ZMP
ENSDARG00000088310
Ensembl ID:
Human Orthologue:
MLLT4
Human Description:
myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 4 [Sour
Mouse Orthologue:
Mllt4
Mouse Description:
myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 4 Gene
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10884 | Essential Splice Site | Available for shipment | Available now |
sa28787 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13762 | Nonsense | Available for shipment | Available now |
sa15870 | Nonsense | Available for shipment | Available now |
sa16881 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10884
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000124888 | Essential Splice Site | 89 | 962 | 4 | 20 |
Genomic Location (Zv9):
Chromosome 17 (position 6082065)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 6161001 |
GRCz11 | 17 | 6318231 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATGCACWTCTCAAGTTCTTAWCATGTGTATGYCATTCATTTCWGTTTTC[A/G]GATGAGGACTCTTTCTTGCTTTCTGTSATAAACGATATTAAMAGCTCCRC
Long Flanking Sequence:
AATATTATAGAGGCTGTATGAGATCACCTGGACAGAAAAAAAATGATGAGACACTCTAAACCTAAAAGAGCTCTGGAAAGTGCTAAAATAGGCGTGATATAACACAGCACATTATTTCTTATATTTTCTGTTTGTTTTTAATGAAGGGACTGATTGATTAGATATTGTGCAAAAGTCCTAAGGCAACAAAGCTGGTCTGGTGCTTAGGACTTTTGCACAGTACTGTATAATTCTAGCTTTTTGCAAGTTTGCTATTTGCTGTACTGTATTTTGATCATTATATGCCTGTTATACTTAACCACAAGTCAACATCCCCCTTAAAATGAACATTTCTTTTTTTTTTTTTTATTGAAGCACTAAACAAGACGACTTAGAAATGAAGTGGACTCTCCCGCTCAGCATTTCTTTAAAGGAAAAAGGTACAATAAAACCACTCAGTTTGCAGGAATATATGCACTTCTCAAGTTCTTAACATGTGTATGTCATTCATTTCTGTTTTC[A/G]GATGAGGACTCTTTCTTGCTTTCTGTGATAAACGATATTAACAGCTCCACCATTCACTTCAAGCTCTCGCCGGCGTACGTGTTTTATCTGGTCGGACGATTCTTAACCAGCAAAACCAGCCAGAGAAATAAATCCCACAAGCAGACTGAGCAGAAAATCTGCCTGGTGTTTGAAAAGATTGTGCGGATGATTCAGGATGTCATTCAGGTAAATAAAAGCCTGTAAGTGTATTGATCACAATTAAATTCCTTAATCTACACTTGAAGTATTATATAGTAAATTATAAACCCCCTGTGATTTTTTTATTTTTATTTTAATTTTTTATGTTTGATGTTGAACAGATCAAGGAGTTATATTCCAAGGATATTATATTTGTCATGATTATATATCATTAATATCAGTGGAACAAACTGTATTTATCTTTTTATTTTATTTTTTACTTTTTATTTAAGATTTTTTCAATATATTGTTTTACAGAACAACCCCTTCCCCAACCATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28787
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000124888 | Essential Splice Site | 490 | 962 | 11 | 20 |
Genomic Location (Zv9):
Chromosome 17 (position 6064639)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 6143575 |
GRCz11 | 17 | 6300805 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAAGAAACCTTTGCACAGCGGAATGGGAATAAGCATCGTAGCTGCCAAG[G/A]TAAAATAGAAAAAACTAAACTGTTATTGTCACTGGGAAAATATGCGATAC
Long Flanking Sequence:
ATTCAAAACCAGTTATAATAATTATTTTTATTATTAAAACCAAAAGTTGCATCTGTTAACATTAGTTTGTTCACTACTAGGAACAAGTATCAAAAGTAAACACTGTAAAATATACTGCACATTCTTAGTCTGTTAATAATTATAGAATAATAATAATAATTATACGCCATTAAGAAAGCAGACAGACTTTTACATTTTTTTTGCAAAGATATGATAGTTGTACTAATAGTGTACGTTTTATTTGCAAAGGCAGAACAACAGTAACATGCTAGTTGAATCTTCTATTTTTCCACTAACTATCGGAAATGTCTTAATCTCAATGTTGTAACTTCTTCTCCATCACTGTCTGACTCTGATCATTTTTTTATTAACTAAAAACTGAAACTGTTAATCAACTAAAGTAATGTTTTTATTTTCATTGTTAGAAATCTGAACCAGTGAAGATAACTCTAAAGAAACCTTTGCACAGCGGAATGGGAATAAGCATCGTAGCTGCCAAG[G/A]TAAAATAGAAAAAACTAAACTGTTATTGTCACTGGGAAAATATGCGATACTGTCATTGAGTGTTGAAATTAACGATATTTTAACAATATAACTAACTTGCAAAATGCTGTTTCATTAGCAATTAAAAAAACTTTTATTTATGTAACAATCATACTATTAAAGAGGTAATACAGTATATACTATTCTGAGCTAATTGAATCAAAAAAATGTCAAGGTGCAAATATTTAAACATGATGGGGTCTATTTTGGCGTTCCATGCGCAAATTGCAAAACGCACGGCGCAAACGCATTAGGGGTTATTTTCTTAATGAGTTATGGGTGTGTTTTGAGAATAAACCAATCAGAGTCTCACCTCCCATTCCCTTTAAGAGTCAGTTGCATCGTACCATGGTGCATTAGCTATTTACATGACGACTTTGTAAGTGGAAAAACTAAACACTTCATTAGCGAGAAAACAGTTAAACAGAGGATCTGCAGCGCTGTTGTAGATAGGGAAACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13762
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000124888 | Nonsense | 629 | 962 | 15 | 20 |
Genomic Location (Zv9):
Chromosome 17 (position 6057674)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 6136610 |
GRCz11 | 17 | 6293840 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAGCAAACCCCAAACAAAACCAGGAGCTGCTCAAGAAGACGCTGGAGTA[T/G]CGCTCAAAYCCYAACCTGACATGTGAGTGWTTGGATTMTTTTGTGTGTGT
Long Flanking Sequence:
TTCGGTTTCCCCTATAGTCCAAATACATGCGATACAGGTGAATTACTTCGGCTAAATTGTCCGTAGTGTGTGAATGTGTGTTTGGATGTTTCCCAGAGATGGGTTGCGGCTGGAAGGGCATCCGCTGCGTAAAAACTTGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGCGACCCCAGATTAATAAAAGGACTAAGCCGACAAGAAAATGAATGAATGAATGTTGTTGTTTTTTTGGGCGAACTATTCCCTTAATACATTAACTGAACCAACAATATTTGTTCTGTTGCAATATTAGTCAAGACATCAGATTATCCATGCATGCTTGTGTCACATTTGTTAGATCCTGATAGCAGTGGAGCATCCAAAGAGAAGATCGGCGCCTTTGATGTCCATGACCGAACTGAAGCATGTGTTTCAGAAACCACCAGAATCCAGAACAGCATCAGCAAAGCAAACCCCAAACAAAACCAGGAGCTGCTCAAGAAGACGCTGGAGTA[T/G]CGCTCAAACCCCAACCTGACATGTGAGTGTTTGGATTCTTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTGTTTGTGTTTGTGTGTGTGTGTGTGTGTGTTTCTTTTTGTTTTGCGGATGTTAACAAGAGCTTAGTGTTGTCGCCTCACAGCTGGTCGCTGGTTCAAGTCCCAGCTGGTCAAGTTGGTATTTCTATCTGGAGTTTACATGTTCTCCTCAGAGGAAACTCACGCCAACACAGGGAGAACATGCAAACTCCCCACAGAATAGCCAACTGACCCAGCCAAGGCTCACACCAGCAACCTTCTTGCTCTGAGGTGGCAGCGCTACCCACTGCGTTACCGCATCGCCCCTGTTCTCTTTAAACCCTATTTAAATTTCCATTAGATAACCAGGAAATGCCTGTGGATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15870
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 |
---|---|---|---|---|---|
ENSDART00000124888 | Nonsense | 711 | 962 | 17 | 20 |
Genomic Location (Zv9):
Chromosome 17 (position 6056085)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 6135021 |
GRCz11 | 17 | 6292251 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAGAACCACTGAACAGCCTCTGCATATTGCTGCATTCTCCAGGGATCAG[C/T]AGAAGATCAACTTCATGGTATTTTGTGTGTCTGTTTTATTGCCCTGTTTG
Long Flanking Sequence:
CAAGTAAGACTTTCTCCAGAAGAAAAAAATACTAGCAGACATACTGTGAAAATTCTCTGCTCTGTTAAACATCATTTGGGAAATATTTAAAACAGATTTTTTTTTACTAATTCTGAATTAAACTGTATATTAGCATTTTTCATATTGATTTTAAAAATATATTTTATTTAATTTTTTTATTAATTGTTTTTAATTTAAATTTTATTTGTTGCTTAATTTTTTTTGTTATGATTTTGGTGTTTGTTTTAGTTCATAATCATAACCCTGGTATACAGATCTTTTTAAGGCATTCATAAACAGTCCCGTTCTTATTCTTTTTATGTTGATATCGTTTGATATATTTCTACATCTCACCCCAGGGGAAACCTTCAAACGCTTCTTTAAACACAGATATTTATCAGAGAGAATATCTGACCCTGCCGTCCTCCAAACTGCACAGCAATAAAGCACCCAGAACCACTGAACAGCCTCTGCATATTGCTGCATTCTCCAGGGATCAG[C/T]AGAAGATCAACTTCATGGTATTTTGTGTGTCTGTTTTATTGCCCTGTTTGATATTTGTGCTTCCAAAAGTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCGTCGATCTGTCTGTTTGTGTCATCCATCCATCTATTATCCATCCATCTATCATTCTTTTTATCTATTGTCCGTCCATTAATCTATCATTCTTTCTATTATTCTATCTATATCCATCCATTCCTCCATCTGTCTCTATTTATTTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16881
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 |
---|---|---|---|---|---|
ENSDART00000124888 | Nonsense | 819 | 962 | 18 | 20 |
Genomic Location (Zv9):
Chromosome 17 (position 6054768)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 6133704 |
GRCz11 | 17 | 6290934 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATTCAGCACCTTCCGCCRGCCTGCAGAYAGCAGAAYTACWTCCCAAACR[C/T]AGCATCTGKATCAATGCTTCGGTGCTTCAGCGTCTCAGAGCAAGGTATTW
Long Flanking Sequence:
TAACTTTTGGACTAAACCAACAGCTGGGTTATTTTTTTAAGCCGAATGTTTGGGTTTTTCATATTTTATCCAATTTGGGTCGAACTAACAATACCTTTACTTGTTCCAACACTTTAGTGTTGAGTAAATGATGACAGAATAGTCTTTTTTAATTGAACTATCCTTTTACAGTAATAATGGTTGTATCCACACAGAAACAGGCGCATTCTCATGATGACCTGTGGAGTGCAGAGAAAGGGCACTCTCTAGTGGACAAACAGAAGTACTTGAAGAAACAGCCTGAAGTGAGCAAATGGATCAGTCTTGCAACTATCAGTCCAATAAACTCCAGTTTCTCCAGCATGGGACACAGAAATGAGCTGTGGAAAATCCCGACAGCTGCCCAGTCTGTGCCTCTGTCACAGCCGAAGCGTCTGGACGTCCCGTATTCACCACAAACCAACAAACCTTCATTCAGCACCTTCCGCCAGCCTGCAGACAGCAGAATTACATCCCAAACG[C/T]AGCATCTGTATCAATGCTTCGGTGCTTCAGCGTCTCAGAGCAAGGTATTTATATTAGTTTTGAAGATTTAATTTCAATATTATCTTTTTAAAGGTCCCATGAAATTAAAATAAAGTTTTTTAGATGTTAGTATTGTTTGTTTTTAGGATACCTACAAGCTAAAACAGTGGCAAAAAGCATGTTTGTCACTTCCGCATAAATGGATCAATGTAGGGCTGGGCGATATAGCGAAAAAAAATAAATAAATCACGATATCATGTTTCATATCATTCGATATCGATAATTATCGAATATTTATAGCAATACATTAAGAATATTAGTTTTTTTAACCACTTTATTTGTGTTTACCAACATCAATCAGGCCTTTATTTGTCACATACACTTTCATATAGTGAAATTTAACCCCCCGACCATACACAAACATCACAATTTTCAGGGGAAGACATTTAGAAAAAGGAAGTAAGATACATTTCAGGAGAGGGAGGCGAAGAAAAACTCCC
Associated Phenotype:
Not determined