ZMP
mad1l1
Ensembl ID:
ZFIN ID:
Description:
mitotic spindle assembly checkpoint protein MAD1 [Source:RefSeq peptide;Acc:NP_957206]
Human Orthologue:
MAD1L1
Human Description:
MAD1 mitotic arrest deficient-like 1 (yeast) [Source:HGNC Symbol;Acc:6762]
Mouse Orthologue:
Mad1l1
Mouse Description:
mitotic arrest deficient 1-like 1 Gene [Source:MGI Symbol;Acc:MGI:1341857]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa19431 | Nonsense | Available for shipment | Available now |
| sa14241 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19431
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 |
|---|---|---|---|---|---|
| ENSDART00000048610 | Nonsense | 374 | 717 | 10 | 17 |
| ENSDART00000103478 | None | None | 323 | None | 9 |
| ENSDART00000103479 | None | None | 323 | None | 9 |
| ENSDART00000147904 | Nonsense | 374 | 717 | 11 | 18 |
The following transcripts of ENSDARG00000033852 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 8897163)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 9136968 |
| GRCz11 | 1 | 9821079 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTTCGCTCTGTGGAAAAGGCCCGCTCTGAGCTCCTGACCGAGATTGCT[C/T]AGCTGCGCGCCAAGGCTCAAGAAGAACAGAAGAAACGAGAGAACCAGGAC
Long Flanking Sequence:
AACAGACGTTTAAAAATGTATACAGAATACATATATGGTCTTTTTATGCTGACAACAAGGTCCTCAATATGAGAAATATTGCAGTCCTGGCAATACTGGTCTCAAATGAGAACCAAACTGAAGTGTGCACATTCAGACTAGTTGGTGCCCATTTAGAAAAATATTGTATGGATTAATCACCATCAGACATACACATTCATTTACCGTCCCCAGGGCTTTATTCAGGTCTCTTTCAAAGAATTGTTTATGGCTCACTGTCTTTCAAACATTGTGCACCATTTCCCTGAATGGCCCAGCAACAAAGACCGTATACTCTACTGTGAACACTGAGAAGGCAGCTTTTATGTTATAAGGAAATGACCTTCCAGGATGTAGAGGATGCAGTTCTTTGTGTTCTCCCCAGAGCTGCTCCATCTTAATGTTCTGGCTTTTTTCTATCTGTCTCTTTCAGTGTTCGCTCTGTGGAAAAGGCCCGCTCTGAGCTCCTGACCGAGATTGCT[C/T]AGCTGCGCGCCAAGGCTCAAGAAGAACAGAAGAAACGAGAGAACCAGGACTCACTGGTCCGTCGCTTGCAGAAGAGAGTCTTACTGCTCACCAAGGTAATACAAAAAGTATTGGTTTCCACATTTAGTTACACTTGTCAAAACTAACTGGTTTAAACTTCCTAGTTTAAATAGATAAACTATTGCTTTTAAGCAAGTGAAATAGCCATGAGAGGTCTGATATGACCCATTATCTCCTAGCTGTACCTCTTATAGAAATCTAGATCATGTCCTTCCTCCTGACTTAAAGTTTTCTCCAAAGGCAAGGATGAGTTGTAGATAAATTACTGTGGCAGAAACTCATTGGACTCGCGAATAATACTCCTTGTTCTTTGTTTGTCAACAGCTTGCTTAATTAGTAATTAACCAAAGCCTTCAATAAACTCCAATCATGTTTCCTAAATGGGTGGTATATGTTTTAATGAGGTCAGTGCTTGAGTGTAATGATGTCTACACTGGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14241
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 |
|---|---|---|---|---|---|
| ENSDART00000048610 | Nonsense | 568 | 717 | 15 | 17 |
| ENSDART00000103478 | Nonsense | 174 | 323 | 7 | 9 |
| ENSDART00000103479 | Nonsense | 174 | 323 | 7 | 9 |
| ENSDART00000147904 | Nonsense | 568 | 717 | 16 | 18 |
The following transcripts of ENSDARG00000033852 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 8869337)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 9109142 |
| GRCz11 | 1 | 9793253 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGGCAAAGCAGCAGCGRGCGGATGAGGTGGAGCAGCTCAGGGTGGAGTG[T/A]CAGCGTTTGAGGGACCGACTCCGCAAAATCGARRTGGCTGGTGGCATGAC
Long Flanking Sequence:
AATTTCTTTGCTCTGTTAAACATCATTTGGGAAATATAAAAAAATCAAAGGGTGCTAATAATTCTGACTTCAACTGTATAGGCAATATGTCTGAATGGTAACGAACTCAACTAATAAAAGATGATGTCCGCCATTCTCTAATTCTCGTACAGCTATCTCAACAAAAATGCTTGCTGTAAACCAACAGCTTTATTGTATTGGCCCTGACAGCATGGCGGGGAAAAACATGCAACAAACCCCGTGCATCATGGAAACAAACTCGTACGACTAGGCATAGTACGAGTTTCAAGGTTTACTGCGGTTTGGAAAAGTCAAGATTTTAAAACCGCAAAAATTACCACATATTAATTGAATCCCAATTTTCAGACTCTCTGCATCTCTTTCCTTCATTAGGGAGACTACGACCCTGTTAAGACGAAGGTGGTCCACCTGCAGATGAACCCCACCAGCATGGCAAAGCAGCAGCGGGCGGATGAGGTGGAGCAGCTCAGGGTGGAGTG[T/A]CAGCGTTTGAGGGACCGACTCCGCAAAATCGAAGTGGCTGGTGGCATGACAACAGATGACACTACCCTCATCATCCCACCGTCACAGGAAATACTGGGTAAATACCTTTTTTACACAAGCCTTTAAAGCATGAGATTTATGGTAAAGACAATCCATCACATTTAGTTGTCTATTCTTAATACCATTGCTGGCTTTCTTTTCTCTGTTCACCAGAAGTTGATGTAAAACATGTTGTGCCTCAAAATATAATTATTGGGTTTTGTTTAAATTACAGAACAAAATACATAAAACAAATAAATTAAATTAAATAAATACAATACATTAAATTATTTAAAAATATCTATAAAATTATAAAATAAAAACTTTTGAAATATTGAAACATCAGGAATTGTTACAAATTGTTAAAAAAGGTGAAAATAAATATATAAATAGATTCTAACAATATATAATAAAAAAAATAATAAATAACACCGTTCAGTTTATATTTTTGTATAAAAAAA
Associated Phenotype:
Not determined