ZMP
nol9
Ensembl ID:
ZFIN ID:
Human Orthologue:
NOL9
Human Description:
nucleolar protein 9 [Source:HGNC Symbol;Acc:26265]
Mouse Orthologue:
Nol9
Mouse Description:
nucleolar protein 9 Gene [Source:MGI Symbol;Acc:MGI:1921285]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24337 | Nonsense | Available for shipment | Available now |
sa9241 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa1022 | Nonsense | Available for shipment | Available now |
sa43985 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa24337
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 |
---|---|---|---|---|---|
ENSDART00000111755 | Nonsense | 22 | 713 | 1 | 12 |
ENSDART00000136941 | Nonsense | 22 | 175 | 2 | 3 |
ENSDART00000142124 | Nonsense | 22 | 713 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 23 (position 25244410)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25030530 |
GRCz11 | 23 | 24957071 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACACAAGGTTCATTCTCGGTCCCAACAGAGGCAGCGAAATGCATCTAAA[C/T]AACATGGCAAGAATAAGTGGAACAAAAAAGTGCGCAGCCTGGACTCAACG
Long Flanking Sequence:
TTAGATAAAAATATCAGTTTTACAGTATTTTGATTACTGCTCTAAATATATTCTTTTCAATGTCTGCATAAAAACACATTTGATCCCAATATATTTTGTTTTGAGAAACACTTAAAATATTTTGGAACAGTAAACATGTCAGGCTAAATAATTCAAATGAATTAATGACATCTGCTGTCTTCATTAGTTTCCAAAAGACAGATGTTTTCTGCTGCAGATACCATTGTCCTTAAAAAAAAAAGTAAATAAAAAATCTGAACGTATAGCAAAAAATGTTGGTGGTTTTAAAACTTTGGCTTTTACAAACCGCGCTATACCTTGAAACAGTTATCGTCCCATACCTAACTTCAAGTAATTCTGTCATAACTACTCATTTGTTCACAGGTGTTTCCTAGCTCTGGATTTATGTCGTTTATAGTCTCGTTGGGGGTCAGCGGATGACAATGAAAGTACACAAGGTTCATTCTCGGTCCCAACAGAGGCAGCGAAATGCATCTAAA[C/T]AACATGGCAAGAATAAGTGGAACAAAAAAGTGCGCAGCCTGGACTCAACGCTCCTTAATACCAGCTCAGGAACTGCAAAGTTGGAACAAGAGATAGCCAAAAAGGAGAAACCAGCAATAAAACGGTTGAAGAAGTTGTATGCGAAGCCTGTGACTCTTCTCTCTGATAACAACTGTGCAGACGAGGATAAAGTTAAACCCACTTCTGTGACTTTTGCTCATGTCCACACAAATGGAGGCACAGAACTGGATGACAGCAGCAGATCAGTGGACTCACAAGAATGGAGTGAATATGCCAACAGTGTTCTTCAGAACGGCATGGAGACTTCAACATTACCTGACTCAGACCAGGCGGAGGATGGGCTTCAATTCCATGCCCACCTTGATCATACCAAGAACCGTGCAGTGTTAGTCATGAAACAAAGTCAGGTAGGTTTACAGTACTCGAATACCAGAATGTCTAAATTTTGAATTTTTAGTTGTGTTTTTATGTATATCCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9241
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111755 | Essential Splice Site | 164 | 713 | None | 12 |
ENSDART00000136941 | Essential Splice Site | 164 | 175 | None | 3 |
ENSDART00000142124 | Essential Splice Site | 164 | 713 | None | 13 |
Genomic Location (Zv9):
Chromosome 23 (position 25244840)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25030960 |
GRCz11 | 23 | 24957501 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTTGATCATACCAAGAACCGTGCAGTGTTAGTCATGAAACAAAGTCAGG[T/G]AGGTTTACAGTACTCGAATACCAGAATGTCTAAATTTTGAATTTTTAGTT
Long Flanking Sequence:
TCAGCGGATGACAATGAAAGTACACAAGGTTCATTCTCGGTCCCAACAGAGGCAGCGAAATGCATCTAAACAACATGGCAAGAATAAGTGGAACAAAAAAGTGCGCAGCCTGGACTCAACGCTCCTTAATACCAGCTCAGGAACTGCAAAGTTGGAACAAGAGATAGCCAAAAAGGAGAAACCAGCAATAAAACGGTTGAAGAAGTTGTATGCGAAGCCTGTGACTCTTCTCTCTGATAACAACTGTGCAGACGAGGATAAAGTTAAACCCACTTCTGTGACTTTTGCTCATGTCCACACAAATGGAGGCACAGAACTGGATGACAGCAGCAGATCAGTGGACTCACAAGAATGGAGTGAATATGCCAACAGTGTTCTTCAGAACGGCATGGAGACTTCAACATTACCTGACTCAGACCAGGCGGAGGATGGGCTTCAATTCCATGCCCACCTTGATCATACCAAGAACCGTGCAGTGTTAGTCATGAAACAAAGTCAGG[T/G]AGGTTTACAGTACTCGAATACCAGAATGTCTAAATTTTGAATTTTTAGTTGTGTTTTTATGTATATCCACACAAGAATGGCCATTATAATTCGCTTGTTAAGTGTGACGTCATGCAAAGCAGTTTCCAGGTCCAATCCACATATATATTTATTATTATTATTATTTATTTATTTATATATATTTTTAATGCCCTATATCTGATAGCTAGAAAATGACTAATTTTTTATAAGTTGTTAAAATATTGGTGTCTGTAATGCTGCAAGTCCAGAGTTTGTTGTGTACACCATGATTTTAAATAAAATTCTCACTTTTTAATCTGTGCTATGACTAAAAAGGGAAAAAGTGGTCATAAACCAATATTTTCTTAATTCAGATGAGTAGCGGCTTGGACCTGGAAACAGTATTTTAGGGAGTTATGTAGTTGTTATATATTGTTATGAAGTTTATATTGTCTTGTCACAACTTAACAATTGGATGTTCATAAATTCTTCACCTAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1022
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 |
---|---|---|---|---|---|
ENSDART00000111755 | Nonsense | 195 | 713 | 2 | 12 |
ENSDART00000136941 | None | None | 175 | None | 3 |
ENSDART00000142124 | Nonsense | 195 | 713 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 23 (position 25246709)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25032829 |
GRCz11 | 23 | 24959370 |
KASP Assay ID:
554-0926.1 (used for ordering genotyping assays)
KASP Sequence:
GGTCATGTAGAAGTGCTGGGCTTCACCATAGAGGAGGGTCAACAGCCTTA[C/A]CCTSTGTTTTCACCACCGACCCACTGCCCGCTCACTATCACGGCCTTAGG
Long Flanking Sequence:
CAAAAAAATTAAATATCCCAATATATTTTCCAACATCGTGCAGCCCTATTAGTTGCTATAACAAAGACAGCAAAAGCTCTGAGATCAAATTCCCATTTCCACATGCACAGCAAGGTGTTACGAGTCAGCCTAGAAGTCTTATCACAAAAAAACTCCTATAAATCACGAACAGAGAACTGCAGATGTTAGTTGAGATCAGAAAGGCTCCAAAAGTACAATCTAAAGTAATTCTTTTTCACAGTTGTCTGTCTTCATTTTAACCATGGTTGCCAATATAAGTAAATGGTACTGTATTCGAGGTTGTCATCAAACCATTGATGAAATTAAATGAGAACACATTGGCACTGTCAGCCAATTTGTATGTTTTGGTTGGTTTACCAGTAGTTTATGCTAGTTTTGTCTCTGCAGGTCTTGTGTTTTCGTGGGAAGTGCCTGCTCACTTGCCTCTATGGTCATGTAGAAGTGCTGGGCTTCACCATAGAGGAGGGTCAACAGCCTTA[C/A]CCTGTGTTTTCACCACCGACCCACTGCCCGCTCACTATCACGGCCTTAGGAAACAACCAGTCCTCCAGCAAGAACAAGAAAGAGGGCCAGCTGGAAGCAAAAGCCATTGTTCGCAAATATTTCACAACAGGTAGCACTTTCACTTATAATCTTAATGACTTTCTTTCTCTCAAATCTGATTTTAAGGCAAAATATTCCAGGTTAAAATTTTACAATTATTTAATAATAATAATGATTTGTTGATTGGGTGTTTTTTTTTTTTTTCAAAATAAAACATGAATTCTGTCTAGAATTTTTTTTCAATTGAAATGGCTTTAGTTTACTTTCATTCTAAAATAAACAGACATAAATTAACAAATAAAATTGATAAAAGAAAATACCAAAATAGAAATGCAAGCACACAAATTGTTTAGTTTACTTTAATTTAAATTTAATTTTACCTAAATCTAAAATAAACATCCCTAAATTAACAAATTAAATTGTTTAATACATTTTTTTAA
Associated Phenotype:
Data not yet available
Mutation Details
Allele Name:
sa43985
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111755 | Essential Splice Site | 282 | 713 | 3 | 12 |
ENSDART00000136941 | None | None | 175 | None | 3 |
ENSDART00000142124 | Essential Splice Site | 282 | 713 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 23 (position 25247775)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25033895 |
GRCz11 | 23 | 24960436 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTCTCTCCAGCTTTTCTGAACTCACTGAGCTATTCGGCCTCAACTCGG[T/C]AAATATAGTGCTATTTCAGATATTACACTCTGACATTTTAGTCACTGATG
Long Flanking Sequence:
TAACAAATATTAATAGTTACATAAATACATACATTAAGTTACGTTAGTTACTCTGTCCTAAAAAAACACAGTTTTTAATGCATTTCTTGAGTGCAAATGTAAATGATGGATAAAGCCAAGTTGAAAATAGGAAATTATGAATTGTTTACAATAATTTTATCAAAATACTTTAGAGTCCTAGGCTTTAACTGAGGGGATATTTTATCCCCCATTATCTCAGAAAAATCTTGTCATAAAGGCATTCTTTATGAAAAGCTAAAATATCAAAACAGTCCATGAAAAAAATGTTTCTGCACAGATTTTTTTCTGCACCTGCTTTCCAAAGATCAGCTGCAATTTTTCTCTCTTTTTGTCTTTTCTTTTTGTAGAGCCGAGTAAAAAGCTGATGAATGAGGTGGATTCGGATTCCTGTGTGGTGCTTCTGGAGTCTCTGGACACACCACTCACTCGCTTTCTCTCCAGCTTTTCTGAACTCACTGAGCTATTCGGCCTCAACTCGG[T/C]AAATATAGTGCTATTTCAGATATTACACTCTGACATTTTAGTCACTGATGTGTCTGTTTCAATGTTAGAATGATGAGGTTTTATGTGCAGAGGCGGCTGTAAAAAGGCATTTGTAGTTTGACTCTTCAGAAGAATGTAAACACTGACTGTTGCCTTTGACGTTGTTTGTTTGAACACCCTGGCATAGCAACATGGATATATTTGTGTTTGTTTATTCGTCCTGCAGAAGGAGTTGAAGTCTCAGGCTGCCATCTATAGCCCTGTCCTGTCCGCTGTGGGTGTAACGGCTCTGCGTGGGCCTTGTGCACAGGGTCTGGTCATGTCACGCAGCTACAAAGAAACTATAAGCAGTTTGCTCAGTGCCTGGGCAGGTAAATAATGTAAAATAAAATTGAGAGGTAGTTAATCCAAAAAAAAAAAACTAATTGACTTTTTTTTATATCCTTACCAAACATGCATGTATTTGTAAAATAAAAAATAAAATAAAAATAAAAAAGTTA
Associated Phenotype:
Not determined