ZMP
si:ch211-278j12.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate myeloid/lymphoid or mixed-lineage leukemia (Trithorax homolog, D
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 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37140 | Nonsense | Available for shipment | Available now |
sa11362 | Essential Splice Site | Available for shipment | Available now |
sa11351 | Essential Splice Site | Available for shipment | Available now |
sa11340 | Essential Splice Site | Available for shipment | Available now |
sa37139 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37138 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37140
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 |
---|---|---|---|---|---|
ENSDART00000039754 | Nonsense | 192 | 1813 | 4 | 33 |
ENSDART00000126343 | Nonsense | 226 | 1912 | 5 | 33 |
Genomic Location (Zv9):
Chromosome 20 (position 43275098)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 43346257 |
GRCz11 | 20 | 43243335 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACAAGGACCATTTCTAACCCCGAGGTGGTGATGAAGAGAAGACGACAG[C/T]AGAAGCTGGAGAAGAGGATGCAGGAGTTTCGGAGTGAAGACGGTCGACCC
Long Flanking Sequence:
AAATGTTTTTTCATAATGGATTTATTATTATGCATCGGACTCAGTGTGCACACATGAATACGAAAAAAACGCATATGAACATTTCAGACTTCTGAGAGCAAAGACTTTTACAGGTATGAAAGCACCCTAATCTCTTACAAACAAGTATTTCTCTTGAAATAAACAATGGAGCAAAGTCTGGATTAAATTGTCTCTGGGTCTGAATCCGGGCTTTAAGAAGCCCTGTATTAGAGCATCTAGTGTACTCATCTTTTTATTTTGTTTTGATTGTCTTAATAATTTGTAAAAAAAAAAAAAAAAAAAACAGGTTTTAAATTTCTCTTTCTGTGCTACCTTGTCTGACTTAATTGGCTGCCTTTTAAATACATCTTTTTTGTTGTTTGTCTACCTGATATAGAGAGAACTCCAGATTAGCAGCTGAGGTTTATAAAGACATGCCGGAGACCAGTTTCACAAGGACCATTTCTAACCCCGAGGTGGTGATGAAGAGAAGACGACAG[C/T]AGAAGCTGGAGAAGAGGATGCAGGAGTTTCGGAGTGAAGACGGTCGACCCGACTCAGGTTTGTATTAACGATTACAAACTTCCCCAATTGGCGAAAGTAAAGGCAAAAAAACCTTGAGAATAACCAGACTTAACCATTTTTCCTCTGGCCATAATAATAATGTCATAAAACTCTTTAAAAATGTATCCATTTGTTCATTTTCCTTTGGCTTAGTCCCTTTATTCATCAGGGGTCACTACTGTGGAATGAACCGCCAACTATTCCAGCAAACGTTTTGCATAGCGGATGCCCTTCTAGCTGCAACCCAGTACTGTGAAACACCCATACACTCTCACATGCGCACAAACAAGCACTACGCCCGATTCATTTTATTTAATTCACCTGTTGTGCATGTATTTGGACTGTGGGGTAAACTGATTACCTGGAGGAAACTCACGCCAACACGAGGAGAACATGCAAGCTCCTCATAGAAATGCCAACTGACCCAACCAGGACTCGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11362
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039754 | Essential Splice Site | 471 | 1813 | 10 | 33 |
ENSDART00000126343 | Essential Splice Site | 505 | 1912 | 11 | 33 |
ENSDART00000039754 | Essential Splice Site | 471 | 1813 | 10 | 33 |
ENSDART00000126343 | Essential Splice Site | 505 | 1912 | 11 | 33 |
ENSDART00000039754 | Essential Splice Site | 471 | 1813 | 10 | 33 |
ENSDART00000126343 | Essential Splice Site | 505 | 1912 | 11 | 33 |
Genomic Location (Zv9):
Chromosome 20 (position 43258838)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 43329997 |
GRCz11 | 20 | 43227075 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCCAAAAGAGACCCCGGGCCCATGATGAAAGGCAGGCACAARTCAGGG[T/G]GAGACATTTTTTTTTTTCTNNTCTTTTAATAGCAAAAGCCTCAAAAATCWCA
Long Flanking Sequence:
ATGTGTATACTGAAATTTGTTTGGTAAAAGTGTTCATCTTAGCGAAAACTTAATCTTTTATGCAAATCTTTTCTGTCAAATTAAAAGTTAATCCTACTCTGTAATGAGCATATGTTTTTTATGAGTCTTTTTAAAATGTATGCGCATCTTAGCATTTCTATCAACCGATTTATATTCAAAATGTGCATAAAAATAGGTGGATGGAAGCATAGCTTATGTTTCTCTTCTGCTTGATCCTCATGCAGCTGTTTGGGCCTGGGATTCTCCCTCATCACTGTGACCTTATGCATGCGGACGGCTTGGTGACCATAACCCCAGCCAATATGGACGCAGAGACATTTGTGGATGGACAGCGGATCGCTGACACTACAGTTCTGCGCAGTGGGGTGACCGTCCAGTTCGGAGCAACTCACGTCTTCAAATTCGTAGACCCCAGTTATGACCAGAGCATGTCCAAAAGAGACCCCGGGCCCATGATGAAAGGCAGGCACAAATCAGGG[T/G]GAGACATTTTTTTTTTTCTTCTTTTAATAGCAAAAGCCTCAAAAATCACAGCATTGTGAAAATGTAGCCCTTTATACATTTCTGGATGTTGCAAATTATGTAGCCGGAGAAATGTATGGCTGCTTTTTATCTTTAAAACCGGTTAATCGTGCTTTTGAAAACACTATCAGTTGGGTTTAGGGTTGGCTCTAGTGGATTTATGTGAGAACAGCAGGTGTGAATTGCAGTCAGAGAAATTTGAGATATTATAAAGCGTACACAGCAGCCTCTGGTGGATTCATGAAAACAAAAACTGCAAAAAACGTTGATCCTGGGACATATTTGCCGCTCTCCAGAAATGTTCACTGTAGTACGTTTTCAGAAGGAGTCTAGATTGAAAAATCCGGCTGTTGAAGACCATGTTGGTTGAAATGTCAAATTAAATTTGTCTTTTAAGAGCTGAAGTGGAAGTGGGCCGAATTTTTTTATTTATTTTTTTTACTTCATGGATTGTGTTTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11351
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039754 | Essential Splice Site | 471 | 1813 | 10 | 33 |
ENSDART00000126343 | Essential Splice Site | 505 | 1912 | 11 | 33 |
ENSDART00000039754 | Essential Splice Site | 471 | 1813 | 10 | 33 |
ENSDART00000126343 | Essential Splice Site | 505 | 1912 | 11 | 33 |
ENSDART00000039754 | Essential Splice Site | 471 | 1813 | 10 | 33 |
ENSDART00000126343 | Essential Splice Site | 505 | 1912 | 11 | 33 |
Genomic Location (Zv9):
Chromosome 20 (position 43258838)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 43329997 |
GRCz11 | 20 | 43227075 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCCAAAAGAGACCCCGGGCCCATGATGAAAGGCAGGCACAARTCAGGG[T/G]GAGACATTTTTTTTTTTCTNNTCTTTTAATAGCAAAAGCCTCAAAAATCWCA
Long Flanking Sequence:
ATGTGTATACTGAAATTTGTTTGGTAAAAGTGTTCATCTTAGCGAAAACTTAATCTTTTATGCAAATCTTTTCTGTCAAATTAAAAGTTAATCCTACTCTGTAATGAGCATATGTTTTTTATGAGTCTTTTTAAAATGTATGCGCATCTTAGCATTTCTATCAACCGATTTATATTCAAAATGTGCATAAAAATAGGTGGATGGAAGCATAGCTTATGTTTCTCTTCTGCTTGATCCTCATGCAGCTGTTTGGGCCTGGGATTCTCCCTCATCACTGTGACCTTATGCATGCGGACGGCTTGGTGACCATAACCCCAGCCAATATGGACGCAGAGACATTTGTGGATGGACAGCGGATCGCTGACACTACAGTTCTGCGCAGTGGGGTGACCGTCCAGTTCGGAGCAACTCACGTCTTCAAATTCGTAGACCCCAGTTATGACCAGAGCATGTCCAAAAGAGACCCCGGGCCCATGATGAAAGGCAGGCACAAATCAGGG[T/G]GAGACATTTTTTTTTTTCTTCTTTTAATAGCAAAAGCCTCAAAAATCACAGCATTGTGAAAATGTAGCCCTTTATACATTTCTGGATGTTGCAAATTATGTAGCCGGAGAAATGTATGGCTGCTTTTTATCTTTAAAACCGGTTAATCGTGCTTTTGAAAACACTATCAGTTGGGTTTAGGGTTGGCTCTAGTGGATTTATGTGAGAACAGCAGGTGTGAATTGCAGTCAGAGAAATTTGAGATATTATAAAGCGTACACAGCAGCCTCTGGTGGATTCATGAAAACAAAAACTGCAAAAAACGTTGATCCTGGGACATATTTGCCGCTCTCCAGAAATGTTCACTGTAGTACGTTTTCAGAAGGAGTCTAGATTGAAAAATCCGGCTGTTGAAGACCATGTTGGTTGAAATGTCAAATTAAATTTGTCTTTTAAGAGCTGAAGTGGAAGTGGGCCGAATTTTTTTATTTATTTTTTTTACTTCATGGATTGTGTTTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11340
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039754 | Essential Splice Site | 471 | 1813 | 10 | 33 |
ENSDART00000126343 | Essential Splice Site | 505 | 1912 | 11 | 33 |
ENSDART00000039754 | Essential Splice Site | 471 | 1813 | 10 | 33 |
ENSDART00000126343 | Essential Splice Site | 505 | 1912 | 11 | 33 |
ENSDART00000039754 | Essential Splice Site | 471 | 1813 | 10 | 33 |
ENSDART00000126343 | Essential Splice Site | 505 | 1912 | 11 | 33 |
Genomic Location (Zv9):
Chromosome 20 (position 43258838)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 43329997 |
GRCz11 | 20 | 43227075 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCCAAAAGAGACCCCGGGCCCATGATGAAAGGCAGGCACAARTCAGGG[T/G]GAGACATTTTTTTTTTTCTNNTCTTTTAATAGCAAAAGCCTCAAAAATCWCA
Long Flanking Sequence:
ATGTGTATACTGAAATTTGTTTGGTAAAAGTGTTCATCTTAGCGAAAACTTAATCTTTTATGCAAATCTTTTCTGTCAAATTAAAAGTTAATCCTACTCTGTAATGAGCATATGTTTTTTATGAGTCTTTTTAAAATGTATGCGCATCTTAGCATTTCTATCAACCGATTTATATTCAAAATGTGCATAAAAATAGGTGGATGGAAGCATAGCTTATGTTTCTCTTCTGCTTGATCCTCATGCAGCTGTTTGGGCCTGGGATTCTCCCTCATCACTGTGACCTTATGCATGCGGACGGCTTGGTGACCATAACCCCAGCCAATATGGACGCAGAGACATTTGTGGATGGACAGCGGATCGCTGACACTACAGTTCTGCGCAGTGGGGTGACCGTCCAGTTCGGAGCAACTCACGTCTTCAAATTCGTAGACCCCAGTTATGACCAGAGCATGTCCAAAAGAGACCCCGGGCCCATGATGAAAGGCAGGCACAAATCAGGG[T/G]GAGACATTTTTTTTTTTCTTCTTTTAATAGCAAAAGCCTCAAAAATCACAGCATTGTGAAAATGTAGCCCTTTATACATTTCTGGATGTTGCAAATTATGTAGCCGGAGAAATGTATGGCTGCTTTTTATCTTTAAAACCGGTTAATCGTGCTTTTGAAAACACTATCAGTTGGGTTTAGGGTTGGCTCTAGTGGATTTATGTGAGAACAGCAGGTGTGAATTGCAGTCAGAGAAATTTGAGATATTATAAAGCGTACACAGCAGCCTCTGGTGGATTCATGAAAACAAAAACTGCAAAAAACGTTGATCCTGGGACATATTTGCCGCTCTCCAGAAATGTTCACTGTAGTACGTTTTCAGAAGGAGTCTAGATTGAAAAATCCGGCTGTTGAAGACCATGTTGGTTGAAATGTCAAATTAAATTTGTCTTTTAAGAGCTGAAGTGGAAGTGGGCCGAATTTTTTTATTTATTTTTTTTACTTCATGGATTGTGTTTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37139
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039754 | Nonsense | 1016 | 1813 | 24 | 33 |
ENSDART00000126343 | Nonsense | 1050 | 1912 | 25 | 33 |
Genomic Location (Zv9):
Chromosome 20 (position 43192663)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 43263822 |
GRCz11 | 20 | 43160900 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTTACTCTAAGATGTCTCTGTCTTGTAGAGCGGCAGAATTGATGACA[C/T]GAACTGGGTCTGTTGTAACGCTTGAGGTGGCCAAACAAGGAGCCATTTAT
Long Flanking Sequence:
AATAGACAGTTTAAAAGTTCATTTCTGACACTGATGTCATGATGTATAGTCTTGGATTTAACTTGCAAGCATATTTATTTTCAGTCATTTACGCCGTGGCTTATCTGTGCTTTACAAAGCAGTGAAATGCTTTTCAAAAATTGACTTGCGTTTAAGCATCTTGCGTGTGGTTTTAAGATTCAGTGGACTCAATGAAACTCTTAAATCTGCGGATTTCAATGAAATGAGAAGCATGTGGCTGGAAAGGCTTATGAATGGACGCAACAGAAGTTGCCTTTGGGATTGGTTCCAGTGGTCGTCTTTTTGAAGCATTTGTTTACAGTTAGCTGACGGCTAATCCAAACACGTGTACTATGAGATTAGTCTTTTTAAAGCATCTCTCATGGGATTGCGACATTGTATTGCTAATGCTTTGAACGTTAAATTCATTCATAATAGCCTGCAGTTTTGTGTTTTACTCTAAGATGTCTCTGTCTTGTAGAGCGGCAGAATTGATGACA[C/T]GAACTGGGTCTGTTGTAACGCTTGAGGTGGCCAAACAAGGAGCCATTTATCACGGTCTGGCCACACTTCTTAACCAGCCATCCCCCATGATGCCTCGCGGTAAGCACAAACTATGGGACAAACACAAATACTGTTTTATTTTAATATTGAGAATGTTGGGTCTAGCAAAAAAAAAAAAAAAATGCCTGCGTGCTAGCATGAGTAAATCCTTAAAGAGGTGTAAACAGTGGCATAGCAGACGGGCATGCAGGCCTCACGCTGCAGTGTTAAAGTTGTCATTTTTTAAAATTGTTTGTTAACCAAATAAATAGATTGTTCAATTTGATTTAATGACCATTAAAAAATAAATACCCATTAAATTCCATACATAAACTATGTTTTAATTAAATAATCCATACATTAACAAAAAACACATTTTAAATAAGAACTACATGACAAAACTGCGCCTCGAAATCCTGTTCTCTTTCTCTCTGTTTAAAGAATACAAGTGAAATATTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37138
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039754 | Essential Splice Site | 1204 | 1813 | 27 | 33 |
ENSDART00000126343 | Essential Splice Site | 1238 | 1912 | 28 | 33 |
Genomic Location (Zv9):
Chromosome 20 (position 43183253)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 43254412 |
GRCz11 | 20 | 43151490 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTCTTCCCCCTATGGATAACCACTCCAACAACAGCATGGTTATGCAGG[T/C]TAGCCTTTTTAGGAATTGAATGCATGGTATCCAGGGGCCACAGACAGTCA
Long Flanking Sequence:
AGCTTGTTTATGATTTATATAATATCACAAACATTGATCCGGTTGTTGCATAGAAAAAAAAATTGCATTACCATATCTTATAAAATACACTGACATATAAAGTAAATTGGAACTCAAAGCTTTTACTGGGGCCCCTGTGTATACCCATTCTTGTCTCTGGACAACCTTTTTGATCCACTTCAAATTTTGACAGCCTCTATGTATAAAATTTGTTTTATTTTTATTTGCTTTTGTCTCTGTTTCATTTCTTTTCTGAATATATATTGGCTTTTAAGAAGCTGTCTAATCTGTCAATACCCTATTTTTCCCACAGGAGGAGCCCTCTCCACCCCGTCCAGAGGCCTATCCCATCCCCACTCAGACTTACCCTAGGGAATACTTCACCTTCCCAGCCTCCAAATCTCAGGACAGGATGGGCCCTGGCCAGCCCTGGCAAAACAACGAACAAGAGCCTCTTCCCCCTATGGATAACCACTCCAACAACAGCATGGTTATGCAGG[T/C]TAGCCTTTTTAGGAATTGAATGCATGGTATCCAGGGGCCACAGACAGTCATTGTGGAACACACACAGCTTTTGTCAAACTATAGTACTGTGTAGTTAATTTCACTTTATGGTAGTTACTTATTAATTTAGCTTTAAAATATGTTTATGTTTATTTATTTGGTTTTAAGTTATTTATTTATTCATTTTATTATTTATTTTATCTTACATTGTTAAAATTCACACTGCTGTTAATAAGTTTGGGTTTTATTTATTTATTAAAATAAAAAAGATATTAACACTGTTATTTAGATGCTAAAAAGTGTCTGTAAAAACATTTCTAATGTAACGTAAAGGCTCTATTACAATAATTTTTTATGTAAATCATTATTAATAATAATTATTTCTTATTATTCTTATGATTATTAATAATAATGATTTCTGAAGGATTGTGTGACAAAAAAAGGAGTGCGAATGAAAGCTTTGTGACTTTTTTTCCCCCAATGCAATTAAAAAGTATAGT
Associated Phenotype:
Not determined