ZMP
si:dkey-91i17.1
Ensembl ID:
ZFIN ID:
Description:
Si:dkey-91i17.1 protein [Source:UniProtKB/TrEMBL;Acc:Q5CZR4]
Human Orthologue:
NOP2
Human Description:
NOP2 nucleolar protein homolog (yeast) [Source:HGNC Symbol;Acc:7867]
Mouse Orthologue:
Nop2
Mouse Description:
NOP2 nucleolar protein homolog (yeast) Gene [Source:MGI Symbol;Acc:MGI:107891]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36089 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16537 | Essential Splice Site, Missense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36089
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000063573 | Essential Splice Site | 546 | 658 | 16 | 18 |
ENSDART00000114272 | Essential Splice Site | 551 | 739 | 15 | 16 |
ENSDART00000130222 | Essential Splice Site | 551 | 739 | 14 | 15 |
The following transcripts of ENSDARG00000043304 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 19297241)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 17327564 |
GRCz11 | 16 | 17235541 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCAGAGAAATTATAAAGTGCATTTTGAAAATCTTGATCTCTTCTCTGTA[G/A]ATTCAAAGAGAAACGTTTCCATCCTTCTCTTAAACTGTCTCGACGATTCT
Long Flanking Sequence:
CACTTCATGGCCTCAAAGTTTTACAGTCTAAAAATTGTATACAAATCTTAGTTTCAAAACAATAAAGAAGCAACCTGTGAACTAAATCTGAGTTGATGGTGAAAGCCTTTTAAGTTTCTGTCTGATTATGGACTAAAGCAGATATTGCAACATTTTAGAGGAAAAGTGAAACAGGTAGATGTAAAATGTATTAATCTATATTTTAAAAGCTAAAGTATGTCTGCTGAAATATGCCAATTTTCTGTCCATTTGGTATGAGATTTGATTTGTCTCTATAGGTGGAAGAGAATGAGTGGGTGGTAGATTATGCTTTGAAGAAGAGAAATGTTAAGCTTGTCCCCACTGGATTGGACTTTGGCAAAGAGGGATTTACCAGGTAATGAGATCTTATTTGAAATTCATCAACAGTAATAAAGGTTATAGTCCTAGAAATTAAGTTCAAGTGTGTTTGCCAGAGAAATTATAAAGTGCATTTTGAAAATCTTGATCTCTTCTCTGTA[G/A]ATTCAAAGAGAAACGTTTCCATCCTTCTCTTAAACTGTCTCGACGATTCTACCCTCACTCTCACAACATGGATGGGTTTTTTGTGGCCAAGCTAAAGAAGCTGTCTAACACCATCCCTACTGCTCCAAAAGAAACAGGTGTGTGCTTATTTCAAAAGATTTTATCCACAAATTTGTATTGTATTTTATTTAAAATTTTTAAACATATTCCTTAGAAAATCAAGAAGAATCACTTGTAATGGAGACTGCAGCTTCATCAGAGATGAAAGAACAGAAGCCTGCTTCAACTCCAGAAAAAAGCAGCTTTGAAAAGAAACAGAAATTGAATCCTCAAACATCCAAGCCACTCATCGTTAAAAAGAAAGCTGAGAATAAAAAAACTGGCCCCAAAAAAGCCAAAATTGCCAAGCTGGATAGTGAAGCTGCAAAAAAGTTTGAGAAACCTAGCAAAAAACAGAAGGGAAAGCAAATGAATGGCAATCCAACAACAGAGGGGATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16537
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:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000063573 | Essential Splice Site | 651 | 658 | None | 18 |
ENSDART00000114272 | Missense | 657 | 739 | 16 | 16 |
ENSDART00000130222 | Missense | 657 | 739 | 15 | 15 |
The following transcripts of ENSDARG00000043304 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 19296846)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 17327169 |
GRCz11 | 16 | 17235146 |
KASP Assay ID:
2260-9473.1 (used for ordering genotyping assays)
KASP Sequence:
ACTCATCGTTAAAAAGAAAGCWGAGAATAAAAAAACTGGCCCCAAAAAAG[C/A]CAAAATTGCCAAGCTGGATAGTGAAGCTGCAAAAAAGTTTGAGAAACCTA
Long Flanking Sequence:
AATTCATCAACAGTAATAAAGGTTATAGTCCTAGAAATTAAGTTCAAGTGTGTTTGCCAGAGAAATTATAAAGTGCATTTTGAAAATCTTGATCTCTTCTCTGTAGATTCAAAGAGAAACGTTTCCATCCTTCTCTTAAACTGTCTCGACGATTCTACCCTCACTCTCACAACATGGATGGGTTTTTTGTGGCCAAGCTAAAGAAGCTGTCTAACACCATCCCTACTGCTCCAAAAGAAACAGGTGTGTGCTTATTTCAAAAGATTTTATCCACAAATTTGTATTGTATTTTATTTAAAATTTTTAAACATATTCCTTAGAAAATCAAGAAGAATCACTTGTAATGGAGACTGCAGCTTCATCAGAGATGAAAGAACAGAAGCCTGCTTCAACTCCAGAAAAAAGCAGCTTTGAAAAGAAACAGAAATTGAATCCTCAAACATCCAAGCCACTCATCGTTAAAAAGAAAGCTGAGAATAAAAAAACTGGCCCCAAAAAAG[C/A]CAAAATTGCCAAGCTGGATAGTGAAGCTGCAAAAAAGTTTGAGAAACCTAGCAAAAAACAGAAGGGAAAGCAAATGAATGGCAATCCAACAACAGAGGGGATAAAGGAGAAGAAAGAGGGCAGTCCATTCAAGAAGAAAGAAAACAAAACCAAAAAGAAGAACCTGCTGAAGAAAAAGAAGAACAGAATGGGGAAAAACAAATTTAAGAAGTTAAAAAGTATGCTTGGACAGCAAGAAAGTGGCCAGTGAACTTTAGTCATCTGACAGTAAATTGACATGGACCTATATGCTCAGGACTGGGATCTGTCAGTGGTTTGACCCAAGACAGTAAGTTAAACCAGTCCCAGCTTGCTGTTGGGGACTCAAAGATCATTCTTTAGTAACTTACACAGTGAATTTGTGTATTTATACTGCTTTTCAAGACTGTCAACCTTACTGATTCACCAAGAAGGTTACTTCAACCTTCTTGTGATATAAATGTCATAAATGTAAATGTCAT
Associated Phenotype:
Not determined