Busch Lab

ZMP

traf2b

Ensembl ID:
ENSDARG00000017812
ZFIN ID:
ZDB-GENE-030131-5345
Description:
Novel protein similar to vertebrate TNF receptor-associated factor 2 (TRAF2) [Source:UniProtKB/TrEMB
Human Orthologue:
TRAF2
Human Description:
TNF receptor-associated factor 2 [Source:HGNC Symbol;Acc:12032]
Mouse Orthologue:
Traf2
Mouse Description:
TNF receptor-associated factor 2 Gene [Source:MGI Symbol;Acc:MGI:101835]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa17008 Nonsense Available for shipment Available now
sa33738 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa17008
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
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Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000074731 Nonsense 9 532 1 10
ENSDART00000146296 Nonsense 9 532 2 11
Genomic Location (Zv9):
Chromosome 5 (position 63021300)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 53779876
GRCz11 5 54426469
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGTTGTGGTCTACRTTTTTMYAGATGATCAGCGCTGCAGGCAYTCTGTG[T/A]AAATGGAAGGATATGGAACGWCCATCTTTACCATCTTCTCTGGACTCAAC
Long Flanking Sequence:
TGGTTTAGCTTTGAATTAATAATGTAACAAGGGTGTAATGCACTGGATGGCTGGCCAATCAAAGCATACAATGATTATTAGAACAATGAGTTTTGTAAAGCTTGGCATTTTTCTAAAAGGTCAAGCAGAGATAAGCTGCAATATGGAATGTAATTTTTTTTAACCTTAATTTTAAGACGTTGCACTACACCAAATAATATTTTTTAGTCACGTCATATAACCCTCTTAAAATTGGGCAGGAATGCTGAAAATGATCCATAATAAATGAATAATGCCATAATGCTAGTTGCTAGTATTGTAATGATTATGGGTATTGACATTAATAGTAGCAAATATGAAAAAGATATACTTACACAAGAACACACTGACATAACAGTGTCTATTTACTATGTTATTAAATTATATTAGGTCATATTTTCAGTAAAAATGAGAGAAATTCATGTTGAAATCAAGTTGTGGTCTACGTTTTTACAGATGATCAGCGCTGCAGGCACTCTGTG[T/A]AAATGGAAGGATATGGAACGTCCATCTTTACCATCTTCTCTGGACTCAACATTGCCTGGGATATCTCGAGAAGTGCTGTCGGTGTCCATGGAACCGAAATATCAATGCCAGCAGTGCAAAGATATTCTTAGGAAACCTTTCCAAGCACAATGTGGACATCGCTTCTGTGTGTTCTGTTTCAAACAACTGACCAGGTACCCAGAGCAACTCTCTGCCTCATGCTCTGCTTTATTTCTTTCCTCTCCATGGACATTCCCAATCCTTTTAATTTCTCGCTGGCTGTAGCTAAATTGTTGACCCACTCTTTGCCTCTTAATCTAAAGCCTGGTTTATACTTCTGCATCAAGTGACCGGCGTAACCAATGGCGCATGCAACGCGCGTAGCTGTGCATTTATACTTCTGCGCGCTGTCTCTGTTGGTCTGCATTAACACTTCCAAAACGCTAGTTGGCAGTGAGGTGTTAATGTTCCTCTGTGTCGAGTTTCTTCACCTGTGTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33738
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000074731 Essential Splice Site 411 532 9 10
ENSDART00000146296 Essential Splice Site 411 532 10 11
Genomic Location (Zv9):
Chromosome 5 (position 62995465)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 53805711
GRCz11 5 54452304
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAGTTAACTCATTTTTGATCCTGCCTGATGACTTTTCTTTGTTCTTCA[G/A]CATTTTACTCCAGTAAATATGGGTATAAGATGTGTCTGAGACTGTACCTG
Long Flanking Sequence:
TTTTGGTGAAATAAGCGTCATCTAGAGGTCTTCGCCTTTCATATAAGCCACTTCTGATACCAAATGATCAACTTGAAGTCCAGTTATTATTTGATGTTCCTAAAACTTGGATAAGGTGACCAGAATTTTGTCAGGTAGTTTACATATATCCTGTATTATCAGATGGCCATAAAGTGATTAATTTTTTCTAAATTGTTAAAATATTGGTCAAGTCCAGAGACACCTTGATTTTGAAAAAAAAAAAAAAAAAAAGTAATAAGTGGTCATAAATGACAATTTTTTCAATTCAAATGAGTAGCTACTTGGACAAGTGCATAGTACAGTGATTAACTTGGAAAAAAATTAATGATATTAATTCAAAAGTTTGCCATTCCCACCTTACATATGCCATTTTCAACTTTGTCAGTTGAGGAATTGTGAAATTTAATCAGGTAATTTTTAGTTTATTTGTGCAGTTAACTCATTTTTGATCCTGCCTGATGACTTTTCTTTGTTCTTCA[G/A]CATTTTACTCCAGTAAATATGGGTATAAGATGTGTCTGAGACTGTACCTGAACGGTGATGGCACAGGTCGAGGCTCTCATCTCTCTCTGTTCTTTGTGGTCATGAAAGGCAAATATGATGCTCTGCTGAAGTGGCCCTTCAGCCAGAAGGTAAATCTTCTTTTTACTATTTAATTTTCTCTTATAGCCTTTAAAGATGCCATAATATGAAAATCTGGCTATACCTTAGCATATCTGAATAACAGTTCACATAAATTGAGCTTTATACACTATAGCTTCCTTGTACTTATGTAAGTCCTGTGAATGTAAAACAGGCCAATTGGAACAAAACACAAATTCTGCCTATATACATCATTAATATGGACGCCCCGGCTATATGTTTGGCCACAATTCCTAGTGAGATTACAACAATTGTATATTTGTTTCTTATTTTTAAGTTGATCTAAGCTTCTGTTAAACAGATCATGTATGTGTTATTTTGAAATCGGGACAGTTTATGTA
Associated Phenotype:
Not determined