ZMP
wu:fc39c11
Ensembl ID:
Description:
protein AF-9 [Source:RefSeq peptide;Acc:NP_001017819]
Human Orthologue:
MLLT3
Human Description:
myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 3 [Sour
Mouse Orthologue:
Mllt3
Mouse Description:
myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 3 Gene
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31559 | Nonsense | Available for shipment | Available now |
| sa13570 | Nonsense | Available for shipment | Available now |
| sa34031 | Nonsense | Available for shipment | Available now |
| sa14211 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31559
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000021502 | Nonsense | 58 | 555 | 3 | 13 |
| ENSDART00000053278 | Nonsense | 90 | 587 | 3 | 13 |
| ENSDART00000054998 | Nonsense | 90 | 269 | 3 | 8 |
| ENSDART00000113593 | Nonsense | 26 | 523 | 1 | 11 |
The following transcripts of ENSDARG00000006754 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 20042131)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 18575160 |
| GRCz11 | 7 | 18827427 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAAGAGTCTGGATACGCTGGCTTTATCTTGCCTATTGAAGTTTACTTT[A/T]AAAATAAGGTATTGTTTTTCCTCTCTTGTGGATTATTGCCTGTATAAACC
Long Flanking Sequence:
ACTGTAGATCAGTGGTTGCCAACCCTGTTCCTGGAGAGCCACCTTCCTGCAGATTTCAGTTGCTACCCATATCAAACACACCTGAACCAATTAATTAGTACCTGAACACCACGTGATAATTACCGGCAGGTGTGTTTGATATGGGTTGCAAATGAAATCTGCAGGAAGGTGGATCTCCAGGAACAGGGTTGGCCACCCCTGCTGTAAATTCTAGCAAATTGTTAACAGTAATCTAAAACCTAATGAAAACGTGTTGGTATTTATAGGCACTGGTGTATTTTTTTTATTCATTAAAACACTCCCTAAACACAACCTAAAAACACTCTAAATATGTGTTTATATTCTCAATATAGCACCTATTAGTCTCTTATTGCTTAAAGTAGAAATGCTTTTCATGCTGAAGTCTGTCTTTTGCTCTTTTTGCAGTGTGCAAAGATCCACCATATAAAGTTGAAGAGTCTGGATACGCTGGCTTTATCTTGCCTATTGAAGTTTACTTT[A/T]AAAATAAGGTATTGTTTTTCCTCTCTTGTGGATTATTGCCTGTATAAACCTAAGTTCGACCCGTTGTGTAACCTAAAACTCATCCAGACACCATTGTGACATGGACGAATGTAATATCCCTGTCACTTTTCACCAGGAAGAACCCAAAAAAGTGCGCTTCGACTACGATCTGTTCCTGCATCTGGAGGGTCACCCGCCTGTCAATCACCTGCGCTGTGAAAAACTCACCTTCAACAACCCCACGGAAGAGTTTCGCAGGAAGCTGCTCAAGGCCGGAGGGGTGAGTGGTCGTTAATATAGCTTTAATGCAAGCTTACATGATTGATTAAAAATTATAAAAGAGCAGAAGCTTCACTGCGCTAAATAAACAGGTTTTATGGGTCATTTGATGCTGCGTTTCTCAACCACGTTGCTGGAGGACCACCAACACAGCATGTTTTGGATGTCTCCTTTGTCTGTCAAACCCATTACAGATCTTACAGTCTGTGCCAATGAGCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13570
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 |
|---|---|---|---|---|---|
| ENSDART00000021502 | Nonsense | 314 | 555 | 7 | 13 |
| ENSDART00000053278 | Nonsense | 346 | 587 | 7 | 13 |
| ENSDART00000054998 | None | None | 269 | None | 8 |
| ENSDART00000113593 | Nonsense | 282 | 523 | 5 | 11 |
The following transcripts of ENSDARG00000006754 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 20025485)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 18558514 |
| GRCz11 | 7 | 18810781 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTCCTGCCCTGCTGCAGCAGCAGCACCATMATTCKGATAAAAAGGTTT[T/A]GAAAGACAAGCCDCAGATCCGGCATAATCGATTACAAAACAGTGAACTTT
Long Flanking Sequence:
TGGATAGAATGCTGAATTAGTTCAGTCTAACATCATCTTATTCTCGTTATAGGACGGCTCCAAAAGCAGCAGTGCTCTTACAACTACCAACAACATCAGCAGCAGCTCCCTCAAGCTCCACAAACCACCCAAGGACCACAAAGACCACAAGGATAAGCCTTCTAAAGACTCAAAAGAGTCCAAAAGTGCCTTCAGAGATTTCAGCAAGGACTCTGGAAAACTCTCTAAAGATTCCAAAAAACCCAAAGAGAATCAACCAATTCAGGAAGATCGGCCTATTCCTCAAATGGGGTTCAAGGAGCCCAAGAGCGCGTCGAAGGAGCAGCGCTCATCCGAGCTCAGCTTCTCAAGCCTGAGTCAAAGTAAACGGCGGCCTGTGCTGGACAATGAAGGCCATGTTACCAAAAAACGGAAAAGCAGTTTTTCGGAGAGCTCGCAAAAGCAGCAAGCGTGTCCTGCCCTGCTGCAGCAGCAGCACCATCATTCGGATAAAAAGGTTT[T/A]GAAAGACAAGCCGCAGATCCGGCATAATCGATTACAAAACAGTGAACTTTCAGAGAAGAAAAAGCTGCAAGCATTACCGCCCTTCCAGAATGTGTTGGACCCCAATGACTCTGATATGGATGACAACACCTTCACAAGATCAGATGTAAGTCGCTTTTAGATTATTACGACTAAATCAAAATGAGTCTTTGATTTTTGCGTAGTTGGTTAGTTGTAGCACAAGATGGTGATATTTGTAAGCATTTGATGAGCTTTATCCTACATTTTTATGGAAATACAGTTTGTAACGGCAAAATTGCCACCAATTCCTCTGTCTCTTCATACTTTCATGCCTTCATCCATGCTATGGAACTATTATCTCTCTGTTGTTTGCTTCTTCCTTCTTTTTCTGTCTCTTCCTGTCCATTTTTTCCCTCCCTCTTTCACTCCATCCATCCATCCATTCAACCCAGGATTCATTTTTTTATTAAATCCAGCCCTCAATTCTTCCATTTGTCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34031
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 |
|---|---|---|---|---|---|
| ENSDART00000021502 | Nonsense | 346 | 555 | 7 | 13 |
| ENSDART00000053278 | Nonsense | 378 | 587 | 7 | 13 |
| ENSDART00000054998 | None | None | 269 | None | 8 |
| ENSDART00000113593 | Nonsense | 314 | 523 | 5 | 11 |
The following transcripts of ENSDARG00000006754 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 20025389)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 18558418 |
| GRCz11 | 7 | 18810685 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTTCAGAGAAGAAAAAGCTGCAAGCATTACCGCCCTTCCAGAATGTGT[T/A]GGACCCCAATGACTCTGATATGGATGACAACACCTTCACAAGATCAGATG
Long Flanking Sequence:
CAGCAGCAGCTCCCTCAAGCTCCACAAACCACCCAAGGACCACAAAGACCACAAGGATAAGCCTTCTAAAGACTCAAAAGAGTCCAAAAGTGCCTTCAGAGATTTCAGCAAGGACTCTGGAAAACTCTCTAAAGATTCCAAAAAACCCAAAGAGAATCAACCAATTCAGGAAGATCGGCCTATTCCTCAAATGGGGTTCAAGGAGCCCAAGAGCGCGTCGAAGGAGCAGCGCTCATCCGAGCTCAGCTTCTCAAGCCTGAGTCAAAGTAAACGGCGGCCTGTGCTGGACAATGAAGGCCATGTTACCAAAAAACGGAAAAGCAGTTTTTCGGAGAGCTCGCAAAAGCAGCAAGCGTGTCCTGCCCTGCTGCAGCAGCAGCACCATCATTCGGATAAAAAGGTTTTGAAAGACAAGCCGCAGATCCGGCATAATCGATTACAAAACAGTGAACTTTCAGAGAAGAAAAAGCTGCAAGCATTACCGCCCTTCCAGAATGTGT[T/A]GGACCCCAATGACTCTGATATGGATGACAACACCTTCACAAGATCAGATGTAAGTCGCTTTTAGATTATTACGACTAAATCAAAATGAGTCTTTGATTTTTGCGTAGTTGGTTAGTTGTAGCACAAGATGGTGATATTTGTAAGCATTTGATGAGCTTTATCCTACATTTTTATGGAAATACAGTTTGTAACGGCAAAATTGCCACCAATTCCTCTGTCTCTTCATACTTTCATGCCTTCATCCATGCTATGGAACTATTATCTCTCTGTTGTTTGCTTCTTCCTTCTTTTTCTGTCTCTTCCTGTCCATTTTTTCCCTCCCTCTTTCACTCCATCCATCCATCCATTCAACCCAGGATTCATTTTTTTATTAAATCCAGCCCTCAATTCTTCCATTTGTCTGTCTGTTTCATCTTTTAAACCTTCTTTTTGTCTATCCATCATCCATTCTTCTTCAGATCATCCATCTATCCATCATCTCATCCATCACTATTTCTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14211
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 |
|---|---|---|---|---|---|
| ENSDART00000021502 | Essential Splice Site | 466 | 555 | 10 | 13 |
| ENSDART00000053278 | Essential Splice Site | 498 | 587 | 10 | 13 |
| ENSDART00000054998 | None | None | 269 | None | 8 |
| ENSDART00000113593 | Essential Splice Site | 434 | 523 | 8 | 11 |
The following transcripts of ENSDARG00000006754 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 20004391)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 18537420 |
| GRCz11 | 7 | 18789687 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGCTACYCCATAATGATCCTCCGCCGTTGCTGAAAAACAGCARTAACCAG[G/A]TGAGCTGCAGTCGCCTTCTGTCYCATTCAGTCCACAGGTGAGGATTTCCG
Long Flanking Sequence:
TATTATTAGCCCCCCTAAGCAATATTTTATTTTGATAGTCTACAGAACAAACCATCATTATATAATGACTTGCCTAATTACCCTAACCTTAACCTAATTAAGCCTTTAAATGTCACTTTAAGCTGTATAAAATTGTCTTGGAAAATATTTAGTGAAATATTATTTACTGTCATCATAGCAAAGATAAAATAAATCAGTTATTAGAGATGAGTTATTAAAACTATTATGTCTAGTAATGTGTTGAAAAAATCTTTCTGTTAAACAGAAATTGGGGGGAAAATATACGGGGGGGCTAATAATTCCGGAGGGCGAATAACTCTTGAGTTCAGCTGGATGTCCATGACTGCATATCATGTTGACGTGTGGATAATGAATGGTGAAAATGTCATGTGTTTTGCAGGGTGAGTTTAAGTGACGGCAGTGAGAGTGAAAACAGCTCTGGCTCGTCACCGCTACCCCATAATGATCCTCCGCCGTTGCTGAAAAACAGCAGTAACCAG[G/A]TGAGCTGCAGTCGCCTTCTGTCTCATTCAGTCCACAGGTGAGGATTTCCGTCGGCCGTTTATCAGCTCTCGTGCTTATCAAGAGAACCAGGTGGAAATTATATGTGGAAGAAAGGTGCATTACAGGTGCTTGACAGAATAAATGTGAGCTGAAGGAATAAGAAAGTCATTTTATATATACAGTTTTATCAGAATTAATAGCCCTCCTTTTATTTATTTATTTATTTTTTTAAATATTTTCCAAGTGGTGTTTATCAGAGCAAGAAAATTTTCACAGTATGTCTGATTATATTTTTTCTTCTGGAGAAAGACTTTTTTGTTTTGTTTCAGCTAGAATAAAAGCAGTTTTTAATTGTTTAAAAGACAGTTTAAGGTCAAAATTATTAGCCCCTTCAAGCTATATATTTTTCTACAGAACAAACCATCATTATACAATAATTTACCCTAACCTGCCTAGTTAACCTAATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGC
Associated Phenotype:
Not determined