ZMP
cul2
Ensembl ID:
ZFIN ID:
Human Orthologue:
CUL2
Human Description:
cullin 2 [Source:HGNC Symbol;Acc:2552]
Mouse Orthologue:
Cul2
Mouse Description:
cullin 2 Gene [Source:MGI Symbol;Acc:MGI:1918995]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25203 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44070 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24431 | Nonsense | Available for shipment | Available now |
sa44069 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25203
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 |
---|---|---|---|---|---|
ENSDART00000013257 | Nonsense | 272 | 764 | 10 | 22 |
ENSDART00000138432 | Nonsense | 253 | 745 | 9 | 21 |
ENSDART00000140125 | None | None | 93 | None | 4 |
Genomic Location (Zv9):
Chromosome 24 (position 2331934)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 2301932 |
GRCz11 | 24 | 2297976 |
KASP Assay ID:
554-7805.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACAGGTTTTGGGCAGGTTGAAAGATGAGGAGGTGAGATGTCGGAAGTA[T/A]CTTCACCCCAGCTCTTACTCCAAAGTCATCCATGAATGTCAGCAGAGGAT
Long Flanking Sequence:
TCAGATTGTACAAGAAGCACTGCATTAAATTACATTTCCCCCCGCCATGTCTTTAAAATATAAACATTTATTTGACCCCAGTTTATTCAATGGAGCTTCTGCGCTAGCCTGCCGATTGTGACGGGCGCGTGTGAGTAAACGGCTTTTTGTCTCGTTTTACTCTTGAGCAACTAAATGAATGCCCGAGTATGTTTAACTGATTGTATTTTAACTGCATTACAACATCGATGCTGTTGAAGGTATTGTATAAAATGGAAAAAAACTAACAATAACAGCTCACCAGAAGTTTATCCGCATGGGAACAACACTTGCTCGGCATATAGCCTATTGTTTTATTTACAGGTCAACAGCGCACAGAACTGTCATATGATCATTCTTTAAAAATGTGGCACATCCACATCATTTGTGCAAGTTTGTAATAGAAATGTTGTGTATGTGTGTTGTGTTTTGTGACAGGTTTTGGGCAGGTTGAAAGATGAGGAGGTGAGATGTCGGAAGTA[T/A]CTTCACCCCAGCTCTTACTCCAAAGTCATCCATGAATGTCAGCAGAGGATGGTGGCCGATCACCTGCAGTTCCTGCACGGAGAGTGTCAAAATATCATCCGGCAGGAGAAGAGAGACGGTCAGCACTCCATACACTCACACACACTGCCAATGCTCACGCATCGCTTATGGCTTGATGTTTGTCATTTCTATTGTTTATTAATAAATTGAATTTATGTAATTATCCATTGTTTAATTCTCGTTGTTTTGACTCAGATTAGGTAAGAAGAACTGAGCTCTTGCCATATTTTACTACCATTTCATTCATTCATTCATTTTCTTGTCGGCTTAGTCCCTTTATTAATCTGGGGTCGCCACAGCGGAATGAACCTCCAACTTATCCAGCACATTTTTACGCAGCAGATGCCCTTCCAGCCACAACCCATCACTGGGAAACACCCACACACTCATTCACACACATACACTACGGACAGTTTAGCCTACCCAATTCACCTGTACCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44070
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013257 | Nonsense | 532 | 764 | 16 | 22 |
ENSDART00000138432 | Nonsense | 513 | 745 | 15 | 21 |
ENSDART00000140125 | None | None | 93 | None | 4 |
Genomic Location (Zv9):
Chromosome 24 (position 2324087)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 2294085 |
GRCz11 | 24 | 2290129 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCAGGAGACGGTAGTGGACCTGGGCATCAGCTTTCAGATTTACGTTTTA[C/T]AGGTGAGCGAGAGATTTATTAATCATACACAAAATTAGTTTGCTGCAGTG
Long Flanking Sequence:
CTAACATTGTTGTGTTGTAACCATTGCTATGTTGCTTGTCTTGTGCGGTTTTTGAGTTTTAATTGACTCTTGCGGTGTTTTTTACTGTTTACTGCTAGATTTACGCCAGAATGCTTGCGAAGAGGTTAATACATGGGCTTTCGTTATCGATGGACTCAGAGGAAGCCATGATCAACAAGCTGAAGGTACAGTCGTCTCTGTGGTGTAAGAGCTCACTGACATGTCTTGTTATGTCCTGGTTTTGTGCACAGGGGTTTTAGTTGTTGTTTGCTGTTGTGTTGTCGTTGCTGTGATTTAAAGCACTTTGCTTTCCTCGTTTCTTTCCCCTGGTCTGCTCTTGGGTCTTCCAGCAAGCGTGTGGTTACGAGTTCACGAGCAAACTGCACAGAATGTACACAGATATGAGCGTCAGCACCGACCTCAACAACAAATTCAACAACTTCATCAAAACCCAGGAGACGGTAGTGGACCTGGGCATCAGCTTTCAGATTTACGTTTTA[C/T]AGGTGAGCGAGAGATTTATTAATCATACACAAAATTAGTTTGCTGCAGTGATGTATAGTGTTTGTGTGTGTGTGTGGTGTGTTTTAGGCAGGTGCATGGCCCCTCACACACGTCCCCTCGTCCACGTTTGCGATCCCGCAGGAGCTGGAGAAAAGTGTACAGATGGTAAGAGTTCATCTAACCTTCCTTCATGAGGTTTTAGATCAGTGAACTGAGATTTACTGATGTTTTCTGTTTGCAGTTTGAGTTGTTTTATAACCAGCACTTCAGCGGCAGGAAGTTGACCTGGCTACATTACCTCTGCACAGGTACAGCAGCTCCCATTCACACGTGTACTTCTATTCAGGAACTTTGGGTCTGTACTGTTTTTACTATTCTTACCATTGGTTTGTTTGTCTCAGGTGAGGTAAAGATGAATTACCTGTCTAAGCCGTATGTGGCGGTGGTGACCACCTATCAGATGGCGGTTCTGCTGGCGTTCAACAACAGCGAGACTGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24431
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 |
---|---|---|---|---|---|
ENSDART00000013257 | Nonsense | 619 | 764 | 19 | 22 |
ENSDART00000138432 | Nonsense | 600 | 745 | 18 | 21 |
ENSDART00000140125 | None | None | 93 | None | 4 |
Genomic Location (Zv9):
Chromosome 24 (position 2323572)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 2293570 |
GRCz11 | 24 | 2289614 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGTTCTGCTGGCGTTCAACAACAGCGAGACTGTGAGCTATAAAGAACTG[C/T]AGGACAGCACACAGATGAACGAGAAAGAGCTCCAGAAGACCATCAAATCT
Long Flanking Sequence:
TTTATTAATCATACACAAAATTAGTTTGCTGCAGTGATGTATAGTGTTTGTGTGTGTGTGTGGTGTGTTTTAGGCAGGTGCATGGCCCCTCACACACGTCCCCTCGTCCACGTTTGCGATCCCGCAGGAGCTGGAGAAAAGTGTACAGATGGTAAGAGTTCATCTAACCTTCCTTCATGAGGTTTTAGATCAGTGAACTGAGATTTACTGATGTTTTCTGTTTGCAGTTTGAGTTGTTTTATAACCAGCACTTCAGCGGCAGGAAGTTGACCTGGCTACATTACCTCTGCACAGGTACAGCAGCTCCCATTCACACGTGTACTTCTATTCAGGAACTTTGGGTCTGTACTGTTTTTACTATTCTTACCATTGGTTTGTTTGTCTCAGGTGAGGTAAAGATGAATTACCTGTCTAAGCCGTATGTGGCGGTGGTGACCACCTATCAGATGGCGGTTCTGCTGGCGTTCAACAACAGCGAGACTGTGAGCTATAAAGAACTG[C/T]AGGACAGCACACAGATGAACGAGAAAGAGCTCCAGAAGACCATCAAATCTCTGCTCGACGTCAAGATGATCAGCCACGACCTGCAGAAAGTATGTAGTACCCCTTTTTCTGGAACATTCAGATGTCTTTCAAGCTCTACTGATGCTGGTGAGGAAATTAATTATGAATAAATGGGTTGGGACAGAACTCCCTCTTGTCAAGGACTGGATAATCCTGATAATCCTGAAACCATAGCTGTGGGAAATTCTGCTGACCTGTCTTGGCATTGATTATTAATCTATTATTTATTTATTTTGTGTTTTTATTTATTTGTTTCTTTGTTTCTTTGTTTATTTATTAAACTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACAGTTGAAGTCAGAATTATTAGCCCCCCTGAATTATCAGACTGCTTTTTTATTTTTTCCTCTTTTTCTGTTTGACAGAGAGCAGATTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44069
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013257 | Nonsense | 647 | 764 | 19 | 22 |
ENSDART00000138432 | Nonsense | 628 | 745 | 18 | 21 |
ENSDART00000140125 | None | None | 93 | None | 4 |
Genomic Location (Zv9):
Chromosome 24 (position 2323488)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 2293486 |
GRCz11 | 24 | 2289530 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGACCATCAAATCTCTGCTCGACGTCAAGATGATCAGCCACGACCTG[C/T]AGAAAGTATGTAGTACCCCTTTTTCTGGAACATTCAGATGTCTTTCAAGC
Long Flanking Sequence:
GCCCCTCACACACGTCCCCTCGTCCACGTTTGCGATCCCGCAGGAGCTGGAGAAAAGTGTACAGATGGTAAGAGTTCATCTAACCTTCCTTCATGAGGTTTTAGATCAGTGAACTGAGATTTACTGATGTTTTCTGTTTGCAGTTTGAGTTGTTTTATAACCAGCACTTCAGCGGCAGGAAGTTGACCTGGCTACATTACCTCTGCACAGGTACAGCAGCTCCCATTCACACGTGTACTTCTATTCAGGAACTTTGGGTCTGTACTGTTTTTACTATTCTTACCATTGGTTTGTTTGTCTCAGGTGAGGTAAAGATGAATTACCTGTCTAAGCCGTATGTGGCGGTGGTGACCACCTATCAGATGGCGGTTCTGCTGGCGTTCAACAACAGCGAGACTGTGAGCTATAAAGAACTGCAGGACAGCACACAGATGAACGAGAAAGAGCTCCAGAAGACCATCAAATCTCTGCTCGACGTCAAGATGATCAGCCACGACCTG[C/T]AGAAAGTATGTAGTACCCCTTTTTCTGGAACATTCAGATGTCTTTCAAGCTCTACTGATGCTGGTGAGGAAATTAATTATGAATAAATGGGTTGGGACAGAACTCCCTCTTGTCAAGGACTGGATAATCCTGATAATCCTGAAACCATAGCTGTGGGAAATTCTGCTGACCTGTCTTGGCATTGATTATTAATCTATTATTTATTTATTTTGTGTTTTTATTTATTTGTTTCTTTGTTTCTTTGTTTATTTATTAAACTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACAGTTGAAGTCAGAATTATTAGCCCCCCTGAATTATCAGACTGCTTTTTTATTTTTTCCTCTTTTTCTGTTTGACAGAGAGCAGATTGTTTCAACATATTTCTGAACATAATAATTTTAATAACTCTTTTCAAATAACTGATTTATTTTGTCTTTGTCATGATGACAGTTAATA
Associated Phenotype:
Not determined