ZMP
LOC796144
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19944 | Nonsense | Available for shipment | Available now |
sa15819 | Nonsense | Available for shipment | Available now |
sa11571 | Essential Splice Site | Available for shipment | Available now |
sa38372 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19944
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 |
---|---|---|---|---|---|
ENSDART00000123809 | Nonsense | 413 | 1649 | 14 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 7321497)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 6860641 |
GRCz11 | 3 | 6746481 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAGCAGAACCTGATTCTGAGGAACCAGATCCAGCAGGCGTTTGTGGAG[C/T]GAGACATCCTGACCTTTGCTGAGAACCCGTTCGTGGTCAGCATGTTCTGC
Long Flanking Sequence:
TCCCCACAAGATCAAAATGTACTGATATTGCTATACTTGTGGGGACATTCGGGAATACTTGCACAGTCACTCACTCATCATCATTTTCAGATATCCTGGTGCTATTTCAGAGAAATGATGTTACAAGAGTATAATGAGGATGTGCAAGAGAGCGTGATGGGATTTTGAAGGGATTTTCTCTTTTCCAGGGAAAAATGAAACCCATGAAGCCACCAGGAGAGGCAGATTTCCAAACCATCAAACTCATCAGCAATGGAGCCTACGGGTAAACTAACACACACTGTACAGACTGTGTCCAATTCCAAACACCCCAGCACCCCAGTTTATTTACATTTGTACAGTTGTGTGTAGATACTGTACACATGACAGAGGTTGCTTTGTGTTTTTTCAGCGAGGTGTATCTGGTCCGTCATCTGGAGACCCGGCAGCGCTTCGCGATGAAGAAAATCAACAAGCAGAACCTGATTCTGAGGAACCAGATCCAGCAGGCGTTTGTGGAG[C/T]GAGACATCCTGACCTTTGCTGAGAACCCGTTCGTGGTCAGCATGTTCTGCTCCTTTGAGACCAGAAGACACCTGTGTATGGTCATGGAGTATGTGGAGGGTGAGACGCAGCATAGTATCATTCTAGAACAGGGGTGGGCAAATTTGGTCCTGGAGGGCCGGTGTCCTGCATAGTTTAGCTGCAACACTAATCAAACACACCTGAACATAGTGTTTTCAAGATCACTAGAAATCTATTAAGCAGGTGTGTGTGATTAGAGTTGGAGCTCCACCGGCCCTCCAGGAACGAGTTTGCCCAGCCCTGTTCTAGAAACTATTCCAAACACCCCAGCAACTGCATAGCAACATTCTAAAAAGTGTTCTGAGCACCTTAGTAACCACAAAGCAACATTCTAAATCAGTACCAAACACCTCAGCAACCACATAACAACATTCTAAAAACTGTTCCAAACATCTTAGCAACCACAAATTGTGACAACATTCTTAAAATGTTATAAACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15819
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 |
---|---|---|---|---|---|
ENSDART00000123809 | Nonsense | 866 | 1649 | 23 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 7308032)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 6847176 |
GRCz11 | 3 | 6733016 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGCRCATGCCGGAGCCCTTCAGTGCACGAGTAGGAAGTGACCTCGTCT[T/A]ACGAAGAGCACGACATCATCAGATACCGAGCKACAGTGAGAAACGAACCG
Long Flanking Sequence:
TGTCCGCGACACCTCCCTCTCTCAGCACCCGCGCGTCCTCAGTTATATCCGCGCATAGAGCGCCGGAAAAGAGGTCCGCGACACCTCACTTCATTTTCATAACCGGTCACTTTCGTTTTCACATTGGGGTTGAGGGCGGCGTGATCGTCCTCTGCCTAGAGCGGCAGTTCAGCTTGCTCCAGCCCTGCATATGACCTACAGTTAATATGGCTGCCAGTTTCTTCGCTTGTCAACATTGCTAGCATGGCATTGACCGTGGTCAACGTGTGACCGAAACATTTACCTTTTTTTTTTTTTTAGTAAATTGCTTGTCATTTCATCTCGCTTGTTGATTTTCGGAAGTTTTTCAGCTCACTTTTTCCCCAGAGGAGTCGAAACTCCCATTAATCTCGTGTGATCTTTCTGCTTCTCAGACAAGCTTCTGCGTCCCGCTGAAGGTCCATCAGCTCCTCTGCACATGCCGGAGCCCTTCAGTGCACGAGTAGGAAGTGACCTCGTCT[T/A]ACGAAGAGCACGACATCATCAGATACCGAGCGACAGTGAGAAACGAACCGCCACTCGCTCCGGCACAAAAGTCATCAAGTCGGCCTCCGCCACGGCGCTGTCTGTCATTATACCTGCAGGTGAGACTTTAGATTCTACTTTATAACCATTACAAATATCAACAAACAGTAACATTAAATTAAATTAATTAATAGTGACACAGTAAAGTGGACACTGGACACCTTAAAATAAAATCTAACTCTTGTTTTTGGCCTGTAAGCTTTCGTAATATTACTGTTTCTTCATTTTGTCGTTAGTTGAGCAGCATGGTACGTCTCCGCTGGCCAGTCCCATGTCTCCTCGATCCGTCTCATCCAATCCCTCGTCTCGTGACTCATCTCCGAGTCGTGATTATTCGCCTACGGTCAATGTCCTGCGCTCACCGATCACCATCCATCGCTCTGGGAAGAAGTACGGCTTCACTCTGCGAGCCATCAGAGTCTACATGGGCGACAGTCACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11571
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 |
---|---|---|---|---|---|
ENSDART00000123809 | Essential Splice Site | 1069 | 1649 | 26 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 7306263)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 6845407 |
GRCz11 | 3 | 6731247 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGATGGCCAGACGCAACAAGAAATCAGCAGCAAAAGATGGACAAGAGAG[G/A]TCAGAAACTGGGAATGCCTTTACATCATGGGTCAAACTCARCTCCTGGAG
Long Flanking Sequence:
CCTTTAATAAAATGCATGTTTTTAGGACTGTTTTTAATTTGTGATATCTTTTTTATTCTTACTGTTTTTTTTGTTCTACTGTGCTTAGAAAAGCGCGTTATAAATAAAATGTATTATTATTATTATTATTGTCATCATCATCATCATTATTTCTTTTTCTCTGAGCATATGGAGAGGAAGAGAGTGTGTCCTACAGGTGGTTTGTCAAGTCCACTCACCTGTGTGGAGCACACTCAGAATTGAACAATGTTTTTTAAATAGCATAGGGTGCTTATTAGAAGTTGTCTGGTGCATATGGAGAGGAAAAGAGTGTGTGACCTATTTCAATGCTGTCGTTGACCATTCATTGCTTTGGATTTTCAGAGTGGCAGCAAAGTAACAGTGACGACTACTCCGTTCGAAAACACCTCCATAAAGATTGGTCCCGCCAGGAAGCTGAGCTACAAAGCCAAGATGGCCAGACGCAACAAGAAATCAGCAGCAAAAGATGGACAAGAGAG[G/A]TCAGAAACTGGGAATGCCTTTACATCATGGGTCAAACTCAGCTCCTGGAGGGCCGCAGATCCGCACAGTTTTGCTCCAACCCTAATCAAACACAGCTGATCCAAATAATCAAGGTGTCTTGAACACCTTCATTAGTTGCATCAGCTGTGCCCTTCCAGCGGCAACCCATCACTGGGAAACACCCATACACTCTCATTCACAGACACATACACTATGGACAACTTAGCTTACCTATAGCGCATATCTTTGGATTTGTGGGGGAAACCGGAGCACATGCAAACTCCACACAGAAATGCCAACTGACCCAGCCAAGGCTCTAACCAGCGACCTTCTTGCTTTGAGGCGATTGTGCTACCCACTGCCCCACCGTGACGCCCTATAGAGAATATGGGTCAGTGACAAAACAGGTTTGGCAAGATGGGAAATTTAAAAATCTTTTACAAAGTTGATTTAAAAGCATCCGTCAGATATTTTAAAATGTACAGATTGTATTCATGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38372
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 |
---|---|---|---|---|---|
ENSDART00000123809 | Nonsense | 1344 | 1649 | 28 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 7300956)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 6840100 |
GRCz11 | 3 | 6725940 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAACTCGGGAGGCAAGACTCAATCATGGATAGAGAGTTTGAAGGGAAAT[C/A]GAAGCAGGCTGACTCAAGCGAAGCAATTTTGAAGACTGCATCAAAAACTG
Long Flanking Sequence:
TGCCGGGAATATTCCTCTGTCCCCATTGGCTCACACACCATCCCCGACTTCGTCCTCTCCACCACCCATAGCGGGACACATCGTTGGCAGCTCCAACACCACCCAGGCCTTCCCTGCAAAGCTTCACGCCTCCCCTCCAATAACACGTCCACGACCTAAAAGTGCAGAACCACCCCGTTCCCCTCTTCTCCAAAGGGTGCAGTCCGCCGAGAAGCTCGGTCCACCTTCTCCGCCATCCTCGTCATCTTCTGATAGGAAGGGAGGGCTTGGCATTAGAAAGCATGGTTTGGATGTTGTGCATGCCGAATACCGCCGGGAGTCCTTCCACTGCGAGCATGCCCTCCAGAGCTTGATGGAGATAGAAGGAGAAAACACGCCCAGTGCTCTACCCTCTCCACCTGATCAAACGCCAACGCACATGCCCATCAAGCACACGTTGAGTCCAGCAAGGCAACTCGGGAGGCAAGACTCAATCATGGATAGAGAGTTTGAAGGGAAAT[C/A]GAAGCAGGCTGACTCAAGCGAAGCAATTTTGAAGACTGCATCAAAAACTGAACCAGTAGCAATCATTGTAGATCTTAAATCAACCCCGTTGGGTGAAACAACCCAGAGGGATAAAGTAGCCTCTAAGTTTGAGTCTTCCCAAGTTTCAGTTGCCTCAATGGGGAAGGTTGTAGCCAAGGATGTGGGAAAGATTGAATCTTCTAGTACTTTGGTAACTGGCCCCAAGATCCCAGATTGGACGCCAATTGTCCAGAGCTCTGGAGTACAGGAACTCAAACCTCATCAAACCGAGAGTCCTAAAGGGCTGGAGAATGGCAAAGACATTGGAAAGATCCCAGTGAAAGAGAAAACCCAATTGACAAAGACTCCAGAGGCAAGCAAGTCAAGTAAAGGACCTTTAAATGTTGAGGGGACTGGATCTGGTTCTATTGGTACACCTAAAGTCTCAGAAGCAGTTCCAAGCCAGTCTAAGAGCATTCAGGAACGGGCTCAAACTCCAT
Associated Phenotype:
Not determined