ZMP
dot1l
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate DOT1-like, histone H3 methyltransferase (S. cerevisiae) (DOT1L)
Human Orthologue:
DOT1L
Human Description:
DOT1-like, histone H3 methyltransferase (S. cerevisiae) [Source:HGNC Symbol;Acc:24948]
Mouse Orthologue:
Dot1l
Mouse Description:
DOT1-like, histone H3 methyltransferase (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:2143886]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37502 | Essential Splice Site | Available for shipment | Available now |
sa1413 | Nonsense | Available for shipment | Available now |
sa17639 | Nonsense | Available for shipment | Available now |
sa17278 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37502
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089076 | Essential Splice Site | 42 | 1523 | 2 | 28 |
ENSDART00000142046 | Essential Splice Site | 51 | 1122 | 2 | 27 |
Genomic Location (Zv9):
Chromosome 22 (position 21136744)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 20791420 |
GRCz11 | 22 | 20816398 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCAGGATAAACATCATGATGCTGCACACGAAATCATCGAAACCATTCGG[T/C]GAGTCCATTACCTGTTTTGATTTGATATTATTATTATTATTATTATTATT
Long Flanking Sequence:
CTGACATGGAAGAATGAATGATTAAAATAAAAATACAACCTGAAATATTTAAATAGCTAATATAAACTTTTAATTACTTCTATAATAGTTTTGTATTTTAAGCAACGGAGATAAATAATTATCGAAAATAAAAATGAAAGTAGACTAAAGACTTTTTTTTTTTTTTGTACGCTCTTGTGCTTGGATAGAATTTTGCTTTGCATTCACTAACTTTAAACATACGGGATGGCTCAGGGTGATCTAATATACTTATCTGAACCCGTGTGCCTGATGAACTTGTCCAGCAGCTTGAAGGCGCACTGTGTGTTGCAGAATAAGCAACAGTCGTGATCCGTGACCTAGAACCAACTGAAGAGGTCAAGTTTCTGTTGTAGAAACTAAGAGACGTACAACTACAGATCACATGTTAATGAACTTTGCCTATAATTGAGCTTTTCTTTTCTATCCTTCTCCAGGATAAACATCATGATGCTGCACACGAAATCATCGAAACCATTCGG[T/C]GAGTCCATTACCTGTTTTGATTTGATATTATTATTATTATTATTATTATTGTGTGTGGTTTGCTGATTAAGTTTTGTTATTATTGACTAATTGTTGGTATTCTAAAAGTAATAGTGATTCTTTTAACAATATCAGTGTTGAGTTCCTGCTTCATAGATGTGGAAACTGATGCATTATTGTTTTTAGGATTCTTTGATCCTAGTCAACTTTAAGAATTTATTTGCCATTTTTAGATCATAAAAATCTTTCACTTTTGAAAGCTTTAATCCTTCATAAGCAAAAGTAATTTATTTTAATGGTACTTTAGAATGGGACTTTTACAGAGTTTCCAAAAAAAATATGATGCAACTCAATAGTTTTTGATTATAATTCAACAGTGATGGTTCTAATACACGTTTCTTTAGAAGCAGAGAATGCATCATATATGAATGTGAGACTCAAAATTGGAGTAATGATGCTAAATGTTCTGCTTTAATTCACAGAGATAAATACAATTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1413
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 |
---|---|---|---|---|---|
ENSDART00000089076 | Nonsense | 180 | 1523 | 6 | 28 |
ENSDART00000142046 | Nonsense | 189 | 1122 | 6 | 27 |
Genomic Location (Zv9):
Chromosome 22 (position 21133124)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 20787800 |
GRCz11 | 22 | 20812778 |
KASP Assay ID:
554-1334.1 (used for ordering genotyping assays)
KASP Sequence:
TTGCAGGGGTCGGTCAGGTGGTCCTGCAAGTTGCTGCGGCCACCAATTGT[A/T]AACACTACTATGGCGTGGAGAAAGCAGACATTCCAGCTACCTATGCAGAA
Long Flanking Sequence:
AATGGCTGAATCAAGACCAAAGTTAATCTTAATGGACGTTAATTTACACATAATTGGAAAGTACAGCAAAAACTCAAAAAAAGCAAAATAATAAAAATAACGACAAGTAAAAAAGAAATGCAGTTGTGGATTGTAAAATGCATCAGCAAATTTGGCTACTACAATTTATTATAAATGGGCCTTTAGGGGTGAAGTACAATAGAAATGCAACGGCAAATAAAAACAATTAATTAATTAATAAATAAAAAAAACATCAAGTCCTGGACCGGTATCGGTCCGTGGATCAATTGGTACCAGGCAACACAAGAAATCATTAATCATTTCCGTTTTTATTATTATTTCTGTCTGAACATATTTTTCAACTGAAGTGCATCTCAGAACTCTTAACATGATCTTAAAATCCACGATACATACATCTTCAAATTTAATGTACAGCTTTCATCTCCTCCTTTGCAGGGGTCGGTCAGGTGGTCCTGCAAGTTGCTGCGGCCACCAATTGT[A/T]AACACTACTATGGCGTGGAGAAAGCAGACATTCCAGCTACCTATGCAGAAGTACATACATAAAATACTCCTTAAATAGCCCAAAAAAGTGGACGTTTTACATTTAATCTTTACATCTGAATGTCTTTACAGTCAATGGACAAAGAGTTTAAGAGGTGGATGAAGTGGTATGGCAAAAAACATGGCGAGTACACGGTGAGCTTGTTCAATTTTTGTTTATTCTAAACTCATTGTGGCTTATGGGATGAAATATATCAATACTGATGTCATTTGGGCAGCTGGAAAGGGGAGATTTCCTTTCAGAAGAATGGAAGGAACGAATAGCCAGTACAAGGTATGATCAAATACAGGCTAGTAAGATTTACAAGCTTTAATAATCTTGTTTTGCTCTTTTGCTCGCATGTGTGCATATGTCTTGTGTAAGTCTGTAGTATGATGTGTTCTTTTGCAGTGTTATTTTTGTGAATAACTTTGCCTTTGGTCCTGAGGTGGACCACCAGT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa17639
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 |
---|---|---|---|---|---|
ENSDART00000089076 | Nonsense | 338 | 1523 | 13 | 28 |
ENSDART00000142046 | Nonsense | 347 | 1122 | 13 | 27 |
Genomic Location (Zv9):
Chromosome 22 (position 21129133)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 20783809 |
GRCz11 | 22 | 20808787 |
KASP Assay ID:
2261-6783.1 (used for ordering genotyping assays)
KASP Sequence:
CTAWTTCTCTTCCCACAACAYATGCGGTGTGTTTTTGGTTCCAGGAGGAA[C/T]AGGAGGTTGCCAGAAGGCGCCCACAGAAGGACAGTAAAGAGAACAAGAGC
Long Flanking Sequence:
GTGATCTTGTCTTTACATTTGATGCCTATATGTAACAGGCTTTTTCTTCATGCAGATATTGGCACAATAATGCGAGTTGTGGAGCTGTCCCCTCTGAGGGGTTCGGTGTCCTGGACAGGGAAGCCAGTCTCGTACTATCTGCATACAATAGACCGCACCATAGTAAGTGTGCTTTCATTCGTGACAAGCTGCTTTTGTTGTTCCTCTTGGTGTACAGTGGAAGTCTAATTTGCATTAGCCCTTATTGCTAGGCAAATGATGTTAGACAGGCCTTTATGTTTTTGTGAAACACTGAATTTCACATGTTTGAGTATTTACACAAATCTGACTAAATACTTTCTATTTGCAGCTTGAAAACTATTTTTCTAGTCTCAAAAATCCTAAACTCAGGGTAAGCCTTTTCTGTTTGATCTACGATGTTGTTCATGAGTTTTTGGACAAAATGTGAAGCTAATTCTCTTCCCACAACACATGCGGTGTGTTTTTGGTTCCAGGAGGAA[C/T]AGGAGGTTGCCAGAAGGCGCCCACAGAAGGACAGTAAAGAGAACAAGAGCAACACCACCACCCCGACCAAGCCTAAAGAGCACAAGGTAGACCTGCAGGACAATCATTCATTCACATCTGCAGAGTAAAATCATAGTTTGTTTATGGATAGTTCATTAATTCATTCACTTGTTCATTCATTCACACAACTGCATGGTAAAATCATTGGTTATTTGTGAATAGTTTGTTCGTTCAATCATTCATTCACGACTGCATAGTAAAATCATAGCTTATGCATAGTTCATTCATTCACAACTGGATAGAAAAATCATAGTTCGTTTATGCATAATGCATTCATTCCCAACTGCATAGTAAAATCAGTTCATTTATGGATTGTCAGTTCATTCATTCGCTGATTCATTCATTTATTAATTAATTCATTCACAATCGCATAGTACAATCATAAATCATTTATGGATAGTTAGTTAATTCATTCATTCAATCCTTCATTCAAATCATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17278
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 |
---|---|---|---|---|---|
ENSDART00000089076 | Essential Splice Site | 782 | 1523 | 20 | 28 |
ENSDART00000142046 | Essential Splice Site | 790 | 1122 | 20 | 27 |
Genomic Location (Zv9):
Chromosome 22 (position 21117601)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 20772277 |
GRCz11 | 22 | 20797255 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCAGGATTCAGCCGCAAACCAGTTYCGGGCACTCGGAAACAWCCATCGG[T/G]GAGTGAAAGTTAGCCAATTAGTTSAGTAAGTACTTATCTATTGGTCACTG
Long Flanking Sequence:
CTCTCTCCTCCACTGAATCATTGGCTCCCCCTGCTGTTTGTTTCCAGATCAGTATAGTTGAACTCGAGAAGAGCCAGCGACAGCAGGAGCTCCTTCAGCTCAAGTCATCCTACAGCCCTTGTGAAGTGTCCCCCTACAGAAAAGCCCTCCCTGGCCCTGATCCTCGGCCCACACTGGACCCGGATACCCCAAAACTCACCCCGCAATCCTCTATGGGGCTGAACGGCCTCAGTCCTGAACTCTCTATCAACGGCACTGCCTCTCCGGGTTATGAAAGATGCACCGGAAGTGCAATGGGCAAAAACGAACTCCTCACCCACTACCTGCCCATTTCTCCAGACCACGAAATTGTGCCGCCAACCCCGGACTCCAGAACCAGGCAGCTTGGGCAACCCCTGCCCGACTACACCCGCTTTTCTCCAGCAAAGATCGCCCTCCGCAGGCACCTCAACCAGGATTCAGCCGCAAACCAGTTCCGGGCACTCGGAAACATCCATCGG[T/G]GAGTGAAAGTTAGCCAATTAGTTGAGTAAGTACTTATCTATTGGTCACTGATCACTCACGGGTGTTTTCAGGGGCGACACTGGTGCCATTTCATCTCCAACACTGGGCTTTAAACAGGCTTCACCATGTTCCTCGGAAGTTCAAGCGGTCACCACAGCCAAGAGCACAGATAGGGTAATAAACGGTGTCTTTATGTGAACTAGAGGTTAAACGGATCAGCAGAAGTCACGGTTGGGATCATGTTTTAGGTTTTGCAGCATGAATTGGGTCTTTTTTTTTTTTTTTTTTTGACTATTAGGCAACGCAAGCAAAGCGCAGATTTTATTTGGGGATATATTGGTAACACTTTAAGATAATGGTCTATTAGCTAATGTACTTTCTATTGTTAACAAACAATGAGTAGTATGTTTATTAGGTTATTTAAATTGAAATAACATTTGTTGATATTAATTCAGTTCTTTAAGGCTGCGTTTACACAGATCTTGATGGTCAATTCTGAT
Associated Phenotype:
Not determined