ZMP
suv420h2
Ensembl ID:
ZFIN ID:
Description:
suppressor of variegation 4-20 protein-like 2 [Source:RefSeq peptide;Acc:NP_001091656]
Human Orthologue:
SUV420H2
Human Description:
suppressor of variegation 4-20 homolog 2 (Drosophila) [Source:HGNC Symbol;Acc:28405]
Mouse Orthologue:
Suv420h2
Mouse Description:
suppressor of variegation 4-20 homolog 2 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2385262]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17369 | Nonsense | Available for shipment | Available now |
| sa20036 | Nonsense | Available for shipment | Available now |
| sa33199 | Nonsense | Available for shipment | Available now |
| sa20035 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17369
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 |
|---|---|---|---|---|---|
| ENSDART00000109104 | Nonsense | 70 | 2065 | 3 | 9 |
| ENSDART00000113053 | None | None | 37 | None | 2 |
| ENSDART00000121907 | Nonsense | 70 | 2065 | 2 | 8 |
| ENSDART00000124458 | Nonsense | 70 | 519 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 3 (position 31031051)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 30749090 |
| GRCz11 | 3 | 30879932 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTGCGGTTCAAGCGCACGCATGACTTCCAAGCCAYCTTTGATGCTCTGT[T/A]GGATGGAGAGTGGGTYAGCGACTATTTCGCTGGGCTGGGTTCACACCGRC
Long Flanking Sequence:
TCTTCAATCAGGGCATATACAATGCACAACACAAAAAGAATGAAAGTCTCTCTATTTTGTTTTTCAATGCGAATATTTAAATATTAAATCAAGATAAATTTACTGGAGATTAAAAACAAAGTTTTTTTTTTTTTTTTTAAAAAGGAAATAAATAGATTTAAAGCTTTATACAAGAGCAAAAGTGTGAATGGATTTTTCTAAACTCACTGGCAGTTATTTATTTATTAATCTATTTGTGAGAAACATAAATACAACATGAATACATACAAACACAGTACATTTTGGGGAACAATTATTTAAATAAAAAAAATCTATTTCCCAAAATGTATTATTATCATAAGGCTGTTAAAAATGTATTGCATAATAAATGTTATCTCTACTTTATAATTCTTTCTTTGATGCAAGTACTCCCCCTGAGATCCGGCGATGGGGGTACCTCAGAGAGACACTCCTGCGGTTCAAGCGCACGCATGACTTCCAAGCCACCTTTGATGCTCTGT[T/A]GGATGGAGAGTGGGTCAGCGACTATTTCGCTGGGCTGGGTTCACACCGACAGGAGCTGTTGAAGCAGCACGTGAGTATCATGTTTAATCTAGAATAGCGTAACAATCATCCTTTCCTGTTTCTACACAGAGAGTTTTGTCTATGTGGCTGTTCAAGTCTAGTGTTGTAAATGATGGTTTGGCTTCACTTAAAACATGATAGTGTTTGGTGGATTAGGTGTTTGCTGTCTTGATGAATACAGTCTCTTCACTTATTTAAATGGGCTGAATTTAATTGCAGTCTTTGATTAATAATCACGCAATTTTCCAAGAACAGAACATTTTAAGGGATAGGATTAGACTTTTGCTATTAAATTTTCTTTGCTGAGCACCCATGATACCACAGAGCAGAAGCGAATCCTTTCTTTATTTGTTTTTTCATTTATTCTTCTGCTAGTCTGTTTGTTTTGTGCTCACTCCATAAGCGATGTGGGTTCCTTGTATAATTTGCAGTGGTTGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20036
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 |
|---|---|---|---|---|---|
| ENSDART00000109104 | Nonsense | 1056 | 2065 | 9 | 9 |
| ENSDART00000113053 | None | None | 37 | None | 2 |
| ENSDART00000121907 | Nonsense | 1056 | 2065 | 8 | 8 |
| ENSDART00000124458 | None | None | 519 | None | 9 |
Genomic Location (Zv9):
Chromosome 3 (position 31022594)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 30740633 |
| GRCz11 | 3 | 30871475 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATCCTAGAAGTGAAACATCCAAAATTAGGAAAAGAGTCAAATACATCT[T/A]GGAAGAGGATAACCAAGTGGAAAATGAGAAAGAAGTTGAAGAAAGAACAA
Long Flanking Sequence:
AGAGAAAAAAGACAAGCATGATACACTTAAAAACAAATGTGAGCATCCTAGTCAGGGACTCACTGCAGCTAATCAGCCAAATAAAGATGACACTTCAATTTCGTTGGAGCCTTCGTCCATGTGCATGGTGTCTCTGGATAATAGTCCCCAGAGCAGTATTCCCCTAAAGAAACGTCAGTTTCGAGAATCAGTGGACACCGACCCAGAACAGGATGTTAATGTAGCTGCAACACTGTGTACAGATGGCAGTAATGACACTGAGCCCAACTCGGACAATCTGTTACCTAAGCCTCGTGAAGGAGGCCATTTGGAATCAAGTTTAACTTATAAAGACAATGTTGGTGTTGAGTCCAAAAAATGTGGCTCGTCCAAGTTGTTAAAGACTTTGCCAAAACGATGTTGTAAAGGTCTTCAAAGTGCTCAGCATGACCCAGCGAGAAGGACAATCAATGATCCTAGAAGTGAAACATCCAAAATTAGGAAAAGAGTCAAATACATCT[T/A]GGAAGAGGATAACCAAGTGGAAAATGAGAAAGAAGTTGAAGAAAGAACAAAGGCACCTAGGAACTCTAAGACTGGACTTTATATAGAAGATGCCAGAAATGAGTCGACTACCTCAGATGACAAGTCTGAAGAAGATCAGAGGTTAAATGTCAGAATCCGCCTTAAGAGAAAAAGAGGAAAAGAGTGGGAAATGGAAAGTACAGATGAAGCAGAAGGTGTTGTAGACAAATCAAACCCTTTGTCTTTAGTTGACCCCTTTAGGGCCATTTTGGATTCAGTCTCAATTTTAAATGCAGAAATGGAGAGGATTAGGGGTCATGGGGAGGACGATAATGGTATAGGGTTGGAGAAAGCCACCAAAGCAGTCCAAGATGTGCTAGAGCATTGTAGAAAAGAATGTGCAACTAAGCCATGTAAAAGACAGCAAAAAGCGTCAACTGTTGGAATTCGAAACAGAAATCTTAACACACCAAAAGAAACTGTTCAAGACAGTAGTAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33199
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109104 | Nonsense | 1486 | 2065 | 9 | 9 |
| ENSDART00000113053 | None | None | 37 | None | 2 |
| ENSDART00000121907 | Nonsense | 1486 | 2065 | 8 | 8 |
| ENSDART00000124458 | None | None | 519 | None | 9 |
Genomic Location (Zv9):
Chromosome 3 (position 31021303)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 30739342 |
| GRCz11 | 3 | 30870184 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATACAGGATCCTTCAGTAGCCCTTTCTCCCAAAGTCCTGCTGATGCGTG[G/A]AATCCAGAGACTCCTTACCTTGGATCCCCAAGTCCAGTGAGTAACTTTAG
Long Flanking Sequence:
GGTACAGAGACATTCAAAGATCCAGTGAGTTTTGAGACTTCACCTTTACCATTATCCCTTTCACCTTTGTCGCTTTACTCTCCCTGTTATGATGGACTCACGGGAGTTGGTAAAGTCAGTGGAAGTATTCAAGCAAAAGAGAATGAAAATAAAGGAAAGAATGACACTTCTTTGAGCCACAATTTGCTTCAGATTAATAAAAGTCTGTCAAGACTCCAAGCTCTGAGTCACCCGCAGGTATGCGAGAAAAGTGTGCCAACCAACACTAGTACAACCTCTTCTCAGATTCAGTCCCCACCTATATCTCCATTTACAACAGAGTGCAGCTTTAGTAACTATTCTGAGGATGTACTTGACTTTCCTTGTTTAAATCTGGAAAACTACGATCAGATGCCTGCACAAAACAGCTTGGCTAACACCTTAATTGATTACTGCCCTGGCGAACCACATAATACAGGATCCTTCAGTAGCCCTTTCTCCCAAAGTCCTGCTGATGCGTG[G/A]AATCCAGAGACTCCTTACCTTGGATCCCCAAGTCCAGTGAGTAACTTTAGTAGTGGTGATGACCTAAACTTCCCAGACATTGTCTTTGCTCAGTCTGAAACGTCCTCTTCTGTCGGTGCTCCTCAAATGGTCTTCAAAGATAGATCATGTAATTCTGCCACAAGTTCTGCTCCTCTTCAAGACCCTGAGAAAAATCTGTACTTATCTGATGGTGAGTTGTCCAAAAGTCCCATAGAGCTTCAGGTTCAGGAAAATTCAGCAACAGCGTTTCTTCCAAAAGACTTGTCAATATTTAACAATGCAAATGCTAAACAGGCCATTCACACAGCTGGGCGTTTATATCCTCAGGATAGAAAGTTAAACTTTCTTGATTCCATTGTTAAGTCTTCAGAGGCAAGCCTTGCTAAAATTGAGGCTAAAGATAAAACTCACGGACCTCTCAATTTACATAACTCGAGTGCAAAATCTGAATCTGTTTTTCCAAGTCAGACAACACAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20035
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 |
|---|---|---|---|---|---|
| ENSDART00000109104 | Nonsense | 2063 | 2065 | 9 | 9 |
| ENSDART00000113053 | None | None | 37 | None | 2 |
| ENSDART00000121907 | Nonsense | 2063 | 2065 | 8 | 8 |
| ENSDART00000124458 | None | None | 519 | None | 9 |
Genomic Location (Zv9):
Chromosome 3 (position 31019572)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 30737611 |
| GRCz11 | 3 | 30868453 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACTGAGGCTTGTGGTGACTGACGGTACAGTGGATCTGGACCTACAATA[T/A]ACCGATTAATAATGACGTCTTTTATTGATATGCTGACATTTATTTATTTA
Long Flanking Sequence:
GTGTCACAGCACAACAGTCCTCATCTGGGCTACAGAGAATCTCTGATCCATGAGGCCCCACTAAGTAAAACACAGTCATCCACTTTTGAAAACAGTCAACATCCTCAACAGTCTTATGTTGTGAACTTCACCGGAGATCATTCTCTCACCCTTGGATACAGCGAGGATGGTGAACGCTCGAATTACACTGGTTCAGGTCCTGCAAATTACACTTATCATTGTCTTATGGAGCCTTCAGGAACTCAAGGAAGGCTGGTTGTTGAAGCGTGTGGTCCCTCAAACTTCTCGCCTTCTACACCTGTGAGTAGGTGTCCTGGGTCTAAAGTCCATGGAGGCCAAATTTGTAAGGATCCTCAGCAGACTCAGCAGCCTGGAACTCACCCATATAATTCTGTACACTTTACCACCTCCCACTCTCAAAGCACCCCCATAACAGATCGCAAGCCTAAGAGACTGAGGCTTGTGGTGACTGACGGTACAGTGGATCTGGACCTACAATA[T/A]ACCGATTAATAATGACGTCTTTTATTGATATGCTGACATTTATTTATTTAAATCGACTTCAGTGTAATAAGGTGTTCTGTTTGTTTTTCATTAAACTTGTATGGATCGTCCAGTTCTTAGCATTAAAGCAGAATTTTTCTTGAAATATTTAAAGACATATTTTTATTAGCAAACTTGATTGCTTAATTACTTGTATGCTGCATTTAATGTTTTAGTACATTACATATAGAAGATCATATTTTTCATGCTAGTGGTTCCTGTAAATATTATAACAGGAAAAATGGATGTTCTGTTCACCCTGTAGTACATAATACTTGCCACATGATGGTGGTGCGGTTCTCCACCACATGGAAATTCACTCGATTTCCTCATAGCCTTTTGAGTTCAGAGTTTGTAATCTAGATTGCTGTTGTTAAGAGTTTGTATGTGTGGCAACTTTCATAGTTCAGTGGGTTTGCACATGAAGGACCAGAGCATGGTTCATCTGATTTCTTAAATGT
Associated Phenotype:
Not determined