ZMP
si:dkeyp-72h1.2
Ensembl ID:
ZFIN ID:
Description:
tumor necrosis factor, alpha-induced protein 2 [Source:RefSeq peptide;Acc:NP_001025387]
Human Orthologue:
TNFAIP2
Human Description:
tumor necrosis factor, alpha-induced protein 2 [Source:HGNC Symbol;Acc:11895]
Mouse Orthologue:
Tnfaip2
Mouse Description:
tumor necrosis factor, alpha-induced protein 2 Gene [Source:MGI Symbol;Acc:MGI:104960]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa32285 | Nonsense | Available for shipment | Available now |
| sa23665 | Nonsense | Available for shipment | Available now |
| sa13685 | Essential Splice Site | Available for shipment | Available now |
| sa13324 | Nonsense | Available for shipment | Available now |
| sa36998 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32285
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 |
|---|---|---|---|---|---|
| ENSDART00000063736 | Nonsense | 321 | 547 | 4 | 13 |
| ENSDART00000126959 | Nonsense | 321 | 701 | 4 | 13 |
The following transcripts of ENSDARG00000043416 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 18745352)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 18773609 |
| GRCz11 | 20 | 18673192 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACTGCAAGAGCTTACCAGGTCCAGTATTGAGTTTGAGGATTGCGCCTA[T/A]ATACTGAGCTGGATAAAGATCTACTACCCAAAGTAAGATTGATGTCTTAA
Long Flanking Sequence:
GGCAGGACAGAAGATGAAGAGGACAAGCTCCTGAGAGACTCAGAGATATTCAGGGAGCGACTAAAGTTTGCCATTCTTGACTCTTTCAATGAGGAAAATCAGGAGACACTTAAGAGTGCGTTGATTTCAATACTTCAAGAGGAGGCACAGGACAGACGTTGGGCAGAAGTTTCTGAAAACCAGCGTCCAATATGGAGGCCCACAGAGTGCAGACAAAAAATCCATGATCCACTGCTTAAGACTTTAGTGGAGACACGATTGAAAAATGCAGATGGACAGGAGAATAAAGCAGACAAGCTGTCCACTTCCTTAAAGAGAGAGGTGTGCCGAACAGGCAAACAAGTACAAAAAGACCTGCTGATTGTGGTCCGAAATCTAAAGGAGTGTTATCCAGCAGACTTTGACATCTGCAGAACATATGCTCAACTTTACCATCAGACCTTCTCCGCCAGACTGCAAGAGCTTACCAGGTCCAGTATTGAGTTTGAGGATTGCGCCTA[T/A]ATACTGAGCTGGATAAAGATCTACTACCCAAAGTAAGATTGATGTCTTAAAAGCACATTCATTTACATGTCAGCTATCTATTTGAGCTGTGGGGATAAATTGTTTGAGAAATCAATTCTGCTTCATAAATTCTGAGATGCTCAAAATGCATCGCTACTCTCTCTCTTTAATTGATGCTTTATCAAAGAGGGTTTTTGATTATGGGTTTTTGAAAATGACCATAAATGCATTGTATATCACAGCTCTAAGTCAGGGGTGCATGGCCTACCCTGTTCCTGGAGAGCCACCTTTCTGCAGATTTCAGTTGCTACCCATATCAAACACACCTGAACCAATTAATTAGGACCTGAACACCAAGTGGTAATTACAGGCAGGTGTGTTTGATATGGGTTGCAACTGAAATCTGCAGAAAGGTGGCTCTCCAGGAACACGGTTGGCCACCCTTGCTCTAAGTAAAGGAAAACATTCAGCTGAGGTTTAAATATGAAAGTGCACAGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23665
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 |
|---|---|---|---|---|---|
| ENSDART00000063736 | Nonsense | 361 | 547 | 5 | 13 |
| ENSDART00000126959 | Nonsense | 361 | 701 | 5 | 13 |
The following transcripts of ENSDARG00000043416 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 18749580)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 18777837 |
| GRCz11 | 20 | 18677420 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACAGTTCATTACTTGGACCTCTGTTACCTGAGGAACATCTTAAAAGAT[T/A]AGAGGATCAGTACTTCTCATGCAAGGAGGTAATTTTATCAAAGTCATTAC
Long Flanking Sequence:
AGCTGAACAAATAATATACGAGTCAGGATAGTTAATTAAGAATAAATGCATGTTATAAGACAATGAAAGTTTTATTTTTTTTTTTGTCTTGGCTGTTGTTGGAAACCCCCAAAACCAAAATATGACCTTTTATAATGCATAATAGTAGCTTTTTAATGATTATTTTAGGCATGAGGGGTATTTGTAAGGAATTGGATGCAAGCAGAGTACTGCTGTTTCATAAAGCATAAAGCACCATCTGCTGTTAAAAAACTAAACTCAGAATCCATTCAAAAGAGAATAGCAATGCATTTTGATAGAATTGATGTAAATTTCTTAAATGATTTTTTTTCTTAGCTCTATATTATCTTTATTATAAACATTCAGTATTTTCTGACACTGTTTATGAATATTAATGTTCTTTTTTCATCTTAGAGATGTACTGAAGCACAAAGAACTGGAGCAGCACATCAACAGTTCATTACTTGGACCTCTGTTACCTGAGGAACATCTTAAAAGAT[T/A]AGAGGATCAGTACTTCTCATGCAAGGAGGTAATTTTATCAAAGTCATTACCAAATAGTTTTATCAATAGTCAACCTCATATGCATTTGACACCATAGTGCTCACTTGTGTTGGCATTGTGAGATGATCTTATTATTAGATCTTATCTTCTACAGTGACATGTTGTGGTTTAATGATTATTTGTTCTAATTAGAATGAAGTCAGAAATTGGTTATCCAATGCTTTTGATAAAGAAGTGGATAAATGGAGTGATGGCTTTGAACCTGAGCTCATTGAAGGATGCTACTTTGGTAACCTTGCTGTCGATGTTTTGCCGGTAAGCTATGGGCTCTGTTGACATGCTATGCAGTATGTATTAAAAATATACAGCAGCATTTCATAAAATGTAAATGTTTTTGCTTCCAAGCTTATTGAAGGAACTGTGAAAGAGGTCAATGCACTTTTGGAATGTGAAAGTAAATCCTGGAGTCTTCTATGTCTACTGGATAGCTCTCTACTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13685
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 |
|---|---|---|---|---|---|
| ENSDART00000063736 | Essential Splice Site | 370 | 547 | 5 | 13 |
| ENSDART00000126959 | Essential Splice Site | 370 | 701 | 5 | 13 |
The following transcripts of ENSDARG00000043416 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 18749610)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 18777867 |
| GRCz11 | 20 | 18677450 |
KASP Assay ID:
2261-4118.1 (used for ordering genotyping assays)
KASP Sequence:
TGAGGAACATCTTAAAAGATTAGAGGATCAGTACTTCTCATGCAAGGAGG[T/A]AATTTTWTCAAAGTCATTACCAAATAGTTTTATCANNAGTCAACCTCAWA
Long Flanking Sequence:
GTTAATTAAGAATAAATGCATGTTATAAGACAATGAAAGTTTTATTTTTTTTTTTGTCTTGGCTGTTGTTGGAAACCCCCAAAACCAAAATATGACCTTTTATAATGCATAATAGTAGCTTTTTAATGATTATTTTAGGCATGAGGGGTATTTGTAAGGAATTGGATGCAAGCAGAGTACTGCTGTTTCATAAAGCATAAAGCACCATCTGCTGTTAAAAAACTAAACTCAGAATCCATTCAAAAGAGAATAGCAATGCATTTTGATAGAATTGATGTAAATTTCTTAAATGATTTTTTTTCTTAGCTCTATATTATCTTTATTATAAACATTCAGTATTTTCTGACACTGTTTATGAATATTAATGTTCTTTTTTCATCTTAGAGATGTACTGAAGCACAAAGAACTGGAGCAGCACATCAACAGTTCATTACTTGGACCTCTGTTACCTGAGGAACATCTTAAAAGATTAGAGGATCAGTACTTCTCATGCAAGGAGG[T/A]AATTTTATCAAAGTCATTACCAAATAGTTTTATCAATAGTCAACCTCATATGCATTTGACACCATAGTGCTCACTTGTGTTGGCATTGTGAGATGATCTTATTATTAGATCTTATCTTCTACAGTGACATGTTGTGGTTTAATGATTATTTGTTCTAATTAGAATGAAGTCAGAAATTGGTTATCCAATGCTTTTGATAAAGAAGTGGATAAATGGAGTGATGGCTTTGAACCTGAGCTCATTGAAGGATGCTACTTTGGTAACCTTGCTGTCGATGTTTTGCCGGTAAGCTATGGGCTCTGTTGACATGCTATGCAGTATGTATTAAAAATATACAGCAGCATTTCATAAAATGTAAATGTTTTTGCTTCCAAGCTTATTGAAGGAACTGTGAAAGAGGTCAATGCACTTTTGGAATGTGAAAGTAAATCCTGGAGTCTTCTATGTCTACTGGATAGCTCTCTACTGAGGTAGGTAATATTTATATTACTAATTTTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13324
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000063736 | Nonsense | 400 | 547 | 6 | 13 |
| ENSDART00000126959 | Nonsense | 400 | 701 | 6 | 13 |
The following transcripts of ENSDARG00000043416 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 18749862)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 18778119 |
| GRCz11 | 20 | 18677702 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAGTGGATAAATGGAGTGATGGCTTTGAACCTGAGCTCATTGAAGGATG[C/A]TACTTTGGTAACCTTGCTGTCGATRTTTTRCCGGTAAGCTATGGGCTMTG
Long Flanking Sequence:
GCAATGCATTTTGATAGAATTGATGTAAATTTCTTAAATGATTTTTTTTCTTAGCTCTATATTATCTTTATTATAAACATTCAGTATTTTCTGACACTGTTTATGAATATTAATGTTCTTTTTTCATCTTAGAGATGTACTGAAGCACAAAGAACTGGAGCAGCACATCAACAGTTCATTACTTGGACCTCTGTTACCTGAGGAACATCTTAAAAGATTAGAGGATCAGTACTTCTCATGCAAGGAGGTAATTTTATCAAAGTCATTACCAAATAGTTTTATCAATAGTCAACCTCATATGCATTTGACACCATAGTGCTCACTTGTGTTGGCATTGTGAGATGATCTTATTATTAGATCTTATCTTCTACAGTGACATGTTGTGGTTTAATGATTATTTGTTCTAATTAGAATGAAGTCAGAAATTGGTTATCCAATGCTTTTGATAAAGAAGTGGATAAATGGAGTGATGGCTTTGAACCTGAGCTCATTGAAGGATG[C/A]TACTTTGGTAACCTTGCTGTCGATGTTTTGCCGGTAAGCTATGGGCTCTGTTGACATGCTATGCAGTATGTATTAAAAATATACAGCAGCATTTCATAAAATGTAAATGTTTTTGCTTCCAAGCTTATTGAAGGAACTGTGAAAGAGGTCAATGCACTTTTGGAATGTGAAAGTAAATCCTGGAGTCTTCTATGTCTACTGGATAGCTCTCTACTGAGGTAGGTAATATTTATATTACTAATTTTACAAATTCTTCTTATTTAATTACATTAAAATAGTAAGGCTGATGGTATTTTCCCCATTTTCTCCAATGGCAGCTATGGGACAAGTCTGAAAGAACTTGTCAAAAGAAAACAAGAAAACATTCCTAAAATTCTCAGGGATAGCTTGGTGAATATTTACGTTTTTAAGTGAGTTTCACTGACTTTCTATACTGCAAAAAATATGTTCCTATATATCATATTCATATTATCATCTTATTCACATTATTATTTACTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36998
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 |
|---|---|---|---|---|---|
| ENSDART00000063736 | Essential Splice Site | 411 | 547 | 6 | 13 |
| ENSDART00000126959 | Essential Splice Site | 411 | 701 | 6 | 13 |
The following transcripts of ENSDARG00000043416 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 18749897)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 18778154 |
| GRCz11 | 20 | 18677737 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCATTGAAGGATGCTACTTTGGTAACCTTGCTGTCGATGTTTTGCCGG[T/A]AAGCTATGGGCTCTGTTGACATGCTATGCAGTATGTATTAAAAATATACA
Long Flanking Sequence:
AAATGATTTTTTTTCTTAGCTCTATATTATCTTTATTATAAACATTCAGTATTTTCTGACACTGTTTATGAATATTAATGTTCTTTTTTCATCTTAGAGATGTACTGAAGCACAAAGAACTGGAGCAGCACATCAACAGTTCATTACTTGGACCTCTGTTACCTGAGGAACATCTTAAAAGATTAGAGGATCAGTACTTCTCATGCAAGGAGGTAATTTTATCAAAGTCATTACCAAATAGTTTTATCAATAGTCAACCTCATATGCATTTGACACCATAGTGCTCACTTGTGTTGGCATTGTGAGATGATCTTATTATTAGATCTTATCTTCTACAGTGACATGTTGTGGTTTAATGATTATTTGTTCTAATTAGAATGAAGTCAGAAATTGGTTATCCAATGCTTTTGATAAAGAAGTGGATAAATGGAGTGATGGCTTTGAACCTGAGCTCATTGAAGGATGCTACTTTGGTAACCTTGCTGTCGATGTTTTGCCGG[T/A]AAGCTATGGGCTCTGTTGACATGCTATGCAGTATGTATTAAAAATATACAGCAGCATTTCATAAAATGTAAATGTTTTTGCTTCCAAGCTTATTGAAGGAACTGTGAAAGAGGTCAATGCACTTTTGGAATGTGAAAGTAAATCCTGGAGTCTTCTATGTCTACTGGATAGCTCTCTACTGAGGTAGGTAATATTTATATTACTAATTTTACAAATTCTTCTTATTTAATTACATTAAAATAGTAAGGCTGATGGTATTTTCCCCATTTTCTCCAATGGCAGCTATGGGACAAGTCTGAAAGAACTTGTCAAAAGAAAACAAGAAAACATTCCTAAAATTCTCAGGGATAGCTTGGTGAATATTTACGTTTTTAAGTGAGTTTCACTGACTTTCTATACTGCAAAAAATATGTTCCTATATATCATATTCATATTATCATCTTATTCACATTATTATTTACTTTAAAACAAGTATAAATGACATGCAGTGCATTGTTGAC
Associated Phenotype:
Not determined