART00000048855 | Nonsense | 232 | 1416 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 1 (position 15283259)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 15848427 |
| GRCz11 | 1 | 16541364 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAGACACATCTGAGGACCTACAATCGGATGTGTCTAAAGGGTGTTTGT[T/A]GAATGAAACCAACAGGGAAGTTGTCAACGAAAAAGGGGAAGTCTCTTTAG
Long Flanking Sequence:
TGAGACGTCACCTGACTCCGTGCGCAGCTTGAGTAGTCTGAGCAGTGTCAGAACCGATAGTCCTCTGGATGTGGACATGCCTGAGGCGGAGATGGGAAAAGTAATGGCCAACAGTGATGATTCAGGCATACAGAGCCCAGACTGCAGACCAGACTATGCAGAGGACGACAACTCTGTGTCAGTCTATCTGGATGCTAATGAGGACTGCTGGAGTGACAACGACAACCATAATGTAACTTCGGTGGTATCGCAGAAGGTCAGTCAAACTGATGGCGATGATACATCCTTGTGCTCTTCAGAAAACGGTGACGATGACACCAAAGATGAGGAGGAAGAAGAAGACTCTTTTCTTTCTTTAGTTTCGGTAGAAGTGATGATGAAGAGCCAAGCTGGAGTCTCAGGTCTGGAGGGCTCTACTGTATCTCAAGTGGCAATACCAAAAGCTGGTTTACAAGACACATCTGAGGACCTACAATCGGATGTGTCTAAAGGGTGTTTGT[T/A]GAATGAAACCAACAGGGAAGTTGTCAACGAAAAAGGGGAAGTCTCTTTAGCCATTCAAGAAACTGATGTTGTGAATGAGACATTTGCGTCACCTGAAAGTTCTGAGGATATTAACGTCTCCAGTTTCATAATAGGTACCAGATCCATCTTAAAAGATGACATCCAGCAACACTCTGATGAACATCCAGAAGACGTCTTTAAAATGGATGTGGTGTTTGAACCCAATGAGGAAGTTGTCCACAAAAAAGGGGAAGACTCTATTGAGTCGCCTTTAGCAATTCAAGATATGGATGTCATGAGGGAGACAGGGGTGTTTTCTAAAGGTTCAGAAACTAATGAAGTCTCCAGTCTCATAGCAGATTTAAAAAATGTAACTTCTTGCTTGTCAGCCTCAAAAGATGATAATCAGCCAAGGGCTAATGGCCAACAATCAGAAATGGTTACTTGTATTGTACCCAACATAGAGCTTGTCCACAAAAAAGGGGAATACTTTGTTGAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12425
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 |
|---|---|---|---|---|---|
| ENSDART00000048855 | Nonsense | 248 | 1416 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 1 (position 15283307)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 15848475 |
| GRCz11 | 1 | 16541412 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTGAATRAAACCAACAGGGAAGTTGTCWACGAAAAAGGGGAARTCTCTT[T/A]AGCCATTCAAGAAAYTGATGTTGTGAATGAGAYATTTGCGTCACCTGAAA
Long Flanking Sequence:
CAGAACCGATAGTCCTCTGGATGTGGACATGCCTGAGGCGGAGATGGGAAAAGTAATGGCCAACAGTGATGATTCAGGCATACAGAGCCCAGACTGCAGACCAGACTATGCAGAGGACGACAACTCTGTGTCAGTCTATCTGGATGCTAATGAGGACTGCTGGAGTGACAACGACAACCATAATGTAACTTCGGTGGTATCGCAGAAGGTCAGTCAAACTGATGGCGATGATACATCCTTGTGCTCTTCAGAAAACGGTGACGATGACACCAAAGATGAGGAGGAAGAAGAAGACTCTTTTCTTTCTTTAGTTTCGGTAGAAGTGATGATGAAGAGCCAAGCTGGAGTCTCAGGTCTGGAGGGCTCTACTGTATCTCAAGTGGCAATACCAAAAGCTGGTTTACAAGACACATCTGAGGACCTACAATCGGATGTGTCTAAAGGGTGTTTGTTGAATGAAACCAACAGGGAAGTTGTCAACGAAAAAGGGGAAGTCTCTT[T/A]AGCCATTCAAGAAACTGATGTTGTGAATGAGACATTTGCGTCACCTGAAAGTTCTGAGGATATTAACGTCTCCAGTTTCATAATAGGTACCAGATCCATCTTAAAAGATGACATCCAGCAACACTCTGATGAACATCCAGAAGACGTCTTTAAAATGGATGTGGTGTTTGAACCCAATGAGGAAGTTGTCCACAAAAAAGGGGAAGACTCTATTGAGTCGCCTTTAGCAATTCAAGATATGGATGTCATGAGGGAGACAGGGGTGTTTTCTAAAGGTTCAGAAACTAATGAAGTCTCCAGTCTCATAGCAGATTTAAAAAATGTAACTTCTTGCTTGTCAGCCTCAAAAGATGATAATCAGCCAAGGGCTAATGGCCAACAATCAGAAATGGTTACTTGTATTGTACCCAACATAGAGCTTGTCCACAAAAAAGGGGAATACTTTGTTGAGTTGCCTTTTGCAATTCAAGATACTGATGTTATGAATGAGACAGTGGAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25552
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 |
|---|---|---|---|---|---|
| ENSDART00000048855 | Nonsense | 467 | 1416 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 1 (position 15283964)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 15849132 |
| GRCz11 | 1 | 16542069 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATGCAGCTTCTTCTCTCTTAAAAGAGGAGTACCAGCCAAAACCCATGT[T/A]GAAAATGGCTGCTGGGAATAAATCCAATAGGAAAATTGGCCACAAAAAGG
Long Flanking Sequence:
GGATGTGGTGTTTGAACCCAATGAGGAAGTTGTCCACAAAAAAGGGGAAGACTCTATTGAGTCGCCTTTAGCAATTCAAGATATGGATGTCATGAGGGAGACAGGGGTGTTTTCTAAAGGTTCAGAAACTAATGAAGTCTCCAGTCTCATAGCAGATTTAAAAAATGTAACTTCTTGCTTGTCAGCCTCAAAAGATGATAATCAGCCAAGGGCTAATGGCCAACAATCAGAAATGGTTACTTGTATTGTACCCAACATAGAGCTTGTCCACAAAAAAGGGGAATACTTTGTTGAGTTGCCTTTTGCAATTCAAGATACTGATGTTATGAATGAGACAGTGGAACTCAACATGGAGGTTGTACATGAAAAAGGAGATTCCTCTACTGAGTCCATCCAAGAAACCAATGTTATCAATGAGACAATGGTGTCTACTCAAAATAAGGATTCCAATAATGCAGCTTCTTCTCTCTTAAAAGAGGAGTACCAGCCAAAACCCATGT[T/A]GAAAATGGCTGCTGGGAATAAATCCAATAGGAAAATTGGCCACAAAAAGGGAGAAACCTCCATTGATCCAATTCCATTCAAAGAAACAATGGTGTCTCCTAAAAATTCACAAGCTAAAAAAACCTTTACTGCTGTAATTGGTACCGTAAAGATAGTTTCTTCCTGCTCAAAAGATGACAACCAGCCAAAAGCAAATGGTCAACAATCAGAACTGGCTACTTTTGCTGAACAAAACATGGAGGTTGTCCATGAAAATGGAGAATCCTCTGTTGAGTCCATCCAAGAAACCAATATTATCAATGAGACAATGATGTCTCCGGAAAATCGAGAGGATAATAGCATAACGAGTACCAAAAATGCAGCTTCTTCCCTCTTAAAAGAGAGCAACCAGCCAAAACCCAAAGACCAACCAGAAAACGTGTCTAAAATGGCTACAGTTAATAAAGCTGTCCCCAATAAAGAAGAATCCTCCGCTGGTGCAATTCGATTCAAAGAAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6577
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 |
|---|---|---|---|---|---|
| ENSDART00000048855 | Essential Splice Site | 1090 | 1416 | 6 | 14 |
Genomic Location (Zv9):
Chromosome 1 (position 15332550)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 15897718 |
| GRCz11 | 1 | 16590655 |
KASP Assay ID:
554-4418.1 (used for ordering genotyping assays)
KASP Sequence:
TCGGCGTCTGGAGGCTCTCGCTCTGGTCGTGCAGCACATCTTCAGTGAGG[T/C]TGGAGAGCTTTATTRTTTCTTTCTTTCTAGATACTCCTCTGTGGAGTTTW
Long Flanking Sequence:
ACTTTTTTTCCAGCATCAGCCCAAGAGGGCGTATGTTGTTTGTGGGACAGACTTTGTTGCTTAAAGCTTTTGTTGCAGATCTTTCCTATTAGTCATGATATTTTCTTTCTTACGATTTCATTGAAGTATTTTCTTGTGGTTTGTGGGTGTGATTGTGTTTAGCAGATGCTTTCATCATCACTGGTTGTTGTACTGAGGAGTAGATGTGGTTCTGGACTCTGAAATCATGCTGAATGTAATGACCGCACTGAACACGCGCTCTTTTACAGTGGACAAGAGCTCCAAGGGGTCCAAAGCTGCAGGGCCCACGGCTGGACGGACCCCACAGCACAGCCCAGCCTGTCAAGCAGGACCGGTGGAGGAAGAGGATGAGAGAGAAGATCTCCGTCTTCAAAACGAGAAGAAGAATCAATGCATTCTGCACCTTCGTAAACTCATCGCTAATGGCAATCGGCGTCTGGAGGCTCTCGCTCTGGTCGTGCAGCACATCTTCAGTGAGG[T/C]TGGAGAGCTTTATTATTTCTTTCTTTCTAGATACTCCTCTGTGGAGTTTATTTTAATAATTTTTTTGGTTTGCTTAGAAATATGATAGTGATATTTTTTTTATATTCTTGATTTTTTTTATACATTATTGATCTGCTGATTCACAGATAGGTCAGAGTGCAAATGTGTGCTAAAGCCGATAGATTTCATTATTAGTGATGATAACCTATAGATTTACTCATCACTATAGACACATTTCCGGATAGCGGAATTATTTTACTTTATTAATTAATTACTTTGTTTATTATATTGTGATGAATGAAGTGATTTTTTTTTTACATTTACATTTTACATTTAGTCATTTAGCAGACGCTTTTATCCAAAGCGACTTACAAATGAGGACAAGGAAGCAATTTACACCACTAAGAGCAACAATGAATAAGTACTAAAGGCAAGTTTCAGGTCTGTAAAGTCTAAGAAGGGAAGTGTTAGTAATTTTTTTTTTTTTTTTTTTTTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1312
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000048855 | Essential Splice Site | 1113 | 1416 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 1 (position 15346044)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 15911212 |
| GRCz11 | 1 | 16604149 |
KASP Assay ID:
554-1227.1 (used for ordering genotyping assays)
KASP Sequence:
CAGAGGGAAGAACTTTCTGTCCAAATCAACAACCTGCGAGAGCAACTGAG[T/C]AAGTAACACATGTCCAGTCAATTACACAGAGACTCGGTTCTTGTGTCCGT
Long Flanking Sequence:
ACTAAAAACAGCATTGGAACATGAATATTTAAACATTTAAAAGCCAATTTAGGATAATTAAATTTAATTAAACCATTAAAACTAAAAAGGTTATGTTTACAGAAAACCTCACAATGATGCTATCGCATAGGCTTTAACTTCATTATGTTTATATATCCAATAAATATGACTTCAGTGTAGTTAAAGAGGTGTATTATTTGTGTCTATTCATTAATTAGTAAATAATTAAGCTGTTTACTCCATTTTAACTAGAATATTTATCATTTTAAATCAAATTTAGTTATTACTTTTATTTAGAATTTTTGATTCTATTTACTTAAGTCTAATTATTCTAGAAAAAACCTTTGTTAAACATGTAATCTTCATCTATCCTTGTATGTGATTGCCCTGGATGACTGTTGATGGTTTTGTTTCTTCTGTCTTTTGTTACAGCGCGAGTCGGCAATCAAACAGAGGGAAGAACTTTCTGTCCAAATCAACAACCTGCGAGAGCAACTGAG[T/C]AAGTAACACATGTCCAGTCAATTACACAGAGACTCGGTTCTTGTGTCCGTTCCTTAGACTCACAGAGCATAAGGCTTTCATCTTGCTCGGATAGCTGTCATTTAGCAGGTGCTTTTGTTCAAAGTGACTGGAAGAACACTTATCTGTGAGAAACCTTGGGAGAACTGTCTTGCTCAAGGGCACAGTCCTGATAAAATAGGGCTGAGTGAGTGTTTAGTTTCGGGGTCACACCTACTTAGGATTGCAGTTTTCTTTTTTTTCCACAGATAATTTAACCAAGCAATATTTAGAATCCGGAATGTCATGAAAAACTAGTGGCACCTTAGGAACTACATTTTAATACCATCAAAACAATTTACCAACTGCACTGCAACATCTTAGTATTGTGGCAGAATCAAAAATTATTATTGAATATGTGAAAAAACAAAACTAAAATCTCTAGGAGCAATTACTATATGTCGAAACCTATTAAAAAGATATATATTCATATACATGATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1993
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000048855 | Essential Splice Site | 1220 | 1416 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 1 (position 15354131)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 15919299 |
| GRCz11 | 1 | 16612236 |
KASP Assay ID:
554-3080.1 (used for ordering genotyping assays)
KASP Sequence:
ACTGAGCAAATAGCAACACTGAAACATGAACATGAGACTTCACTCACAGG[T/C]GATTTCACTGCAGTSATCRACAGTTTCTGCTTTTGTTTAATGTACTGTAT
Long Flanking Sequence:
TCCCTCCCTACCGCATCTCTCCTCGCTCTTCAGACACGTCGCTGGCCAAACAACTTGTCAAACACCACCAAACCACCACCTCCCCTGACAGCTGAGCGGGACTCACCAAAATAAACCGTGAATCTCTGACCAATGTAAGGAGAGTTTATTCACACGTGACTTGTTTTAGCCCTTTTGGTCTGATTAGAAACTTTGCAGTGTAAAAGCGAACCGCACCAAGAGCAAAGAGCAACAAAGTAACAATTTCAATCCCTGTTTTGGAACAAATGAATCGATTCACAGGTGAAAGCACCCTAAGAAGCACATCTGGAGAATGGCAGAGTTGCTAATATTAGCTGAAGGCGCTGCATGTTTAGTGTTTTCATTGTTGATGGGTATGATTTCTACTGACAGGTGGAGGATGTGAGGTACAAACAAGAAGCACTGAGGAAGCAGCAGGAAGCGGCACACACTGAGCAAATAGCAACACTGAAACATGAACATGAGACTTCACTCACAGG[T/C]GATTTCACTGCAGTCATCAACAGTTTCTGCTTTTGTTTAATGTACTGTATTTTGAATTTGATCTTGATCTTCCTGTATGACAAAGATTTTTTTCTTCTCCCCTTTTCCAGAGCTCAAAAAGGCTTATGAAAATGACATGCAAGAACTTGACAAAACGCTTAAGGAGTCTGAGGCCATGCTTAATGTATGCATCACCATCTCATCATTTCCCTTACTGTTTAACTTGGAATATTTGAGATCTTTACTCAACTTGCAAATTGAAAATACTTTGTGTCTTTGCTTTTTTTTGCTAATTGTTTATTTGATCGCTATTGTCTTAACTACAGGAGAAGATTGAGACTTTGACAGCAGAAAATGAGGCTTTGAAAGAAAGACTGAGAGAGGAGCAGGAGTGGAGGAGAGCTGCGGCTGACAAAAGCCAGGTAGGTGTACAATGAAATGCATTATTCTCAATACAACTTTAGGGATGATTTACACTTTGCATTATTGAATAAATTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19459
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 |
|---|---|---|---|---|---|
| ENSDART00000048855 | Nonsense | 1282 | 1416 | 12 | 14 |
Genomic Location (Zv9):
Chromosome 1 (position 15355773)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 15920941 |
| GRCz11 | 1 | 16613878 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTCAAACTAAGCAGCTGTTTCTCTGTGTGCAGAAGGACGCGCATACAT[T/A]GTATTTGGAGCAAGAACTGGAGAGTCTCAGAGCTGTGCTGGAAATAAAGA
Long Flanking Sequence:
CAAACCTTTATGAGTTACATTTTCTGTTGAACACGCACAAAAAAAATAACAGATATCCATAGAAAAAATACAGTGAATGAAATTGGCTACTGGTTTGCAATATCTTTTGAGTTCAACAGAGCAAAGAAACATGTTTGAAATAAATGCAGGATGAGAAAAATTTTGCACAATTTTTGTGAGTTAAATTCAGTCTTTTTTTTTTGTGAAAAACATTACTCATATGTGTTCAAAAAAATGAATAAATATTTATTTAATTCATTATACTTGTTTAGTTCATTATACATATTTATATTTTCCTGCTACTTTATTTCATAAAGCTTTTAAAAAAATATCCCTACCTGTAGTGTCAATGGGGTTAGTGTGATTTCAGCTTAGACCATGTAAAGCCTGTTACAGTGACCCTTAGGAAGCCTGTAAACTGCAGAGATGCTCAGTCACTTTACGTGGTGAATCTCAAACTAAGCAGCTGTTTCTCTGTGTGCAGAAGGACGCGCATACAT[T/A]GTATTTGGAGCAAGAACTGGAGAGTCTCAGAGCTGTGCTGGAAATAAAGACCAACCAGATACACCAGAAAGACAAGAAACTCATGCAGATGGACAAACTGGTGAGGACTGATAATAAATGTACACATTTGATGTCCTTATAGACCCCTCATTGCATTATGAGTCAGTTTAGTTTAAGTAGCCATATGGACCAAAGTTTTTTTAACGAACCTCCATTAAAGAGTCTGCTGTGACATTGTTTTTACTTAACTACCATCACAATAATTAGTTTCATTATCAGATATTTATTGAATAATACAAAATATGGCCTTAAATGTTAGGGCAATACCATGCATTACAGAATAAATGAATGACATAGTCTAAAGGAAAAACCCAATTATTTTGTTCACCCCACTGGCAGATGAATTTGCTTATTTCAAGGAAAAATTTTATTAATTTTGACATTATCTCTTAAAACAAGACTTTTTTGCTTTTCTAAAAATGCTTCCTGATTTAAGAATT
Associated Phenotype:
Not determined