ZMP
si:ch211-69k21.4
Ensembl ID:
ZFIN ID:
Human Orthologue:
MTUS2
Human Description:
microtubule associated tumor suppressor candidate 2 [Source:HGNC Symbol;Acc:20595]
Mouse Orthologue:
Mtus2
Mouse Description:
microtubule associated tumor suppressor candidate 2 Gene [Source:MGI Symbol;Acc:MGI:1915388]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11453 | Nonsense | Available for shipment | Available now |
sa9452 | Essential Splice Site | Available for shipment | Available now |
sa9606 | Essential Splice Site | Available for shipment | Available now |
sa34904 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11453
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 |
---|---|---|---|---|---|
ENSDART00000090059 | Nonsense | 282 | 1303 | 1 | 14 |
ENSDART00000141387 | None | None | 243 | None | 4 |
Genomic Location (Zv9):
Chromosome 10 (position 24996076)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 24595428 |
GRCz11 | 10 | 24564880 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCATAAAAGTGCATAAATTCCCAATGGAAGCGGAGSARAATACTGGATA[T/A]AAATGGATGTCAACTGAGGTGCCRAAAGGTATGGTGAGGGTACAACCTTC
Long Flanking Sequence:
AGGAAGTTGACTTTTGGATCCCCTTGGAAAGACCACAATGAAAACCACAGTGTGGATGGAGATGCAAATGAGAACTCACAGCCCCTTGACCTCAGGACCTCTAGCTCTCGCTCTGGTGCAAACCGAACCCTGAGAGATGGCCGAAGTGGATCTGAAAGCAATGTCTTTTCATCTTCTCTTTCTGCAGTGACCAGCCTCAGTGGAAGTTTAGCCAGTGCCCTGGACACTGCAGGCTGCACACAGCCTCTCTATTCCCAGTTCACCAAGTCTACCTCAGGCAAAGGCAGGAACCAGCAACCAGCTACTACTGAGTCCTTCATCCACTCAGAGAGAAACAGGGATCTTCCCAGGGATTTGGACCAAAACCATAACTCTACTATACTGCCTCAGGAACCACAATATGACCGAAGTAAGCTAATCACTCCAAGTGGTGCATATCCTTCAAATGGAACCATAAAAGTGCATAAATTCCCAATGGAAGCGGAGCAGAATACTGGATA[T/A]AAATGGATGTCAACTGAGGTGCCGAAAGGTATGGTGAGGGTACAACCTTCTTGTCGGCAGCTTGTCCGCCCTCTTTCTACAGAAAAGCGATTAACCTCAGGATATCCCAACAGTGACCAGGCAGACCAACAACAATCCCACTATTCAGAGACCTGTCATGGACATCAACAAGTGCTAGCTTGTACAGAAGTCAACAGTAATCCCAACACAGGCACAGAGATGGTTCACAACCAGACCTTTACCAGAGAAGCCCAACGTATAAAGAGGCAGAGCTCAGCAGATCGTGCCGCAAGTCCCTCCAGCCTTGAAAGAAAGACACACTTCAGCCGCCGGGCCTACAGCAGTCCAAGTAGACCATCCCCTCCTCCATCCCCCAAGACCACAAGGTCTCCTCAAAGGCATCCTTCATCATCACCCATCAAAACTTTACCCTCTCGAGCTCCACAGTTGGGTTATGCTGGGTACACTTCAGGCTTAAGAGCCCCAGTGAAAACAACTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9452
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 |
---|---|---|---|---|---|
ENSDART00000090059 | Essential Splice Site | 678 | 1303 | 2 | 14 |
ENSDART00000141387 | Essential Splice Site | 86 | 243 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 10 (position 24997400)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 24596752 |
GRCz11 | 10 | 24566204 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCAATGCAGGCAGTTAACCCAACCACTCAAACTCCTCAGGAAACACAAG[G/A]TAAGATCTATCGCACAGTTCCATTTATATGGCATGTTTTACATCGCTTTC
Long Flanking Sequence:
GGTCTGGGATTAAACCACCCAGCAACACCATGCCTCACAAAATGGCTGGCAGATCGGACAGCTTCTACGGGTCTCTTAACAAGCCTCTATCTGCAGCAGTAAGGAGTGATTTACAATTGAGAAATATTTTGTTATTAATTAAATGCTTTTATATCCATAAATATTAGTTTGTGTGTATTGGGAGAGTTTATATTCTGCAACCTGGGGTCATGTTTTTGTTTTTTAAAATTAGGTGGGACGATCCGCAGTTGGCCTTGGGTCTCCAGTGTCTGCAGCTGAGGACCCATCTGGATCACCTATGGGAGCACAGGATACAGGGAGTCTTTTTCGTTCACCACGGGGCCTAAGACCTCAACTTGGCGTTGGTGCTGTAAACAGGACTCCTTCTGTACTTGCAAAAGGCAGGATGACCTTAACAAGTCACCCAAAGTCACCACTGACCATCAGTCAACCAATGCAGGCAGTTAACCCAACCACTCAAACTCCTCAGGAAACACAAG[G/A]TAAGATCTATCGCACAGTTCCATTTATATGGCATGTTTTACATCGCTTTCCATCAGTAAAGCTATCTCACATAGCACACTAGTGCAGGTTCGGTGTTTAAAAATGGTTTTCAGTGATAGAATCACCAAGGCTTTGTCCTAAAGGCAAAACTGACTCTGGAGTGTTTTGAGATGAGTAGATGTAAACAGAAAGAAGGAAGAGAATGCCATAAGTCTTCGCATCCCTGCCAGTAATGCATTTGTAATTGTAAGAGATAAACTCATCCCAGCCTCTCGTCAGTAGAAAATACACTTTACCTCCTGGCATTTAGTTGAATATAAATAAAGTTCACATTCATCTTGTGCCATGAGGGAGTTCTGTCTGAGCTTAAAAATTCCCTACCATTTCTAAAGCGCACTTTATTTCCAACAACTTTGCCTGTCAAGGTGAAGATATGAGTTATTTCATCTTAAATCCACTACCAACATTGCCATCATCCTCTGTGTTTTTTCTAGAGGGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9606
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 |
---|---|---|---|---|---|
ENSDART00000090059 | Essential Splice Site | 803 | 1303 | None | 14 |
ENSDART00000141387 | Essential Splice Site | 211 | 243 | None | 4 |
Genomic Location (Zv9):
Chromosome 10 (position 25036548)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 24635900 |
GRCz11 | 10 | 24605352 |
KASP Assay ID:
2260-3244.1 (used for ordering genotyping assays)
KASP Sequence:
TTCAGTTAATTCCCACACACTGCCATTAACTSTTGTCTTTCTTTCTCCGM[A/T]GTATCCCGTAAGGAATTCCAGAAGAGTTCGGATGGCTCCCGTTCATCCCA
Long Flanking Sequence:
TAAAAAGTCTATTTTATATCATCATGCACATCAAGGGATATTCATATATATATATATATATATATATATATATATATATATATATATATATATATATATTCTACACTCTTTTTTTTCTATTCACCATGAGCTGACAGACCTGGGATTTGTGAGATGCATGAATTTTTATATATATTAGAACTATATTCTGTACTGTAAGTGTTGGTCCAAAGATGCCTGCGGCCTCTCTGAATGACATATCTTCAAGTCCATGTCAGCCAGACCCTGGCAGCTGCGTTATTTTGAGGTTGGCTGCCTCTTATTGGAATCGATCCACGGACCACTGAGACTATATTATGATCCATGGAAGGGGAGAGCGATACGAGCAGCAGAGTTGGAGAAGGGTTTACTGTTACAAACCCTTTCATAGATTGCTGTACTGTATGTGTCCCTAGAGCGAATATCCTTTAATTCAGTTAATTCCCACACACTGCCATTAACTCTTGTCTTTCTTTCTCCGC[A/T]GTATCCCGTAAGGAATTCCAGAAGAGTTCGGATGGCTCCCGTTCATCCCAGTCATCCCCTAAGAGACTCGCTGTAGTGTCTCCTAAACCACAATCTCCAGGTAAACCAACCAAGACAAAGATCAAGCTAAGATATTGCTTTCGTCCCCCGCTGCTCTATAGAGTACAGTGCTGCCATTAGATGATGCTATTGGATAAATCTCATCTTACGTCTGGCACTGTAACCCTCTCTATTTTCCTTCTCTCTACGCACACACACTTAGAATGAGAGGGTATTTCATATACGATGCAATCAGTTTGGCCACTGGGGCCAAGTTCAGCTGACATGTTGAACAAAATGAAGCAATACTCCTGGTTTAGGGCATCAACGAACCTAATTAGAGCTTAAATTGTCTTGAAGGATTTGAAATGGTTAGTTCACCTTAAAGCTGTAGCCACTTCAGAATGGGAACTAGGTAATAATGTTTTGTTATTTGAGTTGTACTTTTTCATTGGAAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34904
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 |
---|---|---|---|---|---|
ENSDART00000090059 | Nonsense | 1059 | 1303 | 10 | 14 |
ENSDART00000141387 | None | None | 243 | None | 4 |
Genomic Location (Zv9):
Chromosome 10 (position 25048142)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 24647494 |
GRCz11 | 10 | 24616946 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGACAGAAATGGGGAGAAGAGCTCAATCTCATTTCGTTTATCTTAGATT[T/A]AAGGAAAGCCCATGAGCAGCAGAAAGCCAGTCTAGAAGAGGACTTCGAGA
Long Flanking Sequence:
GAAAACATGTTAAATGAGAATTTGAAATATTTTATAGCATACTTTAAAAAAAATAAATATGATTTAGTATTCAAAATATTTTAATTTGATAATGTATTTAAATAAATTGCTCTTACACTTACTTTTACACCGTTACTTTTACCGTAAACCGACATGCCAACCATTTGTTAGAAGTTAATATTTTTAAAACGATGGGATGTGTTGGGAAAAAAATGCATTGAGTGTGTTAACTAGCGACATTAGGAGTTAGGAAATGCAATCCAAAAATGTTTTTCTTGGTGGGCCAGCTAAAGGGTTAATGTGGTTTTGTGTGTAGATTGAAGAGTTGACTGCCAACCATGAGGCTGCCCTTGAAGACCTGAAAACCATGCACAACATCACTATGGCAACACTCCAGGAGGAACATGCCAGGACGATGAGAGGTGAGTGTCTGATTCATAACATCACCAACAGACAGAAATGGGGAGAAGAGCTCAATCTCATTTCGTTTATCTTAGATT[T/A]AAGGAAAGCCCATGAGCAGCAGAAAGCCAGTCTAGAAGAGGACTTCGAGAAACTGCGCCTCTCACTTCAGGTGATTTGATTCAAGGTTTGTTATGAAGGTTTTTGCTCTTCATTTGAGGTCATTAGTAACAATAATGTTTTCTTCAGGATCAGGTGGACACTCTGACATTCCAGAACCGGACTCTGAAAGACAAAGCTAAGCGTTTTGAGGAGGCACTGAGGAAGAGCACTGATGAACAAATTGTGGTATGTTTCTTTGAAGTCGTCATGAAAAACTATATTCTATCTATATATTTCTGTAATTTTTGTCCCTAATGTGTGATGCACATCTAAATCAAACAGATTCTTTAATGAGAAAAAATGTTCATCAGGACAAATCAAAATAAAAATGATGGACAAATCAGCTGATTTTGAATTATATAGCTGTTTTGCTATAGGTGAATTTCATTTGAGTGACACATTGCCTCGCACTTACATGTCATTAAAGAAAGGCAGAGATG
Associated Phenotype:
Not determined