ZMP
ikbke
Ensembl ID:
ZFIN IDs:
Description:
inhibitor of nuclear factor kappa-B kinase subunit epsilon [Source:RefSeq peptide;Acc:NP_001002751]
Human Orthologue:
IKBKE
Human Description:
inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase epsilon [Source:HGNC Symbol;Ac
Mouse Orthologue:
Ikbke
Mouse Description:
inhibitor of kappaB kinase epsilon Gene [Source:MGI Symbol;Acc:MGI:1929612]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35071 | Essential Splice Site | Available for shipment | Available now |
sa2615 | Nonsense | F2 line generated | Not yet available |
sa30946 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35071
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 |
---|---|---|---|---|---|
ENSDART00000080116 | Essential Splice Site | None | 721 | 2 | 22 |
ENSDART00000129062 | None | None | 721 | None | 20 |
Genomic Location (Zv9):
Chromosome 11 (position 22236807)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 21243038 |
GRCz11 | 11 | 21403606 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTCTGACTGTTGTGTTTAAGAGAAGTGTTAAGTTCAGGAATAAAACGG[T/A]AACGTAACGTAATTCACTTTTTAATTGGATGAGAGACATGTTTATTTTGA
Long Flanking Sequence:
TGTTAACATTTTAAAGATTAAGTAATCTTGTGAGAGCAAAAACACACACAGACGCCCAACAAGGAAGTTCCTGACAGCAATGAAAGGAAAGTTGCTGCTGAGTTTCCGTCAAGCTGCTCTCTTTACTTCAGTCTGAGGACTGCAGGTGTAAAAAGTTTGTACAATAACTCAGTTTGGATTGAAGAGGAAAATGCGTCGCCATCAAACACACAAATGGTTAGTTGATTGTTTTTTGTAGTTTTCTGTTGTCGGTCAGTCAGAATAATGACGACGACGATGATGATGATGATGATGGTGCGAAGGGGAAATTCTTAACGCTATTGTAAGTTGACACGTTTTCCCTAATAAGTACGTTAACATTACATTTAAGAAACATGTTTATTTTTTACAAAATATGATTAATCTGCTTTTAGGTCATACAGGAAGGAAGTGGACTTTATTCGACTCTTCTGCTCTGACTGTTGTGTTTAAGAGAAGTGTTAAGTTCAGGAATAAAACGG[T/A]AACGTAACGTAATTCACTTTTTAATTGGATGAGAGACATGTTTATTTTGATTGTGTTTGCCTTATTTTAGCACCTAAATATTATTTAATAACCTTAAAACTCTATTTGATGTTACAATTGGCTAATTATAAACAGAAACTAACGAGAAGTTCACTGACAGCATAATTTACATATTACCAGAGCTCAGTTATGTATTCAATCTGAAGGGAAATTGAACTAGAGATAGTCAAATAGCTAGCTTAGCTAATAACTAATTTTGATTTGACTAAGATTCGTCATGAAAAGTGTCTTAAATGTTTAAATACTTTATAATGTGGATAATTTAATACTCTTTTGAGCAGAATTTACTTTAAATAAAGAAGTAACACAACATGGTAGCCGAACACACTGTGGTTATGCGACCCTTACCATAGTTTAATCAAAGCATTTGTAGTAATACTGTGATTCTACACATGGTTATCAGTCTGCCTAAAAACAGTTACCACAAACTTCTGTTAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2615
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000080116 | Nonsense | 351 | 721 | 10 | 22 |
ENSDART00000129062 | Nonsense | 351 | 721 | 8 | 20 |
Genomic Location (Zv9):
Chromosome 11 (position 22214544)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 21220775 |
GRCz11 | 11 | 21381343 |
KASP Assay ID:
554-3333.1 (used for ordering genotyping assays)
KASP Sequence:
CAATCTTTTTTGAGGATGTTCAGGCCCAAACTGGAATTGAACCTGCGGCT[C/T]AACAGTATTTATTTCAAGGCCATCCTCTCATATTAGATCCAAGCATGAAA
Long Flanking Sequence:
AAATAATTTATAAATTTATAAATTAGTTTTATTCTGTCTAGCTTATTTTGGGAATGTCTTTTTGTAATAATAAAGAAATATATTGGCCCATGGTGTCCGACCTGAAAGTCTCTTTTGCAGCTCAGCCCTTGCCTACACTCAGCTAATGTTGTTATTTGCCGGCTTCAGCCATGGTCTCTCAGCCACCATGTCTTTCCAATAACAGATGTTTACTAGAAGTTAAACAAAAGTAAAAATTGTTTTAAATTTGAAAGTTGAAGTAGTTTTTTTTTAACCTCACTGTTTCCAAGTAGACAAAATAAGTTTAATTTACCCTGATCTCAATATACAGTATTTACCACCATAGCTCTTTATATATCGTTTTTCAATGATTGTTGTTTTGTTCTGAATTATTTTTACACAGTGATTCCACACTGAAAATTGTATTTTGGTGTTTTCTTTCAAGGGTCTCAATCTTTTTTGAGGATGTTCAGGCCCAAACTGGAATTGAACCTGCGGCT[C/T]AACAGTATTTATTTCAAGGCCATCCTCTCATATTAGATCCAAGCATGAAAGTAGTGAACATTCCCCATACCAGCTCAGATAAGCCCATGATTCTGATCAGCCGGCGACTGGAAAGGATAATTGGATATCCCTTCGAAGAACGTAAGGACACAATACATATTTGGTTAAGACTTTAGTACACAGCAGGGAAGCATATTTACTTTGACATTTACCTCAAAAAACTCCCAGATTATGGTTTCGTTATCATTATAGGAAATGTTCATGCCGAATAAAACCATGTCCTAACAACATGCAATGTGACAAGATTCCAGAGAGGAGCAGTTTTGCTGTCTGCACAAGACGCCACTGAGGCATTTACACTAACCGGCCACTTTATTAGGTACAGATTACTAGTAACAGTTTTTTTCCTATAGAACTGTCTTAGTCCTTTGTGGCTTAGATTTAACAAGGTACTGGAAATATTCCTCTGAGATTTTGGTCCAAACTGACATGATAGCATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30946
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 |
---|---|---|---|---|---|
ENSDART00000080116 | Nonsense | 558 | 721 | 16 | 22 |
ENSDART00000129062 | Nonsense | 558 | 721 | 14 | 20 |
Genomic Location (Zv9):
Chromosome 11 (position 22208527)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 21214758 |
GRCz11 | 11 | 21375326 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATTCAGAAGATGGAGGTTTTGTTGTCGCAGATTGTTGATGTACATTTC[C/T]AGTACTTCAGGGACAGACAGACAAGAAGTAAGTGGATGTGTGTTTACCTC
Long Flanking Sequence:
ATGATTTTAGTTGATTAATGTGCATAAATTATAGAGTATAATAAAAAAAGTTTGTTAAGGTAAACAAAATATTTTAACTATATTTAAACCCCTATATAGAATTTAAAAAATACACTATAAAAATAAATATTTTTAAAAATAAAAGTACGCTAAAGTCAGTATGCGAGCCGAGTAGAATGTCCGAATTCCATTCATACTTTCACATTCATACTGTATAGAACATACTTTTCTAACGGCCGAGTAGTACCTTTAAATTCAAATGCAGTACATACTTAGTAGGCGGTTTCGGACGCAGCCTGGGTCTTTAGAGAAGAAATCATTTAGGACTATTTCAGGGTCTAGAACGTCAAAAGGCTTGTAAATAAACCAAATAAACACTGTTGAAAATAAATAATGACTTCATTAATATGTATCCCATTATTAATTCAATTACATTTTCTCTTCAATGCAGCATTCAGAAGATGGAGGTTTTGTTGTCGCAGATTGTTGATGTACATTTC[C/T]AGTACTTCAGGGACAGACAGACAAGAAGTAAGTGGATGTGTGTTTACCTCCCACAATGTCACACAGCACAAATTATAGATGCATATTTACTGTAACTGCTGGAATGTTCCACAATTGGACATATAATGGCTCTTACTCTTTTTCCTTCATCTTTGATAAGGTGCTTTTACACAATCCACACTAGAAAAAAAGCGCTATAGAAATACGGATGAATTGAATACTTGACACCTATCAAAAGACTGATTATGCTATAGCTTTCAAGTTTTTATTAAAGAACCCTCTCCACTAGTCAAATGGTTTCAGGACACATCAAAAATTCACTAAATGATGTGAGAATATCAGTGACCCATTTCTATCAGTTGCGAGAAAGCTGGACGTGGAGTATGATGACTGGAGCCAGTGCTGAGATTAGTGAGATTAGCGTGTTGCTCGTACCCGCTGCGAGTAGAGGAGGCAGTGTTGTGCTTCCTTATCTGACAGCAAGGACCATTCCAGACAGA
Associated Phenotype:
Not determined