ZMP

suv39h1a

Ensembl ID:

ENSDARG00000026799

ZFIN ID:

ZDB-GENE-040801-111

Description:

Histone-lysine N-methyltransferase SUV39H1-A [Source:UniProtKB/Swiss-Prot;Acc:Q6DGD3]

Human Orthologue:

SUV39H2

Human Description:

suppressor of variegation 3-9 homolog 2 (Drosophila) [Source:HGNC Symbol;Acc:17287]

Mouse Orthologue:

Suv39h2

Mouse Description:

suppressor of variegation 3-9 homolog 2 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1890396]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa16242	Nonsense	Available for shipment	Available now
sa44685	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa16242

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC
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Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000038955	Nonsense	22	411	2	6

Genomic Location (Zv9):

Chromosome 8 (position 24248709)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	23374527
GRCz11	8	23395766

KASP Assay ID:

2260-0539.1 (used for ordering genotyping assays)

KASP Sequence:

TTAAGATTGCAGGGTGCCYTGTAARCTTTTGTTGGAGGACMTTCAGGCTT[T/A]GTGCCGAAGAAAAAAACTAGTTTGCAAGCAGCTGAGTGTGACAAAGAACA

Long Flanking Sequence:

TTTGTCACTTTCCACACTGAATAAAATATAAAATAAAATAATAAAATGAAATAAATAAATAAAATACTGACAGCAATTCATCGACTTTCCCCCCACCTCATGTACGCTATCAGAGGGACTGACCAATGAGCGTTAGATATTGTTCTCCTGGCTACAGCTCAACCAATCATTAACGCGAATACCTTAACGCGGGCTTCCCTTCATTGAGAATCATAAACAATCCATCTAGCTTGAAGTGACGAAGCGAACATGGCGCGAGATCTAAAAGGTAAGATGTCTGTGCTTTCTTTAAGTTTTTACTAACTGTCCCTTTATACACGTCCCAAATAATTTGCCGCAAATAAACGGGCTGTTTTAAATAAATTGCATTGTTAATAGCATTACTAGTGTGCAGAAAGTGCTCATTACACATGAAACTTAAACGACATCATCGAGCCATGTTTATGTTCTTTAAGATTGCAGGGTGCCCTGTAAGCTTTTGTTGGAGGACCTTCAGGCTT[T/A]GTGCCGAAGAAAAAAACTAGTTTGCAAGCAGCTGAGTGTGACAAAGAACAACTTTAATGACTATGAAGTGGAGTATCTGTGTAACTACAAAAAACACAAGGTCAGATTATTATGCTTTTAAAGTATATCATGAACGGCTGTGGTGAGGTCAGAAATGTTAAAATAAGATGGACCTGCAGGGCATCTTAATCTAAAATGCAAAATTTTACATAATTTCTATGATGAGGTAAAACTTTTCACAGATAAAAATGGCATTAATATGTTTTAGTTTATCGTATTTTTGTTAGCATTGTCTCTACTAGCAAAGCTTTTGGGGATCTGGGATCCAATCGCATTGTTTTCTTGAACATATTCAACTGAATCTGAATCTCAGGTAAGGTTGTTTGGTAGATTTATTAAATAGAGACTAATTCGGGACAGATTTACTGCAAGAGAGCGCTTCTGTTGGATTGAGCTCTGGGCTGGGCGATTTGGCCCTAAAATAAAAATCTTGATTAACG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa44685

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

C > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000038955	Nonsense	67	411	3	6

Genomic Location (Zv9):

Chromosome 8 (position 24250284)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	23376102
GRCz11	8	23397341

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AATATGCCTGTTCAGGGTCGAGAGTTCTTCCTGGTGAAGTGGAAAGGCTA[C/G]GAGGAGTCAGAAAACACCTGGGAGCCTCTTAAAAACCTTAAATGCCCAAT

Long Flanking Sequence:

AACAGAGTAAGGTCTCATGACTCCACATGCGATAAGGAAAGTAATTAAAAAAAATTGACCTGTAAAAATTAGATTGATTATAGGTTCTGAAAGTGGATTACGATTACTTTGAGTAATTTTCCCAGCCCTAGATTGAGCTCCATTGAGCTCCTAATCGACAGCTTTGGCAATTACCATTTTCCCTAAAATAGAAGCTCGGATATAGTAGATCTGGGCTCATCTCTTAGAATCTAACCATTTTGACTTAATCTACACAGACTTAATATAAAGAAATGTTCTTCCTTTCTTCAATACATTTTTGTCTCATTTAATTGGGTGGACTAGCTATCAATCTGATGGGGTCAGTGCCACCCTGGCCCTTTTGTAGCCTTGCTACTGGCCTCAGCTGTTTCTACTTATCCATATTTCATATCCCCAATTTATAAGATTTACCTCACAGTAACCTTTAGAAATATGCCTGTTCAGGGTCGAGAGTTCTTCCTGGTGAAGTGGAAAGGCTA[C/G]GAGGAGTCAGAAAACACCTGGGAGCCTCTTAAAAACCTTAAATGCCCAATACTGTTACACCAGTTCCGAAAAGACATGAAGGCAGCTCTGCTTCAGGCCAACGAACCACTTGATTCTGCATCTTTGAGTGGCCCTATCATCTCCTTCCTTCGCCAAAAGGCCACACAGCGCATTAGGCTTAAAAAATGGGAAGACCTCATGAACCAGACCTGCTGGCACAAGGGCCGAATATTTGTCTCAAATGAGGTAGACATGGATGGACCTCCCAAAAACTTCACCTACATTAATGAGAATAAGTTAGGGAAAGGAGTAGATATGAATGCAGTAATAGTGGGCTGTGAGTGTGAAGACTGCGTCTCTCAGCCAGTTGATGGCTGCTGTCCAGGGCTGCTGAAGTTTCGGAGGGCATATAATGAGAGCAGGCGGGTGAAAGTGATGCCTGGTGTACCCATTTATGAGTGTAACTCCAAGTGCCGCTGTGGACCAGACTGTGCCAACAG

Associated Phenotype:

Not determined