ZMP
mll5
Ensembl ID:
ZFIN ID:
Description:
Myeloid/lymphoid or mixed-lineage leukemia 5 (Trithorax homolog, Drosophila)Novel protein (Zgc:64223
Human Orthologue:
MLL5
Human Description:
myeloid/lymphoid or mixed-lineage leukemia 5 (trithorax homolog, Drosophila) [Source:HGNC Symbol;Acc
Mouse Orthologue:
Mll5
Mouse Description:
myeloid/lymphoid or mixed-lineage leukemia 5 Gene [Source:MGI Symbol;Acc:MGI:1924825]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20276 | Nonsense | Available for shipment | Available now |
sa13142 | Nonsense | Available for shipment | Available now |
sa45175 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa20276
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 |
---|---|---|---|---|---|
ENSDART00000066903 | Nonsense | 89 | 334 | 4 | 9 |
ENSDART00000123369 | Nonsense | 89 | 1265 | 4 | 21 |
ENSDART00000126732 | Nonsense | 89 | 1375 | 3 | 23 |
ENSDART00000130072 | Nonsense | 89 | 381 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 4 (position 21381169)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 22724504 |
GRCz11 | 4 | 22445479 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCGCCGGCGTCCCCACCTCCCTCGGTGCTGATCCGGCCGGGCGAGAGCT[T/A]GTTTGTGTCCGGAAGCCGGCCTGGTGAGAACTTGTTTGTGCCGGGCGGGC
Long Flanking Sequence:
TGTCAAAATATGCATGACTGGTGCAAACAAAACAGTTGATTCGTTGGTGAACTTCTCACTAAGAAGCGTGGATTGTTAATGTTCATTCTTCCTTTTCCTTTTGTTTCGCTGCTGTTAAACCTGTTTTTTTTCTGTATACTTCAAAAACACCTTGTCAGACTTGTTCCTCATTCTGTCCTCTCTCTCTCTCTTTTTTTCCCTTGTGTGTTTATGTGCATGGAGCAGACCAGAATCTGTGGAGGCGAGCTCTGTGGTAGTTGAGAAGTCCACCTACCCTCACCAGATTTACAGCAGCAGCTCCCACCACTCCCACGGATACATCGGTCTGCCTTACGCCGTGAGTATCAAACACACTCACACCTAGCTTATCTACATCTCATTAACTTTCTAATCCATTTTTACATGTATATTTTGGTAGGACCATAATTATGGGGCGCGACCCCCACCCACCCCGCCGGCGTCCCCACCTCCCTCGGTGCTGATCCGGCCGGGCGAGAGCT[T/A]GTTTGTGTCCGGAAGCCGGCCTGGTGAGAACTTGTTTGTGCCGGGCGGGCAGGACGAGGCGTCGCGTGGCACCACGCTCAGCACCTCGGAGGACGGCAGCTACGGTGCTGACATCACACGCTGCATCTGTGGCTTCACCCACGACGATGGCTACATGATCTGCTGCGACAAGTGCAGGTAAGACTTTGATGCCCATTTAATATGTTCAATTGAGTTGGATGTAACGCCTTCCACAGTAACATGTTACTGAATTCTCATTACATTTCTGTACGCATTAATGTAATAAATTACATTTTAAATTTGTATAATTTGATTACAGTTACTAAAGTCACAGTAATTGCGTTACTTGTGTTACAATTATAGTTTTTAGAAGAAAAAAAATGCTTCTTTTAAAGCACGTTTTCCACTGCAACATCCGTCAATAAGCATGTGCTTTTAAATAGCTGGAGAGCGTGAGCTGAAATTGTTGCTGTCAAGAGTGCTTGCTTCAAGTGGAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13142
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 |
---|---|---|---|---|---|
ENSDART00000066903 | None | None | 334 | None | 9 |
ENSDART00000123369 | Nonsense | 487 | 1265 | 11 | 21 |
ENSDART00000126732 | Nonsense | 487 | 1375 | 10 | 23 |
ENSDART00000130072 | None | None | 381 | None | 9 |
Genomic Location (Zv9):
Chromosome 4 (position 21374414)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 22717749 |
GRCz11 | 4 | 22438724 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTGCTCAAGCAYAACCTGGAGCCCACAGAGAATCTWGGCTCTAGCACA[C/T]GACGGCGAGGCCGTAAGGACAAAGAACCATCGCGGGACGAGAGCGGACAA
Long Flanking Sequence:
TGGGTGTTATCCACTGTATGTGTGTATGCAATAAGGTCTGGTGGGAGTGGGTAGTCTTGATGGAATTCATGGATAGCGATTGGTAGCCGTGATGCTTTCAACTCTTGTGCGTGACATGTACTTTGTATGCACATTCATACTGGCAGATACAATTAAAGAGCTTGAAAGCTTATTAAAGCATTTGCATTCAACATGTTATTGGGTTACTGGGCAAAATCTACCTGTTATATAGAGCTTTAAGCTGTTTTTGATCTTTAACTGATAAAAGAAATCAGAGTAACATGTTTACATTACAATCCACATATCAGTTTATAAGTGTTTGCATGTAAACACATCTTTATTTTTGTATATAATCAACTGTTTGCACTTTTCTCACTACTTTCGTTCTCTTTTCCTTTGCTAGTAAATATAAGGTGGACTGTGCTTGTGTAAAAGGCAATCCGGAGTGTCCTGTGCTCAAGCATAACCTGGAGCCCACAGAGAATCTAGGCTCTAGCACA[C/T]GACGGCGAGGCCGTAAGGACAAAGAACCATCGCGGGACGAGAGCGGACAAAATCAGAACCTCACTATGGACTGTGACGGGTCCAAGGGGAAAACGCTTAATGACGCCAAACAGAGAAAACTCTCTCCTCTCAGGCTCTCAATATCTAACAATCAGGTACCGTAGACACCAGTCAGTGTCATTCCAACCCACTTAAATTTCATCTCAAAAGAACACCTCACACAAGTTTTCATTCTTGAAAAGGTACTACTGGCTTCAATGTACAATTAACTAATTAGAAAAACCGAACTGAGACATAGTTGATAGATCGTAACAGTAAGTTTTGATGAAACTAGGTATAATGAACAAAACTCTAGCTTTTGTTTTAAATTCTGGGTCCCATTGTTGGCTGAGAGTCATCCATAAACGTCGAAAAACCCTTCATGTTTGCATATAAATATTATCCGTTTATTAATCTGTGCATGATTCTTTCTCTGTTTGGATATTTTCAGTCATTCTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45175
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066903 | None | None | 334 | 9 | 9 |
ENSDART00000123369 | None | None | 1265 | None | 21 |
ENSDART00000126732 | None | None | 1375 | None | 23 |
ENSDART00000130072 | Nonsense | 364 | 381 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 4 (position 21361273)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 22704608 |
GRCz11 | 4 | 22425583 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCACACCACCGGATACTTGGGCACAGGATGGCACTGACCACACCCACC[A/T]AAACCCCGCCCTCCAGACGGACTCTCTCAGAGAGGGGGCGGAGCTACATC
Long Flanking Sequence:
CCTCCCCACCCGCAGCCTGGCCCCACCTTACTGCATGTCAATCTGCAACCTCCTTCACTGCAGCAGCATCAGCTCCTGCTGAGCTCCGCCCCACCTCCGCCTCCTCCTCCACCTCCTCAGACACAGAGTTCCCAGCAGCCCCCGCCTAACTCCGGCACGCTCCTGTCAATCAAACAAGGACCACACCCACCCCTTCCACCCCCTCCTCCAGCTCCCTCCACTAACGCACCACCGCACCCGTTCCAAAACATCAGTGGCTTTCAAACCACTCTACTCCACCAGTCTGCACCAGCCAACCCCTCAGTAACCGCATCTACTTATCAACAAACTGTATTACCCCCTCCTCCTCCACCTCCCCCCCAACAAACTCCTCCCACACAGACCCCGCCCAATCCGAGCATCCCTCAGATCGCAGGTGGCAATCGAGGACCCGCTCCTTCCTCCGCCTCTTTCCACACCACCGGATACTTGGGCACAGGATGGCACTGACCACACCCACC[A/T]AAACCCCGCCCTCCAGACGGACTCTCTCAGAGAGGGGGCGGAGCTACATCTTGTAACATACAGCACCACTGTAAATATTTTCTATGTACCTTTTCACAAAGGCTAATGTAACCTGGTGGGGGTACATTTTAAGAAGAAAATGAGGACTGTAACAGAGTAGACTGTGTGTAAAAGATGATGGTTAATGAACCCTGGTGCTCATCACAGTCCCCCACACCTCCCGTCACAACCTCGTACTGCCATCCTGTCTTTTCCAGACGTCTTTTTTTACTTTGAATGTTTTTATTCATTTTAATCGCACCTTTCCGCCGTCTTTTCCTGTTTTGTCCTCCCAGCGCAATGGGACATTCCAGTTTCTTCCCTACCGTTTCCTAATCTCCCCCTGTTTTTTCACTCATCAGTTATTTGTTTTATCTAGGCGCTCATTATATAGCAAAAAGGTTTTGTATAGAGAAAAAATACAGAATCATTATTTTTTTTATTCCTTCATGTAAGAGAAA
Associated Phenotype:
Not determined