Busch Lab

ZMP

si:ch211-278j12.1

Ensembl ID:
ENSDARG00000029472
ZFIN ID:
ZDB-GENE-050419-52
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
sa11340 Essential Splice Site Available for shipment Available now
sa11362 Essential Splice Site Available for shipment Available now
sa11351 Essential Splice Site Available for shipment Available now

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.
Availability:
Order Allele From ZIRC
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:
sa11340
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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:
sa11362
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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