ZMP
u2af2b
Ensembl ID:
ZFIN ID:
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43235 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa3012 | Essential Splice Site | F2 line generated | Not yet available |
sa14700 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43235
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
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 |
GRCz11 | 19 | 10310694 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCAGGCTCGCAGACTTTACGTTGGCAACATCCCATTTGGCATCACAGAG[G/T]TGTTGAACGAACACTATTCGCACACTAGAATTACTCTGCGGGGCTTTTGT
Long Flanking Sequence:
TTCAAAAAAGAAATCAATGGATCAAAGGTACGATAATTCTCCGAAATATTGCGCAGCTCTAATCAGTCTAAATTTTTCTGTCCACATGGATGGTGCTCAAACCAAATTAGTGAGGTGACTGTTGAAGCAGAACGAGTTCAGTGTGTGATAATCGGCATGTGCTAAACTCTTCCATCTGTGCTCATCCTCGGTTAAGTAAGCTGCACAGACACGGATGTTTGCGAGAGAGCCCAATGCAAAAATTAGTGTACATAGCCCTTAACTACGTTTTATTCTCTTTCTGTCTTCTATTACTACTCAGTAACACATATATAATTTATGAATTCATATTTTGTTGTTTTCCCTCAGCTGCTGGTCAAATCCCCGCTACCGCTTTGCTGCCCACCATGACGCCAGACGGCCTGGCAGTAACGCCGACCCCGGTGCCTGTAGTAGGCAGTCAGATGACTCGCCAGGCTCGCAGACTTTACGTTGGCAACATCCCATTTGGCATCACAGAG[G/T]TGTTGAACGAACACTATTCGCACACTAGAATTACTCTGCGGGGCTTTTGTAAACTGATCCAAATAGAGAACACTAGCATGCTTGGATGCATTATGCAGAAGCATATTGGATATTTATTTTAGCATACTCCGATATTTTCATATTTAGATTATTTTACATTCATCTACAGCTCACCTAAAGTTAATCAATCTTTAGCTAATTTAAATTTGTTAATATTACACTACCAGACAAAAATCTTTTCGTCGATCCCAGCTGTAGGAGCAACAAGTTATAACTTGACTTCTGGTCAAAAAGTAGCAATTTTCAGATGAATTATCTAAAGAACTGCAACCTAATCATCACAAATAGTGCAGAAGACCTACTAGAACCCACATAGACCCATGATTCTCACAGATGTCAGTCAGGTTTGGTGAAGGAAAAATCATGGGTAGGGGTTACATTCAGTATGGGGGCGTGCAAGAGATCTGCAGAATAGATGGCAACTTCAACAGCCTTAAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3012
Status:
F2 line generated
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
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 |
GRCz11 | 19 | 10306817 |
KASP Assay ID:
554-2772.1 (used for ordering genotyping assays)
KASP Sequence:
CTATCAGCCATTACCTGGCATGAGCGAGAACCCCAGCGTTTATGTGCCAG[G/A]TAAACCCACAATACAATTCTCTTCTAAGATATCAAACTACAACAAATATG
Long Flanking Sequence:
ATTTATTACCCTTGGTCCGGACCAAATGAAGCGAACTACAGATGTGAAAGAACCCATAGACTTCCTGATAAACTGACGCCAAATATCAAAGAGAAAATGGACTTTGCTATAGTAGGAGAAGCCGCTGAGGGCCTTTTTCTTATAAAATAAATATATGCACCTCAGAAGACGAAATGCAATGAACGCATGGTGGTGCCGATTTTATTATGCACATAATGCCAATTCCATTTGTTATACAATATTCCAATAATGCACATAAAAAGATGAGTAGATAAAAAGAAAGCTACTCACAGGGGCTTATGTTGCCTATGATTTGGTATATTTGGTTGTTGACTGTATTCTTCTTTCATTAATTCATCAGTTCCGATCAGTGGATGAGACCACGCAGGCCATGGCATTCGATGGCATCATCTTCCAGGCACAGAGCTTAAAGATTCGCAGACCGCATGACTATCAGCCATTACCTGGCATGAGCGAGAACCCCAGCGTTTATGTGCCAG[G/A]TAAACCCACAATACAATTCTCTTCTAAGATATCAAACTACAACAAATATGACTTTTGATTTTTATTTTTTTCCTTTATTACAAATGTCTGGTGTCCTTATGCATCTGTAAAGCAGTCCAATTTCAGGGTAAACTTATTTTCATTTAAAGTTGACTTTAGGAAAATCTTGCTGTTATTTCTTATTCATTTAAACCCTTTTACTTTAGTCTCTTATTCACCTTTTTTTTGTGCCTGCCAGTTGTGTGTTGATGAATGTTGTCCATCTGCTCCACAGGTGTGGTGTCTACTGTTGTACCAGACTCTATTCACAAGCTGTTCATTGGAGGTTTACCAAACTATCTCAATGACGACCAGGTTGGTTACAAATGCTTTCTGGTTGAAAGTCTGTGACGCATGCATTGGCAGTCATAAATTTATAAGATGTTTTGTACTTGCATTAAAGGGATTTCTCATTTTGAAAAATGAACATTTATACAACATCAATGGTTCCAAACCTTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14700
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:
T > A
Consequence:
Nonsense
Transcripts:
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 |
GRCz11 | 19 | 10301257 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGGAGTACGAGGAGATCGTGGAGGACGTCAAAGAGGAGTGCTCTAAATA[T/A]GGCCAGGTCAAGAGCATAGARATTCCCAGACCCGTCGATGGCCTTGATAW
Long Flanking Sequence:
TGGGCACAAAAATCTATGTTTCGAGGTATAAAAAATTTGCATTTAATTATTTAAACAGAAAAATTATACTTATTTAGAATTTTTGTCTTGTTTCTAGTTCAAATAACTACATTTCAAAGCAAAACTCCCCAGAAAACCATCAAATAGTGCTATTTTAACCATCTTGAGAAACTATTCATATCGCAATATTAATTGTAGAAAAATAAAATATTGCCGATTGTAATATATATCAGATTTTTCCCAATATAGCACAGCCCCAATTCTAATCATCCTTAAATTGTCTGTATTTCCCCTCTTTTCATTATCCATCTGTAGACGAGTATAAACGAGACTCCAGTGACGTTGCAAGTGCCTGGCCTCACATCCAACCCCATGATCCAGATGGGCGGTATTCCCACTGAGGTCCTGTGTCTGATGAACATGGTGGCTCCAGAGGAGCTTATCGACGATGAGGAGTACGAGGAGATCGTGGAGGACGTCAAAGAGGAGTGCTCTAAATA[T/A]GGCCAGGTCAAGAGCATAGAAATTCCCAGACCCGTCGATGGCCTTGATATACCTGGAACTGGCAAGGTAAGCCTTACCAAAGCAGCTCGAGTGGGCTGCAAACTTTTTTTTTTTAACACTTTTATTGTTTCAGAAAAATGTGATACATACATACTGTATTAGTAACCAAATACCAGTCAAAGAACACCTGCCCCGTCCTGACATTCAAATAAAAAAAATAATTTAAAAAATGCATTCTCATGCGAGGAAATAATACATAAACAAATAAATAGAAAATAAAGATTAACTAAAATAAGATAAAATAATAATAAAAATTAAAAAGGGCAATTTTGTTAAAAATAAAAAATATATAAAAAATAAATACCATTAAAAAAATTGACATTTCAACATATACATTCTAGTGAAAGTGAAAAGTATATTAAAGTTAGTCATTACAAACAGTGAATTTTAACAGTCACATTGTTTGGGATTACTAAACGGTCAGTCCACTCTTATTTAAA
Associated Phenotype:
Not determined