u2af2b

Ensembl ID:
ENSDARG00000011740
ZFIN ID:
ZDB-GENE-040426-1881
Description:
U2 small nuclear RNA auxiliary factor 2b [Source:RefSeq peptide;Acc:NP_991252]
Human Orthologue:
U2AF2
Human Description:
U2 small nuclear RNA auxiliary factor 2 [Source:HGNC Symbol;Acc:23156]
Mouse Orthologue:
U2af2
Mouse Description:
U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) 2 Gene [Source:MGI Symbol;Acc:MGI:98886]

Alleles

There are 3 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa43235 Essential Splice Site Mutation detected in F1 DNA During 2016
sa3012 Essential Splice Site F2 line generated During 2016
sa14700 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa43235
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
G > T
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000023571 Essential Splice Site 165 475 6 13
Genomic Location (Zv9):
Chromosome 19 (position 10933230)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 10391769
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GCCAGGCTCGCAGACTTTACGTTGGCAACATCCCATTTGGCATCACAGAG[G/T]TGTTGAACGAACACTATTCGCACACTAGAATTACTCTGCGGGGCTTTTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa3012
Current Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
G > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000023571 Essential Splice Site 250 475 8 13
Genomic Location (Zv9):
Chromosome 19 (position 10929353)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 10387892
KASP Assay ID:
554-2772.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
CTATCAGCCATTACCTGGCATGAGCGAGAACCCCAGCGTTTATGTGCCAG[G/A]TAAACCCACAATACAATTCTCTTCTAAGATATCAAACTACAACAAATATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14700
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000023571 Nonsense 409 475 12 13
Genomic Location (Zv9):
Chromosome 19 (position 10923793)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 10382332
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GAGGAGTACGAGGAGATCGTGGAGGACGTCAAAGAGGAGTGCTCTAAATA[T/A]GGCCAGGTCAAGAGCATAGARATTCCCAGACCCGTCGATGGCCTTGATAW
Associated Phenotype:
Not determined

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