ZMP
tnfb
Ensembl ID:
ZFIN ID:
Description:
tumor necrosis factor (TNF superfamily, member 2) [Source:RefSeq peptide;Acc:NP_001019618]
Human Orthologues:
LTA, TNF
Human Descriptions:
lymphotoxin alpha (TNF superfamily, member 1) [Source:HGNC Symbol;Acc:6709]
tumor necrosis factor [Source:HGNC Symbol;Acc:11892]
tumor necrosis factor [Source:HGNC Symbol;Acc:11892]
Mouse Orthologues:
Lta, Tnf
Mouse Descriptions:
lymphotoxin A Gene [Source:MGI Symbol;Acc:MGI:104797]
tumor necrosis factor Gene [Source:MGI Symbol;Acc:MGI:104798]
tumor necrosis factor Gene [Source:MGI Symbol;Acc:MGI:104798]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22693 | Essential Splice Site | Available for shipment | Available now |
sa22694 | Splice Site, Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22693
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017569 | Essential Splice Site | 60 | 242 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 15 (position 33996070)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 34841846 |
GRCz11 | 15 | 34699815 |
KASP Assay ID:
2260-8809.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTTGGCCTCTGCGTTGTGGCTGCATTTTTCTTCACCTGGCATGTGATG[G/A]TAAGACTGAAATTTCATTGAGGGATGATCATTGGAATAATGAAACATTCT
Long Flanking Sequence:
CACATTTAATCTACTAACAGGTTTTTGAAAGTGTAAAGTGAAAAGCCTATTATATTTACTACTATCTTTCCGGCAGAAGTGTGAGGGTGTGTATGTGCAAGCGCCGTGTCTGGAGGTTTGTGTGTGGGTGGAAAGTTGGTGTTTGAGAGCTGAGGGTGTTCTTTCCCCTTTCAAACCAACCTCTGTTCCTGAAGCCGCTTGCTGGCTTACATCACTGGAGTTTCCCCTATCTTTAGTGTATATAAATGACAGAGCAGACAAGTTCAGTTCATACACAAAAACTCAGTAAAAAAAGGAACACAGCAAGGAGAACTAGCAGCATGGTGAGATACGAAACAACATTAGTAGATATGGAAGCCGGTGTCGGGGGAGTTTATCAGACAACCGTGGCACCTGTACCGGTTAATTCTTCAAGAAGCTGGATATGGAAGACACTCGCTGCAGTTGCTTTTGTTGGCCTCTGCGTTGTGGCTGCATTTTTCTTCACCTGGCATGTGATG[G/A]TAAGACTGAAATTTCATTGAGGGATGATCATTGGAATAATGAAACATTCTTGAAATACCTTATTTAAAAAGCAATGTCTTTTGCAGAAGCCAAACGAAGAAGGTCAGAAACCCAACAGAGAACATCTAAAACAACAAATCACCACACCTTCAGGTTAATAACATTCCCAGTATTCCATCTTGTACTTTTGTTTTGCTTTTCTTTTTCTAAAACAACTCCTTTTTGGGCATTGATGGTTACATTTCTATACTTAATAACACTTAGAAAAAAACATGACTTCTTTTAGAACTGTTCAATGAAAATTTAAGAGTTAATATCATTAAACAAAGTGTAACTATTAAACTTGTAACCCAATGTTGGACAATATATGGACAACATACAGCCAAACTGTCTTGTTTTTGGGATGTTGCACATTGGTCAGTCTTGTGGCTGTTTTAAATGTGCTAAATCAATAATCTTAAGCTAGATTTGTCCATATTTGATCCAACATTGGGTTTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22694
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 > A
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017569 | Splice Site, Nonsense | 82 | 242 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 15 (position 33996221)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 34841997 |
GRCz11 | 15 | 34699966 |
KASP Assay ID:
2260-8810.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTCAGAAACCCAACAGAGAACATCTAAAACAACAAATCACCACACCTT[C/A]AGGTTAATAACATTCCCAGTATTCCATCTTGTACTTTTGTTTTGCTTTTC
Long Flanking Sequence:
GAGGGTGTTCTTTCCCCTTTCAAACCAACCTCTGTTCCTGAAGCCGCTTGCTGGCTTACATCACTGGAGTTTCCCCTATCTTTAGTGTATATAAATGACAGAGCAGACAAGTTCAGTTCATACACAAAAACTCAGTAAAAAAAGGAACACAGCAAGGAGAACTAGCAGCATGGTGAGATACGAAACAACATTAGTAGATATGGAAGCCGGTGTCGGGGGAGTTTATCAGACAACCGTGGCACCTGTACCGGTTAATTCTTCAAGAAGCTGGATATGGAAGACACTCGCTGCAGTTGCTTTTGTTGGCCTCTGCGTTGTGGCTGCATTTTTCTTCACCTGGCATGTGATGGTAAGACTGAAATTTCATTGAGGGATGATCATTGGAATAATGAAACATTCTTGAAATACCTTATTTAAAAAGCAATGTCTTTTGCAGAAGCCAAACGAAGAAGGTCAGAAACCCAACAGAGAACATCTAAAACAACAAATCACCACACCTT[C/A]AGGTTAATAACATTCCCAGTATTCCATCTTGTACTTTTGTTTTGCTTTTCTTTTTCTAAAACAACTCCTTTTTGGGCATTGATGGTTACATTTCTATACTTAATAACACTTAGAAAAAAACATGACTTCTTTTAGAACTGTTCAATGAAAATTTAAGAGTTAATATCATTAAACAAAGTGTAACTATTAAACTTGTAACCCAATGTTGGACAATATATGGACAACATACAGCCAAACTGTCTTGTTTTTGGGATGTTGCACATTGGTCAGTCTTGTGGCTGTTTTAAATGTGCTAAATCAATAATCTTAAGCTAGATTTGTCCATATTTGATCCAACATTGGGTTTTGACAACCCAACATTGGTTTAGAGTGTATTCATTATGTGATTTGTACAGAAAAAGGGAAGCATATAGACTTATAAAACAAACATAGAAGTCACTTATTCAACAAACATACACTGTTAAAGTATCCTGGTTGCCTTCAATTTTTAAGCTGAATCA
Associated Phenotype:
Not determined