Busch Lab

ZMP

cul4b

Ensembl ID:
ENSDARG00000060510
ZFIN ID:
ZDB-GENE-041008-208
Description:
cullin-4B [Source:RefSeq peptide;Acc:NP_001116316]
Human Orthologue:
CUL4B
Human Description:
cullin 4B [Source:HGNC Symbol;Acc:2555]
Mouse Orthologue:
Cul4b
Mouse Description:
cullin 4B Gene [Source:MGI Symbol;Acc:MGI:1919834]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa14313 Nonsense Available for shipment Available now
sa19087 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa14313
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085295 Nonsense 199 885 3 21
Genomic Location (Zv9):
Chromosome 14 (position 34466179)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 33150879
GRCz11 14 33491193
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTACACAAATGAGACCTGGCAGAAACTAAAGGAGGCAGTAGAGGCCATA[C/T]AGAACAGCACTTCAATAAAGTACAATCTAGAGGAGCTCTATCAGGTCGGT
Long Flanking Sequence:
AAATGAGTCTTCGAAGCTATATCATGCATATTAATGAAGTCGCATCTCATTCACAATAGAGTGCGCTGATTGGTTCAAACCAAGTCTTTCTCATGAATTAATAGACAGATGTGCTGAAAACTCAATGTCGCTTTGTACCAGCCGGTACAGACAGCCAATCTCTATGCTGGAATTTACACAATGATCTTATCGCTGTGACATTGCTTTAAAATGTCTTTTTAAATCGGAAGAACAAATTTTCTCCAAACAGCGCAAAAACAACCATTTTTAACTTTGTAGTCAAATGCTCTTTGGTGTTTAGTGACCCTTTGACTATATGCTTTAATATTATGGAACTTTTTTACCTTAACCCTGGATCACCAAATCCTGACATTGTGTGCTTACTGTTTTTACTCATCTCCTTTTTTATATAATGTTATACATTTTCAGAAAAGCCCAAATTACCAGAGAATTACACAAATGAGACCTGGCAGAAACTAAAGGAGGCAGTAGAGGCCATA[C/T]AGAACAGCACTTCAATAAAGTACAATCTAGAGGAGCTCTATCAGGTCGGTGCTATAATAAACTAGCTTTAATATTTTTTTGTAATATTATACGTGGAATCTAATGTTTACTTGTTCTTTCAGGCTGTTGAAAACTTGTGCTCTCATAAGATATCTGCCAAGCTGTATAAACAGCTCAGAGTGGTTTGTGAAGACCACATCAAGGCACAGATTGACCAGTTCAGAGAATATCCTTTTCCTTGCTACACTTTGTATTTATTAATCTGCTGGAATGTTAGATTTTGAGTAAAAGAGAAGAGCACAAACCTGGGCTCAACATACACAAATCTGCAGGCCAATAGTTCTGCTTTTCTTTTTAATTAACATAGTGTTATTATGCTCTCTCGTTCAAGCGTTTGGGGTACATCATATTTTTGAAAGAATCTTCTTTCAAAGTTTTCACATATTTACATTTAATTACAGCAAGGTTGTATTTTCACATTTAAGCATTTATAGCATTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19087
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From EZRC
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085295 Essential Splice Site 672 885 16 21
Genomic Location (Zv9):
Chromosome 14 (position 34474622)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 33159322
GRCz11 14 33499636
KASP Assay ID:
2260-7736.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGCTATTGGCCAACATACGTCCCTATGGAAGTACATCTGCCAGCAGAG[G/T]TCAGTTCTGAGAAATATGTAGGGATGTAGCGATTCACCATGAGCCGGTTG
Long Flanking Sequence:
TTAAAGGCAAAGATGTTTTTGAAGCCTTCTACAAGAAAGACTTAGCGAAGAGGTTACTGGTGGGAAAGAGTGCCTCTGTAGATGCAGAGAAATCAATGCTGTCAAAACTGAAGCATGGTAAATTACATTTCTCCTTTTATGTTTGATTCCAAACCCTCGCAAATCTTTCTGTAGACTGTAAACTAAAAATGGCAAATTGTGTTTCTTTTTTTGTAGAATGTGGAGCAGCATTTACTAGTAAACTGGAGGGAATGTTCAAAGACATGGAGCTGTCGAAAGATATTATGGTGCAGTTCAAACAGGTAAGGGAGCTTTTATTTTCTTTCTATTATTCATGTTCTTTGGTGTCTCGTTTTTATCTAGCAAATCTCTGTTTTCATTCTGTATTTCAGCATATGCAGTGCCAAAATATTCCTGGTAACATTGAGCTGACAGTGAACATCCTCACTATGGGCTATTGGCCAACATACGTCCCTATGGAAGTACATCTGCCAGCAGAG[G/T]TCAGTTCTGAGAAATATGTAGGGATGTAGCGATTCACCATGAGCCGGTTGAAAATCAATTAAAATGTTATGATTCAAACCTGTAGAAATGTTGAACGAATTGTGATACATTTTTTCAATAGAGGGGGCGCTGTGCGGCGAGCAAGAGGTGGGGTGGCAGTAAAATGACATCGGTGAAGTGATGCAGACGAAAAAACTGTTTGCAAATACTGCAAAAAGACGCTTACTTGTACCAACAAAACAATGAATATGATGCACATAAACAGTCAGCACAGTGAAAAACTACTGTCACAGATGACTATACGCAAAAAGACTTAATAAATCAGATGATTTGCAGCGCTGTTTCCTCCGACGAGTGCACGGTGCATAGCGAAAGTATGAAGATGTTATTCAGACTGAAAGAGAAAGTTGTTCTGTTACAGAAGCAGGTATTAGATTATTATACCCTCTCCCTTTCAAATAAGTTTATACTTATTTTAATAATTTGCATATTATTATTGA
Associated Phenotype:
Not determined