Busch Lab

ZMP

traf7

Ensembl ID:
ENSDARG00000060207
ZFIN ID:
ZDB-GENE-070112-2212
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.
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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