ZMP
traf7
Ensembl ID:
ZFIN ID:
Description:
E3 ubiquitin-protein ligase TRAF7 [Source:RefSeq peptide;Acc:NP_001073654]
Human Orthologue:
TRAF7
Human Description:
TNF receptor-associated factor 7 [Source:HGNC Symbol;Acc:20456]
Mouse Orthologue:
Traf7
Mouse Description:
TNF receptor-associated factor 7 Gene [Source:MGI Symbol;Acc:MGI:3042141]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa30605 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa14681 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa30605
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084579 | Essential Splice Site | 18 | 639 | 2 | 20 |
ENSDART00000132703 | Essential Splice Site | 18 | 639 | 3 | 21 |
The following transcripts of ENSDARG00000060207 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 35697175)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 35482371 |
GRCz11 | 3 | 35611879 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGCTGGTTTTGGATCCACGTTTCCAGCAGTCCCACAAGTAGCAAAAGG[T/G]CAGTATTAACTGTTGGACCACATGAATCATATTAGAGCTGTAAAATGCTC
Long Flanking Sequence:
TTACTTATAGTGCCTTGCACACAATTAATATTGTACGTAGTAAAATCGGTCATGGTGGGGTATTTCATTTTGTGCTGTTGTGCTTTTTTCACTAGTTTGTGTTGTTTTTAAACAGGTTACAATTTTTTATTGTCTTTTTAAATTGAATTTATTGTCAGCTAGTTTGCATTATATATTTATTGTTAGTGAGAGATCATGTTTTTAATTATTTTCCCCTTATCCACAGGCTACAGCAGGTATTTTGCTCAATGCTTTGCTGTATTATGAGTGTTAGTAAACCATCGCGCTTTGACTGATTCTCGGGAGGATCCGTGGCAATTGCCACTACCACTGTACCTTCACCGGACATCACCAACAAGGTAGTCTGATATGAATTGTCAGCTATTGTGTTATTTGAAGAATTTACTAGTAAAAACGACTTGTATAATTATCTGTATGCAGGCCAAAATGGATGCTGGTTTTGGATCCACGTTTCCAGCAGTCCCACAAGTAGCAAAAGG[T/G]CAGTATTAACTGTTGGACCACATGAATCATATTAGAGCTGTAAAATGCTCATGTAAAACTTTGGTATGCAAAATACTGACCTACACTTGAAGTCAGAATTATTAGCCCCCCCCCCCCCTGATTTTTTTTTTTTCTGTTTAACAAAGAGCATTTTTTTTATGCATTTCTAAGCATAATAGTTTTAATAACTTTTAATATAAAGTTAAAATAACTCTCTAATAACTGTTTTATTTTATCTTTGTCACGATGACAGTAAATAATATTTTACTAGATATTTTTCAAGACACTTCTGTACAGCTTAAAGTGACATTTAAAGGCTTAACTAGGTTAATTAGGTTAACTAGGCAGGTTAGGGTAATTAGGCAAATTATTGTATAACGATGGTTTGTTCTGTAGACAATCGTAGAAAAAAAAAGTCTAAATGGACTAATAATTTTTTCCTTAAAATAGTTTTCAAAAAATTAAAAACTGCTTTATTCTACTCAAAATAAAACAAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14681
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 |
---|---|---|---|---|---|
ENSDART00000084579 | Nonsense | 436 | 639 | 15 | 20 |
ENSDART00000132703 | Nonsense | 436 | 639 | 16 | 21 |
The following transcripts of ENSDARG00000060207 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 35710869)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 35496065 |
GRCz11 | 3 | 35625573 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGACAGTAACTAATACACNNATNNTCACTTGCTCTTCCTCAGGTTTGGGATATC[C/T]AGACCCTTCAGAAAGTGAACACCATCCGGGCACACGATAACCCTGTGTGC
Long Flanking Sequence:
AAGAAAAATGACTATTGTTCCGAACCAGCTTTACAAATTAAAATAATCATATAAATATGTAATCTGATGCACTGCACTGATTTTTATGTGGACATAACCATGTTTTACGAATGACACACAGTCACATCCATTTTGTGCATTTTAAAAAGCACCAAACAAAAAGCTGTATGCTTTTATTTTGAAAGCACTGAAAAAACAATTATGAAGTGTAGTTTTAGGCTCTGGTTACAGCTCTAATAAAAATATACAATATTTAAAAAGAATTTAACAAAGTAAAAACGGTTGCAAATGTCATGTTCATGTTGTCTTTAAATGGACAAGGGAACTTACAAATTCTTGCACATTTTTTTTTGTTTCTGCAGGAACAAGCTGTATAGTGGCTCAGCTGATTGTACAATCATTGTGAGTGTCCCTGAAGTGCATTTAAAAGAGGAATCAAACTACTGATTCGGACAGTAACTAATACACATTCACTTGCTCTTCCTCAGGTTTGGGATATC[C/T]AGACCCTTCAGAAAGTGAACACCATCCGGGCACACGATAACCCTGTGTGCACTCTAGTGTCCTCACACAACATGCTCTTCAGCGGCTCTCTCAAAGCCATTAAGGTCAGTATCGTCTGTTGTAGAGATGATGTGCGCGTCTGCAAACACATGCCCAATCAAGCAGCTAATGTCAAGCTTCATTCTGCCCCATTTGGTGATGTGCATGTTGGCTCTATAAACCTCTTTTGTGTGAAATTTGGCTGACAATTAATTGTCTAAGAAGTAATTGCAGTTACAGACAATAATTGTATATTTTGGAAATATGCTTTTCATATAACTAGCTAATTCAAGAATTTTTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACCTGTAGAAAAAAGTGAATTGTGCACAGTTGTTTGCCTTTTAAGTAGTTGAAGCATTTAAGTTACTCACTTTTGC
Associated Phenotype:
Not determined