ZMP
suv420h1
Ensembl ID:
ZFIN ID:
Description:
Histone-lysine N-methyltransferase SUV420H1 [Source:UniProtKB/Swiss-Prot;Acc:Q5U3H2]
Human Orthologue:
SUV420H1
Human Description:
suppressor of variegation 4-20 homolog 1 (Drosophila) [Source:HGNC Symbol;Acc:24283]
Mouse Orthologue:
Suv420h1
Mouse Description:
suppressor of variegation 4-20 homolog 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2444557]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36641 | Essential Splice Site | Available for shipment | Available now |
sa23293 | Nonsense | Available for shipment | Available now |
sa36642 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18386 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36641
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 |
---|---|---|---|---|---|
ENSDART00000060191 | Essential Splice Site | 52 | 808 | None | 10 |
ENSDART00000123099 | Essential Splice Site | 52 | 808 | None | 9 |
Genomic Location (Zv9):
Chromosome 18 (position 20895418)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21125641 |
GRCz11 | 18 | 21114707 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCTTCGCCAGAACAAAGGCTCCCCGAGTGTCAGAAGATGCAGTCGACG[T/G]AAGTTCATAAAACAATTTATTGTATTTTACCAGTAGTTAGTTTTTCTATT
Long Flanking Sequence:
CCAAAAGTAGCCACGTGGTGGCGCTATGCACCTAAGAATAATTTAAAAGTAATCATCTCAAACATTTGAAGTGAATTCATAGTTCATGGCATGCTGGTAATGAAATGAACCTGTACTGTTTGTGTTGAAGTTGTTGAAGTATTATTGGCAATATAATCATATCAAAAGTACATTAAACAACGTTTTTTTTTTTTTGAACAGGTGAAGTCAAATCTAAAGAAACAATTAAAGACGACAGATCTGACCTTATTCCCATTGTACCTGTCGCTGTCTTGTTGAATGGTTTCTCACAAGCACACAGAAGCTCAATGCGCCTTCTCCATACCGCCAGCTGGTATGAAGTAGATGGGAGAATCCAAGAACATGGTGCTGAATGGCAGGAGACATGGCAGAAAGTTCTCCAGTAATCAGCCCGTAAGCAAATCCAGGCTGCAAAACACACAGAGATCCCATCTTCGCCAGAACAAAGGCTCCCCGAGTGTCAGAAGATGCAGTCGACG[T/G]AAGTTCATAAAACAATTTATTGTATTTTACCAGTAGTTAGTTTTTCTATTAGTTATTCATGTCAAATGTTCAAACAGGTTGTGGTGGGGCGCCCCCGGAGGCAGAAAGGCGTCATGTTCCTTCATCGGGAATGACTGCCAAGGAGTTGTGCGAGTATGATGATCTGAGCACCAGTCTGATCCTGGATCCATACCTTGGCTTTCAGACCCACAAGATGAACACCAGGTTTGTGCTTGGTGAATTTGAAAATGGTATTTTACAGTTAACAAGAGTTTTTTTATTTATTTATTTTTAATACATATATTTTTAAGGTTTCGACCAATCAAAGGCCGGCAGAGGGAGCTGAGGGAGATCATTGAGCTTTTCAAGAAGCATGACAACCTGGAGAAAGCTTTTCAGGCTCTGACATCTGGAGACTGGACCAGACATCATTTTCTCAACAAGACCAAGTCCCAGGAGAAGCTCTTCAAAGCACATGTAAATTTTAGCTAATGAATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23293
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000060191 | Nonsense | 280 | 808 | 8 | 10 |
ENSDART00000123099 | Nonsense | 280 | 808 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 18 (position 20897442)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21127665 |
GRCz11 | 18 | 21116731 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTGTGTAAAGGTTCTACGGGACATTGAACCAGGGGAAGAGATCTCCTG[C/A]TACTATGGAGATGGATTCTTTGGAGAAAACAATGAATTCTGTGAATGCTA
Long Flanking Sequence:
TTTCATCATATGCTTTTTATTTGCACATTTCAGGAAAAGGAATGATAAAATCGAACATCTTGTGGGCTGTATTGCTGAGTTGTCTCCCAGTGAAGAGCGGATGTTGCTTCGACATGGAGAGAATGATTTCAGTGTCATGTACTCAACGCGCAAAAACTGCGCACAGCTCTGGCTGGGACCTGCAGCTTTTATTAACCACGGTTTGTCTCTTCTAGATTCTGATCAATATGATGTGATCAATAAAAAATTTCCAATTATCATATGTTGTCCTTAATAATAAAAATATTAATATTATTATTTTAATTTCTTACAGATTGCAGGCCAAACTGCAAGGTAAGTACATGTGATTGGACTCTGCTTTCTCAATAATGAAGATTAATGAGGAATGGAAAATACAGTTTTGCTGATGTGTGGCATTTGTTCCAGTTTGTGTCAACAGGCCGAGATACCGCCTGTGTAAAGGTTCTACGGGACATTGAACCAGGGGAAGAGATCTCCTG[C/A]TACTATGGAGATGGATTCTTTGGAGAAAACAATGAATTCTGTGAATGCTATACTTGTGAAAGGTATCATGTGCTGCATTCCTTTAGTTTCTCGGGTTTCTTTGTGTGTTGTTGGTGGGAATTAGAAACAGCAATTCATATCATATTTTTAAATAATTATGCAAAGAAATGGTTTGTTTTGACATGCATATGCTTGATGTAGAAATTAATATGCAAATATGAATATGTAAAATTCAGCACTCTTTACACTTTAAAACATTTTCTTGTGTATGATGATAATGATGATGATAATATTAATACTAATAAAATGCCATGTTTTTATACACCCTTATGTTTTAATTTTTAGCCAGTGTTTGAACTTAGTGAGTTAAGATAATAAAAATTTGATAAAAAAAAATCATAGGTTGTGACCAAAAAAAGTGCTTTTCCATCAAATTAAAAGTTGTCATTTTTTAATAAATAAATAAAATTAGGAAGAAAATTCTAATAATATAATAAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36642
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 |
---|---|---|---|---|---|
ENSDART00000060191 | Nonsense | 366 | 808 | 9 | 10 |
ENSDART00000123099 | Nonsense | 366 | 808 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 18 (position 20898337)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21128560 |
GRCz11 | 18 | 21117626 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCTGTCAGTTCCAATGCAGAGGCAGACTCTCAGGAACCAACCACTGTA[C/T]AAACATGTGAGAGACCTGTAATACCAGACGTTTGATGCTAATAATACTGT
Long Flanking Sequence:
AATCATAGGTTGTGACCAAAAAAAGTGCTTTTCCATCAAATTAAAAGTTGTCATTTTTTAATAAATAAATAAAATTAGGAAGAAAATTCTAATAATATAATAAATCAATAGAAAATAAAAATTCAAGTGGTCTCTTCATTTTTTTCCCACCAAACCTGTATGAAATATATTTGGCAATAGTGTTTATAAGCATAACCTTGTTGCTTTATTTTGATATATAATCTATTTGGTATTATACACTGTCACATAATTGGATCGAATAGTCATCTATTAAATGACATTTTTAAATGAAATATTTATGTTTCAGGCGTGGCACTGGAGCTTTTAAATCGAAACCAGGGTTACCTGTTGAAGCTCCAGTGATCAATAGCAAGTACGGCCTCAGAGAGACAGACAAGCGTCTGAACAGACTGAAGAAGCTGGGGGAAAGTTGCAGGAACTCTGACAGCCAGTCTGTCAGTTCCAATGCAGAGGCAGACTCTCAGGAACCAACCACTGTA[C/T]AAACATGTGAGAGACCTGTAATACCAGACGTTTGATGCTAATAATACTGTTACGGCTCAAGCTCATCATTTCTTTTCTCTTTCTTTCATGTTTCTCCAGCATTACGTAAGAGAACTTCACAGTCCTGTGTCAAAAAGCACGGAGAAGCTAAGGCTGTAACAAGGCAAACTCTGTCAAGCACTCCTTCTTCTACCTCATCCTCTAAACGAAGTCAAGCGAATATTTCAAGTTTACCAAAGAGACTTAAGTCAAAGCCCACACAGACTTTGTCTAAAGGAAGACGACGCTGTCGAGGCCTATGGACGAAAGGTTCTAGCCGAGTGAGCGCTAGCGGAAATCTCAAAGAGTCCTCTAGACGAGACACAGACAGACGTAGATCTGCAAGCAAAGGCAGTGTTGCGCGTTCATCAGAAAACAATCGGAGCTCTTCAAAGGGTGCTTCCCCATGCAAGGACAGCACACTTTGCCCTTACAGAACTCGTAGGTCCACGAGGACTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18386
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 |
---|---|---|---|---|---|
ENSDART00000060191 | Nonsense | 625 | 808 | 10 | 10 |
ENSDART00000123099 | Nonsense | 625 | 808 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 18 (position 20899207)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21129430 |
GRCz11 | 18 | 21118496 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTCTAAGAGCAGCAAGRCCCTCCGTCGAGGGAAAGGCAAGAAGAARCGA[C/T]AGATCACAYGCTATGACGCTCAGCTGATTCTGCAGAATAACTCRGGCATC
Long Flanking Sequence:
GACGTAGATCTGCAAGCAAAGGCAGTGTTGCGCGTTCATCAGAAAACAATCGGAGCTCTTCAAAGGGTGCTTCCCCATGCAAGGACAGCACACTTTGCCCTTACAGAACTCGTAGGTCCACGAGGACTTCTCTTGGTGCTCAGGGGGCTGAAGGCACAGAGGCTTCAAACCACCCGGCGAGCCCGAGCATCGTCCTCAAGTCAGAGCCTGGAGAGTTCATTCCTGTGACACTTGGGCACCAGATGAGCACTCCTAGTTTGGACTCCAGCTGTCCCAAGAAAGGGACTTGTCCTAGACGCAGAAGGACAGTAAAACAGGAAGACTCCTACGGCGAGTCCTTCGTCCAGGAGGGCGTTCCAGATCTGCGGCACGCGGTTCGGGCTGCAGATGTAGCAGACTGTGGGAAGGTGGTGCTCGGCCTTCCAGACCGCCACCAGCACTACAACGGCTCCTCTAAGAGCAGCAAGGCCCTCCGTCGAGGGAAAGGCAAGAAGAAACGA[C/T]AGATCACACGCTATGACGCTCAGCTGATTCTGCAGAATAACTCAGGCATCCCCAAGATAACACTACGCCGGCGTCGAGACAGCAGCAGCAGCAAGAATGAGCCCAGAGAGACCAGCTCCTCAAGCTCCTCCAAAATCAGCATCAAGTTCAGCAAGGAGCACGAGAAGGACCGGAGCAGCTCGTACGTAGCCAAACTCAACAACGGCTTCAGCCACGGACCGCACAGCAGCTCCACCAAGCTCAAGATCCAGCTGAAGCGGGAGGAAGACCCCGCCAGCTTGCACCGCACTTACCCGGAGGACGTCACCTTGGGCATCGTGCAACGAGACGCTGCGGACGTCCTGGATCACAAGGCAGCCGCTCAGGTAGGTCAGGACATGGAAGTGGAATCGATGTCGTCAGAGGACGACGACGATGACTACTTTGATAACGAGGATGATTTCATCCCGCTCCCACCAGCAAAACGCCTGCGCCTCATCGTGGGCAAAGATTCCATAGAC
Associated Phenotype:
Not determined