Busch Lab

ZMP

mnat1

Ensembl ID:
ENSDARG00000002077
ZFIN ID:
ZDB-GENE-041010-203
Description:
CDK-activating kinase assembly factor MAT1 [Source:RefSeq peptide;Acc:NP_001006100]
Human Orthologue:
MNAT1
Human Description:
menage a trois homolog 1, cyclin H assembly factor (Xenopus laevis) [Source:HGNC Symbol;Acc:7181]
Mouse Orthologue:
Mnat1
Mouse Description:
menage a trois 1 Gene [Source:MGI Symbol;Acc:MGI:106207]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa42235 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa1249 Nonsense F2 line generated Not yet available
sa35529 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa42235
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000006648 Essential Splice Site 106 309 3 8
Genomic Location (Zv9):
Chromosome 13 (position 31881673)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 31527621
GRCz11 13 31658071
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTCTCTGACTGAGTATAATGACTATCTGGAGCAGGTGGAAGACATCGG[T/C]GAGATGTATATACAGCATTAAATCATTTATATTTTTGCCCCTGTTCTACT
Long Flanking Sequence:
TTTGGAAAGTTTCTAAGGCCAGATTTTACCCTCTGAAGCAACGAGATGATTGAAATGTGTGTTTGTGTGGAATCGCTTCTGAAGTTTTTTTCCAGCAGATTTCACATTTCATTACTGTTGTTTTTGACTGTCTTTCAGCTGACCTTCTGCCAGTGCGAGTAAAAAGTTTGCATGTGTGTGTGTTTCAGGTGTGAGAGCTGTGTGGACATGCTGTTTGTCCGTGGTTCTGGTAACTGTGTGCAGTGTGACACTCCTCTCAGAAAGAGTAATTTCCGTGTGCAGCTCTTCGAAGATCCAGCCATCGATAAAGAGGTGGAGATTCGCAAGAAGGTCCTCAAAATGTATGCAGCAGAGAAAGTGCACTCAAAATACTCTTAATGCCTAGTTTTTCGTATTTTAATAATGTGTGTCTTTTCATCTTTCAGTTATAATAAGAGAGAATTCGATTTTTCCTCTCTGACTGAGTATAATGACTATCTGGAGCAGGTGGAAGACATCGG[T/C]GAGATGTATATACAGCATTAAATCATTTATATTTTTGCCCCTGTTCTACTTTTTCAAGTATTACACAGTGTAATGCTGCACTATGTGAATCTAAAAGGCCTGCAAAGATCTAAGTGCACAACAAATAAAGTCATAATGTCACCTAAAAAGAAATGAATCAATTTTGAACTGTAGAAACGAGTCGTCAGCATTCCCAGTTTCAGTGTAACCGTGTACATAGAGCTGTAATGATTCTGCCCATCAACAACATCCACTTTGACCTGCCCTCAAAACTTTGGTTCATGTTGTCAGCAGCTTTTTGAGAAGCAACTTTTGTTACTGAGATGAAAAATTTACTCTGTCACAATTAGGGAGGTCAGAAGCATCTTCAATATAAGTACCAATCAGTACTGAAATTAACTAGATTTAACAATAGCAGCTTTCCCCATGAATTATGAGCACTGCTTTGTGGATTCTTGAACACAGCTGATTGGCTATTGTGTTTGTGGCTTTCAAATGCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1249
Status:
F2 line generated
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
ENSDART00000006648 Nonsense 124 309 4 8
Genomic Location (Zv9):
Chromosome 13 (position 31883270)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 31529218
GRCz11 13 31659668
KASP Assay ID:
554-1164.1 (used for ordering genotyping assays)
KASP Sequence:
TTAACCTGGCCAATAACATGGATGTAGAAATGACCAAGCAGAAGATGGAA[C/T]AGTATCAGCGAGATAACAAAGATGTTATACAGAGAAACAAAGCAAAACTG
Long Flanking Sequence:
CAAACTAAATAAATAAATATTTTTTGCTGAAAATATCTCAAGTAAAACTTAAGCCAATGTAAAAAAAAATAATAATAAAAAATAAATATATATATATAATGTTTTTTATGAAATACATTGATAAATATTAATTTGATTTAAAAATGTTTCTTTGAGGATTTAGATAACCACTTTAGCTTCTTATTTTTTTTATTATTTTTTTAGTTTTTATTATTTTTTTACAATAATGTATTATCTGATGTATAAATGTACACATAAAACGTAAAAAGTGCCAGTGTAAGCATCTAAAGAATCTCTAAAAGCAATTAGTGCTTTCAAACATTGGATGGACTGTAAACCTCTTGTAGGACCTAATCAAAACTGAAAAACAGCATAATTGTTGCCCTTTAAAATGATTTCCTTTTGTGATGTTTTTTTAAATGTTTAACTGTTTTCAAATGTTTCCAGTGTTTAACCTGGCCAATAACATGGATGTAGAAATGACCAAGCAGAAGATGGAA[C/T]AGTATCAGCGAGATAACAAAGATGTTATACAGAGAAACAAAGCAAAACTGGTAAGCGTGCGTGTGTTTCTGACTAATTTATTTTTTTTTGTCTTAATGAGTTGCCCATGTGCTTCAGACACATTTGACTGTTTTGTATCCTTAAACTTTTATTTTATATTTTTTAATATTCTTTTTTTTTTTTTTTTTTGTTAATTGGATTTTTACAAGTTAAATACAATATAGAACAAAGTGCAGCAGATCTATCATCACCAAATATACTACCCCATGCATGCCCTAAACCTCCAACCCTTAGTGCCATAGGTGATATCTAAGCATTCTGTCCTGTTATACCCAAGTAAGATATAAAGCCGCCCCAGTATTTGACAAATAAATCTTGACGGTTTTTCAAATGAAATGCATTTTTTCCAAAAACATGTAGGATGGCACTTCTTTAATCCACGTAGGATTTAGTAAATCAAATTTTATTTTCTATTTTATTTGATCAAATTGTACCTCTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35529
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000006648 Nonsense 270 309 7 8
Genomic Location (Zv9):
Chromosome 13 (position 31893596)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 31539544
GRCz11 13 31669994
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTACATTGACACATATGGGCCGCCTGTTCCAGAATTGGATCAGCTAGGC[C/T]GAAAAGGGTAAGAATCACTTGCACTTCCTAAATGTATTGTGTTATATGTA
Long Flanking Sequence:
GACTCCATCTCAGACAGAATGTCTGTTGGTGCTGTTTAAATGAGGTCATATGCATTAACCGTTCCAAATATACCCAGTGAGTGTGTTAAATACTCACCTCCAATGGTGCTGTATGATGCCAATTAAAAAATGAAGCACGCTGATTGCAACGTTCTAGTGCTCTGAACATCTAAATGTACTTATTTACTTTCAAATGATTCTCCAAACACCCTAAACTAAAAGAAGTGTCAAAGGTGCGGTCAGAGCTCTTAACCAATAAAAAAAAGTCATGCTAACATTTTTTTTTACATTTGCTACATTTTTTTTATTTGCACATTTTTCATACTGCAAAAAAAAAAAAAAAAAAAAAAACTGAAAAAATGTTTCTTTCCTTTTCTTTTCTTTAGGGTCAGACCGTATCTTTGGCTTCTGTGTCCCGCGTGGAGGAAGTTTTATATGTTTATCAGCCTCTGTACATTGACACATATGGGCCGCCTGTTCCAGAATTGGATCAGCTAGGC[C/T]GAAAAGGGTAAGAATCACTTGCACTTCCTAAATGTATTGTGTTATATGTAAGGGATAATGTATATCCAGCCGGTTGTTATCGCAGAGTAACTCTGAGCTATACTAATGCACTAACTATTTAAATAAATGGAAAGTTTTCTAAAGAAATATTTGTTCTTAACAAACGCCTGGATGCAGCCTACATGAACCTTTTTATTATTATTATTATTATTATTATTATTATTATTATTAATACAGTTTAATCATGGCTCTTAACAATGAAGAAGAGCAGAAGGATATATATGAAGAAGTGTCATAAGGATATAAATATTTTCATTGATGGTCAAGATAATTTCCCGGATGAGCTTGTGTTATTAGTTTAATCAGTTGTTATCTGGGATTAACATACTGTGGAATGTCATAATTTTTTTACCAGAATTAAGTATTCTATTGAGCTGTATTATATTACATTACATTACAATATTACTCCTCCTCAGTCCATCCAGAGTGGATTTATTAAA
Associated Phenotype:
Not determined