Busch Lab

ZMP

mtmr10

Ensembl ID:
ENSDARG00000010601
ZFIN ID:
ZDB-GENE-061103-52
Description:
Myotubularin-related protein 10 [Source:UniProtKB/Swiss-Prot;Acc:A0JMF6]
Human Orthologue:
MTMR10
Human Description:
myotubularin related protein 10 [Source:HGNC Symbol;Acc:25999]
Mouse Orthologues:
Mtmr10, Sbf2
Mouse Descriptions:
SET binding factor 2 Gene [Source:MGI Symbol;Acc:MGI:1921831]
myotubularin related protein 10 Gene [Source:MGI Symbol;Acc:MGI:2142292]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa40920 Nonsense Mutation detected in F1 DNA Not yet available
sa40921 Nonsense Mutation detected in F1 DNA Not yet available
sa18004 Nonsense Available for shipment Available now
sa7597 Missense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa40920
Status:
Mutation detected in F1 DNA
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
ENSDART00000085716 Nonsense 22 752 2 16
ENSDART00000127131 Nonsense 22 765 2 16
Genomic Location (Zv9):
Chromosome 7 (position 32062993)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 30455335
GRCz11 7 30726485
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCATACTTGTACAGTGAGTTATAAGTGTTTATGTTTCACAGACCGATT[T/A]GAAGAAAAGTCCACAACTGCCTATCAAGAAGCTAGAAGCAAAACTTTTAC
Long Flanking Sequence:
ACTCGGTTGGATAACTTTGGTGTCAGTTCTTCACTGTGGTAACTTTTAAGGTAATAACTATAATAAAAAAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATGGTACTTCCATGAGACATGGAGTAAGATACAGGGGAAATGCCAACTTTATAAGGATGAAAATGTGTAACCTATTTAGATATACATTCAACTTTACATAACTTAATAACAAATAAGTAGCCAGGATGTTTAAAATTTAACTCATGGGGTAATGAATTATTATAACCCCATGGACAGTGAAAAAAAAGCTTTTTCTCCTCTAATCTAACATTAATGTCCACAAATTCCTTATTCATAAAAAAAACTCTGATTTTCAACATAATACAATGTGGTGCTGTTGCTCACTATTTTTTTAGACCCATAATTAGATAATTTAGCTTCATTATGACTATCATTGTATTGCATACTTGTACAGTGAGTTATAAGTGTTTATGTTTCACAGACCGATT[T/A]GAAGAAAAGTCCACAACTGCCTATCAAGAAGCTAGAAGCAAAACTTTTACCGGGTGAGTGATTTCAAAACTACTTCTATCACAACAGCTCACAACCTTCAAGGTTAGGTTGGTGTGGGTGACTATTTGAAGTTTCACAGAGTATGTTTGATAGTTCAAACCACCAGTGCGTATTTCAGGAAACACGATTTCAGTGACTACCCTGGTAAATTAAAATTTAACAAACTCTGGTTATTCATGTTCAAAATGATGAGTTGATTTGTGCTACTTCTCTATTTCATTGTATGCTGCACGACTAACCATGCTTTGGAGCAGGTTTTTGTTCTTGTTTTGATCTCACAAACTGATCAGCTGTCAGCAAAGTGACAGATGTCTGACAGTGAAATAACTTCACTATGTATTGCTATGTAGTCCCTTTATTAATCTGGGGTTGCCACAGCGGAATGAACCGCCAACTTATACAGCATATGTTTTACGCAGCGGATGCCCTTCCAGCTGCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40921
Status:
Mutation detected in F1 DNA
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
ENSDART00000085716 Nonsense 375 752 12 16
ENSDART00000127131 Nonsense 375 765 12 16
ENSDART00000085716 Nonsense 375 752 12 16
ENSDART00000127131 Nonsense 375 765 12 16
Genomic Location (Zv9):
Chromosome 7 (position 32099561)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 30491903
GRCz11 7 30763053
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTTTCGTTTAACAGGACATTTTTGCGGCACGCAGTGGAGGTAGTCTA[T/G]ATGCTTGAGAGCAGGCATGTGTCTGTCATACTCCTTGGTAAGAAGCACTT
Long Flanking Sequence:
CTAAATAAGACTTTAACTGTAGGAAATCCTCTCAGGCTTAACACTGGGCTACAGTAAGGGCCAGGAATGTTTTTGGTTATTTCAGGAATCCCCCATACTGTTTCCTGGTGCCATTGAAAACATGTTAGCTGGAAATACACTTTTAAAACATAGCTTAGGTCTATACAATGTTCCAAAAGAGCTAAGCAGTCTGATGGTGTAATCATATGTTTTTTGCCTCCTGCCTCACTCTGGCTCTAATGTGCCTTTTTGCTCACTTTTGTATAAATATGCAGAGTCATTTGAGGAGTCTGAAGAGAAATGGCTGTCATCCTTAGAGAGTTCAAGATGGATGGAGTACGTCAGGTATGATTGAGGAGTGTTCAGTAGTAGCTTCTGCCAGAAATGGTTTCTGTTTTTGCATGCTTAGGTGTTTATTTAGGCCTCAACAGTTTTGAGATTGTTGTGGTATGTTTTTCGTTTAACAGGACATTTTTGCGGCACGCAGTGGAGGTAGTCTA[T/G]ATGCTTGAGAGCAGGCATGTGTCTGTCATACTCCTTGGTAAGAAGCACTTTGTACACACACATTTATGATGTATATGATAAATATTTTAGTTACTTGTACTTGCAACTTCTCAGTGTTTATTTAAAATATCTTAGTTTAACCATGGAATGACATGAGGGAATGATGACAGACATTTCATAACTGAGTGAATTTACTTAAAGACAAACATGTAATCCGTTTAAGTCTTATTTTGTCTATATGTGTTTGCATGTGCAGAGAAGGAGGACCGGGACCTGAGCTGTGTGATTTCCAGTCTGGTGCAGCTGATGTGTGATCCACACTGCAGGAGTCTGCATGGCTTCCAGGCTCTGATTCAAAAGGAGTGGGTGATGGCTGGGCATCGTTTCCTGGATCGCTGCAACCATCTGAAGAAGAGTGATAAAGAGGAGGTAGTGCAGCGCATATATACTGTATATCAAATGTATTTCAGCATCATATTTCTTCATCTATAAAGGGGCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18004
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085716 Nonsense 375 752 12 16
ENSDART00000127131 Nonsense 375 765 12 16
ENSDART00000085716 Nonsense 375 752 12 16
ENSDART00000127131 Nonsense 375 765 12 16
Genomic Location (Zv9):
Chromosome 7 (position 32099561)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 30491903
GRCz11 7 30763053
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTTTTCKTTTAACAGGACATTTTTGCGGCACGCAGTRGAGGTAGTCTA[T/A]ATGCTKGAGAGCAGGCATGTGTCTGTCATACTCCTTGGTAAGAAGCACTT
Long Flanking Sequence:
CTAAATAAGACTTTAACTGTAGGAAATCCTCTCAGGCTTAACACTGGGCTACAGTAAGGGCCAGGAATGTTTTTGGTTATTTCAGGAATCCCCCATACTGTTTCCTGGTGCCATTGAAAACATGTTAGCTGGAAATACACTTTTAAAACATAGCTTAGGTCTATACAATGTTCCAAAAGAGCTAAGCAGTCTGATGGTGTAATCATATGTTTTTTGCCTCCTGCCTCACTCTGGCTCTAATGTGCCTTTTTGCTCACTTTTGTATAAATATGCAGAGTCATTTGAGGAGTCTGAAGAGAAATGGCTGTCATCCTTAGAGAGTTCAAGATGGATGGAGTACGTCAGGTATGATTGAGGAGTGTTCAGTAGTAGCTTCTGCCAGAAATGGTTTCTGTTTTTGCATGCTTAGGTGTTTATTTAGGCCTCAACAGTTTTGAGATTGTTGTGGTATGTTTTTCGTTTAACAGGACATTTTTGCGGCACGCAGTGGAGGTAGTCTA[T/A]ATGCTTGAGAGCAGGCATGTGTCTGTCATACTCCTTGGTAAGAAGCACTTTGTACACACACATTTATGATGTATATGATAAATATTTTAGTTACTTGTACTTGCAACTTCTCAGTGTTTATTTAAAATATCTTAGTTTAACCATGGAATGACATGAGGGAATGATGACAGACATTTCATAACTGAGTGAATTTACTTAAAGACAAACATGTAATCCGTTTAAGTCTTATTTTGTCTATATGTGTTTGCATGTGCAGAGAAGGAGGACCGGGACCTGAGCTGTGTGATTTCCAGTCTGGTGCAGCTGATGTGTGATCCACACTGCAGGAGTCTGCATGGCTTCCAGGCTCTGATTCAAAAGGAGTGGGTGATGGCTGGGCATCGTTTCCTGGATCGCTGCAACCATCTGAAGAAGAGTGATAAAGAGGAGGTAGTGCAGCGCATATATACTGTATATCAAATGTATTTCAGCATCATATTTCTTCATCTATAAAGGGGCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7597
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085716 Missense 720 752 16 16
ENSDART00000127131 Missense 733 765 16 16
Genomic Location (Zv9):
Chromosome 7 (position 32104800)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 30497142
GRCz11 7 30768292
KASP Assay ID:
554-4352.1 (used for ordering genotyping assays)
KASP Sequence:
GCTCCWCCAGRATACCTCAGCTCCTCGTTTCCCTTCTCTCCTGTGGGCAA[T/G]CTGTGTCGGCCCGGCATTTTGGGGACTCCTCTGAGCAAGTTYCTYAACGG
Long Flanking Sequence:
AACTACAGTTCCACTGTGCGCGGTTTGCCTTCACTCATGCGCAATGGATCTCTTGGGCCGAACGACACCCTGACCCGCCGAAACTCTCTTGTGCTGCGTCTGCGTTCTGACTTGTCTCAGGTGCGGGAGCAGCCGGAGACTCCGTCAGAGCGCTTCGTTCGGGACTTCTTTTCTCGGGCTGTCGATCTGCAAGGCCTGCTGCTCCCCCAGCTCCTCCCATCTCACCTCTCCGTCTGGAAGCTGTACTTCCTACGCTGGGTCCCCGAGGCCCAGATCCCACACGGCGGGCCTGTCACTGCCTTCCACAAGCTCTCAGTGCTCACAGACGAGATCGAAATGCTCCAGAATCAGCTGAGGCAGTACAAAGGAGCAGCCGGGACTGCTAACACATCCCACGCGGAGCACAGCAAAATGTACTTTAAGGCCACTTCCACTCCTCAGCAGTGCCCTGCTCCTCCAGAATACCTCAGCTCCTCGTTTCCCTTCTCTCCTGTGGGCAA[T/G]CTGTGTCGGCCCGGCATTTTGGGGACTCCTCTGAGCAAGTTTCTCAACGGGGCCAAGATCTGGCTCTCTACAGAGACGCTGGCCAATGAGACCATCTGAAAGTGGATCAACATGAAGATCTTGCGTGATGTGAATGTGCAGGCTTGTGGTACGGACACGTTTTTATTCAGTCTGTTGAGAGCCGTCGGCTGGTGAGGTTTTTTTAATTTTTTTTTTATTCTTGCACATGATTAAATATAATGCTCCAATCGCACATCTTTCTGACTTGGGATTGTTTGGATCTGTTCTACCTGTGTTGTGGTGGATTTTATTTTCCTTGTAGAGTTTGTGGCATTAGATGGAAAGGAAGGTAAACCGGTAATGCTTTGCATATTTATGGTTCAGTTTGTTTACATTAGATAAAGCATTAGCTATCATGAACAAACTATAAATGGTTTATAGAACACAAATTAGTATGTACATTTCACATTTCAAATGTTTTTACAACTTTTACATTCATT
Associated Phenotype:
Not determined