ZMP
MAST3 (1 of 2)
Ensembl ID:
Description:
microtubule associated serine/threonine kinase 3 [Source:HGNC Symbol;Acc:19036]
Human Orthologue:
MAST3
Human Description:
microtubule associated serine/threonine kinase 3 [Source:HGNC Symbol;Acc:19036]
Mouse Orthologue:
Mast3
Mouse Description:
microtubule associated serine/threonine kinase 3 Gene [Source:MGI Symbol;Acc:MGI:2683541]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21868 | Essential Splice Site | Available for shipment | Available now |
sa17432 | Nonsense | Available for shipment | Available now |
sa41798 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21868
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 |
---|---|---|---|---|---|
ENSDART00000121872 | Essential Splice Site | 108 | 1433 | 4 | 26 |
Genomic Location (Zv9):
Chromosome 11 (position 13519135)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 13275958 |
GRCz11 | 11 | 13333617 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTCCATCCTCAGGTTACGGGACCAATCCTCCCAGCTCAACAGTCTCAG[T/A]ATGTGCCTCAGTATGAATCAACAATTCCTTCTTACAAAACTGTTCTGATC
Long Flanking Sequence:
ACTGATGGTTTGGGTAGATGTAGACATTAATTATTAAGATGGTTGGGTTAAAAGTTGTAGTAGGTGTAGACATTAATTATTATGATGGTTGGGTTTAAGGTTGGGGTAGGTGTAGACGATAATAATTATGATTGTTCAGTTTAGGTCTGGTGTAGGTGTAGACGTTAATACATATGATGGTTGGGTTTACGGTTGTGGTAGGTGTAGATGTTATTAACAGCGCCATCTTGTTGACAACATAGTTTTGACATCTGGGTCTTCATAACTTCAAGTTAAGTTTCTACTGCAAGTTACGCTGCCTTTGTTACGCCCCTGTCTTGCAGTCCACAGACATGCCCTACTCGACTAAGTGGCCACATACAGGTTTGAGTGACATGGCATCATACTGACTTCTAAAGTGATCTGCGTTTTCTTTTTTAGAGCGGAAGGGAGACGATGGTCTCTGGCTTCGCTTCCATCCTCAGGTTACGGGACCAATCCTCCCAGCTCAACAGTCTCAG[T/A]ATGTGCCTCAGTATGAATCAACAATTCCTTCTTACAAAACTGTTCTGATCCATGACAATAAAATAAACAGTAATGACAAGTCGAAGCATAAATTATGATAGATTTTTCAAATATTTTTCAATTGTTTAATTTAAAGCTCTTTAATAATAAAAACACTGTAAGATGAAGTATTTCTTCTGAATTAATCAGCGGTGTGAAATGTTCTCATATTTTTTAATTCATAAACTTTTTTTTTTAAAGTCTGTGTAAAATGGAAACGTACAATTTTTATTTTGATAGCGCACATTCTTACCGTACGTTCACACCGAAAGCGGCGACAGCGTCAAAGTAGCCGGAAGTCATTCATTTTCAATGAGAGCCGGCGGCGAGGAGCAGCGCGGCGCGTCTTCGCCGGCGTGAGCGTCGAGGAGAGTTGAAATGAAGTCAACTTTATGGTAATGAGCTATGACGCGGTTCAGCGGCAAGCAATCAGAATGAAGACGTCCATCGCTTGATAGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17432
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000121872 | Nonsense | 854 | 1433 | 21 | 26 |
Genomic Location (Zv9):
Chromosome 11 (position 13478021)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 13234844 |
GRCz11 | 11 | 13292503 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGGGGGTCCTCCATGCTTTGGAAACCAGCTGGAGACACCCGACAAACAG[C/T]GACTCTCACCAGGACGCAAAGTCCCCAAATCCGCATCAGTRTCCACTCTC
Long Flanking Sequence:
TGTGTGTGTATACATTTTATTTTTCTCATTTAGTTGCCTTACCACAATTAGGCTTCCCACATCTCGTTCAGCCTTCATTTAAAAATAAAAATCCCTGCAGCACTCAATAATGATGGGGAAAAGGGCTTTTGAATCTGATATGTTTTACTTCTGCTGTCTGATGATTTTCTCTTTTTAAAAATGTATAAAAAATAAAAACAAAAAAAAAATCCTCTCCTCAAAGAAAACCTCTTATGGATTGTGCAGAATTGTATTGAAAATGTGTCCATTAACAATGTTCAGTCTTTAGTCTTTCTATAATAATACTACAAAAATATTAATAATATAATAATGCAGTCACTAAGGTGGATTTGTGTTTTAATTCTGCAGCTGAAGTTGTCGTTTCTAACCTGCGAAGAATCAGGCTACGTAGCAACAGCACAGGAACGAAACACTCGTCTCCAAGGGAACAAGGGGGTCCTCCATGCTTTGGAAACCAGCTGGAGACACCCGACAAACAG[C/T]GACTCTCACCAGGACGCAAAGTCCCCAAATCCGCATCAGTGTCCACTCTCTCACTCATCATTACTCCAGGTCAGACCCCAAACACGGCTACCAAAAAACACAGCTACCATAGCAACATCTCAAAACTGTCCTTTTCATATATAGTAAAATAGTACAGTGGAGATGAAAATTGTAAAACAGTTTATGAACGCATGTAAGTCTTGTAAATTTTGAAGATATTTTTATTTTGATTAAAGCTGCATTTGAATAAATCACATCCGTTAGAAAGACCTTTTTGACGTTTTTCATTTTTTCCCTCAGATGACGGGAGTGGCAGCCTACAGGGACGCTCCATATCCCCTCGTTCATTTTCCTCCAATCCCTCATCGCGAGACTCCTCCCCCAACCGAGACCTGTCGCTCAGCATCAGCAGGCTCCGTCCCCCAATCATCATCCACAGCTCTGGGAAGAAATTTGGCTTCACGCTACAGACTATTCGTGTTTACATGGGGAACAGTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41798
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000121872 | Nonsense | 938 | 1433 | 22 | 26 |
Genomic Location (Zv9):
Chromosome 11 (position 13477536)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 13234359 |
GRCz11 | 11 | 13292018 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAGCTCTGGGAAGAAATTTGGCTTCACGCTACAGACTATTCGTGTTTA[C/A]ATGGGGAACAGTGACATCTACACCATACACCACATGGTCTCGGTGAGCAG
Long Flanking Sequence:
ACACCCGACAAACAGCGACTCTCACCAGGACGCAAAGTCCCCAAATCCGCATCAGTGTCCACTCTCTCACTCATCATTACTCCAGGTCAGACCCCAAACACGGCTACCAAAAAACACAGCTACCATAGCAACATCTCAAAACTGTCCTTTTCATATATAGTAAAATAGTACAGTGGAGATGAAAATTGTAAAACAGTTTATGAACGCATGTAAGTCTTGTAAATTTTGAAGATATTTTTATTTTGATTAAAGCTGCATTTGAATAAATCACATCCGTTAGAAAGACCTTTTTGACGTTTTTCATTTTTTCCCTCAGATGACGGGAGTGGCAGCCTACAGGGACGCTCCATATCCCCTCGTTCATTTTCCTCCAATCCCTCATCGCGAGACTCCTCCCCCAACCGAGACCTGTCGCTCAGCATCAGCAGGCTCCGTCCCCCAATCATCATCCACAGCTCTGGGAAGAAATTTGGCTTCACGCTACAGACTATTCGTGTTTA[C/A]ATGGGGAACAGTGACATCTACACCATACACCACATGGTCTCGGTGAGCAGAGAATCATTAATAAATCTTCCTTTCACAAAGCATCCTGTCTGAATTTAGACACTTAAAGGTGCTGTATGAAAGTTTTTGATTCTTCTAAAGCACAGGTGTCAAACTCAGTTCCAAAAGGGCCGCAGCTCTGCAGTTTAGTTCCAACCCTAATTAAACACACCTGATCAAACTAATTGAGTCCTTCAGGCTTGTTTGAAACCTACAGATAACTGTGTTGAAGCAGGGTTGGAACTAAATTGTGCAGGGCTTCGGCCCTCCAGGAATTGAGTTTGACACCCCTCTTCTAAAGCTTATAAATAGCATAATATGTTTGCAGATAGTAAAGAAACATGCCAAGTAAGCATCCTTTTTTTATCATAAAACAATGCTGAAGTCAGATATACGGCTTTGAAAATGTATTTTCCGTGCCGGATTGCTTTCTTTGTTTTCGTAATATTTCAGCAGCCCGG
Associated Phenotype:
Not determined