ZMP
mast1
Ensembl ID:
Human Orthologue:
MAST1
Human Description:
microtubule associated serine/threonine kinase 1 [Source:HGNC Symbol;Acc:19034]
Mouse Orthologue:
Mast1
Mouse Description:
microtubule associated serine/threonine kinase 1 Gene [Source:MGI Symbol;Acc:MGI:1861901]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12456 | Nonsense | Available for shipment | Available now |
sa16788 | Nonsense | Available for shipment | Available now |
sa32768 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12456
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 |
---|---|---|---|---|---|
ENSDART00000063938 | Nonsense | 78 | 1717 | 4 | 26 |
Genomic Location (Zv9):
Chromosome 1 (position 51849084)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 50696445 |
GRCz11 | 1 | 51340244 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGGCTGATGGCAGAYGCTGGTCTCTGGCTTCTCTTCCCTCGTCTGGATA[T/A]GGGACCAACACACCCAGCTCAACGGTACAAACTCATCCACACAGAGCTGA
Long Flanking Sequence:
AAAATTATTCATTCTTTTTTGGAGGTCACCACAGCGTAATGAACCGCCAACTATTCCAGCATATATGGGAAAGACCTATACAGTCTCATTCACACACATACTCATACACTACGGCCAATTTAGTTCATCCAATTCACCTATCGCACAAGTCTTTGGACTGTGGGGGAAGCCTGAGCACCCAGAGGAAACCCACACCAACACAGAGAGAACATGCAGACTCCACACAGAAATGCCAACAGGCCCAGTCGCGACTTCAACCAGCAACCTTCTTGCTGTGCTAATCACTGAGCCACTGTGTCACCTCCACAAAAATATAAATAAGAAAATCTAAAATTGTTTTTTTTTTTAATCTCAAGATCCACTGGACAAAATCCAGAAGGGCCTGATTAGCTGTGGCTACTGTGCAAAATCTGCTTCTGTATTGTGATGTGCTTGTCTGTTTCTGCCTGCAGGGCTGATGGCAGACGCTGGTCTCTGGCTTCTCTTCCCTCGTCTGGATA[T/A]GGGACCAACACACCCAGCTCAACGGTACAAACTCATCCACACAGAGCTGATGCATTCATGTTTTATTCAAGAAATATTCAGATACTGTGTAACTAAAGTATGCACAAATAGAAAGTCAACACAGGATAATCAAAACAGGTGAAAGTGATGAAGTCGCAAAAACAAATTAGACAAATATCAGGAATATACAGTTGAAGTCAGAATTATTAGCCCCCCTGTTTATTTTTTCCCCAATTTCTGTTTAATGAAGAGAAGATTGGGTAACACTTTACAATAAGGTTCATTAGTTATTGCATTTACTAACATGAACTAATCATGAACAACACTTGTACAGCATTTATTACTCATAATTGAACATTTGCTAATGCATTATTAACATTCAAGTCCATGCTTGTTAACATTAGTTAATGCACCATGAGTTAACATGAACTAACAATGAACAACTGTATTTTCATTAACTAACGTTAACTAACATGAACAAATACAGTAGTAAATGTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16788
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 |
---|---|---|---|---|---|
ENSDART00000063938 | Nonsense | 383 | 1717 | 12 | 26 |
Genomic Location (Zv9):
Chromosome 1 (position 51869710)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 50717071 |
GRCz11 | 1 | 51360870 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGGCACAGAGAAACTCGACAGCGCTTTGCAATGAAGAAGATCAACAAA[C/T]AGAACCTGATCCTGCGGAACCAGATCCAGCAGGCGTTCGTGGAGCGGGAC
Long Flanking Sequence:
AATAGCCTAGAGCCCAGTCTGTTGTTGAAAACTAGCCTAGAGCATTGTCTGCTGTTCAAAACATCTATTTTTAAGCATTGACAGTGTAAAAAAAATATAAACTGTGTAAAAATATTTTTAATTAAAGACTAGCAACACCAACGCAGCAGCAGGGATCCAGGATGAAAGTGATAGACATAAAAAGCCATAGGGAGTGAAATTAGGCTCCAGTCGACTTGTTTCCCGAGTCACACTTTTATCTGTGTGTTTCTCTCAGGGGAAGCTCAAAGCCATCAAACCGCCCTGTGAATCCGACTTTCAGACTATCAAACTCATCAGCAACGGAGCGTATGGGTGAGAATGCGTTAACATCCTTTTGTACTCTGAAATCGCTCAAAGCCATTGTGTAAATATGGATAAAGCAGATTTCGGTCTCTCTCTCTCATTGCGATTGTAGAGCTGTGTATTTGGTCAGGCACAGAGAAACTCGACAGCGCTTTGCAATGAAGAAGATCAACAAA[C/T]AGAACCTGATCCTGCGGAACCAGATCCAGCAGGCGTTCGTGGAGCGGGACATCCTGACCTTCGCTGAAAACCCCTTCGTGGTCAGCATGTTCTGTTCTTTTGAGACGCGCCGTCACCTGTGCATGGTTATGGAGTACGTGGAGGGTACGGCATTACAGAGTTTCAGCAATCTGATTCCAATTGAACGTTATTGAGCTGTATTGAAATCACATCCATTTTCTGATTTAGGTGGCGACTGTGCGACTCTGCTGAAGAATATCGGAGCTCTTCCGGTGGATATGGCTCGGATGTACTTTGCCGAGACCGTTTTGGCGCTGGAGTACATTCATAATTACGGCATCGTGCACCGGGACCTGAAACCAGACAAGTAAGCTGCTAATAGAGCTCCCCCTGCTGGAGCGGAGCTGAAGTATAATAGTGAAAGTAAATTGTGCATGTAGATTTCCAAAGGTTCCAGACTTATGCAATCAATAAATGTCTTATGTACTTTATATGATACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32768
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 |
---|---|---|---|---|---|
ENSDART00000063938 | Essential Splice Site | 652 | 1717 | 17 | 26 |
Genomic Location (Zv9):
Chromosome 1 (position 51877631)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 50724992 |
GRCz11 | 1 | 51368791 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTTCATCCCTCATCTTGAGTCTGAAGAGGACACCAGCTACTTCGACAG[T/C]GAGGACACTCGCATTAGTCTGTCCTTGATAGTCATCGCTCTATATCTCTC
Long Flanking Sequence:
TGTGCCTTTTTGTTGACTGTCGCTTTAAATTCAAATGAGATTGTGCTGTTTTTAAAAGATGCCGGAGCTATAAATGCCTATGTGTATATGGGTCTATATGTATATATATGTGTATATGTGTATAATGGGCGGGGCTTTCCCCTTCTGATGACACGTACAAGGGGAGAATGTCAATCGGAGTGTTTCTACAGACTGTTTTAATCAAGTATGATTATAAAAAATAGACTTAATTCTGTTTGACCATTAGAAGCTGGTTATATTCACAGATTGTTGCAACTGTGTTTAAACCCCTTATAAACGTGATTTTTGCATGATAGGACGTCTTTAAGTTAATTTATTTTCTTGTATAGACGTACATCTCTTTACATTCGTACAGGTGGTGCGTTCGAAGTGAAGCAGCACTCGTTTTTCTCAGGACTGGACTGGAACGGTTTACTCCGGCAGAAGGCCGAGTTCATCCCTCATCTTGAGTCTGAAGAGGACACCAGCTACTTCGACAG[T/C]GAGGACACTCGCATTAGTCTGTCCTTGATAGTCATCGCTCTATATCTCTCACCATCATCTCTCGCTCTCTCTCTCTCTGTCGCAGCACGCTCTGAACGCTATCGCCACATCAACTCCTACGATGAAGACGACACCAATGACGACGAGCCTGTGGAGATCAGACAGTTCTCCTCCTGCTCGCCACGCTTCAGCAAGGTCAGTCTGACACGCGCTTGTATTCATATTTCATGCTTCCTCACAATGGCTACGTTTAAATGGACATCAGTAATCTAATTATTTCCCTTAATCTGAATAAGACAATAATATGATTCATGTGTTTACATTAGTTGCTGTTTGAATGTTCCTTTCATGTGTCCATTTTACATGTCATATTACATATTTTTTATTAACGTCACCATTCAACGCTAGTTTCCACTTCCTCCTTTATTTATTTAATTTTTTTAATATTACGAGACAAAGCTAGGGGGCGACATGGTGGCTCAGTGGTTGCCACATGCTGT
Associated Phenotype:
Not determined