ZMP
ehmt1a
Ensembl ID:
ZFIN ID:
Description:
histone-lysine N-methyltransferase, H3 lysine-9 specific 5 [Source:RefSeq peptide;Acc:NP_001025302]
Human Orthologue:
EHMT1
Human Description:
euchromatic histone-lysine N-methyltransferase 1 [Source:HGNC Symbol;Acc:24650]
Mouse Orthologue:
Ehmt1
Mouse Description:
euchromatic histone methyltransferase 1 Gene [Source:MGI Symbol;Acc:MGI:1924933]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa18521 | Essential Splice Site | Available for shipment | Available now |
| sa40453 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa7277 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa26489 | Essential Splice Site, Missense | Mutation detected in F1 DNA | Not yet available |
| sa25299 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18521
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098364 | None | None | 1059 | None | 23 |
| ENSDART00000125042 | None | None | 759 | None | 20 |
| ENSDART00000125175 | Essential Splice Site | None | 321 | None | 11 |
| ENSDART00000126018 | Essential Splice Site | None | 1058 | None | 24 |
| ENSDART00000126880 | None | None | 807 | None | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 31153120)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 28914477 |
| GRCz11 | 5 | 29514630 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAAACTTTTGAGAWATTGTACAAAAATGCAAGCCATTAKAAGTTAGCCGG[T/A]AAGTATGCRCTAAGCYGCTGWAATTGCAATATGTGAGAWATCTCTAGCCG
Long Flanking Sequence:
ATCCATAAATCCCCGCTTAAACAATAAATAAATAAGCAAATTAAAAAATAATTGATTAAATAAATCCACAAATCCCTGCATAAATAAATAAATACGCAGATAAATAAATAAATATAAGAGTAAACAAATTCACAAAAACCTACATAAATAAAACAAATAAATATGCAGATAAAAAAAAATATATATATATATATATATAAAAATACACAAATTCTTACATAACCGTATTTTTTTATATTTATTTATTTATGGTTTTATTTATGCCGGAATTTATGGACTTTTTTTGACCATTTAGATATTTATAAATTTTTCCTATTGGTTACAGTACAAGCCACTGTGATCAAATGACTATTTGCTTTTTGCTCTCCTTACCAACAGACGGCGCGATGTGGTCACATGACAGACGCAGGGTGCATGTAGCAGGGAAGTGAAGAGAGGAAGAAAAACCTCTAAACTTTTGAGATATTGTACAAAAATGCAAGCCATTATAAGTTAGCCGG[T/A]AAGTATGCACTAAGCTGCTGTAATTGCAATATGTGAGATATCTCTAGCCGTATGTTGTCTTTATAGCTGCACGCACTCGTCTGTTGTCATGCGCGTCGGTCTGTTTGCTACATTGTTTCATTGTGTTTCCGCCCACAGCGAGTGCACTAAGCTACTTCTGTCATAAACACGAGTGAATGTTTTGTTTATTAGTTATTAATACACAAGGAACTACGAGTCTGATACCGAGTTGTCAATGTCAGACCTATTCTGTATTGCACAGAAAGTTAGATTTAGCGTTCTGGAGGGCAAGAAAAGATTTTTTGGCTCAAAATCAGTCAGAAAAGATTTGAGGACCAAAATTCCACATGCATGCAGTTTGCTAATTTTTATGTAAAGCAACCCCTACAGTCGTTGTTATTGTTTTAAATTGGTCGTTTACGAGCTAAATAGCTATTAGATTTCACCATACAGTATAATTCGCTTCATGTTAAATAATACAATTGTATACGATGTTGTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40453
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098364 | Essential Splice Site | 174 | 1059 | 3 | 23 |
| ENSDART00000125042 | None | None | 759 | None | 20 |
| ENSDART00000125175 | None | None | 321 | None | 11 |
| ENSDART00000126018 | Essential Splice Site | 174 | 1058 | 4 | 24 |
| ENSDART00000126880 | None | None | 807 | None | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 31149106)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 28910463 |
| GRCz11 | 5 | 29510616 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACAGCATCTCAGTTTACCTCAGGAACTCAAAGACTCCACACAAACAGG[T/A]GGGATTTTTAGTTAAAAAGCTAAGCATAATTAAATGATATTGTTTAGATG
Long Flanking Sequence:
AATTTCAAACCCCAAGCACTGAACATTTTTTCAATAGAGTAAGTCCTCAGAAATCTCAGTCTTTCAATCTGTATTCATACTTTTATTTTAGATGAGATTAATTGTAAACAATCTTTGCCCAGCACTAGTATTTATACATTATGCGTTTATTATAAAGTATTCTAAAATATTTTTGTCATGCTGCTGTAAATATTTCTGTAAAAACCATGCAGTGTTTTTAAGGATTCTTTGATGAATAAAAAGTTCAAAAGATTACTTAAAATCTTTACGGTCATGTTTGTATGAACTTAATGCACACTTGCTGGAAAATTGTTAGTTAAACTTTCTGGCCCCAAACATCCTGAAAAAGACTTGTATATTAAATGTACTTGTCTTGTTTTTGTTAATGAAACACCATAGACTTTGAACAGGGAGAGAAGTGGGTATGAGAGAGACGTGGAGTCATCACCCACACAGCATCTCAGTTTACCTCAGGAACTCAAAGACTCCACACAAACAGG[T/A]GGGATTTTTAGTTAAAAAGCTAAGCATAATTAAATGATATTGTTTAGATGAAAAAACGGGCCCGTCCCTTTGTTTGTGCTGTATCCCTCTGCAGCCCCCAAGAAGAAGAAAAGAAAAATGGGTTTATATAATTTTGTTCCCAAAAAGAAACCGAAAGGGTCCAAGAAAGCGAATGTGTCGTTATCCTCCTCAAATCTGCAGGTCTGAAATCTTGCCCGTTAGAAACTTCTTGCATGAAACCAAGTTATTCTTCTCATTCCAATCTGGACTTTGTTTCCAAACCCTGCAGGAAGCTTTACGTATGACCGGGTCCAAGGGTGGACAGATGTCTATTGAGGAGGCATTCAGAAATAAAGCTAGTTCTGAGAAACCAGAGAAACAGACTTCAACTGCTGTGATAGAGGATGCAGAACCGCACCAGAACAAAGAAACTGAGGATGCTCCAGAAGGCCCTGCTGAGGAATACACAGAGCTGCCTTTACATGCTCTGGCTCATGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7277
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 |
|---|---|---|---|---|---|
| ENSDART00000098364 | None | None | 1059 | None | 23 |
| ENSDART00000125042 | Essential Splice Site | 152 | 759 | 5 | 20 |
| ENSDART00000125175 | None | None | 321 | None | 11 |
| ENSDART00000126018 | None | None | 1058 | None | 24 |
| ENSDART00000126880 | Essential Splice Site | 200 | 807 | 6 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 31144120)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 28905477 |
| GRCz11 | 5 | 29505630 |
KASP Assay ID:
554-5452.1 (used for ordering genotyping assays)
KASP Sequence:
GTGCAAAATAGGTTATTTTAAAAAGTTGGCTTTTATGTYAMAAGATTTAT[G/A]TAAACAAAGCTCACTATGAGCGCTCTTGTWATTGACCTAAACTTTTTGAT
Long Flanking Sequence:
GCCAAAATATTACACATTTTTAAAGTGCAATAGTATTAAAATTTCACAATAATGAAAATTATTATATTTTATTATATTAATATTATTAAAAGTAGATTCATCTACAACTAGCCCAAACGTTGATCACACTACAAACAAGTCATAACTAAAATGATATGGAAGAGATTGTTTACCTGCTCTTTTGTTTATGATTTGGTCAGCTCACATCTTCTGACATGTCTGCAAAATTAAATCGTTCATTCACGTGATAACTACTTGCCACAGTGGCTGATGATCAAAAGTTTATGTCAAGCCCTGACCATAATCATAAATATGAACACAACACTGGACACAAGAGCTATTTTAAACCTATACTTAACTAAAATTCCAGAGAGCTAAACTAACTATACTAACTAATGGTATAAATACTTAAAATATAGTATAAACAACTACAGTATATAGATCAATATTGTGCAAAATAGGTTATTTTAAAAAGTTGGCTTTTATGTTAAAAGATTTAT[G/A]TAAACAAAGCTCACTATGAGCGCTCTTGTAATTGACCTAAACTTTTTGATACTTTTCTTAATGATTATTTTAGGTTCAAGTTGTCTTTGTAAGGATTTGGATGGTAGCAGAGTTTGACTTTTTGTAAAACATACAGCTCCATCTTTTGTTAAAAAACTGAGCTCCGAATTAATAAAAAAGAGAATAGGCCTATTTCACAAATATAGCAATCGAGACCGATATAGGGAATGCCAGAACAGGTTAAAATGACCACTACAATAATGAAATAATAACTGATAAGAAACTAAACTGTTCACAGTCTATTATAAGAAATGGCAATCGTAGCACCAGCTGAGCCACTGGGAGCAATGCTTCCCTGTTCTGGTCTCTTTAAAAATATATATATATTATTATTTTTTATATACCACAGCCCTAGTATTTAGTCTTGTCCACTTGTTATGGGATTGACCATTTTGATTCCAGGTGAAAACAGGGCTTTGTGTTGTGATGTGTTTGCTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26489
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 > A
Consequence:
Essential Splice Site, Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098364 | Missense | 718 | 1059 | 16 | 23 |
| ENSDART00000125042 | Missense | 420 | 759 | 13 | 20 |
| ENSDART00000125175 | Essential Splice Site | None | 321 | 4 | 11 |
| ENSDART00000126018 | Missense | 718 | 1058 | 17 | 24 |
| ENSDART00000126880 | Missense | 468 | 807 | 14 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 31136942)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 28898299 |
| GRCz11 | 5 | 29498452 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTCATGGAAATGCTCTTCTCTAGGTTGTTTCTGTCTCGAGGAGCGGA[T/A]GTAAACCTGAAGAACAGAGATGGCGAAACTCCTTTGGGCTGCTGTAATAT
Long Flanking Sequence:
ACATTTTACATTAGTATAAAAAAATTCAAACATAAATTGATTAAAAAATATATTTAAAAAATGCAAACATGTAAAACAAACTACAGAATATTGAATGGTATAAAAATATTTAATAATTAAATAATTAAGTAAAATTATAAATTGAGTCTTAATACAAGAATCTGTACAGATGCATTTTATATTTAAGATTGTAGTTCCTCATGCAATAATATTTCAGCAATTTTTTATCACCTATGATGTCAGTAAATGATTGATTGGCATGGAGGTAAATAAATACTGAAACATTTAAAACATACATAAGCTTATTTTAATTTTAAACACTTCTAATTTTAGGTTACTTTTAAATTAAAACTGTTATGATTTAGCTCAGTAGTAGCTTTTCCTCTTCACTAGCCCCCTCAGACATGTATAAACCCCAATTTGAAAATCCCTGAATTAATCTGATGTTCATTTTTCATGGAAATGCTCTTCTCTAGGTTGTTTCTGTCTCGAGGAGCGGA[T/A]GTAAACCTGAAGAACAGAGATGGCGAAACTCCTTTGGGCTGCTGTAATATAAACTCCAAAATGTGGACAATCCTGAACACCAATAAGAAGCTGACTGATGCGAGGAGAGGACGAGAAAGCCTGAGAGAGAGACTCCTCTGCAGGTAATGTTTGTCATCTTGAGGTTCATCGTCTTCAAAGCAGACGACCTGATCGTTTTTCCCTTCAGTGTTTATCATTGAGTAGTAACTGCTGCATTCTGGATGTTATTCAGGGTTGTAATTGTAGACCTACCTAGGCTATTGTGTAAATAATATAATGATATTGTGTAGTCCATAACGCGTATGACGAAGCCACTGACAATATGCAAGCTTATGAAATTGTTTCAAATGCGTGCTGCTGTGCACACTTTTTTCACACTCACAATTGCATGTCACGACCACGTGCGCTCTATGTACATTATAGATAAAGCCAGGATGCACGTTTGTTATTATCCGCTGCAAGTCATCTGCTCTTGTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25299
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 |
|---|---|---|---|---|---|
| ENSDART00000098364 | Nonsense | 965 | 1059 | 22 | 23 |
| ENSDART00000125042 | Nonsense | 671 | 759 | 19 | 20 |
| ENSDART00000125175 | Nonsense | 227 | 321 | 10 | 11 |
| ENSDART00000126018 | Nonsense | 964 | 1058 | 23 | 24 |
| ENSDART00000126880 | Nonsense | 719 | 807 | 20 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 31130555)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 28891912 |
| GRCz11 | 5 | 29492065 |
KASP Assay ID:
554-7768.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTTAGCAGGTTTATGAATCATCTTTGTGAGCCCAATCTATTCCCAGTA[C/T]GAGTGTTCACCAAACATCAAGACATGCGCTTTCCTCGTATTGCATTCTTT
Long Flanking Sequence:
CCTTTGCCTGCATTCTGAAGAAGCCTCCTACTGACTCCAGTGTCATGGGTATTCATTTAATGTGAAATTTTCTGCAAAAATGAAAGCCATTAGGGGAATTATTAATTATTTAGACATGATTAATCTCATGCTGCTTTGGTCCAATACTTGCACTGAGGATTTTGTTCTGTGCAGGTTTGCTGGTGAAATAATTTCCGATGGAGAAGCTAACATTCGGGAAAACGACTCCTACATGTTCAACCTAGACAATAAGGCAAGTTAAGAGGTTTGGCTTGTCAAGATTATTTTCATTAAGCTAATTCTACTCTAGTCATACTTGTGGCCTTCAGGGGGCGCTAAAGTATATCAAAATGCCAATAATATTGAAGCAGCTTTATATTTGTGTATTTAATGGCGACCTTTTTTTGTAGGTTGGAGAGGCCTACTGCATTGATGGACAATTTTATGGTAATGTTAGCAGGTTTATGAATCATCTTTGTGAGCCCAATCTATTCCCAGTA[C/T]GAGTGTTCACCAAACATCAAGACATGCGCTTTCCTCGTATTGCATTCTTTGCAAGCAAGCATATTCAAGCTGGAGATGAGCTTGGGTAAACCTTTATAAGTTTATTATTATTATTATTATTATTATTACTATGTGCTTCCATAAGGCTCCTGCAACTTTAGTTTCTGTCTTCTTTGTCTGCATTTGTAACTATTTGAAATGAATCTTCTTTCTCCTCAGGTTTGACTATGGGGATCATTACTGGCAAATCAAGAAAAAGTACTTCCGCTGCCAATGTGGCTCTGGAAAATGTAGGTACTCTGAGGTCGTTCCGGACCGGAACCATGCAGAAAGCTCAGCCCAAACCCTCAGTAATCAGACTGTTGCTCAGGTGGAACACATTCAGTCTTCTAACACTGCTATAGCAATAACTCAACCCTGAGCCTTTCACGCATATAACAGGATACGCTGAGGCCTTTAACAAGTAAATATTGTCAGGAGTTCAACGCATCATTTGCTGA
Associated Phenotype:
Not determined