ZMP
si:ch211-274c22.6
Ensembl ID:
ZFIN ID:
Human Orthologue:
TNFAIP3
Human Description:
tumor necrosis factor, alpha-induced protein 3 [Source:HGNC Symbol;Acc:11896]
Mouse Orthologue:
Tnfaip3
Mouse Description:
tumor necrosis factor, alpha-induced protein 3 Gene [Source:MGI Symbol;Acc:MGI:1196377]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22193 | Nonsense | Available for shipment | Available now |
sa35393 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35394 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22194 | Nonsense | Available for shipment | Available now |
sa10832 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22193
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033528 | Nonsense | 33 | 762 | 1 | 8 |
ENSDART00000147959 | Nonsense | 28 | 756 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 1054254)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 1052062 |
GRCz11 | 13 | 1182353 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTCCTGAAGGCGGTCAAAATCAGAGAGCGGGTGCCCAATGATGTGGTC[A/T]AACCCTCGGCAGGCGGCAGCCTGATCCATCACCTGCGGAGCATGCACCGT
Long Flanking Sequence:
TAAAGCCGAGGAGAAAGGGGTTCAGGGGGGACCATTGGTGGCGTTCTGGCGGGATAAGTTGTCCCTAAAGAACCCCACACAAATAAACGGCGCCCTTGCTAGTCAAATGGCGTTTTCTGAACACACACACACACACACACATACACACACACACACACACACACACACACATCTATCGAGATTTATTCACTGTTATGTGGGAAATTCATAAAAATTTTGACCTTAAAGGGCCTACGAGGAGTACGTCATCAGGGTCTTTTTTTCTAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTTGTGGTGGTGGTTCATTTGTAGCACATGGTTGAGCAATCCTGACAATGGTGTTTCTGTCTTCTTCTTCTTCTGGCAGAGATAGATTGGTTATCCGGAACGCCATGTCTCAGGGCCAGAACTTCCTGCCCAAGTTCCTATTCGTCAGCAATCTCCTGAAGGCGGTCAAAATCAGAGAGCGGGTGCCCAATGATGTGGTC[A/T]AACCCTCGGCAGGCGGCAGCCTGATCCATCACCTGCGGAGCATGCACCGTTACACACTGGAGATGATCCGAATGAGCCAGTTTCCGCAGGCCTTCAGAGAGGTCATCCAGGCGGCCATCTTGGACAGGGCAATGCAGAGCTCGCTGGAACAGGAGAAGAGGCTGAACTGGTGCCGTGAGGTCAAGAAGCTGGTGCCGCTCAGAACCAACGGTAACAGCGGGCTTAATTTCTTTAGCTCTGGCTTTCTGACAATTCTTCCACATAACCCAAGACAAATGGGCTAAACCAAGATGACTGGGCTGATATATGCTGTATGAATGCCCGGTCACTCACTCTAGATAGTAGGCAATGTACAGTATTCAGATTCATATTGTTAGGCTCTTAGTGTAGGGGTGATTAAACATCATCCAGGATAATTCATCAACTACTCTTTGGTCTCAGTAATAATATTTAAACCTAAACTCGTCGTTTCACAGGTAAAAAAATAAAAAAAATGTATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35393
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033528 | Nonsense | 248 | 762 | 4 | 8 |
ENSDART00000147959 | Nonsense | 243 | 756 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 1073970)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 1071778 |
GRCz11 | 13 | 1202069 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGGGAATATACCTGCCTTTGCATTGGCCTCCAGGTGAATGCTACAAATA[T/A]CCCATAGTGCTCGGCTACGACTCGCAGCATTTTGCACCCCTGATCACAAT
Long Flanking Sequence:
ATTCTTATTATATCCTATATATATCTTTAATATTTAAATGTTTTCATATGTAAAGATATTTGCCTATTTCTCTCTTGTGTGTATTAAGCAGTGTGTAAGCGAGGTGCAACTCTGTGCTGGAGTTTAGACCGGGTTTGTTTTGGTCTAATGAAAAATCTATTTTAGTTTCTCAAAATAGCAACGCGCCAGTGGTGCGCCTCAGAACGCCTTCCTTTTTACACCAGAACGCCTATGGGCGCACATATGAGCGCTAATGCATTTGCTATTTAAACAGCGTAGCGCAACGCCTCAAAACCACTCTTGCGCCAAGCTGAAACTAGCAAACAACTATTGCGCCGCACCTTGCGCCACACTGCGCCTTGACTATAATATATGCTTGTTTTTTTTTTCTCAACAGATCAAGTACTCCGAAGTATGAAGTCTGGTTCCTCCTTTTCCCCCCTCAATGTTGGGGGAATATACCTGCCTTTGCATTGGCCTCCAGGTGAATGCTACAAATA[T/A]CCCATAGTGCTCGGCTACGACTCGCAGCATTTTGCACCCCTGATCACAATCAAAGACAGCGGCCCAGGTACAGTATGCTCTACATCTCATATCGTACATTGCACGCATTTTCCATTCACTTTCCTTACTGGGATGATATACAACAAGCAAACCGAATCAGTTTCATTCATTCATTTTCCTTCAGCTTAGTCCCTTATTCATCAAGGGTCACCACAGCGGAATGAACAGCCAACTATTCCAGCATATGCTTTACGCATGGGATGCCCTTTCAGATGTAACCTAGTACTGGGAAACACCCATACATACTCATTCACACATGCACTACAGTTCATCAATTCCCCTATAGCGCATGTGTTTGGACTGTGGGGGAAACCCACACCAACACGGGGAGAACATGCAAACTCCACACAGAAATGGCAACTGGCCCAGTTGGAGCTCAAACCAGCGAGCTTCTTGCTCTTGGGCAACCATTTTAACCACTGAACCACCGCACCACCCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35394
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:
C > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033528 | None | None | 762 | None | 8 |
ENSDART00000147959 | Splice Site, Nonsense | 311 | 756 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 1076920)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 1074728 |
GRCz11 | 13 | 1205019 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGTTTAAATCCAATTAATCATGATTAACACCACTAAACCTAAAATCTAG[C/T]AGCACGTTTGCCTTTTTAAAATCTCGAATGCTTTTTCCTCCAGACTGGAT
Long Flanking Sequence:
ATGAACCGCCAACTTATCCAGCAAGTTTTTACACAGCGGATGCCCTACCAGCCGCAACCCATCTCTGGGAAACATCCACACACACACTCATACACTACAGACAATTTAGCCTACCCAGTTCACCTGTACCGCATGTCTTTGGACTGTGGGGGAAACCAGAGCACCCGGAGGAAACCCACGCGAAGGCAGGGAGAACATGCAAACTCCACACAGAAACGCCAACTGAGCCGAGGTTCGACCCAGTGACCTTCTTGCTGTGAGGCGACAGCTCTACCTACTGCGCCACTGCCTCGCCAGTAAGGACTTTCATGGCACTAAATATACTGGGGTATGAATTACAAAGGGGCTTGATTTAAAAATATTGGTTCTTTTAAAAGTCTTTGAATCTGCCGTTCATGAAAGTGTGGGAACCCTGTCTCAAAACAAAAAGTAAAAAACTCTTTATTTGCACCGTTTAAATCCAATTAATCATGATTAACACCACTAAACCTAAAATCTAG[C/T]AGCACGTTTGCCTTTTTAAAATCTCGAATGCTTTTTCCTCCAGACTGGATGAAGGGAATCTACCTGAGGATATGAACCTGATGGAGGATTACCTGCAGCTGGTGAACCACGAGTACAAGCGCTGGCAGGAGGACAAGGACTCTCTCTGGGCCCCGCAGTCCCAGCGTCCGCCACCGTTCTCCGTCTCTCAGCTCTCCTTAATCGAGATCCGCTGCGCCACGCCGAGATGCACTTTCTACGTCTCTGTGGACACGCAACCACACTGTCACGAGTGCTTCGAAAAGAGGCAGGCGGGACGCAAACCTGAGGCCATTTCTACAATAAATCAAACCTCATCCTCAGATACTGAAAGTCGCGGGAAAATGGAGCGCTCCATCCTGCCTAGTCCGAGGTCAGCGCCCCCTACAGCTCCAAGTTTAAGCCTATATAGTGAAACTCATGCTATGAAGTGTAAAACTCCCGGCTGCTTATTTACGCTCAGTGTGGAGCACGATGGTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22194
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 |
---|---|---|---|---|---|
ENSDART00000033528 | Nonsense | 355 | 762 | 6 | 8 |
ENSDART00000147959 | Nonsense | 349 | 756 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 1077036)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 1074844 |
GRCz11 | 13 | 1205135 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGATATGAACCTGATGGAGGATTACCTGCAGCTGGTGAACCACGAGTA[C/A]AAGCGCTGGCAGGAGGACAAGGACTCTCTCTGGGCCCCGCAGTCCCAGCG
Long Flanking Sequence:
AGTTCACCTGTACCGCATGTCTTTGGACTGTGGGGGAAACCAGAGCACCCGGAGGAAACCCACGCGAAGGCAGGGAGAACATGCAAACTCCACACAGAAACGCCAACTGAGCCGAGGTTCGACCCAGTGACCTTCTTGCTGTGAGGCGACAGCTCTACCTACTGCGCCACTGCCTCGCCAGTAAGGACTTTCATGGCACTAAATATACTGGGGTATGAATTACAAAGGGGCTTGATTTAAAAATATTGGTTCTTTTAAAAGTCTTTGAATCTGCCGTTCATGAAAGTGTGGGAACCCTGTCTCAAAACAAAAAGTAAAAAACTCTTTATTTGCACCGTTTAAATCCAATTAATCATGATTAACACCACTAAACCTAAAATCTAGCAGCACGTTTGCCTTTTTAAAATCTCGAATGCTTTTTCCTCCAGACTGGATGAAGGGAATCTACCTGAGGATATGAACCTGATGGAGGATTACCTGCAGCTGGTGAACCACGAGTA[C/A]AAGCGCTGGCAGGAGGACAAGGACTCTCTCTGGGCCCCGCAGTCCCAGCGTCCGCCACCGTTCTCCGTCTCTCAGCTCTCCTTAATCGAGATCCGCTGCGCCACGCCGAGATGCACTTTCTACGTCTCTGTGGACACGCAACCACACTGTCACGAGTGCTTCGAAAAGAGGCAGGCGGGACGCAAACCTGAGGCCATTTCTACAATAAATCAAACCTCATCCTCAGATACTGAAAGTCGCGGGAAAATGGAGCGCTCCATCCTGCCTAGTCCGAGGTCAGCGCCCCCTACAGCTCCAAGTTTAAGCCTATATAGTGAAACTCATGCTATGAAGTGTAAAACTCCCGGCTGCTTATTTACGCTCAGTGTGGAGCACGATGGTTTATGCGAACGCTGTTTTACTGCGAGGCAAAACCGAACGGCGGGACCGTCTCACGGCTGGTGGGCGTCGGGCGGTCGGGAAAGAGAACGGGACACAGAAAAATGCGTGATGTGCCGGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10832
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 |
---|---|---|---|---|---|
ENSDART00000033528 | Nonsense | 570 | 762 | 6 | 8 |
ENSDART00000147959 | Nonsense | 564 | 756 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 1077679)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 1075487 |
GRCz11 | 13 | 1205778 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCAGCAGGAGCCCAGGACGGAGGGTTCGGTSTGGGCAGAACGCAGTGGG[C/T]AGACCTGGCAGACGCCCGCRGCCMGACAGTGCAAACGCTCTGGATGCCAG
Long Flanking Sequence:
CACACTGTCACGAGTGCTTCGAAAAGAGGCAGGCGGGACGCAAACCTGAGGCCATTTCTACAATAAATCAAACCTCATCCTCAGATACTGAAAGTCGCGGGAAAATGGAGCGCTCCATCCTGCCTAGTCCGAGGTCAGCGCCCCCTACAGCTCCAAGTTTAAGCCTATATAGTGAAACTCATGCTATGAAGTGTAAAACTCCCGGCTGCTTATTTACGCTCAGTGTGGAGCACGATGGTTTATGCGAACGCTGTTTTACTGCGAGGCAAAACCGAACGGCGGGACCGTCTCACGGCTGGTGGGCGTCGGGCGGTCGGGAAAGAGAACGGGACACAGAAAAATGCGTGATGTGCCGGCAGGAGGTGTTTAGGATATTTAATGGCCTCTGCCCACCGTGCATGCAGAGGACGGCTGTTTCTGAGCGGGAGGACACCCAGCAGCAGCAACAGCAGCAGCAGGAGCCCAGGACGGAGGGTTCGGTGTGGGCAGAACGCAGTGGG[C/T]AGACCTGGCAGACGCCCGCAGCCAGACAGTGCAAACGCTCTGGATGCCAGTTCTTCGGGACACAGGAGAAGCTGGGATTCTGCACCATATGCTATCTAGACTACCAGACCAATCACCGTGAGTGTTTTACGTAATATTGTCATGATAGTGGAATTTACAACTTCGATACGATACCTTGAAAAATATCGATATGCCAATATTCGTGACACTAATTCTCATAGCTACTCTTTAAGTTGAGTGTCCACCGAAGTGTTTTTTTGCACTGCAGAAATATGACTCGATATGCTAGCACGATATGGTATCTAGACTACTAGACCAATCACAGGCAGTGTTTTACGTAATATTGTCACGATAGTGGAATTTACAACTTTAATACGATACCTTGAAAAATACCAATATTCATGACAACACTGATTCCCATAGCTACTCTTTAAGCTGAGTGTCCACCGAAGTGTTTTTCTTTGCACTGCAGAAATATGACACATTATGCTAGCATGATA
Associated Phenotype:
Not determined