ZMP
IRF2 (1 of 2)
Ensembl ID:
Description:
interferon regulatory factor 2 [Source:HGNC Symbol;Acc:6117]
Human Orthologue:
IRF2
Human Description:
interferon regulatory factor 2 [Source:HGNC Symbol;Acc:6117]
Mouse Orthologue:
Irf2
Mouse Description:
interferon regulatory factor 2 Gene [Source:MGI Symbol;Acc:MGI:96591]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12780 | Nonsense | Available for shipment | Available now |
sa9417 | Nonsense | Available for shipment | Available now |
sa19076 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12780
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 |
---|---|---|---|---|---|
ENSDART00000059230 | Nonsense | 19 | 330 | 1 | 10 |
Genomic Location (Zv9):
Chromosome 14 (position 4291729)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 4006252 |
GRCz11 | 14 | 4113231 |
KASP Assay ID:
2260-7212.1 (used for ordering genotyping assays)
KASP Sequence:
GTGGAGAGAATGCGCATGAGGCCGTGGTTGGAGGAGCAGATAAACTCTTG[T/A]CAAATACCGGGACTYAAATGGGTCAACAAGGTACGACTGTGAGAACGGCG
Long Flanking Sequence:
GATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATTGATAGATGGATAGATTGATAGATAGATAGATAGACAGCTCTTATAAATTGTTTGCAAGCACATACCTTAAAAATTGAGTAAATCCAGTGAATCATTTTCTCAGTGTATCTGTGATGTCATCTGTAGCTTGACTCATGCATTTCATTCATTCACTTTCAGTAAACAGTGATTCAGACGGACTCCCCTGGAGAATTGTTGTTTTTTAGAAATAGGGTTCAAGTTTATCACGCTTCCTGGAGAATCACGGAGGAATGTACAACCTGTTCTAGGAGGAAAAGCAGCTGTCAAACTTTGACACATTCCAGATGCTTCTTTGTGTTTTTACTGTAGGTCAGCATGCCGGTGGAGAGAATGCGCATGAGGCCGTGGTTGGAGGAGCAGATAAACTCTTG[T/A]CAAATACCGGGACTTAAATGGGTCAACAAGGTACGACTGTGAGAACGGCGGTCTAAAACATGTCTTCTTCATCATTGTTTTGATTAAGCAACAAATAACAGTCTTGCTCACGGTGGTTGAAAGCGTATTGTTGGTTAATTAGGGCTGTGTGTGCACTTTGGGTGTGTTGTGTAATATTTTGCATGTTGTTTGCCTGCAGGAGAAGAGAATATTCCAGATTCCGTGGATGCATGCGGCGCGGCACGGATGGGACGTAGAGAAAGATGCTCCTCTTTTTCGAAACTGGGCCATACATACAGGTAAACATGCCGATAGATGCAAATGATCCCCCCTCCCAGTTAAATGAAATCATGGAACATGTTCAGTTTAAAGGGATAGTTTCCACAAAATTCACTTTTACTCAAACACGAAAACTCAAGAGAACTCAAGTTTTCGTATGGTTCAAAACTTTATGAGTTTCTTTATGTGCTAGGATTTTGCTGTTTGGTTGCTAGGATCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9417
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 |
---|---|---|---|---|---|
ENSDART00000059230 | Nonsense | 173 | 330 | 6 | 10 |
ENSDART00000059230 | Nonsense | 173 | 330 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 14 (position 4279374)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 3993897 |
GRCz11 | 14 | 4100876 |
KASP Assay ID:
2260-7211.1 (used for ordering genotyping assays)
KASP Sequence:
ACACAAGTATTTAATAAATTAAGAACAACATGGATTAAATTGACCGGCTA[T/A]ATCAACACATTCACAGTTCATGCAAAAYAAAAATGTMAAAAATTSTAATG
Long Flanking Sequence:
AACTAAGTTTGATGAAAGCTATTTGCTATTTGCTATGAAAGCTAAAGCTATTTAAGTGTCACTGGTTCGAGCCTCGGCTGGGTCAGTTGGCATTTCTGTGTGGAGTTTTCATGTTCTCCCCGTGTTGGCGTGGGATTCCTCCGGGTGCTTCGGTTCCCCCCACAAGTCCAAACACATGCGCTATAGGTGAATTGGGTAAGCTTAATTGTCCGTAGTGTATGAGTTTGTGAATGAGTGTGTCACTGGGTGTTTCCCAGTGATGGGTTGCAGCTGGAAGGGCATTCGCTGTGTAAACATATGCTGGAATTAAGTTGGCTAATTAAGTTGGTGGTTCATTCCGCTGTGGCGACCCCAGGTTAATAAAGGGTCTAAGTCGAAAATAAATTGAATGAATGAGGATTGTTAATAATGAATCTGAATCTTTAACATAGATTAAATCCTCCCATCCAAACACAAGTATTTAATAAATTAAGAACAACATGGATTAAATTGACCGGCTA[T/A]ATCAACACATTCACAGTTCATGCAAAATAAAAATGTCAAAAATTCTAATGTTTGAGTTGAACACCCAAACGTGTTCCTGGCAGGTTTTCGTAACATTTGTGCTTTTGCGTTTGAGATGGGATGTGATCGCGCTACACCTATCATTCTGTGGTGGACCTGTTTATCCAGATCTCCTTGTTAGCGCGCACGTGTGTGTGTGTGTGTGTGTGTTTCTCACATTCACCGTTCTCTGTTTCCCTCTTCAAATGTGCTGGATTGGGGTAAAAGGTGAGCTTAGCTTGTGTTTGTTTTGTAAGTCAGCGCTGATGTGGAGTCTGTGATACACATCGAATTGCCAAAGCAAAATCAAACTGCAGCGTAATTGATTTACAAAAAGCCTTTCAGCTGCTTCATTTGTTTTTAACCTGATTTCCACTACATCATTTCATTACAGACTCATGGGAAATCCAGCTCAGTTGCAGGGACCGGAGGGATTGTGTCCAGAGTGAAAAATCCCTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19076
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059230 | Nonsense | 173 | 330 | 6 | 10 |
ENSDART00000059230 | Nonsense | 173 | 330 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 14 (position 4279374)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 3993897 |
GRCz11 | 14 | 4100876 |
KASP Assay ID:
2260-7211.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACAAGTATTTAATAAATTAAGAACAACATGGATTAAATTGACCGGCTA[T/A]ATCAACACATTCACAGTTCATGCAAAATAAAAATGTCAAAAATTCTAATG
Long Flanking Sequence:
AACTAAGTTTGATGAAAGCTATTTGCTATTTGCTATGAAAGCTAAAGCTATTTAAGTGTCACTGGTTCGAGCCTCGGCTGGGTCAGTTGGCATTTCTGTGTGGAGTTTTCATGTTCTCCCCGTGTTGGCGTGGGATTCCTCCGGGTGCTTCGGTTCCCCCCACAAGTCCAAACACATGCGCTATAGGTGAATTGGGTAAGCTTAATTGTCCGTAGTGTATGAGTTTGTGAATGAGTGTGTCACTGGGTGTTTCCCAGTGATGGGTTGCAGCTGGAAGGGCATTCGCTGTGTAAACATATGCTGGAATTAAGTTGGCTAATTAAGTTGGTGGTTCATTCCGCTGTGGCGACCCCAGGTTAATAAAGGGTCTAAGTCGAAAATAAATTGAATGAATGAGGATTGTTAATAATGAATCTGAATCTTTAACATAGATTAAATCCTCCCATCCAAACACAAGTATTTAATAAATTAAGAACAACATGGATTAAATTGACCGGCTA[T/A]ATCAACACATTCACAGTTCATGCAAAATAAAAATGTCAAAAATTCTAATGTTTGAGTTGAACACCCAAACGTGTTCCTGGCAGGTTTTCGTAACATTTGTGCTTTTGCGTTTGAGATGGGATGTGATCGCGCTACACCTATCATTCTGTGGTGGACCTGTTTATCCAGATCTCCTTGTTAGCGCGCACGTGTGTGTGTGTGTGTGTGTGTTTCTCACATTCACCGTTCTCTGTTTCCCTCTTCAAATGTGCTGGATTGGGGTAAAAGGTGAGCTTAGCTTGTGTTTGTTTTGTAAGTCAGCGCTGATGTGGAGTCTGTGATACACATCGAATTGCCAAAGCAAAATCAAACTGCAGCGTAATTGATTTACAAAAAGCCTTTCAGCTGCTTCATTTGTTTTTAACCTGATTTCCACTACATCATTTCATTACAGACTCATGGGAAATCCAGCTCAGTTGCAGGGACCGGAGGGATTGTGTCCAGAGTGAAAAATCCCTTCT
Associated Phenotype:
Not determined