ZMP
nol6
Ensembl ID:
ZFIN ID:
Description:
nucleolar protein family 6 [Source:RefSeq peptide;Acc:NP_001154983]
Human Orthologue:
NOL6
Human Description:
nucleolar protein family 6 (RNA-associated) [Source:HGNC Symbol;Acc:19910]
Mouse Orthologue:
Nol6
Mouse Description:
nucleolar protein family 6 (RNA-associated) Gene [Source:MGI Symbol;Acc:MGI:2140151]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa841 | Essential Splice Site | Available for shipment | Available now |
sa12332 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa841
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 |
---|---|---|---|---|---|
ENSDART00000083294 | Essential Splice Site | 191 | 1153 | 4 | 26 |
ENSDART00000128402 | Essential Splice Site | None | 444 | 4 | 28 |
ENSDART00000083294 | Essential Splice Site | 191 | 1153 | None | 26 |
ENSDART00000128402 | Essential Splice Site | None | 444 | None | 28 |
Genomic Location (Zv9):
Chromosome 5 (position 52558712)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 50225908 |
GRCz11 | 5 | 50872501 |
KASP Assay ID:
554-0744.1 (used for ordering genotyping assays)
KASP Sequence:
CTGCATCAARCCCAGAGTCTRTGTGGACCTTGCTGTCATCATTCCTTCTG[T/G]AAGTTATATGTTCTACTTGTCTTTTTTTCCNNNNNNNNNNTGTCTATATT
Long Flanking Sequence:
TCCACTGCAGCTTATTAAAAATGCAGGTCAGAAATTATGTTATCTCTGTGTTATGTTAGTGGTATAACAATTTATTTCAGCTTTACTAATCACTGATTGATGTTGTTGTTCAGATGGAAGAACTGCTGAAAGAAGTGGCCCTCAGTGAGCACAGAAAGAAGCTGGTGGACTCTTTTGTGCAGCAGGTTACAGAATTCCTGGACTGTGTGCCTGAATCTGAAGTTATGGAGGTCAGAAATGATTGAAAGATTGATCGTTTTTTATTTTTACTAATCTGGTTGCAGTTAACGGCAGTATCTGTTTTGCTTTCTCTTATCTGTAGTTAAATGATGTTTCTTGGTTGTCAAGAGTTGAAGTGCCGTTCTTCCTCGTTCCTGCGGCGGCAACAGGTAAATTTCACATGGAGGCTCCAGCATCAGTCAGCCTGGTGGGAAGTTATCCACTGGGCACCTGCATCAAACCCAGAGTCTGTGTGGACCTTGCTGTCATCATTCCTTCTG[T/G]AAGTTATATGTTCTACTTGTCTTTTTTTCCTGTCTCTATTTGTCTATATTTGCAAACTGTTGTCCAATGTGATGTACACGCAATTGTTTTTATTTATTTGAATTATTATCTCATTAGATGACTCCTTTCTGAATTATTGTTTGTTGTGACATCCATTCACCCATCGTTCTGTTGACATGTCAGAAAAAGAAAGCTTGAGAATCTTGTGAACTTCAATTCCCATATGACATAAATTCAAGTTATCAATGGATTTTAATTTATTAGCAATGTGCAGTTTAACCCCTTAACTGTCATCCCCACATTAGCCCCTTTCACACAGTGATACCGGTAAATATCTGGAAAATTTCCGGAACGACTTTACCGGTATATTCAAAAAAGCGCTGTTCACACAGGCGAGGACGTTACGGAAATTTTCCGGAAAAGAGCATTCACACATCCATTCCAAAATACCGGTAAATTCTGACATCATTCACCTCAAATGAGCTTTTAACAGCTGCGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12332
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083294 | Essential Splice Site | 191 | 1153 | 4 | 26 |
ENSDART00000128402 | Essential Splice Site | None | 444 | 4 | 28 |
ENSDART00000083294 | Essential Splice Site | 191 | 1153 | None | 26 |
ENSDART00000128402 | Essential Splice Site | None | 444 | None | 28 |
Genomic Location (Zv9):
Chromosome 5 (position 52558712)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 50225908 |
GRCz11 | 5 | 50872501 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGCATCAARCCYAGAGTCTRTGTGGACCTTGCTGTCATCATTCCTTCTG[T/C]AAGTTATATGTTCTACTTGTCTTTTTTTCCNNNNNNNNNNTGTCTATATT
Long Flanking Sequence:
TCCACTGCAGCTTATTAAAAATGCAGGTCAGAAATTATGTTATCTCTGTGTTATGTTAGTGGTATAACAATTTATTTCAGCTTTACTAATCACTGATTGATGTTGTTGTTCAGATGGAAGAACTGCTGAAAGAAGTGGCCCTCAGTGAGCACAGAAAGAAGCTGGTGGACTCTTTTGTGCAGCAGGTTACAGAATTCCTGGACTGTGTGCCTGAATCTGAAGTTATGGAGGTCAGAAATGATTGAAAGATTGATCGTTTTTTATTTTTACTAATCTGGTTGCAGTTAACGGCAGTATCTGTTTTGCTTTCTCTTATCTGTAGTTAAATGATGTTTCTTGGTTGTCAAGAGTTGAAGTGCCGTTCTTCCTCGTTCCTGCGGCGGCAACAGGTAAATTTCACATGGAGGCTCCAGCATCAGTCAGCCTGGTGGGAAGTTATCCACTGGGCACCTGCATCAAACCCAGAGTCTGTGTGGACCTTGCTGTCATCATTCCTTCTG[T/C]AAGTTATATGTTCTACTTGTCTTTTTTTCCTGTCTCTATTTGTCTATATTTGCAAACTGTTGTCCAATGTGATGTACACGCAATTGTTTTTATTTATTTGAATTATTATCTCATTAGATGACTCCTTTCTGAATTATTGTTTGTTGTGACATCCATTCACCCATCGTTCTGTTGACATGTCAGAAAAAGAAAGCTTGAGAATCTTGTGAACTTCAATTCCCATATGACATAAATTCAAGTTATCAATGGATTTTAATTTATTAGCAATGTGCAGTTTAACCCCTTAACTGTCATCCCCACATTAGCCCCTTTCACACAGTGATACCGGTAAATATCTGGAAAATTTCCGGAACGACTTTACCGGTATATTCAAAAAAGCGCTGTTCACACAGGCGAGGACGTTACGGAAATTTTCCGGAAAAGAGCATTCACACATCCATTCCAAAATACCGGTAAATTCTGACATCATTCACCTCAAATGAGCTTTTAACAGCTGCGCT
Associated Phenotype:
Not determined