ZMP
zgc:109901
Ensembl ID:
ZFIN ID:
Description:
Nucleolar protein 11-like [Source:UniProtKB/Swiss-Prot;Acc:Q4V9P9]
Human Orthologue:
NOL11
Human Description:
nucleolar protein 11 [Source:HGNC Symbol;Acc:24557]
Mouse Orthologue:
Nol11
Mouse Description:
nucleolar protein 11 Gene [Source:MGI Symbol;Acc:MGI:1916229]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17711 | Nonsense | Available for shipment | Available now |
sa40674 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30872 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33853 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa33852 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa26731 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17711
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 |
---|---|---|---|---|---|
ENSDART00000037709 | Nonsense | 80 | 708 | 2 | 18 |
Genomic Location (Zv9):
Chromosome 6 (position 21587637)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 17903411 |
GRCz11 | 6 | 23001330 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGACAGTTGATCACCTGYCCCGCTGTGTATAACACAAAGTCCCAGGAATA[T/A]GTGGYTGTTACAGATAATAAGGTAAGGTGATATAATATTTTATATTATAA
Long Flanking Sequence:
CGAAGAAGAAGTAATTGTCTCATCTCGCGATAGAAACAACTCGAGGGTAGAAGAAACATGGCAACGCTGTATGAGGAATACACGCTGTGTGGAGTTGGACCAGACAAGAATTCGTCCAGTTCAGGAGTTCTGGGGATTGAATTGGGAAAAGATGTTGACCACATAATTGTCACTCACTCTTCGAGAGCAGTTACAGTTTACAAGGTAAATGAGTAACAAAAATGATTGCACGCGGTGATGGGAAAATTCCAGCGTGTAAGCTAACGTTATATTGACCAAACACAAACAAGTGCATTGCTTTATTATTTGGAATCTAATGCTAATTTTTAACTATATAAAACATGTTTAGTTGGAGATTTAGTAGTTGTTTGTGTAATTGCGTAATTTCATAAGTGTTTTGATGATTAGGTGTCTGATCAGAAGCCCACGGGCAGTTGGACAGTGAAACAGGGACAGTTGATCACCTGCCCCGCTGTGTATAACACAAAGTCCCAGGAATA[T/A]GTGGTTGTTACAGATAATAAGGTAAGGTGATATAATATTTTATATTATAAAGAATAAGAATGCTCCAAGTTCATGTCTTGTAAACTTAAGCATTTTTTTAGGTTATCAGAGTTTGGAAAGAAGACGATGTCAATATGGAGAAGGCGTTTAAAGCCACGGTATGTGGACTAATATTTCATAAGGTTTTATTTGTCAATATATTACACGTTATGTGGTTAAATTTAAGTATTTTTTTCTGGCTTAATCAATTGAAACAGTTTTTCTAGGAATATTTTTGATCGATGTAAACATTACAACCATACAAAATACAAAATCATGAAAACTTGGAGTACAATGCAATAAATAAATAAATAAAAATGGGAGTTTTCAGGTTAGTTCCAGATTCTCTATTAATATATAGTACTGTAAGGCATTTTTTCTTAATTTTAAACGACAAAGTAATAACAAATTTTTGTGAAGCACTTTATAAATTCATTGGTCAAAATGATTTCTCTATAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40674
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037709 | Nonsense | 125 | 708 | 4 | 18 |
ENSDART00000037709 | Nonsense | 125 | 708 | 4 | 18 |
Genomic Location (Zv9):
Chromosome 6 (position 21584931)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 17900705 |
GRCz11 | 6 | 22998624 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTGATGTTCTCAGGGTGATGGCAGCTTCTGACTCTGAACCTGTTGTGT[T/A]GTTTAGTTGTGGGGCTGTCATGTTCTTGGACTCGTTGCTTGCTTCACCAC
Long Flanking Sequence:
TTATTTTCTATTTGATTACCGATGACTGCTTTGCAGCTTTCATTATTGAATTTAATTATTATTTATTATAATCTTTTGTTTGTTTTGTAGCAAAAATATTATTTATTAAATTGACATGCATATAAAAACAATAGTACAGAAATAAATATTATTACTGCAAAGTTTTATTTGTGTTTGATGCAAACCTTAAATGTATTTTTCATAAAGTAATAGTAGGACATTTTATAGCACAAAACTTGCATTCAAGCACATTCAAGGCAGCATGATAATGAGAAATGTAATTCATTGCTAGTATTATTGTCATAATCGTCATCATTAATATTTTATAATTATTAGACTTTCATTTTGGAATCATTTCGAGCCATGAAATGTATTAGGTGAAGCTGATTTTGAAACCATGTTTGGCTTTGTAACCTAAATTGTATTTTTTCCTCACTCGTTTCAGGTTTCATCTGATGTTCTCAGGGTGATGGCAGCTTCTGACTCTGAACCTGTTGTGT[T/A]GTTTAGTTGTGGGGCTGTCATGTTCTTGGACTCGTTGCTTGCTTCACCACAACAACCTATAGAAGGCGTTTTAACAGAGGAAGAGTTCATCAGGTTAGAACATACAAGATTATTTAATTACTTTTGTCCTGAAAACACATTGGTAAACCTATCATTTAATATTGAATTAGCTAAATGCTTTTCTTAAATGTAATGGTCCACAAAAATAATAAAACTTTTGATGGATTTACTGCTCCCTTAGGCAGCCTAAGTCTGCATATGAAATTCACAGCTATTAGCTGAACCATGTAATCGATCTGTTGATGGATCTGCAATTTTGGATTAACACTTTCAGATGGATCAACACTGTCAGAGAGATTTCAAATGGTGTGTCAGTGATGTCATCACACAGGCAGCCAATGGTCTTTTTCACTTTTTGATGGCTCCAAACTGAAAATTTAATTGGCCTGGTTTTAGGCACAGGTTTGTGTTTTTAGTGACACTTATTGTTATTGATGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30872
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037709 | Nonsense | 125 | 708 | 4 | 18 |
ENSDART00000037709 | Nonsense | 125 | 708 | 4 | 18 |
Genomic Location (Zv9):
Chromosome 6 (position 21584931)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 17900705 |
GRCz11 | 6 | 22998624 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTGATGTTCTCAGGGTGATGGCAGCTTCTGACTCTGAACCTGTTGTGT[T/A]GTTTAGTTGTGGGGCTGTCATGTTCTTGGACTCGTTGCTTGCTTCACCAC
Long Flanking Sequence:
TTATTTTCTATTTGATTACCGATGACTGCTTTGCAGCTTTCATTATTGAATTTAATTATTATTTATTATAATCTTTTGTTTGTTTTGTAGCAAAAATATTATTTATTAAATTGACATGCATATAAAAACAATAGTACAGAAATAAATATTATTACTGCAAAGTTTTATTTGTGTTTGATGCAAACCTTAAATGTATTTTTCATAAAGTAATAGTAGGACATTTTATAGCACAAAACTTGCATTCAAGCACATTCAAGGCAGCATGATAATGAGAAATGTAATTCATTGCTAGTATTATTGTCATAATCGTCATCATTAATATTTTATAATTATTAGACTTTCATTTTGGAATCATTTCGAGCCATGAAATGTATTAGGTGAAGCTGATTTTGAAACCATGTTTGGCTTTGTAACCTAAATTGTATTTTTTCCTCACTCGTTTCAGGTTTCATCTGATGTTCTCAGGGTGATGGCAGCTTCTGACTCTGAACCTGTTGTGT[T/A]GTTTAGTTGTGGGGCTGTCATGTTCTTGGACTCGTTGCTTGCTTCACCACAACAACCTATAGAAGGCGTTTTAACAGAGGAAGAGTTCATCAGGTTAGAACATACAAGATTATTTAATTACTTTTGTCCTGAAAACACATTGGTAAACCTATCATTTAATATTGAATTAGCTAAATGCTTTTCTTAAATGTAATGGTCCACAAAAATAATAAAACTTTTGATGGATTTACTGCTCCCTTAGGCAGCCTAAGTCTGCATATGAAATTCACAGCTATTAGCTGAACCATGTAATCGATCTGTTGATGGATCTGCAATTTTGGATTAACACTTTCAGATGGATCAACACTGTCAGAGAGATTTCAAATGGTGTGTCAGTGATGTCATCACACAGGCAGCCAATGGTCTTTTTCACTTTTTGATGGCTCCAAACTGAAAATTTAATTGGCCTGGTTTTAGGCACAGGTTTGTGTTTTTAGTGACACTTATTGTTATTGATGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33853
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037709 | Essential Splice Site | 291 | 708 | 8 | 18 |
Genomic Location (Zv9):
Chromosome 6 (position 21572997)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 17888771 |
GRCz11 | 6 | 22986690 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATCACCATGGGCTTTTGGTGCGATGATCATTATGATGTTGTCATTTGC[A/T]GATTATCTTTGCATCTGGAACAAACATTTCCAAACTCTTCAGGCTTGTAA
Long Flanking Sequence:
TGTAAGAGTCATGTGTTCCTATTTTTTACTTATTTATTTTTATATAATTGCAGATGTTACAGTAGGCTATTTCATATTATCATTGATCTGCAGCTATAATCAAATCCTGTTTATGACCTTAAGTTAATAATTGATGTATAAGTATGTGTGAATAAAGCGTCTGTTTTTTGAGAAGTGGTTCTCATATGTGAACGCTCCGTACAGCTTTACTTTTACATTTCTTTGAAGCGTCAACTGCAGCTTTCTGTCATACACCACACCTTTCAAAAGGGTACAGTTTTTTCAGTGGATACACAAGCCTGATAAATGTGACCCGTACTGTACTGAACTGTACCACTCTGTGTAAACAATAAAAATAAAAACAAGTATAAAGTAAAAGAAACATCAAAGTAAAAGTTTATTCTCAGAGATTTTCTTAACAACCCTTAGAACAACACCCCTTCCTTTCTTTTATCACCATGGGCTTTTGGTGCGATGATCATTATGATGTTGTCATTTGC[A/T]GATTATCTTTGCATCTGGAACAAACATTTCCAAACTCTTCAGGCTTGTAAAGAATTGGCCGGAACAATCTACAGTCAGGTGTGGTTATTACTTATCACCTTTATTGCTATTCTTATTACACTTCTACAAATCTTGAAATAATCTTAATAATTTATTTGTGAAAAATAAAAAAACATGAGGAGAAAACTTTTTTTTCTGAATACAGATCTGGTGTTATTCTGGAAAGCTGTACATTCCTCATGGGAAGATACTATCAGTAATTTCTTTTGAGTGCCAAAAGTCATCTCTCGCGGCTGCCATGGGAAAACTGAAGCAGACAAATCAAAGTGGTAAAGATTTGAAATTTCATTTGAAATATGAAAAAATCTGTCCTAATCTTTTCTTCAGAATATATAAAATGAGGCCAAAATATTAAAGTAAAAATCCCTTTTTCCTTCTCTTCAGAATACAAATCACACACCCCCTTGTCTTCCTGGACGGCTTTGCCGCACAATGACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33852
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037709 | Nonsense | 292 | 708 | 8 | 18 |
Genomic Location (Zv9):
Chromosome 6 (position 21572991)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 17888765 |
GRCz11 | 6 | 22986684 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATGGGCTTTTGGTGCGATGATCATTATGATGTTGTCATTTGCAGATTA[T/G]CTTTGCATCTGGAACAAACATTTCCAAACTCTTCAGGCTTGTAAAGAATT
Long Flanking Sequence:
AGTCATGTGTTCCTATTTTTTACTTATTTATTTTTATATAATTGCAGATGTTACAGTAGGCTATTTCATATTATCATTGATCTGCAGCTATAATCAAATCCTGTTTATGACCTTAAGTTAATAATTGATGTATAAGTATGTGTGAATAAAGCGTCTGTTTTTTGAGAAGTGGTTCTCATATGTGAACGCTCCGTACAGCTTTACTTTTACATTTCTTTGAAGCGTCAACTGCAGCTTTCTGTCATACACCACACCTTTCAAAAGGGTACAGTTTTTTCAGTGGATACACAAGCCTGATAAATGTGACCCGTACTGTACTGAACTGTACCACTCTGTGTAAACAATAAAAATAAAAACAAGTATAAAGTAAAAGAAACATCAAAGTAAAAGTTTATTCTCAGAGATTTTCTTAACAACCCTTAGAACAACACCCCTTCCTTTCTTTTATCACCATGGGCTTTTGGTGCGATGATCATTATGATGTTGTCATTTGCAGATTA[T/G]CTTTGCATCTGGAACAAACATTTCCAAACTCTTCAGGCTTGTAAAGAATTGGCCGGAACAATCTACAGTCAGGTGTGGTTATTACTTATCACCTTTATTGCTATTCTTATTACACTTCTACAAATCTTGAAATAATCTTAATAATTTATTTGTGAAAAATAAAAAAACATGAGGAGAAAACTTTTTTTTCTGAATACAGATCTGGTGTTATTCTGGAAAGCTGTACATTCCTCATGGGAAGATACTATCAGTAATTTCTTTTGAGTGCCAAAAGTCATCTCTCGCGGCTGCCATGGGAAAACTGAAGCAGACAAATCAAAGTGGTAAAGATTTGAAATTTCATTTGAAATATGAAAAAATCTGTCCTAATCTTTTCTTCAGAATATATAAAATGAGGCCAAAATATTAAAGTAAAAATCCCTTTTTCCTTCTCTTCAGAATACAAATCACACACCCCCTTGTCTTCCTGGACGGCTTTGCCGCACAATGACATTATAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26731
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 |
---|---|---|---|---|---|
ENSDART00000037709 | Essential Splice Site | 512 | 708 | 13 | 18 |
Genomic Location (Zv9):
Chromosome 6 (position 21566179)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 17881953 |
GRCz11 | 6 | 22979872 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGACATTCCTGAAGCTGTTACCTGTGCTTATCTCAAAACCATTTTGAGG[T/C]GAGTCTTCAACTAACTTTTTGTTAACATTTGTTACATTTAAAAATTAAGT
Long Flanking Sequence:
TTGCTGTATATTTTTGTATTTGAAGCGGTATATACCCATAGATTATATTCTTTAATTTGATGACCCAATTTACTTATTTACCAGACTGCTGTGGTAGAGGATGTGCAGTCAGCGGTGGGTGAATTTATTCATCAGACTCCTCAGACTGACCTTCAGCTTGCAGCAGGGAAAGTGACAATGGTGCTAGTGTCAAGATCCCAGACAGATGACAGCTTCTACCCTCAGCGTGCATTTCTACAACTGCTAGACACTCGTTATCTCTGCTACAGGTTTGAATATACAATCAGCTCTGTGGACACATTTGTCTACCAGGTACTCCAATGTAAATCTCTATTCATTCATTTGTTTTGTTTGTTTGTTTTTGGATATGTAGTGTTTGCCCAGAATTGTTGTCTCTGGCCATGGCAAAGAGAGATTTTCAACTCTGTCAGATTGCTTTCCAACTTTTTCCAGACATTCCTGAAGCTGTTACCTGTGCTTATCTCAAAACCATTTTGAGG[T/C]GAGTCTTCAACTAACTTTTTGTTAACATTTGTTACATTTAAAAATTAAGTCACCATAATCCATAGGGGTGTAATGTTCAAAACGAACCAAAAAAAATATGGTTTGTACATAGCAAACCGAGGTTCCCCCTCCCATCTGTTTGTGACGCACTGATTGATTGATTTATTGATTTTTAGTTTACTCAGATCACCTGACTGCAATAAACAGACAGGTGAAGCCAATGTATAAAGTTATTTGCACAAATGTCTTTTAAACAAGTTAAAAAAAAACAACTTTTGTTTGACTATAGTACTCCAGACTCTGAGATGGAGACTCTAACCCTTGACACAGAGAGCTTAATCATCATGAAAGAAATGAGTCAAGCTCAAAGTCAAATGGAGGAAGGTGAGCAGCAGAACGAGAACGGTGTCTCTAGCAGCAAACAACAGAGGGATTTCTTGTCCATGGATATGAAGTGTCCTGTGGGATTACACAAGGGTGTCCTTCTGTATCCTTTGTTT
Associated Phenotype:
Not determined