ZMP
cul1b
Ensembl ID:
ZFIN ID:
Description:
cullin 1-like [Source:RefSeq peptide;Acc:NP_998660]
Human Orthologue:
CUL1
Human Description:
cullin 1 [Source:HGNC Symbol;Acc:2551]
Mouse Orthologue:
Cul1
Mouse Description:
cullin 1 Gene [Source:MGI Symbol;Acc:MGI:1349658]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa1559 | Essential Splice Site | Available for shipment | Available now |
| sa24472 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1559
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000024691 | Essential Splice Site | None | 774 | 1 | 22 |
| ENSDART00000122757 | Essential Splice Site | None | 320 | 1 | 10 |
| ENSDART00000134947 | Essential Splice Site | None | 775 | 1 | 22 |
The following transcripts of ENSDARG00000007691 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 17949169)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 17255645 |
| GRCz11 | 24 | 17400064 |
KASP Assay ID:
554-1502.1 (used for ordering genotyping assays)
KASP Sequence:
GAGCGCAGGGCCTCGACCTCACACTGCTCGACGTTACAAACACACACAGG[T/A]AAGACTAAAAATCTTTAAACACGTGTCAGGCGTCCCGGTTTGACATAAAT
Long Flanking Sequence:
TTTTTGGAAGGTTTACTCATACTTTGAGTAATATTTACAACAGATACTTTTACTCTACTTCCACTACATTTTAAGCAAGTAATGGTACTTTTACTTGAGTATGATTTTTCAGTTCTCTTTCCACCACTCACTGACTGAGTAATATTTACAACAGATACTTTTACTCTACTTTCAACTACATTTTTAGGCAAGTAATGGTACTTTCACATGAGTATGATTTTTCAGTACTCTTTCCACCACTGGTGGGTTTTACACACATTTTTTGAGTCATTCGCAGCAGGAATGGTCAAAGTGGTTCCTGGCACCTGAAAGAGTGAAGCTCCTACGCAGCTGGTGTACTACGGTGAGTGGACAGTAGGCGTCGCTGTGTGTCTCTGCGCTGTGGCGTATGACGTTTCACTCGCTCTAATACGGAATTCCCAGTCATCTCCAGTCAAACACACACAGACTGAGCGCAGGGCCTCGACCTCACACTGCTCGACGTTACAAACACACACAGG[T/A]AAGACTAAAAATCTTTAAACACGTGTCAGGCGTCCCGGTTTGACATAAATGAAAACTAAATGGACGTGTCTGGCAATGTGTCGATAAGGAAGAGAGACATTTTTGTGATATTACACACCAGTTAAGAATAGGTAGCCATTTTACATCATTATATCTCAAAAGCCTCGGAGAATAACAGTAGTGGGTTAATAACAAATGTTTGTCTTGATTTTCAGGTTATATTTAAATGACGTACGTTTGGTTGACATTATGGTATTAATAGTTCCTCTTAGCGGCAGTTTACAAGGAAGGGTACCTGAAGCTAACGAGCTTGCTACCTAGCATTGCTAATCTATTGATGCTGTTTACAAAACAATATCGCCATATAAATGTTCATGAATTAAATACTTAGTGCGTTTAATGTGTTAAGAAGTATATTATGGAGACCTAAAGCTGTAAACAAATGCTGAGGCAAAACGAAGAGTCCTTTACACACATTCACATGAATTCTGCTGTCTCAG
Associated Phenotype:
Normal
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa24472
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 |
|---|---|---|---|---|---|
| ENSDART00000024691 | Nonsense | 411 | 774 | 11 | 22 |
| ENSDART00000122757 | None | None | 320 | None | 10 |
| ENSDART00000134947 | Nonsense | 412 | 775 | 11 | 22 |
The following transcripts of ENSDARG00000007691 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 17920972)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 17227448 |
| GRCz11 | 24 | 17371867 |
KASP Assay ID:
2261-8595.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAGGCCTGTGGAAGATTCATTAATAATAATGCAGTAACAAGAATGGCA[C/T]AGTCCTCCAGCAAATCCCCTGAGCTTCTGGCCAGATACTGTGACTCCTTA
Long Flanking Sequence:
TATTTTTGTGTCATATGTAATTAATCATTTATGTGTTGTGCGTAAAGAATGTGTTTCAATCCGGCTACCACCGCGAGTGCATTTCAAACCAGTGTAAAGCACTGGCCAGTAATATTTATCTCCATTAATCCTGGATATCATGTTAGTTTGTTTTTGTTTTTTTTGTCGTGCGTGTTTCCCGGTACATCTGCTCTGCTCAGTTCCTGTAAGGCCTTAATTTGATCACAGTCTGAATTGTCACTTCTTGTTTTTCAGGATCCTAAAATGTATGTGCAAACTACCTTGGATGTTCACAAGAAATACAATGCTCTTGTCATGTCTGCGTTCAATAATGATGCCGGGTTCGTGGCGGCACTGGATAAGGTTGTAAGCTTATATGAGATCTGTTGTGTACTATAGTGGTTATTATTAGCCTCTGGTGTAATTTTCATTCTGTGATCTGTGCTGGTCTTCAGGCCTGTGGAAGATTCATTAATAATAATGCAGTAACAAGAATGGCA[C/T]AGTCCTCCAGCAAATCCCCTGAGCTTCTGGCCAGATACTGTGACTCCTTACTGAAGAAGAGGTGATTCTCTCATTCACATCATTATTGGTGGACCAGACCCCATATCAGGCTTTCATTTTCATCTTTTAAGAGTAGAGTTTTGAATCTTTTTAGTGCAATAAAAATGAGCTGACAATAATATCTAAAGAATGAAAACTGCATTAGCAAGGCTCTATATTTGAAACTGAGGATTTAACCAAGTTTGTGTTGTGTTTAGTTCAAAGAACCCAGAGGAGGCTGAACTTGAAGATACTCTCAACCAAGTGGTGAGTTTTTGTTTTCCACTGATATTACTGCTCATAACAGCGTCTTTTCTTCATTGTAATGAAATTAATTTCATTTACTTTACAAATTTACAAAGCCTAAATATTTATTTCTAGCAGAACTTAATCTAGATTACTATTTAAAGATTGTTTTCAGCTTAATTGAATTCACTTTGCCTGAACTTTTATTTTAAATT
Associated Phenotype:
Not determined