ZMP
zgc:171416
Ensembl ID:
ZFIN ID:
Description:
NF-kappa-B inhibitor-like protein 2 [Source:UniProtKB/Swiss-Prot;Acc:A9JR78]
Human Orthologue:
NFKBIL2
Human Description:
nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor-like 2 [Source:HGNC Sym
Mouse Orthologue:
Nfkbil2
Mouse Description:
nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor-like 2 Gene [Source:MGI
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10341 | Nonsense | Available for shipment | Available now |
sa23005 | Nonsense | Available for shipment | Available now |
sa17406 | Essential Splice Site | Available for shipment | Available now |
sa32125 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10341
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 |
---|---|---|---|---|---|
ENSDART00000105326 | Nonsense | 51 | 1427 | 3 | 28 |
The following transcripts of ENSDARG00000071294 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 8646701)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 8644043 |
GRCz11 | 17 | 8801223 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAATCAGACTTGTTTCCCTAGGTGACTATCAAGCTGCTATTGAAGAGCAT[C/T]GACAGGAATTAGCGYTGTCTGAGATTTTGCACGATGTGATTGGATCTGCT
Long Flanking Sequence:
CAGTTTGTGCAATCAACTGGGGGAGGTGTACGCTAAAACAGGTAAAATGGACTTAAGCACTTAGTACATTTAAAGGGACCCAATAATTAAAATTTCCTCATCATTTAGTCACTTAAATGTTTCCAGACTTGTATGATTTGTTGTCTTCTGTTGAAAACAAAATAAGATTCTGAAGAATGTTGGGGAAAAATTAGCCATCGGCATGCATAAAATACTACTGCTGTTTTTTTCCCCAACATTATTCAGTATATTTTTCTTTATGATCAACAGAAGAAGCTCAAATGGTTTTAAAACAAGTGGAGGATGAGTGAATGATGACTGAATCTTCACTTTTGGTTAAACAATCCCTTCAATAACAATAATCTGGGCTCTTAACCCAAACCCTAAAAGAGTTGCTCTGTGAACGATCTTCTTGATAATTATCTGCATTATTATGTATGAATGTATAGATAATCAGACTTGTTTCCCTAGGTGACTATCAAGCTGCTATTGAAGAGCAT[C/T]GACAGGAATTAGCGCTGTCTGAGATTTTGCACGATGTGATTGGATCTGCTGTGGCCAATAGAAAGATTGGAGAGTGCTATGCAGAGCTGGGAAACATCGAAGCTGCACTGAAGGTTTGGAAACCTACATTTGCATTTATGCATTTGGCAGACAGTTCATCAGTTCTTGCTTTCTCAGGGAATTGAACAGAACTTTGGCATTTCTAGCAACTACTATTTAAGCTACAGTAAACGCATGCATGTATTCGTCTTAGTGGCGGAAAAATGACTGATCTAAAAATGTAGTGCGAGAAAGTATTTGTTTGTAAAATATGAGTTAAGTAGTACTCAAGAGTAGTTAGTATTACGCTGTGAAATTAGTTGACTGTATACTGTATAAGTAGGGCTCGTACGGGTGCTGGCAATGCTGGAAAATGCTAAATATTTAATATAGTGGTGTCAAGATAAGAAAAGTGCTTGGATTTTAGACAAAGTGCTTGTACCTACTTGGAATTGAAATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23005
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 |
---|---|---|---|---|---|
ENSDART00000105326 | Nonsense | 1013 | 1427 | 21 | 28 |
The following transcripts of ENSDARG00000071294 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 8674673)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 8672015 |
GRCz11 | 17 | 8829195 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTCGTGTACAGTTGCGTGGTTGTGTGATCAGGCCGCTCAGCGTTATTA[T/A]CAGATGTGTGGACTGCTGCCTCGTCTGTCTCTGCAGAAAGAGGGCGCTCT
Long Flanking Sequence:
TTGGACTGTGGGGGGAACTGGAGCACCCGGAGGAAACCCACATCAACACGAGGAGAACATGCAAACTCCACACAGAAATGCCAACTGACCAGTCCAGGGCTCAAACCAAACTCACTGCGCAACCGTGACGCCCCCTATTTTAACTCGCAATTCGATAATATGATAATTGAGACATAATTAATTCATTTTTATCAATCAATTAATTAATTATTGGCTATTTAAAGTAATGCCATTGTGTTTTTTTTGTGTTTTTTAAGCCACCGGCGTCTTTCCAGAACCGAGCGGCCCATGTTCCTGCACCAATCAGGATGAGGGTTAAAGTTCAGGACAATGTCTTCTTGATTCCAGTTCCACACAGGTATGATGCAGGTTTATGTGTGTTTATGTTTTGTGTTGGATTATGTGTGTGTCTGAATCTAGTTGTCATGCGTGTGTGTTTGCAGTGAGGCAGACTCGTGTACAGTTGCGTGGTTGTGTGATCAGGCCGCTCAGCGTTATTA[T/A]CAGATGTGTGGACTGCTGCCTCGTCTGTCTCTGCAGAAAGAGGGCGCTCTGCTCTTACCCACTGACCCACTGCTGGCTGTGCTGCACACCAATGAAGAGGTCAGAGACAAATAATGCTGTGCTTTTGTTTTTGGAATCACTGAAGAGCATCAAATACTGGCTTTTAAGTAAACTTAGTTTTCACTCTTTTGTTTTTTTACTCCTTCAGGGTCTTTTAGTGTGTAATGTTGCTGTCTGAGCACGAGAAAAGATCTGCAGAGTTACAAAATGCAAAGTTAATTTGTTATCTAGTTATTTTAGAGTTGTGATTGTGTTTTCTTTATGTCCAAGAAACAATGTACACACATATACAGTGCTCAAAATAATTGAGTACACTCCATTTTGAAAATGAATATTTTCATTGAGTTCTCTGTGAATACAGGTCATATAAATTTTGGTGCATTTAAACAAAACTGATTTTTAAATGGATTTATTTATTAAAATTGTATTTTAGCCACTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17406
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105326 | Essential Splice Site | 1233 | 1427 | None | 28 |
The following transcripts of ENSDARG00000071294 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 8687675)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 8685017 |
GRCz11 | 17 | 8842197 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCGCGTTTCCTCCAGCAACACCGTCTCCTGTTAGCCAACGCCATGGCCAG[T/G]AAGWRCAKAATTATTAGCCYYTAGGCCAGGGGTGTCCAAACTMGGTCCTG
Long Flanking Sequence:
AGAATATACTATTAGTAAATTACCATTACTATTACTTTAGTGTCTTGGTTGTTATCCATGGTAGACTTAAACCAACAACAACAACAAAAAAACACCAAAATATTGTCAAATTGTTGTTCTAAAAATATTGTGACTTTATTTAGTCAGTACTGCACACTGAAGTGATTTGACCTGACACTATTAATTTAGAGTTGTTTGACAGATTCATTTTTTGTTTAGTCAATGATGCTTATTTCCCTGTTTATTACTGTAAAGCTGAATTTAATTACTCTCCATATACATGGGACTTGTATAAAGTTTACTTTGAATACACTCTTCTCTCCATAGTGTCTGGAGGAGTTGAACCTAAGCATGAATCCTCTGGGTGATGGTTGGACACAAGCGCTAGCCAGTCTGTTATCCTCTTGTCCTCTTCTGTCCTCTCTGTCCCTGCAAGCCTGTGGTCTTTCTGCGCGTTTCCTCCAGCAACACCGTCTCCTGTTAGCCAACGCCATGGCCAG[T/G]AAGTGCAGAATTATTAGCCCCTAGGCCAGGGGTGTCCAAACTCGGTCCTGGAGGGCCGGTGTCCTGCATAGTTTAGCTCCAACTTCCTCTTAAACTCCTGCCTGGAAGTCTAGGGCCCCGTTTACACTGCCAGTTAAATGTGAGTCAATTCTGATTTTTTGCGCATTTGTGGCACCGATCGGATCTGTTCTATGACTGTGTAAACATGAAAAAAACGCAAGCATTCGGATATTCAGAGATCGGTTTCAGGCCTCCTTCATATGTGGAAATAAATCCGATATAAATCGGATATGTGACAATGCGACTGTCATGTAAACAGGCAGATCGGATTTATTGAGGCTTTCCGTTTTATATGTTATTAAACTTGCGACAATGTGGTGCTTCTCCCTGGTTTATTGACATAGAAGAAAGAGTGTGTGTGGAGACGCCGACGCGATAAACAACAACAGAGGAAACATGGAGGAGGAAAGAAGTCAGTCACCACAATTTGCTCCCACTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32125
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 |
---|---|---|---|---|---|
ENSDART00000105326 | Nonsense | 1299 | 1427 | 26 | 28 |
The following transcripts of ENSDARG00000071294 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 8692214)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 8689556 |
GRCz11 | 17 | 8846736 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAATGTTGACTGATTTTGTTTTTTAGGGGGATTGTCCACTCACACACT[T/A]AAATCTGTCTGGAAATGGACTTACAGACCACAGCATCCTCCTGCTTGCTA
Long Flanking Sequence:
TTTAAAAAAAAAAAAAAAATGCTAAATTTCCGCAATGACATATGATGGCTTGTGCAGGGGCTGTAGTGCTCTCCCAATTCTTAGGGGTAATATTTGAAGCCATTCCCCTTTACACTCAATGTTAAGGGCCAGGGGGAAGGGGTACAAAAATAGAATTGTGATTGGGCCAGTGTTACAGTGTAATGATTTATAATTTTTTTTATGTTATTATTAATTGTCAATATGAGCTTTTAAATTTAAGTGCGGCCACCAGTTGTTGTTGTTTGTTTTCCCTTTTATTCCGCAAGTATGAGTTTTAATAATGACAGGAAAAGCACAAATTGATCAGATATGAATGATTTCTGAAGGAAGTAACCGTTGTCTTAAATATTGTGATTGAACGAATGATAAAATATATGTAATGGCTTTCAGTCTGTGCTTTTAAAATTGGCAGCGTTCATCTGCTGTGGACACAATGTTGACTGATTTTGTTTTTTAGGGGGATTGTCCACTCACACACT[T/A]AAATCTGTCTGGAAATGGACTTACAGACCACAGCATCCTCCTGCTTGCTAGGTGAGTGATTCAACTATGTTTATTTTTATGCATTTTGCAGACACCTTTATCCAAAAATACTGAAAGAAAACTTATTCTGGCTCTTTCATGCTGTATATGTTTATTGTGTTAGTATGCAAAAGCACATAAATCCAGTGTAAAACTACTCATGAAGGCTGTATTTACACTGCAGATCTTGATGGTCAATTCCGATTTTGTGACTCAGTATCTGATTTGTTTTGATGACCTGCTTACATCATCTTTTAAAAGTGAATTGTCTCCAAACGTCTGCATTTACACAGCACACGGCAAAGGCGCAATGACTAGCAGCTGATAATTAAAGAGTGCTCTTTTCTCTATTCCTGTATGTAATCTGTTCGAGCTTTTGACAAGCTGTTTTACTATAGTTTATGACAGAAAGGTTTTCATTTGTCCATCTTCTTTTGATAAATAGGCTTTTTTAACCTTTA
Associated Phenotype:
Not determined