ZMP
traf3ip1
Ensembl ID:
ZFIN ID:
Description:
TRAF3-interacting protein 1 [Source:UniProtKB/Swiss-Prot;Acc:Q6PGZ3]
Human Orthologues:
AC002365.1, AC003980.1, AC006062.1, AC006999.1, AC007379.1, AC008162.1, AC008573.1, AC009021.1, AC010133.1, AC012596.1, AC016595.1, AC018553.1, AC022409.1, AC022486.1, AC023481.1, AC067941.1, AC092485.1, AC097714.1, AC116351.3, AL121899.1, AL138690.1, AL159986.1, AL357512.1, AL591242.1, TRAF3IP1
Human Description:
TNF receptor-associated factor 3 interacting protein 1 [Source:HGNC Symbol;Acc:17861]
Mouse Orthologues:
Gm10563, Traf3ip1
Mouse Descriptions:
TRAF3 interacting protein 1 Gene [Source:MGI Symbol;Acc:MGI:1921269]
predicted gene 10563 Gene [Source:MGI Symbol;Acc:MGI:3642630]
predicted gene 10563 Gene [Source:MGI Symbol;Acc:MGI:3642630]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31748 | Nonsense | Available for shipment | Available now |
| sa17414 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31748
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 |
|---|---|---|---|---|---|
| ENSDART00000007189 | Nonsense | 180 | 629 | 5 | 15 |
| ENSDART00000136444 | Nonsense | 103 | 220 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 9 (position 46691535)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 45822815 |
| GRCz11 | 9 | 45623294 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAAGGGCATCAAGGAGAGCAGTGGGAGTCGAGAACAGAAAGATCCAGAT[C/T]AACCCAAAGATCAAGAGAGCAAGAGGGACGACAAGGACCGCAGACGAGAT
Long Flanking Sequence:
TATCCCGCCGTGAGTGCGATGACACGTGAACAAAATGCCGGCGCTTTTCCGCGCCTACTTGTGGCTTCTTTTGCGCTCCTCAGAAACTATGGGTGACGTCACAGACACTACGTCTATATATTTTACAGTCTATGGTTTATACCTGCCAACACTCCCATTTTTCCCCGGAGTCTCCCATATTTCAGACCCATCTCCCGTTTCGGTCTGACTCACGGAAAACTCCCGGAATATCACCCCGTAAAACCCCACCCCCCACTCCACCTCCAATGATTTCATTTGTGCTTTAAAAGCATATTCTAAAAATAAACAGATGGTTATCATTTGTCTGTGTGGAGATTAATATATTAACATTAAATCTATTCATATTTATGGTTATCGTACTTGGTGTAAATGGCTATATATTATTAACTGTTTGTTTATTAAAGTTTGTCTTGTCTGTTTTCCAGGAGAGGAAGGGCATCAAGGAGAGCAGTGGGAGTCGAGAACAGAAAGATCCAGAT[C/T]AACCCAAAGATCAAGAGAGCAAGAGGGACGACAAGGACCGCAGACGAGATGCTGAGAGGTCTGACAAAGGCCGAGAAAGAGAGCGAACAAAAGACAGAGATCGAGACAAGGACAAGAGCCGCGATCGGGAGAAAGACAAGACTCGAGAGAAAGAGCGGGAACGAGAGAAGGATCGTAACAGAGAGAAGGAGAGAGAGCGGGATAAAGATCGAGATAAGAAGAAGGAGAGGGAATCTCACAAAGACAGAGAACGGGACAAAGATCGTGAGCGCGAGAAACGGCGGGAGAAAGAGAAGGACAAAGAAAGACCCAGAGAGACTGAGGAGAAACTAAAAGACAGAGGCGACAGAAAGGTTGGTTCGCTCTGCTTTATGACTCTGACACATACTTTAAATTATTCATTTCAAACCTCATTCTGACCCTTTCCCTGAAATTATTCACTACGAAAACACATCGGTTTCACAAAAACATTCATATATTTCAGAAATATTTATTTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17414
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 |
|---|---|---|---|---|---|
| ENSDART00000007189 | Nonsense | 353 | 629 | 7 | 15 |
| ENSDART00000136444 | None | None | 220 | None | 3 |
Genomic Location (Zv9):
Chromosome 9 (position 46698363)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 45829643 |
| GRCz11 | 9 | 45630122 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCTAAAGGACAGCGGCGGAAGCCCAAAACAGGAGGTCAAGGTACTGAA[C/T]AAGGTACTGAGCTGAACTGACTTTGTTAATTATTGATATACAATGCATCT
Long Flanking Sequence:
TTATTTCTGCTTTGAATAAGTAGTTATAAGGGTTTTGCAGCTTGGGTAGCTTTAGAGTTCTTCATTTAGAGTAGTGAAAGGTTTTATTTTTGACTTGTGGCATAGCTGTTCAGAGCTAGTGTTGTATAAATGTAAATGTCAAAGAATTAAGGTTTTCTATTGCGATTTCTCTAAATCCAGCCTTCAGATCTCACTGAAATCCAGGTAATTTCTTGAAGGGAAATTCGTTTTCACCTTCATTTTTTGTTTTGATTTGTTGTCTGGCTTTATTGTGATATTTTTTTGTCTGCAACATTGTTTGTTTCTTAAAGGTTTGAAAAGAAAGCAGGCTCGCATATTCTTGAGAAATGTCAGTTAACGTGCTCCAGGGGAGTTGGTAATACTTGGAAATGAATGCTTTTCCTCATTCCTTTCAGGCTGAGAGTCCTTCCCGGATCCCAAGGCCTTCATCAGCTAAAGGACAGCGGCGGAAGCCCAAAACAGGAGGTCAAGGTACTGAA[C/T]AAGGTACTGAGCTGAACTGACTTTGTTAATTATTGATATACAATGCATCTTGATCTGTTTAGTTGTTCCTGGTCTGAATGCTTAAAAACACAAACTCCGTCTGAATAGAATCTGATGTGAGGATGGAATTATTGTGGGATTATTTCAAATGTATGCACTGTGTATTTTAGCACGATGAAAAACATTTAAGATAAACGTCATTAGATGATGTTGTTTATCTTGAATGTTGATATGGATTGTGTATTTTTCTTTCAGACGAGACAGAGAGTGAAGGAGGTAAGTGTTGTTTTCTTCCGCACCTCTTACCAGACCACAAAACGAATTAATTGTTGCAACTTCAAGTAGCTTTAATATGTTTTTAAAAGCAGTGGAAGACAAACTAGTCATAATATCTGTGTAGGGCTGCATAATTTACCCTAAAACTACTGCTACTATTATTATTTTATACTATTATATTTAATACTAATACTATATTATTACTACTATAAATAGTTTTTTTA
Associated Phenotype:
Not determined