ZMP
nfkb2
Ensembl ID:
ZFIN ID:
Description:
nuclear factor NF-kappa-B p100 subunit [Source:RefSeq peptide;Acc:NP_001001840]
Human Orthologue:
NFKB2
Human Description:
nuclear factor of kappa light polypeptide gene enhancer in B-cells 2 (p49/p100) [Source:HGNC Symbol;
Mouse Orthologue:
Nfkb2
Mouse Description:
nuclear factor of kappa light polypeptide gene enhancer in B-cells 2, p49/p100 Gene [Source:MGI Symb
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22283 | Essential Splice Site | Available for shipment | Available now |
sa22284 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22283
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 |
---|---|---|---|---|---|
ENSDART00000056499 | Essential Splice Site | 185 | 247 | 8 | 10 |
ENSDART00000057672 | Essential Splice Site | 179 | 241 | 7 | 9 |
ENSDART00000078289 | Essential Splice Site | 185 | 902 | 7 | 23 |
ENSDART00000133064 | None | None | 100 | None | 2 |
ENSDART00000134122 | Essential Splice Site | 185 | 902 | 8 | 24 |
Genomic Location (Zv9):
Chromosome 13 (position 22864156)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22593494 |
GRCz11 | 13 | 22723944 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAAAGAAGAGAAGAGGAAGGTGAAAGGGCCTGGATATAAGTTTAGTGG[T/A]GAGAGTTATACTATATCGTATATATATATATACGATAACTATTGAATTGT
Long Flanking Sequence:
TTTTTATTTTGTCCATACTACACATCGTCAAATTGCACAGCCCTACATAGTGAGCGGAATTCACTTTAATATATAAAGTCTTGCTGATATTATAACGTTTTGACTGTTATCTACAGGTGTTAAACTTTGTGGGCAATGCTCGTGTGGAGGTTCAGCTGGTGACACACACAGACCCTCCACGAGTTCACGCACACAGCCTTGTGGGTCGACACTGTAATGAAAGCGGGGTCTGCAGTGTTGATGTCGGGCCTAGTGATTTCACAGCACAGTGAGTGAACGCGATTACTGCTCGTATGATCTTTTTCCTTGTTATTATGATTAAGCTAGATTGTCTGTGCAACTTTGTCATGTGCTGTTTGTGTGTTTATTGTGCAATCTGTGCCTAGATTCAGTAACTTAGGCATCCTGCATGTCACAAAGAGAGGAGTGGTAGAAGTCTTAACGAAAAGGCTGAAAGAAGAGAAGAGGAAGGTGAAAGGGCCTGGATATAAGTTTAGTGG[T/A]GAGAGTTATACTATATCGTATATATATATATACGATAACTATTGAATTGTCTTTTTGCTGCTTGTGTCTTCTTCTGATGTAATGTTTCTTGTTTTCTCACTCTTGCAGATGCAGAGGAAAATGCTCTTATGCAAGAAGCCAAAGAGTTAGGCAAAAACATGGATCTGAACATTGTACGTTTAAAGTTCACTGCCTACCTGCAGGACAGCAATGGGAGTTACACCAGAGCATTGAAGCCTGTTGTGTCCAATCCTATATATGACAGCAGTAAGTCCTGCTACACGAAAACTACACAGTAAAATAAAAAAGAGAGAAAAGTTCATATACAGTTGAAGACAGGATTATTAGCTTGTTTATTTTTTCCCCAATTTCTGTTTACAGAGAGAAGATTTTTTCAACACATTTCTAAATATAATAGTTTTAATAACTCATTTCTAATGACTGATTTATTTTATCTTTGCCATGATGACAGTAAATAATATTTGACTAGATATTATACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22284
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056499 | None | None | 247 | None | 10 |
ENSDART00000057672 | None | None | 241 | None | 9 |
ENSDART00000078289 | Nonsense | 601 | 902 | 17 | 23 |
ENSDART00000133064 | None | None | 100 | None | 2 |
ENSDART00000134122 | Nonsense | 601 | 902 | 18 | 24 |
Genomic Location (Zv9):
Chromosome 13 (position 22869230)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22598568 |
GRCz11 | 13 | 22729018 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACAGCACATATTAAGTTTTTTTTTTTTTTTCACTGTTTACAGGTCAGTA[T/A]CCAGTCCATCTCGCTGTGAAGAAAGATGGAGAGCGTTGTTTGCGATTGCT
Long Flanking Sequence:
CAACAAGCTCAGTCAGGTAATTTACAATAAATATATTGTAGAAATACTTTTAAAATGCATAATCTGATGATTTTATTTTATTATTCATATGTTATATATTCATGTAAATACATACATACATACATATATGTATGTAGCATTTTATTATTATTATTTTTTTTTACATTCTATTTTCTTTCATCTCCAGGCTCCTCTGCATCTGGCTGTGATCACCAAGCAACCCAAGTTAGTAGAGATGTTGATGAAATCGGGTGCAGACCCGAGTCTGCTGGACCGAGAGGGCCGGACAGTGCTTCACTTGGCCGCACATACTGGTGATGATGTCATACTAAGACTGGTCCTGAGCCTGCTAGGAGAGCATCACTCCCATTTAATAAACAGTGCTGACTTCACAGGTGAGACGAGACACACACCTTCTGTTAAAATGTCACTTATGGTTGCATGGAATTTTACAGCACATATTAAGTTTTTTTTTTTTTTTCACTGTTTACAGGTCAGTA[T/A]CCAGTCCATCTCGCTGTGAAGAAAGATGGAGAGCGTTGTTTGCGATTGCTGGTAGAAGCAGGAGCAAAGATTAACATGCCAGAGCAGAAAAGTGGCTGCACTGCACTGCACCTGGCAGTGAGGGACAACCTGTTGAAACTGGCCTGTAATCTCATCACTGAGGTAAAGATGTTGGACCGTTAAGATTTCTCATAGTCCTGTGGTCACAGTTACATTTAATTGTACTTGTTATACTACTATTACAAGTCCAGTTTACCAAGTAGAAAATGTGTATAGTACAATAAATGTTGTTAAAAGCTCTTAAAATAAATATTTCTTAAAATTACCTTCAATGTTGAAAACAACTGTCCTGTTTAATATTTTTGAGTTTTACTCTAATCATTATAAAATTCAAAGGAGCAACATTAATTTGAAATAGAAACGTTTGCAATGTATGTTAATTGATAATGTCATGCTTCCCTGCTAAATCAAAATTTTCTTAAAGAACATTTACTGACCTC
Associated Phenotype:
Not determined