ZMP
nsun2
Ensembl ID:
ZFIN ID:
Description:
tRNA (cytosine-5-)-methyltransferase NSUN2 [Source:RefSeq peptide;Acc:NP_956005]
Human Orthologue:
NSUN2
Human Description:
NOP2/Sun domain family, member 2 [Source:HGNC Symbol;Acc:25994]
Mouse Orthologue:
Nsun2
Mouse Description:
NOL1/NOP2/Sun domain family member 2 Gene [Source:MGI Symbol;Acc:MGI:107252]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14653 | Nonsense | Available for shipment | Available now |
sa15958 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14653
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079181 | Nonsense | 122 | 706 | 6 | 19 |
ENSDART00000140336 | Nonsense | 182 | 766 | 6 | 19 |
The following transcripts of ENSDARG00000056665 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 28349277)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 28279389 |
GRCz11 | 19 | 27863612 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTCTTYATGAATTTNTAWATSTAGATTCTGGACATGTGTGCGGCTCCA[G/T]GATCAAAGACGGCTCAACTAATAGAGATGCTACACTCTGACATGGATGTG
Long Flanking Sequence:
AAAAATCTAAATTTGGTCACTTGAACCATGCAGGGTAAAGGCAGCCTTTGTTTTCAGATTACTTTATTTCATACAGTATGCTTTATCAAATATAAAATGTTTAGTGCAGTACATGTGATTTACTTATTGAACTATTGTTTTTTACCCTTTCACATCAGCGTTTACAACCATTATGTTTTGTGCGTTTTCTGATCTTTTCTCAATGAGTGGAGTAATGGTTAAAAGGTTAATAATGTTGATAAACGTTAATAAATTTGAATTGACCTTTAGTGTGTGATTATTTCCTTCATCAGGGAAATATTAGCAGACAGGAAGCAGTCAGTATGATTCCTCCTCTTCTACTGAAAATTGAGCCTCAACATAAGGTAGGTTTTAAACAACTTCATTAGTTTGCTTGAATACCAGGTGGATGTTTGATGTTTTCTTTGAGTATATTGTTTGTCTCCTCTGTTGTCTTCATGAATTTATATATGTAGATTCTGGACATGTGTGCGGCTCCA[G/T]GATCAAAGACGGCTCAACTAATAGAGATGCTACACTCTGACATGGATGTGCCTTTCCCTGGTAAACCTTTATTAATATTCATTTTTTTATGATGAAGTGAGTACTGTTGTGTGGTTTTAAAATCTATAGTTACTCTCAATTTCTTCTGTGTCTTCAGAGGGTTTTGTAATTGCCAACGATGTGGATAACAAGCGCTGTTACCTGCTGGTTCATCAGGCCAAAAGATTGAACAGTCCCTGTATTATGGTGGTCAACCATGATGCCTCTAGCATTCCACGTCTACACTTTGATAACAATGGGAAGAAGGACATCCTGTTTTATGACCGGATCCTATGTGATGTACCCTGCAGGTGAGGAATCTTCTTTTAGACCCCGACTGTGTTTACATGAGTCCCTTTTTTACCTTATTCTGCAATCTTGAATAAGCTCTTTTTATTAATTATTTATATACTTCTAATTCATTTGCCTGTAGGAAAATGACTTGGAATAACAAATTGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15958
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 |
---|---|---|---|---|---|
ENSDART00000079181 | Essential Splice Site | 142 | 706 | 6 | 19 |
ENSDART00000140336 | Essential Splice Site | 202 | 766 | 6 | 19 |
The following transcripts of ENSDARG00000056665 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 28349339)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 28279451 |
GRCz11 | 19 | 27863674 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTCAACTAATAGAGATGCTACACTCTGACATGGATGTGCCTTTCCCTGG[T/G]AAACCTTTATTAATATTCANTTTTTTATGATRAAGTGAGTACTKTTGTST
Long Flanking Sequence:
TTTATTTCATACAGTATGCTTTATCAAATATAAAATGTTTAGTGCAGTACATGTGATTTACTTATTGAACTATTGTTTTTTACCCTTTCACATCAGCGTTTACAACCATTATGTTTTGTGCGTTTTCTGATCTTTTCTCAATGAGTGGAGTAATGGTTAAAAGGTTAATAATGTTGATAAACGTTAATAAATTTGAATTGACCTTTAGTGTGTGATTATTTCCTTCATCAGGGAAATATTAGCAGACAGGAAGCAGTCAGTATGATTCCTCCTCTTCTACTGAAAATTGAGCCTCAACATAAGGTAGGTTTTAAACAACTTCATTAGTTTGCTTGAATACCAGGTGGATGTTTGATGTTTTCTTTGAGTATATTGTTTGTCTCCTCTGTTGTCTTCATGAATTTATATATGTAGATTCTGGACATGTGTGCGGCTCCAGGATCAAAGACGGCTCAACTAATAGAGATGCTACACTCTGACATGGATGTGCCTTTCCCTGG[T/G]AAACCTTTATTAATATTCATTTTTTTATGATGAAGTGAGTACTGTTGTGTGGTTTTAAAATCTATAGTTACTCTCAATTTCTTCTGTGTCTTCAGAGGGTTTTGTAATTGCCAACGATGTGGATAACAAGCGCTGTTACCTGCTGGTTCATCAGGCCAAAAGATTGAACAGTCCCTGTATTATGGTGGTCAACCATGATGCCTCTAGCATTCCACGTCTACACTTTGATAACAATGGGAAGAAGGACATCCTGTTTTATGACCGGATCCTATGTGATGTACCCTGCAGGTGAGGAATCTTCTTTTAGACCCCGACTGTGTTTACATGAGTCCCTTTTTTACCTTATTCTGCAATCTTGAATAAGCTCTTTTTATTAATTATTTATATACTTCTAATTCATTTGCCTGTAGGAAAATGACTTGGAATAACAAATTGCAGTACATGGTCAAACTACAACTGTTTACTCTACAAACAATTGTGTTTATGACAGAATATTAAAA
Associated Phenotype:
Not determined