ZMP
zgc:109983
Ensembl ID:
ZFIN ID:
Description:
Putative methyltransferase NSUN3 [Source:UniProtKB/Swiss-Prot;Acc:Q4KMK0]
Human Orthologue:
NSUN3
Human Description:
NOP2/Sun domain family, member 3 [Source:HGNC Symbol;Acc:26208]
Mouse Orthologue:
Nsun3
Mouse Description:
NOL1/NOP2/Sun domain family member 3 Gene [Source:MGI Symbol;Acc:MGI:2146565]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa610 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa610
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 |
|---|---|---|---|---|---|
| ENSDART00000023768 | Nonsense | 14 | 367 | 1 | 6 |
| ENSDART00000131664 | Nonsense | 22 | 246 | 1 | 4 |
The following transcripts of ENSDARG00000013023 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 33329977)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 32964728 |
| GRCz11 | 1 | 33697296 |
KASP Assay ID:
554-0520.1 (used for ordering genotyping assays)
KASP Sequence:
TTATTCTGCATGTCAGGCAGTTCATTTCTCTTTCTGAAGTCTATTAAGTG[T/A]ATTCTGTCCTCTTCATGTCATGGCCAAAACACAATCTCTAATACAGTAAG
Long Flanking Sequence:
TTTAGAAAATGTAGTTATTCTGCGTTTACATTCATTGTTCAACTTTCCAACCCTGACTATTTTACCAAAAGGCTAATGTGCATCAGTTATTTTTTATTTAAATATATTCTGTATTTACTGGCTAAATGGCTATGGCTAAATGTGTAATATTTGTTTAGATTACATAATTAATTCGTAGTTTCTGAATACTTTCACTCTCACTCAACAGTTATTTAAATGTTACTTGCGATTAAAAACACATAAAAATAATTTTTTTTACAAATTATAAATTGTACTAAATAAAGGCCGTAAACCGACCATAATACCGATTGATACCGACCCTCAAACACAGAAAAACGGAACTAACATCACAACCCACATTTCCGGGGGAACTCAGTAAGAAGACGGACCGCGGAACAGTAGCTATGTAGTTAGAAATAAATTGCATCAATATCAATGTTTTCACCGAAATTATTCTGCATGTCAGGCAGTTCATTTCTCTTTCTGAAGTCTATTAAGTG[T/A]ATTCTGTCCTCTTCATGTCATGGCCAAAACACAATCTCTAATACAGTAAGCGGACAAAACGTATTACATCTGTGATTTAAATACGACAAAACACATAACACTAACATAATACTACGATAACAACTGCAATTCAATATTTATAGAATTTTATATCAACTACGTATTTAGTAATCAGTAAATGATAATTTCTATATTACATTATATACATTTTAATACTTTTAATTAGTTTTAATATTTAATTGTTCTCCATTTCAGCAGCTTGCAGCACAATATATATCTAAACCCCAGAAGCAGCTTTGTGAGACTGTACTGAAGTATTTTGATAGACAGTACAGTGAAGAGCTTGGAGAGCAGTGGTGGAATGCAAGGTGGGTAATAGGATTTTTAATATCAATTAATGCTGTTAAAAGTTTTATGCTTATTTAAATAAATTATTGTATTTTGATGTCAAAATTTTCATGAGAACATTTAAATGTATTTGCATTTAAATGGTTACTATT
Associated Phenotype:
Not determined