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 |
sa37858 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24472 | Nonsense | Available for shipment | Available now |
sa45827 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
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:
sa37858
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 |
---|---|---|---|---|---|
ENSDART00000024691 | Nonsense | 50 | 774 | 3 | 22 |
ENSDART00000122757 | Nonsense | 50 | 320 | 3 | 10 |
ENSDART00000134947 | Nonsense | 50 | 775 | 3 | 22 |
The following transcripts of ENSDARG00000007691 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 17933679)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 17240155 |
GRCz11 | 24 | 17384574 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTATTCTCTTACTGCCTTTTGACTTTAACCTGCTGTTCAGACATGTGTA[T/A]AACTACTGTACCAGTGTACACCAGGCCAGGCCTACTGGCATCCCCTCGTC
Long Flanking Sequence:
ACTAAATAGTTATAAGAGACATGTTTAAGGCATATATTCAACATCCTTAATTAAGGAAAGATCTCCACTTTACCATTCTTAAAGGGAAAATGTGCTTTATGCAATAGCAAAGTTATATAAATCTTGAAGCATCAAAATCCGTACTCTGTATCGGCCGATCCTCATGATAAAGGAATTGGAACTCTATATCGGCTGCAAAAATCCTGACCAGAGCATGTCTAATAGTTACCGTTTTTCTAGACCGCATAGATAAAATCTTTTTTGACTTGACGGTTTAAGTGTGTCCAGCAGCTTTTTCATGCAAGATAAGAATTGTTAGAAATCATATCTCCATGATTGTTGCTGTATTACAGTAGTATAACTGTTTTTGACTGGTTTAGGTCTGTCTTGCATAAAGAAACAGGACCAAGAAACTGCCAGGAGGTTGCTAATGTTATCAATCTGTCATAATTTATTCTCTTACTGCCTTTTGACTTTAACCTGCTGTTCAGACATGTGTA[T/A]AACTACTGTACCAGTGTACACCAGGCCAGGCCTACTGGCATCCCCTCGTCCAAACCCTCCAAGAAAACACCCACACCTGGGGGGGCACAGTTTGTTGGACTAGAACTCTACAAAAGACTCAAAGATTTTCTGAGGAGCTACTTGACAAACCTTCTCAAGGTAACAGCCTACAGCTTGCATGCATAATATTGTTCAGGATATATTGTTGTTGGTATACATGAAACTACTTTGAATGCTGGCTCGAAATTCATTCATAAGATACGTTTATTCTATTACCCTTTTCTTGAATTCAAAAAAATCTGTATACATTTGTTGTTTCCATAATCACTTGTAATTTGTTGTTTTTCTACTAATGCCATGTTGTATCTGACCATGCACGTCTCAGTAATGAGTAAAGATGAAGTCTTGGAATCGTCGTTTACAGACTGAGGAGTTTAATGAGACATGGAGAAAATGGGGAGAATATATTCTTCCATTAAGACCAGACTTAATATAGAATG
Associated Phenotype:
Not determined
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
Mutation Details
Allele Name:
sa45827
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024691 | None | None | 774 | 22 | 22 |
ENSDART00000122757 | Essential Splice Site | 320 | 320 | 10 | 10 |
ENSDART00000134947 | None | None | 775 | 22 | 22 |
The following transcripts of ENSDARG00000007691 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 17914003)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 17220479 |
GRCz11 | 24 | 17364898 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTGTCTTTATGCCCTTAAGCTGCTCAGGATTGCCATTTACTTTTTAAA[G/T]ATGTAAATAACTGGACATTGAACTAAACTCATAGTGGGACCCAGCGTCAG
Long Flanking Sequence:
TCAGAATATTTTCGAGTGTCCTGGGCTGATTTTTGCTGTTTAATCTGATGAAAATTGAACTTTTTAAATGTTTTGAAATTTTTCCACATTTTTCGAGTGCATGGGACTGACTTTTACTGTTTATTCTGATAATGCCAAAGAGCAGCAACGCATTATTTAAGCTTATTTGCATTATTTGAGCACATTTTGTTTAATTTAGGACTTTTATTATTTCAGAAATGCATTGACATTTTGATAGAGAAGGAATACCTGGAACGTGTAGATGGGGAAAAAGACACGTACAGTTACCTGGCATAAAAACAACATCCTCTGGAGTTTGCCGTCCTTCCTGAGATGCATCTTTTTGAGGAGCGTCAAGAGTGGACGCACACAAACCGAGGACTCTCAAGACATTGCTGAGTAAGACACTGGACCTTTTCCCTTTAAACCCAGACTGCTAAAGCGGCCAGTCTTTGTCTTTATGCCCTTAAGCTGCTCAGGATTGCCATTTACTTTTTAAA[G/T]ATGTAAATAACTGGACATTGAACTAAACTCATAGTGGGACCCAGCGTCAGGGTTGCATGCTATAATGCCTCTCAATATAAAAGGACAAAAACTGATTAATTGTGATTCCGTCTTTTGGGAAACTGACATATTGAAAAAAAAAAAAAAAAAAAAAAGATGAAGACAAGAAATACTGTTAACTAAGAGCAAAGCCAGTAAAATCATGTCAGATCGGCTGTTTAGAGATGCATCGTTTCCAGCCAGGAGAACAGCATTTGTATAGTGCAGCTCATTTTATAAATGTCATGAATAAACTTAATTTTTCTTTATACTTTAGTCTTGCTCATTTATATCAAGGAGAATGCAGCTTTTTAATGTATTCACTGTCTGAAATATAGGTGATTTTTATTTCTTCAGCTGATATGAGAATCATGAAACAAATGAATATCTGGAAGAGTACAGCAGACAGTTATTTTCAATGTTTATTTTCTCACGTTTAACAAGTCCTTGTAAACAATTGA
Associated Phenotype:
Not determined