ZMP
irf2bp2a
Ensembl ID:
ZFIN ID:
Description:
Interferon regulatory factor 2-binding protein 2-A [Source:UniProtKB/Swiss-Prot;Acc:Q6NZT6]
Human Orthologue:
IRF2BP2
Human Description:
interferon regulatory factor 2 binding protein 2 [Source:HGNC Symbol;Acc:21729]
Mouse Orthologue:
Irf2bp2
Mouse Description:
interferon regulatory factor 2 binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:2443921]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35596 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa950 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa35596
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025126 | Nonsense | 74 | 491 | 1 | 2 |
ENSDART00000136991 | Nonsense | 74 | 263 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 13 (position 50422490)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 49153528 |
GRCz11 | 13 | 49444206 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAAAGAGCGCATGGATTTCAGGACGGCAGACCGGCGGGGCCGGGGAAA[C/T]AGTTACCGGGGAAGGAGATCCACGCGTCGGGAGACCCGGGCTCGCGCCCG
Long Flanking Sequence:
ACAGCGCATGCGCCGCAGGGGCTGTTCTGTCGAAGAATCAAGTAAATAGACGCGGAGCGGCGGTGACGTCACTGCTCCACATTGAGCTCCAGCCTGGCCGCGGTAGTAGTGAGTGAGAGAGACCGAGCGCGCGTCGTAGTAAAGCACGCTACTATGAAGTTCTGTTTGTAACTTAATTATTACTTGCGCCACCGCGACAGGAACCTACCTTGTTTTTCCCCAGCATCATTCCACACAGGATTGTGCCGTATTTCGGAGGGGTTTTCGCCCGAGAGAGAGCGATGTCGTCCGCGGCGGTTGCTGCTTCGAGGAGGCAGTCGTGTTATTTATGTGACTTGCCCCGCATGCCGTGGGCTATGATCTGGGATTTTACCGAGCCCGTTTGCAGAGGATGTGTCAACTACGAAGGAGCCGACAGGATCGAGTTTGTCATTGAAACAGCCCGGCAGCTCAAAAGAGCGCATGGATTTCAGGACGGCAGACCGGCGGGGCCGGGGAAA[C/T]AGTTACCGGGGAAGGAGATCCACGCGTCGGGAGACCCGGGCTCGCGCCCGCCGCAGCCGCTGGATCGCTACCCGCTCTCCTCAGAGCGTCCGCCCAGATTGGGAGCCGAGTATCAGTCTGCGAGACAGGCGAACGGCATCCCAGTGCCTAACGGATTCTCAAAACCCGACGATCCTCCGGAGCTCAACCGCCAGAGCCCGAACCCGCGCAGGACTAGCGGCGTGCCGCCCAATTTAGTGCCTTTAGTGAACGGCAGCATGGCGCACGCGATGAACGGCAGACCGGGGCAGATGTCAGATCTCGGAGGGAATAAGCGACCGGCGTCGGTCTCCAGCACAGAGCACGACAAGGACAAGCACAGACCGGACAGCCTGACGCCGGAGATCAGCGACGGCCACAAGACGCGCGCCGACGACTGGCTCAACAAGAACAAAACCGTGCGGGAGCTGATGACGCTCAACCCGTACGACGGCAGATTCAAGAAGGAGCACATGCAGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa950
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025126 | Nonsense | 240 | 491 | 1 | 2 |
ENSDART00000136991 | Nonsense | 240 | 263 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 13 (position 50421992)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 49153030 |
GRCz11 | 13 | 49443708 |
KASP Assay ID:
554-0855.1 (used for ordering genotyping assays)
KASP Sequence:
TGATGACGCTCAACCCGTACGACGGCAGATTCAAGAAGGAGCACATGCAG[C/T]AGAGGGTCATGTACGAGACTGGTCCTGCATCCAAATCAGGTATGCTATTA
Long Flanking Sequence:
AACAGTTACCGGGGAAGGAGATCCACGCGTCGGGAGACCCGGGCTCGCGCCCGCCGCAGCCGCTGGATCGCTACCCGCTCTCCTCAGAGCGTCCGCCCAGATTGGGAGCCGAGTATCAGTCTGCGAGACAGGCGAACGGCATCCCAGTGCCTAACGGATTCTCAAAACCCGACGATCCTCCGGAGCTCAACCGCCAGAGCCCGAACCCGCGCAGGACTAGCGGCGTGCCGCCCAATTTAGTGCCTTTAGTGAACGGCAGCATGGCGCACGCGATGAACGGCAGACCGGGGCAGATGTCAGATCTCGGAGGGAATAAGCGACCGGCGTCGGTCTCCAGCACAGAGCACGACAAGGACAAGCACAGACCGGACAGCCTGACGCCGGAGATCAGCGACGGCCACAAGACGCGCGCCGACGACTGGCTCAACAAGAACAAAACCGTGCGGGAGCTGATGACGCTCAACCCGTACGACGGCAGATTCAAGAAGGAGCACATGCAG[C/T]AGAGGGTCATGTACGAGACTGGTCCTGCATCCAAATCAGGTATGCTATTATTTGTGTTCAGGCGTGCTGCATTTATTTGTTTTTAAAGCTGGATAGACGTAGAAAGGATCAATAACAGTGGCTATTTAGTGTACAACCTAGGTGTGTGTTCTTTATTTCAAGCTGGATGGACTGGAGATTAAAGCAGATCTGATTAACTTGTGTGTGTTTATTCACACATGCAGTGCAGTGCTAGCTTTGAATGAGAGCTCTATGGCATGAGTCAGCTGCGAGAGCAGAAAATTTCTGCTGATCAAAGCTCAACGTGTGTTTGCATGTGGTGCATTTGCAGGCAGCCTCATTGTTGCGTCTGGCACTACAATGCATCACTGCGTCTGCCACATTGTTATTGCATAAAGGCGGCTTTGTGCAGCTCATTCATGCAAGCTCCTGCTCTCTCTTTTTTGCAGATCGAGGCAAACATCCCAAGAATCTGAAGAGAAAAGCTTCTCCGGAGCCGG
Associated Phenotype:
Not determined