ZMP
noc2l
Ensembl ID:
ZFIN ID:
Description:
nucleolar complex protein 2 homolog [Source:RefSeq peptide;Acc:NP_001003830]
Human Orthologue:
NOC2L
Human Description:
nucleolar complex associated 2 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:24517]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39407 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13675 | Nonsense | Available for shipment | Available now |
sa32441 | Nonsense | Available for shipment | Available now |
sa29917 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa18365 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39407
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091662 | Essential Splice Site | 50 | 748 | 2 | 19 |
ENSDART00000122945 | Essential Splice Site | 50 | 744 | 2 | 19 |
ENSDART00000141853 | None | None | 187 | None | 6 |
Genomic Location (Zv9):
Chromosome 23 (position 23472481)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 23251788 |
GRCz11 | 23 | 23178339 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCCTCACCAAAGAAAGGAAAGAGCAAAACGCCTGCACTTCAGAAAACG[T/A]AAGCAAATGCTTTACATTCAGATGGTCATTCCAGTGTTCTGGGCCCAGTT
Long Flanking Sequence:
TATATCATACTGACTGTAGTATTGTGCTATTATGTGTCATCTATTAAAATTAAATGTTTTATTTTAGGCATATTAAGTCTCATTTCATTTTAATCAGTTGTGATGTATTCAGTTATTCAATAAAAATATATAATAGAAGATAATTTAGTTAGAACTAATTAATATATTATTATTAATTATAAAAATATGTTTACTTTCTACAGCACTTAGTCAATCCAAAGAGTGCTAGACGAGCAAATGTAATCAAAACAAGCTAGTAAAAGATACAATCCCAAACACATAATTCCTACTATGGCCACAAATATCTAGACTAACTGTAAACAAAAAAAAGATTGGATTCTTTCATGATATCTATGTTATGTTTTTGCAGAAAGTTGGAGGATCTCAGTGTGGATGAGTTCATGTTGTCTGGGTTTGATTCTGATGAGGAAGATGACTGTGAGGATGAAGAACCCTCACCAAAGAAAGGAAAGAGCAAAACGCCTGCACTTCAGAAAACG[T/A]AAGCAAATGCTTTACATTCAGATGGTCATTCCAGTGTTCTGGGCCCAGTTTTTCAAAAGGTTTAATTCGGATAAAATTGATCCGGATTTAGTCATCCTGTTTTTGCGATCTGTGATCTCGTAATCCAGAGATAATTTTTGAGCCAGTTTTTCAAATCAACATCGGATTGGATCAATCTGTATCGGATAGGAACTTTTCAGGATCACTAAATCTGGATTACCAGTGCTCATTCAGGATAGGAAATCACAATCTATTGATACGTAAAGAGCAACAAGTAGAATAGCCAGTGTGGGGTCAATATAACTTTATTTTTATTTCAAAAGATAACACACACATTTAAAAAAAAACTTAAAACAAGAAAAACCCCAGCCCATCCTTGTACAGCAATCCGCTCATCTGAGACCTACAACACAAACACTGTACATTTGAGGATATTTAACAAGTTTCAAATATAGATGTATTGAATTAAAAAGGCCTTAATGTCAAAACCTCCACAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13675
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 |
---|---|---|---|---|---|
ENSDART00000091662 | Nonsense | 241 | 748 | 7 | 19 |
ENSDART00000122945 | Nonsense | 237 | 744 | 7 | 19 |
ENSDART00000141853 | None | None | 187 | None | 6 |
Genomic Location (Zv9):
Chromosome 23 (position 23467286)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 23246593 |
GRCz11 | 23 | 23173144 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTNATTTTAGATTAGTACTTCCATTTTCAAGTACCAGGTGGCAGAAAAAT[C/T]AGATTGATATTAAGATGTACCTTGCTGGTGTTGTTCAGGTATTTTTTTTT
Long Flanking Sequence:
ACATTTATGAACGTGGTACTTTAGCTTGTGGGAATTTTACCTAACCATATTATTTCTCATAAATATAAAAACAAAAACCAGTATAAGGATATTTTTGCCTTCATAACAATAATAATTGTGGCATTCTAACTGCATTTTATTAGGCTTTGTCATGCAGTGATTTCTCAAGACATTTTTTTTCTTAAATGCATAATAAATGACACCTGATAATGTTTATGTATTTATGATGTTAAATATGCTCACTGGCAGTTTCTCTATTTCCTGTATTTCCAGTGTTCAATTCCCTCGTCCTGTTCTGTATAAGAGACATGCATGCAGCTCTGCAAAAAATGCTGAAGCTGAAAACTCCAGATAAGGACACAAAAAAGTAAAAAAAATCTTTATGTCCAGCTATGTATATATTTTTTAATTGATCTGATTGTTGATAAATTGTGTTTGTTTTTTGTTTTTTTTATTTTAGATTAGTACTTCCATTTTCAAGTACCAGGTGGCAGAAAAAT[C/T]AGATTGATATTAAGATGTACCTTGCTGGTGTTGTTCAGGTATTTTTTTTTCCTTCTAAATATGTTGGATATATGATATATCTTGAACTAATTCTTGACTTTCAGTGCTGACATGTAGAGTTTTGTGATGCATGTTATCATCCTCAGCTCCTCTCCAGTTTAACTCAAGCCACAGTTATAGCTGCAGTTCTCCGTCACGCCAACCAGATGGTGCCGTACTACCTGTGTTTGCCAAAACAGTGCAGGCAGTTTCTCAAAGTAAGCACTGTGCATTCTTAACATAAACTTTATGGTTATGGTTTTATGCAAGCACAAATTCATCATCTGTGCTGTTTTTTTCAATTGTGACACTAGAGTCTGATCAAACATTGGAGCACAGGAGAGGAGACCGTCAGAGTTCTGGCCTTCCTGGCCCTCAACAAAATCTGCAGACATAAACCAGATGCCCACCTGAGCGCTGTTCTTAAAGTAAGTTTGATTTTACAAAGCAATGTGAAACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32441
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 |
---|---|---|---|---|---|
ENSDART00000091662 | Nonsense | 413 | 748 | 11 | 19 |
ENSDART00000122945 | Nonsense | 409 | 744 | 11 | 19 |
ENSDART00000141853 | None | None | 187 | None | 6 |
Genomic Location (Zv9):
Chromosome 23 (position 23465098)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 23244405 |
GRCz11 | 23 | 23170956 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTACAACTGGCAGTATGTGCACTGTCTATATCTGTGGTGTAGAGTGT[T/A]GAGCACTATTTACCCCAGTGAGGTTTTGGAGCCACTGATCTACCCACTGT
Long Flanking Sequence:
TATTGTTATTAAAATCTTATTGACCCCAAACCATTAAGCAGTAGTGCATACTAGAAAAAGGAAGCAAAACATAAGATCAGCTCCATTATAAGTTAAAATGCTTGAAGATGGCAAAGTTTATGATCATTGCTTTTTTTTTATTGTTTGCAGCAAATGTACATTGCCTACGTGCAGAACTGCAAGTTCACGTCCCCCAACACTCTTCCCATGATTAACTTCATGCAGCGGACTCTAGCTGAGATGTACTCACTGGACACACAGGTGTCCTACCAGCATACCTTTCTGTACATTCGTCAGCTCGCCATCCACCTCAGGAATGCCATGAACTTGAAAAAGAAGGTAGTTGGAAGTCTTGTTCTCTTGCACTCTTATCTTTTAGCCATCATATGAGAACTATGTCTAATGTTTTTGGATACTCTGATTCATGCGTTTTCAGGAGACATACCAGTCTGTGTACAACTGGCAGTATGTGCACTGTCTATATCTGTGGTGTAGAGTGT[T/A]GAGCACTATTTACCCCAGTGAGGTTTTGGAGCCACTGATCTACCCACTGTGTCAAGTCATCATCGGCTGCATCAAGTAGGATTTGTAAAAATTATTTATTTATTGTTATTTTTCATTAGCATTTGAGACATCACTATTTTCTAATAATAATAATCTCTTACATTTTATATAGCACTTTTCTGGACAATCAATGCGCTTTACACATTTTTGGGGGGGAATCTCCTCATCCACCACCAGTGATTTAAGAAAGATTTAAACTAGATGTTAAAGATTTAAACACAGGGGTGATAGCGTTCCGGCACCACGCCGGATTTCCGGCGTACTGTGGCAGCGGGGAAAAAAAATCAGGTTCACGGATATTGATCTGTCATGTCTCTAGATTCACAGAATTCACTCACTGCTGAAAGCGCCGGATTGTGTTTTATTAAGCAGGGGCGTAGATTTAGGGTGGTCGGTGGGGACGTGTGCCCACCAATATCCACAAACTACTGAAATGTCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29917
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 |
---|---|---|---|---|---|
ENSDART00000091662 | Essential Splice Site | 633 | 748 | 16 | 19 |
ENSDART00000122945 | Essential Splice Site | 629 | 744 | 16 | 19 |
ENSDART00000141853 | Essential Splice Site | 134 | 187 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 23 (position 23431989)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 23211296 |
GRCz11 | 23 | 23137847 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAACTTCGGGAAAAGGAGATTCAGCTGGAAATCTCAGGAAAAGAAAGGG[T/G]AAAAAAAGCCAAATCCACAGCAATTATCAGGATTAAATCCAAATAATTCA
Long Flanking Sequence:
TTTCCTTCTGGTAAACATTTATTAATGCTGTGATGGAAAAAGGTGTGCACCAAGGGCCTCTACTAGGTCCGCTTCAGTTTTTTAAAAATGGCTAAAATCGACTTGATGCTTAATTAGTTTGACTAAAGGGTATAGCAGTAGACCATACAATATATCAACTTTTTTTAAGTGATGCAGGCGGACTCTGTTTTTCGGGGAGGGGTTATTGATCAGCAATAACAGAGCAGCCCTGTGTGTACTCATCATGTCTTACAATAGTACTTTTCGAGTAACTTCATGGCTTTATTTTGTTGAGAAAGTGTATTGAGATCCCTTTTGTTTAGTTCTCCTATGGGTGAACATGGAGAAGCATTCATTGTGTGTGTTTATTTTGCTGTGTTTACAGGCAGCCTGGGAGAAGCTGGTAGCAGAGGAAGGCACTCCACTCACTAAATATTACAGCCAGTGGAAGAAACTTCGGGAAAAGGAGATTCAGCTGGAAATCTCAGGAAAAGAAAGGG[T/G]AAAAAAAGCCAAATCCACAGCAATTATCAGGATTAAATCCAAATAATTCAAACCACATTTTGCATTTAGACAGAACGTATCTGAACCCTCATGTTTCACAACTAAGAGCCACAGTACAATGCGGTTGTTTGATCTGCAGGAAGAATCAATTTATTTTGATTATGTCATTGAAATTGCTGTTTATCCCATCGCTATGTTAATTCTCCTTCTCTATTAAACGCACAGATGTGGTCCATCTTTGCGAACTAACGTAGTGCTAGTTTTGTCAAAGTACCTACTGTGTGGTTTTGTTTGTGTGTGCGCGTGTGTGGAGAGAGCTGGAGAGTGTCCATAGGGAGATAATGGAGATGACACCAGGCGGAGTGTTGGCGTCTAGGAAGCGGCAGATTGGCGGAGGAGGCGGCAGGGCTATTGCTACAGGAAGAGTATTATAGCGCTCAGGGCTGCGTCCCAGGCTTTGATCCACTGAGTCCCCACGCTCAGATCTGATTACCACTGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18365
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 |
---|---|---|---|---|---|
ENSDART00000091662 | Nonsense | 724 | 748 | 19 | 19 |
ENSDART00000122945 | Nonsense | 720 | 744 | 19 | 19 |
ENSDART00000141853 | None | None | 187 | None | 6 |
Genomic Location (Zv9):
Chromosome 23 (position 23420918)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 23200225 |
GRCz11 | 23 | 23126776 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACCRGAAGCAGCCTTCATCTTCTAAGGGCAAAGCTCCAAAGAAGATGT[T/A]GAGTACAGAGCTGAAACAGGTGGCTGAGGGAGATGAAGATATGGTTGAGG
Long Flanking Sequence:
TTCATCCTTTGATAAAAGTTTCTGAAGGAAAACAAATTGCTTTGGGTTGAATCTTGCAGATAAATTAGAAATGATCTGTTTTGATTTAATGATGTCTTAAAAAATGCTAATTTGATCTGGCTGCTCACCTTACTTGCCTCTGTATTAGTAAGATAAAAGTCCATTTGGATTTGAACTGCAGAGTAATTACATGTTGATCACTGCTTTAAAGATTTTATTTTTTTTTATCTTTTACAGAGGAAAAAGATGATTCTGATGAGGATGATGAAGGCCTGGAGGACCTCACAGACCTTAGTGATGAAGATAACGAAGACGATTCTGGTGATTATGTTTCTGTTTTGAGTGAGGCTAGATATGATTGTTCAAGGAAACTTCTGTGTGTTTTCATTATTCACCTGTATTTGCCTGTTTTTTAAACTGTTCCCCATTCCTGTGATTTTTCTTAGATGGAGACCAGAAGCAGCCTTCATCTTCTAAGGGCAAAGCTCCAAAGAAGATGT[T/A]GAGTACAGAGCTGAAACAGGTGGCTGAGGGAGATGAAGATATGGTTGAGGACCTGGAGCTCTCAGATCAGGACTAAAATCGGTGTTACATCAGAGAGACTTTTCTATTTCCCAAATAATACTGCTTTTAAAGGAACATTTGACTTTTTTTGGAAATAAGCTTGTTGTACAAATCGCCTTCAGGCCTTGCAGAACACTTTTAGCTTAGCATAAATCATGGAGTCAGATTAGACCATTAGCAACGAAAAGTTGCTATTTTCTAGGTCAATATGGCTAGAAACTATCAAGGATCAAACTAATCAAGGAACTTGGCAACCACAGCAACTTTTCATTTCCAGTGATTTAGGCTAAGATAAATATTCTACTGCCAAACCCAGAGAATGGCTAAATGGATTTAAAAACGGTACAAATCCGCTGTTTTACTCTAGGTGACTTTTAAAATGAGACCATTTCCAAAAAAAAAGTGGAGTGTTCCTTTAAAGAAATATCTCCTTTAAGAGT
Associated Phenotype:
Not determined