ZMP
mtmr9
Ensembl ID:
ZFIN ID:
Description:
myotubularin-related protein 9 [Source:RefSeq peptide;Acc:NP_001038535]
Human Orthologue:
MTMR9
Human Description:
myotubularin related protein 9 [Source:HGNC Symbol;Acc:14596]
Mouse Orthologue:
Mtmr9
Mouse Description:
myotubularin related protein 9 Gene [Source:MGI Symbol;Acc:MGI:2442842]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9609 | Essential Splice Site | Available for shipment | Available now |
sa6627 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16766 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9609
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 |
---|---|---|---|---|---|
ENSDART00000035447 | Essential Splice Site | 98 | 549 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 20 (position 19028840)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 19057097 |
GRCz11 | 20 | 18956680 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGTGATCARTGTAGGCTGTCAGTGTTTAYGTTATGAGGATCTCTCCTCC[A/T]GGCTCTGTCCACGCTGGACTCTGTGTCWCTGATGTACCCRTTCTTCTAYC
Long Flanking Sequence:
ACAATGAGGTGTTATTTTTCTCTTCACAGTTTAAATATTAAAAGTTAATTAATTAAAACAAAAAAAATAAAAACTTTTAGCAGACCACGAATATTCCAAAATAACTGAAACATGTCTTCCCACAGCAAAAATAAGGATATTGAATATTACTGTTTTGTTAGGAATACTAAGAGAAAATAATCTGGAGGAATATCCTCAGAAGAGCCGCAAATATGCTTATGATACTAATGTTACAACACAAAGTGTACAATTATTTTCATTATGGAAAACAAATTGGGTCTCAAAGCATGTACCTTTCATTCAGTTTTCACTATGGAAATGGCTTATTTGCTTCACAGCCTTAATATTCAAAATGATTTGTTTCAGTTATTGAATTATTTTAGTTATTTGAATGGAAGTTCCGTTGTGCTGACAATAACACATTTGGTTGATGGTAACCTGAACATTTTCTAGTGATCAGTGTAGGCTGTCAGTGTTTATGTTATGAGGATCTCTCCTCC[A/T]GGCTCTGTCCACGCTGGACTCTGTGTCTCTGATGTACCCGTTCTTCTACCGTCCGCTGTTCGAGGTCATTGAGGACGGATGGCAGTTGTTCGTACCAGAAGAGGCTTTCAAAGACCTGGAGTCAATGGTATTGTTTTATCTCTGGACGTCATGACACTGAGGTTATCAGAAAAATTTGGACAGCTTCTCAGTGTATCAGTGTTCAATTTTTTTAGTTAAGATCGTTCTCTATGTGAACCAGCAGATCAAATCATGCTCGTATTGCATAAATGCGATCTTGTCTTGTAATAATGCGCTCACCACATTTCTCCATTTGTCATTGAAATAACGCTATAGGTAGTTGGTAGATTTGTGTAAAGGTCTGCCGCCACAGCTGGAAAAAATCCTAGAGGAAACACTGCACTGTAATTAAAAAGCTTGATTTTATTTGATAAATGTTATTGTTCATGTGAAATATTTGCAATATAGTTTATTTCTGTGATGCGAAGCTAAGTTGTTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6627
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 |
---|---|---|---|---|---|
ENSDART00000035447 | Nonsense | 288 | 549 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 20 (position 19033936)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 19062193 |
GRCz11 | 20 | 18961776 |
KASP Assay ID:
554-4882.1 (used for ordering genotyping assays)
KASP Sequence:
CTAACATCCTGCAGGAGAGCCTGATAAAGCTGGTGGAGGCCTGCAATGAT[C/T]AGTCTCACAACATGGACCGCTGGCTCAGTAAACTCGAGGCCTCCAACTGG
Long Flanking Sequence:
TTAAATGTTTTTGCCACGAAAATTGCTTTTGTTGCTGATAATTGGCATTAAACAATAAAAATATGATATAATATTTGTGGTTTCTGTGGCTGAATCACATTAAAGGAGAAGCGCAGCAAATATGTACAAATAAACTGTTATTTAATATAAAACAGTGAACAGTTTTCTGGCAGGCCAAAATGTGGAAAATCTATAGCAGATTAAAAAAAGATGTCAAGTTTCTCTAAATTTTATACCGTTTGCTTGGTTTTGTGATTCTGTAATTGCTAAATTCTAGAGACTGCTCAAAGGTTGCCTTCTTTTTTCATAATACATTGAAATTCATCTTCTTAGTAAGTGAAAGTGTTGGGAAAGTCAGGATATTTCACATTTGACTTAGAGAGGGACCCTGTGAATCACAAATGATCTCTGTAAGTGTGACTATAATCTGACCTGTGTTCCTCCACAGATCTAACATCCTGCAGGAGAGCCTGATAAAGCTGGTGGAGGCCTGCAATGAT[C/T]AGTCTCACAACATGGACCGCTGGCTCAGTAAACTCGAGGCCTCCAACTGGCAGAGTCATGTCAAAGAAATCCTGACCACCGCCTGCCTGGCTGCACAGTGCATCGACAGGTACATCTGCTGATGTGTCTGTCTGTCTGTTCTTGTCCATTATTAACACAGTTCTGCAGACGCCATATTGTGCAGCTGTGTTAATTACTGTTTTAGCGCTGTTCAAAGTTAATTAGAAAAGCTGCCGTCTCCCTATTTGCCACTACGTTTGTTGCAAAGCTCATTGTGTCGATAATTAGTGCTGTTGTCGTGCTGTAATCATCATTATGTTAATACCACTCCGGCACTGCTGTTTTAAATGCTGCTTTTGGTGCACAGTTCATTATAAGGTTTGTAGTGCTAGAAGTAAATGTGTTAAATAATCTTAAAATTGAGTGCGCTTTGAGACTGGGATCGGGGGAAGTATTTTTAAGAGCAGAGATGTCCAAACTAGGTCCCACGGGCCAAAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16766
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 |
---|---|---|---|---|---|
ENSDART00000035447 | Nonsense | 427 | 549 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 20 (position 19041032)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 19069289 |
GRCz11 | 20 | 18968872 |
KASP Assay ID:
2261-4123.1 (used for ordering genotyping assays)
KASP Sequence:
AGTTYCCTTGCTCATTTCAGTTCAGCGAGAGCTTTCTCATCATGCTYTTC[G/T]AGCACACCTATGCCTCACAGTTTGGCACTTTCCTCGGCAACAGTGTGGCT
Long Flanking Sequence:
AACTACACACATAACCCAAGACAGACCACTTTTATATTAGGCAGAACAATATTGTGCAAGAGATATTGTGCAAAAGAGGTTGATGAAAACAAGTAGTGCAACATGATTGTGTGGCACATTCACAAGTTAACATTGTTTTCCTGATTGAGTCCTTGCAAGATGGAGTTTAAGAAAAGTGTTCAGTGCATATAGAGAGATGAGTATTTCAACAGGTGGTTTATCAAGCCCACTTGCCTCTTGTGAGATAAAGTCTTACGTTATATTTCTTAAAATATTGGTAATATGATATTTTGATAATATGAAGCACAGGATAACCAGTGACAATTTCTCTTCAGGCTGGTCACCCGTTCCAACAGCGCTGTGCTCAGTCTGCATACTCCAATGGGAAGCCCCGCAGTGAAGCACCGGTGTTTCTGCTCTTCCTGGACTGTGTGTGGCAGATCCTCCGTCAGTTCCCTTGCTCATTTCAGTTCAGCGAGAGCTTTCTCATCATGCTCTTC[G/T]AGCACACCTATGCCTCACAGTTTGGCACTTTCCTCGGCAACAGTGTGGCTGAAAGGTTAGTTATTCCCTCCATCACAGTGCTGTCATTTGTTTACTGTAAAACATCACATACAAAAACACTTCAATTCTATTGTTTGAGCCTCATTTTTAACAAGCCAATACAGGTTCCGTCCCAAATAACAAAACAAAACTAACAAACTGTGTCTTGAAAATGTCTTGAAATTTTAATATGAACCAATACTGGAATATTTGAAATGATTTTATATCAGTTTCCCTTTTTTCATTTATGCAAAGTTTTCAGATACTTTGTACCATGTGCCTTTCGTGCTTCATCAGTTAATTCATCTGGTGTTTGTGCATCTCTTTTTGTTAGTGTGCAAACGTTGAGTTCTTTTTGTGATTTTGTGCATTAAGAGATGCCAAATAACAGTAGGTTACATCTGAAAGTGAAAGTAAAACGTGGGGAAGATAATTCAGCTGTTGTCATGAACATTAATCAA
Associated Phenotype:
Not determined