ZMP
chuk
Ensembl ID:
ZFIN ID:
Description:
Inhibitor of nuclear factor kappa-B kinase subunit alpha [Source:UniProtKB/Swiss-Prot;Acc:Q4G3H4]
Human Orthologue:
CHUK
Human Description:
conserved helix-loop-helix ubiquitous kinase [Source:HGNC Symbol;Acc:1974]
Mouse Orthologue:
Chuk
Mouse Description:
conserved helix-loop-helix ubiquitous kinase Gene [Source:MGI Symbol;Acc:MGI:99484]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35487 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35488 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35487
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000027428 | Essential Splice Site | 159 | 758 | 6 | 22 |
Genomic Location (Zv9):
Chromosome 13 (position 25590725)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 25236385 |
GRCz11 | 13 | 25366835 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGGATCTCAAGCCAGAGAATATTGTGCTGCAAGAAATTAATGGAAAGG[T/C]ATTTACTTTTTAGTGGTTAGAATTTTATTCTATAGACATGCTTTTCAAAC
Long Flanking Sequence:
CTAATCTTTTTTTATCCTACTTCTAAGGCTAAAGCACCTTAATGTTGTCACAGCAAAGGATGTGCCTGAGGAGATGATGCACATTGCCTTGAATGATTTACCACTTTTAGCCATGGAGTATTGTTCCAAAGGAGATCTTCGTAAGGTGTGTGCGTGTGACCATAGGCTTTTCTTTTGTATCTGTCAGATGTGCTCTTATATTAAGTTCATTCTGACTCATTTCTGTTTTTTAATTCTTTTTTTGTAGTTGTTGAGCAAACCTGAAAATTGCTGTGGGTTGAAAGAGAGTGAGGTGTTGTCTCTACTCAATGATGTTGGTAATGTGTCAAAGCCTGTTGCTTCTGTTTTTAGTATTTTTACCATCAATAGCTGAGGGTTGTGTGTCAAACTGAGTGTTTTCTTTTGAATAGGTTCTGGAATCCAGTACCTTCATGAGAATAAGATCATACACAGGGATCTCAAGCCAGAGAATATTGTGCTGCAAGAAATTAATGGAAAGG[T/C]ATTTACTTTTTAGTGGTTAGAATTTTATTCTATAGACATGCTTTTCAAACATGGGTTATGTTTTGTTGTCTATGCAGCTTGTTCACAAGATAATCGACCTTGGTTATGCCAAAGACCTGGACCAGGGGAGCTTATGCACTTCATTTGTGGGGACTTTACAATATCTGGTATGTTTTAACCTGCATTATTTAGAAATATGACAGTTATGGCAATAATCTCACATACACTTTCATATGCTGGAGATTTTTTATTAAGATGCAGGGAATTTTTTGTGTCTAATACCTGTCAGTTTTGAGATTTTGGAGATTGTTCTTTGTACTCATGGGAAAAAAAACATCCACAATGCAATTTTAAGTGTTTATTTTATACTAATTTATAATTATAGAAAAAAATACCATTGTTATTTTAATAACATATTTTTTAAGGCTGTTACCTCAAAATGAGTTTTTCACTTGTAGTGATCCCTGTTTTTACTCCAGTATCACTTACACCAAATTTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35488
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000027428 | Essential Splice Site | 504 | 758 | 14 | 22 |
Genomic Location (Zv9):
Chromosome 13 (position 25596143)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 25241803 |
GRCz11 | 13 | 25372253 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATACAGTACGACTTGGAGAAATACAGTGATCAGATGCAGTATGGCATATG[T/A]ACGTTTTTGAATATGCTGCTTTGTTGATAAAGCTAAAAATGTGTTATTGC
Long Flanking Sequence:
GAAAGTGTCAACTTTATTGGTAAGATATGATTTGGCTTTTCTTTGGATCATTTGTTTAGATGTTATTGCGTGAAATGTGAAGTATTTGTAAACTTTCATTAGAATATTAAAATTCCTTAACTCGTTTTGTGTTTCAGTTCGGGAAACCAAAACTCAGCTCCCACTAAGTACCCTAAAAAAGGTTTGGGGTGAGGCGGTTAGCTACATTTGTGGCCTCAGAGAAGACTACAGCCGCCTCTTCCAGGGCCAGCGTGCAGCCATGTACATACCTTACATTTACTATGCTCGTTAATGTCTCTGTCTTGTGTTTTGTTCTGTTCATAATTGAATCATTTGTTTGTTTGCAGGCTGAGTCTTCTTCGCTTCAATACAAATTTGACAAGATACAAGAACATGATGTTCTCCTTTTCACAACAGCTCAAAGCAAAGCTGGACTTTTTTAAGACCAGCATACAGTACGACTTGGAGAAATACAGTGATCAGATGCAGTATGGCATATG[T/A]ACGTTTTTGAATATGCTGCTTTGTTGATAAAGCTAAAAATGTGTTATTGCATTATTGATTAGTAATAATCCATTTTTTTTGTAGCTTCAGAAAAGATGCTGAAGGCTTGGCACGAAAATGAAGAGAGGGCTGCTGCTTTTGCACAGGTGCTGTGAATGAATGATACACAAAGTAGTTTTAAAACCTTTAATAAATAGTCATCTAAGTGGATTTCACATTTTTGTAAAAAAAAAAATCTTTTTGACCAGCATATCTGTTGTGCAAATGTATTTGTATGTGGGTTTACATTTGTTTTAACTACAACTAAAACAACTTTTTTATCTTCTGAAGGTGGCAGAGATTGGTCATCTGGATGAGGAAATAATGGCGTTGCATTCGGAAATCGTTGAGTTACAGAGAAGTCCTTATGCTCGTCGTCAAGGAGATGTCATGGAGCAGTTGTGAGAACCTTTGTTCAGAAATAAGCTTTGTGAAGTTTATCAGCATTTATTTTGACATAA
Associated Phenotype:
Not determined