ZMP
ireb2
Ensembl ID:
ZFIN ID:
Description:
Iron regulatory protein 2 [Source:UniProtKB/TrEMBL;Acc:Q3YMK8]
Human Orthologue:
IREB2
Human Description:
iron-responsive element binding protein 2 [Source:HGNC Symbol;Acc:6115]
Mouse Orthologue:
Ireb2
Mouse Description:
iron responsive element binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:1928268]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12679 | Nonsense | Available for shipment | Available now |
sa14739 | Nonsense | Available for shipment | Available now |
sa3307 | Nonsense | F2 line generated | Not yet available |
sa5705 | Nonsense | F2 line generated | Not yet available |
sa24600 | Nonsense | Available for shipment | Available now |
sa44228 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12679
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046618 | Nonsense | 37 | 999 | 2 | 21 |
ENSDART00000135808 | Nonsense | 12 | 974 | 2 | 21 |
Genomic Location (Zv9):
Chromosome 25 (position 6607647)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 6127089 |
GRCz11 | 25 | 6254491 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTNCCTAGGAGTTTTTAATCAAAGCTTTTATTCCCTACAGAGCATCCATA[C/A]GGCCATTTGATTGACACTCTCCAGAGCGAACAATATSAAGAGCRGARATA
Long Flanking Sequence:
CTGCTTGCCTTTAATAAAAAAATCTCTTTCACATGAAAACTCAATGTGATGCTTGGTAAGGGCACACTAAACCATCAGGGGGCCGGTTTATGCCGGGTTCTCACCAAATGGGGAATCAGGTATTTTCATGTAAATTGCATATGAGTCGATGCAAACGTAAGAACAGATGCAGATTACGTCCTGGGGTTGAAAAATGTGAAATACACAATACACCCAGTCCTATTGCCCAATCAGAAAGGAGAAAACACTGTGCACACTAAAGTCCTGAGGAGAAAATTCTGGTTGTAGTGTCCCCACGAGCACAGTTTTCCGAAAGTTTTGGTTTTAATCACCCGATGCCCTTTTTTTGTGTAGACAAACAGCAAAACATAAAAAAAAAAAAACCCATTTTCTGCACAAGCCTTTCTGTTCCTGTCTTTCCTACGCCAATCACTTTTATTTATCTGTGGTTTTCCTAGGAGTTTTTAATCAAAGCTTTTATTCCCTACAGAGCATCCATA[C/A]GGCCATTTGATTGACACTCTCCAGAGCGAACAATATCAAGAGCAGAAATATTTCAGCCCACAGAAGCTTAATGATGTCAGATACGGTAAGTAACTGGCTGATTCCTTCATCTTTGCTGACGTCACTTGTTACAATAAAACATAAAATTGAGTATGAAATATTGAAGTGTCATGCTCTTTTTGTTGTAGAGAAACTGCCGTTCTGCATGCGGGTTCTCCTGGAGTCCGCCATTCGGAAGTGTGACGAATTCTACGTGAAAACAGAGGATGTATCCAGTATTTTGGACTGGCAGGTGCAGCAGAATCAAGCAGAGGTTGTGTTCTCGCCCGCCCGGGTTCTGCTGCAGGATTTCACGTGAGTTTGTTTAAATCCATTTATTATTTTTACCCCAGAAAGAGACATTTGTTTCAAAATAACAAATGTTTGCATTTTTATAAATTTAGGTTTGTTGTAGCTTAAGGCCTGGTTTATGCTCTACGCTTTCGCCAGTTTGCTTGAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14739
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046618 | Nonsense | 253 | 999 | 6 | 21 |
ENSDART00000135808 | Nonsense | 228 | 974 | 6 | 21 |
Genomic Location (Zv9):
Chromosome 25 (position 6600303)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 6119745 |
GRCz11 | 25 | 6247147 |
KASP Assay ID:
2261-9337.1 (used for ordering genotyping assays)
KASP Sequence:
GTTTGATGTCTGTCYGACGCACACACAGGCCTGAAACAATGGTCAGAAAC[C/T]AAGAGATGGAGCTAATCAGAAACAAAGAGAGGCTGCAGTTCTTYAAGGTG
Long Flanking Sequence:
GTTGGCATTTCTGTGTGGAGTTTGCATGTTCTCCCTGCGTTCGCGTGGTTTTCCTCCGGGTGCTCCGGTTTCCCCCACAGTCCAAAGACATGCGGTACAGGTGAATTGGGTGGGCTAAATTGTCCGTAGTGTATGAGTTTTTATGGATGTTTCCCAGAGATGTAGCTCGAAGGGCTTCAGCTGCATAAAACATGTGCTGGATGAGTTGGCAGTTCATTCCGCTGTGGCGACCCCAGATTAATAAAGGGACTGAACGAAAAAGAAAATGAATGAATTGAGAGATCACATTTAACTTTTAATATACAGTTTTTGTGAATTTTATTTAATTAAATTATATCTTTGTGTATCATCTCTTGTTGAAATATAAAGTTATATGTATCATGTAATATTTTTATGTATATTGATCTTGCAATAAGTTGCTGATGTGGAAATTAATCAATTAATTAAACTGTTTGATGTCTGTCCGACGCACACACAGGCCTGAAACAATGGTCAGAAAC[C/T]AAGAGATGGAGCTAATCAGAAACAAAGAGAGGCTGCAGTTCTTCAAGGTGAGTTTTAGGGGCTTTCTGTGATGTGCTTTTATTTAGGCTGTCAATGTAAACTTTTATAATAGAATTAATTTGTCACAGGAAAAATGAACATGTTAAAATTATGAATTCAGTTAATACATGATTAACTGTTGTATGATGGAATGCGGTCATAATCAAGATAAAAAGTAAGCTGTTTGCCCCATATGAGTTTCTGTCATATATTTTTGACCCATGAAATTGTTAAATATTATCACACAAACAAGTTTAATATCACACAAGAGCTGTTTTTTTGTCAGATTGTTTAATTAAAAGCATTATTTCATATTTTCTCATTAGTAAAAGTCCATTAAAAATGACATTTCTAGCATTATTTACTTATCTTTGTGTCTTTTATTTTAAACCTCTTTGTATTTATTAATTTTGAAGAACCTGCAAATTATTTTCAAGAATGTTGATAACCAAATAGTTTCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3307
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046618 | Nonsense | 307 | 999 | 7 | 21 |
ENSDART00000135808 | Nonsense | 282 | 974 | 7 | 21 |
ENSDART00000046618 | Nonsense | 307 | 999 | 7 | 21 |
ENSDART00000135808 | Nonsense | 282 | 974 | 7 | 21 |
Genomic Location (Zv9):
Chromosome 25 (position 6599417)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 6118859 |
GRCz11 | 25 | 6246261 |
KASP Assay ID:
554-3079.1 (used for ordering genotyping assays)
KASP Sequence:
AATCTGGAGTACTTGTGTAAGGTGGTGCAAGAAGAGGAGGGCTTTATTTA[T/A]CCWGACAGTGTGGTGGGAACAGACTCTCACACAACTATGATYAATGGCCT
Long Flanking Sequence:
CATTTCTAGCATTATTTACTTATCTTTGTGTCTTTTATTTTAAACCTCTTTGTATTTATTAATTTTGAAGAACCTGCAAATTATTTTCAAGAATGTTGATAACCAAATAGTTTCGGAGCAAATCTGTTAATATGTCTAAATGACAGTTCAGTTTCAACTTCTGAGAAGATTCTGAGAAATTGTTTAAATGGTTTAAAAGAAATCAGTATGTTCATTCAGAAAGGATTTGATAAATTGGTCAAAGTGCTGGTAAATCATGTAAATTGTATCATGTTGAACGAAAGTAACGTCTTTCAAAACCCTTTTAAAAAATCCTACTAACCCCAAACTTTTGGTAATAATTGACGTCCTGCTGTATTTGTTTTGCCGTTATTCTCTTCTCAGTGGTGTTCAAAATCCTTTAATAATGTCAACGTGGTCCCGCCAGACATCAGCACTGTACATCAGCTGAATCTGGAGTACTTGTGTAAGGTGGTGCAAGAAGAGGAGGGCTTTATTTA[T/A]CCAGACAGTGTGGTGGGAACAGACTCTCACACAACTATGATTAATGGCCTCGGGATCCTGGGCTGGGGTGAGTGGGAACACCTCAAAAAAGTGTAAACCAGTAAACCAACTACCTATTTCTCTTAAAAATGAGTTATTGATGTTCTCTAATATAACATCTTTCTTTCTTTCTTTTTGTTCTTTGTTTTTGTCTTTTTTCTTTTTTGTATGTTTTTTTTTCTCACTTTATTTTTTCTGTTTTTGTTTGTTTTCTTTCTTTGTTGTTTCTTTTTTCTTTTGTTTGTGACTTTCTTTTGTTTCTTTCTTTCTGTCTCTTTTTCTTTCTTATATTCTTTCTTTTTTTCTTGCTGCTTTTTCTTTATTGCTTTAAATTTTTCTTTTTATTGTGTTCTTTGTTTTTGTTCTTTTTTCTTTCTTTTGTTCTTTTTAAATTCATTTTGTTCTTTCTTTCCATTTTCTTTTCTTTCTTTTTGTATTTTCTTTGTTTTTGTCTTTTTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5705
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046618 | Nonsense | 307 | 999 | 7 | 21 |
ENSDART00000135808 | Nonsense | 282 | 974 | 7 | 21 |
ENSDART00000046618 | Nonsense | 307 | 999 | 7 | 21 |
ENSDART00000135808 | Nonsense | 282 | 974 | 7 | 21 |
Genomic Location (Zv9):
Chromosome 25 (position 6599417)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 6118859 |
GRCz11 | 25 | 6246261 |
KASP Assay ID:
554-3079.1 (used for ordering genotyping assays)
KASP Sequence:
AATCTGGAGTACTTGTGTAAGGTGGTGCAAGAAGAGGAGGGCTTTATTTA[T/A]CCWGACAGTGTGGTGGGAACAGACTCTCACACAACTATGATYAATGGCCT
Long Flanking Sequence:
CATTTCTAGCATTATTTACTTATCTTTGTGTCTTTTATTTTAAACCTCTTTGTATTTATTAATTTTGAAGAACCTGCAAATTATTTTCAAGAATGTTGATAACCAAATAGTTTCGGAGCAAATCTGTTAATATGTCTAAATGACAGTTCAGTTTCAACTTCTGAGAAGATTCTGAGAAATTGTTTAAATGGTTTAAAAGAAATCAGTATGTTCATTCAGAAAGGATTTGATAAATTGGTCAAAGTGCTGGTAAATCATGTAAATTGTATCATGTTGAACGAAAGTAACGTCTTTCAAAACCCTTTTAAAAAATCCTACTAACCCCAAACTTTTGGTAATAATTGACGTCCTGCTGTATTTGTTTTGCCGTTATTCTCTTCTCAGTGGTGTTCAAAATCCTTTAATAATGTCAACGTGGTCCCGCCAGACATCAGCACTGTACATCAGCTGAATCTGGAGTACTTGTGTAAGGTGGTGCAAGAAGAGGAGGGCTTTATTTA[T/A]CCAGACAGTGTGGTGGGAACAGACTCTCACACAACTATGATTAATGGCCTCGGGATCCTGGGCTGGGGTGAGTGGGAACACCTCAAAAAAGTGTAAACCAGTAAACCAACTACCTATTTCTCTTAAAAATGAGTTATTGATGTTCTCTAATATAACATCTTTCTTTCTTTCTTTTTGTTCTTTGTTTTTGTCTTTTTTCTTTTTTGTATGTTTTTTTTTCTCACTTTATTTTTTCTGTTTTTGTTTGTTTTCTTTCTTTGTTGTTTCTTTTTTCTTTTGTTTGTGACTTTCTTTTGTTTCTTTCTTTCTGTCTCTTTTTCTTTCTTATATTCTTTCTTTTTTTCTTGCTGCTTTTTCTTTATTGCTTTAAATTTTTCTTTTTATTGTGTTCTTTGTTTTTGTTCTTTTTTCTTTCTTTTGTTCTTTTTAAATTCATTTTGTTCTTTCTTTCCATTTTCTTTTCTTTCTTTTTGTATTTTCTTTGTTTTTGTCTTTTTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24600
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 |
---|---|---|---|---|---|
ENSDART00000046618 | Nonsense | 349 | 999 | 8 | 21 |
ENSDART00000135808 | Nonsense | 324 | 974 | 8 | 21 |
Genomic Location (Zv9):
Chromosome 25 (position 6598328)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 6117770 |
GRCz11 | 25 | 6245172 |
KASP Assay ID:
2261-9336.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTATTGAATCTGAGGCGGTGATGTTAGGTCAGCCGGTATCTTTGACTT[T/A]GCCGCAGGTGGTCGGCTGTAAACTTGTGGGGACCATTAATCCTCTTGCCA
Long Flanking Sequence:
TTGTTTTTGTCTTTCTTGTTTCTTTTTTTCTGTCACTACTTTTGTTTTTTCTTCTGTTTCTTGTTTTTCTTTCTTTACTTTTTATTTGCTTTTCTTTTTTCCTTGTTTTGGTCTTCCTTTGTTTTTGTTTTTCTTGTTGATTTCTTTTTTCTTTCTTCTGTTTCTCTCTTTTTCTTTATTGCTTTTATTTTTTCTTATTGTTCTTTCTTTTTGTTTTCGTTCTTTGTTGTTTCTTTGTTGTTTATTGTTTTTGTCTTTTGTTTTTGTTTCTTTTTTTCTTTTTTTTCTTTCTATTTCTTCTGTTTCTTGCTTTTTTATTTCTTATTTTTTTCTTTTCTTTTCTTTTTTTCTCTTTCTTTCTTTGATGTCTTTTTTTTCTCTTTCTTTTCATTCTTTCTTTTTGTGTCTTTTTCTATCTTTCTTTTTTTCTTTCTTTCTTTCAGGAGTTGGAGGTATTGAATCTGAGGCGGTGATGTTAGGTCAGCCGGTATCTTTGACTT[T/A]GCCGCAGGTGGTCGGCTGTAAACTTGTGGGGACCATTAATCCTCTTGCCACATCCATTGATATTGTCCTGGGTATTACTAAGGTAATAATTACGGTGAAAGTTTTTTTTGTATTTTTATTTTTTTTTTTTATTGTCTACAATACTGTGAATATATTTATTTAAATTAGGCCTAATTCACAATGCATGATTTTAATACCTGTCGGATCGCCCGTTGTGTTCATATTGCATGAAAACTACAAACCAATTACAGACAAGTTCAGCTCACAAAAATCACGTGAGAAATGATAAGAACAGGTGCAAGACTGGAAATGGTACCCTGCAGTAAATATTTTAAGTAATCTGCCACTTAAATGGGCCATTCCTGAGTGACTTTTTACAACAAGTAGATATCAGGGTTTAAATCGTGGTAATAGTTTCATATAAATTCAATGAGTAATTATTCAGAGTTACATAGACATGAAATTGTCTTGTAACGTTAGACTTCAATATATGACCTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44228
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046618 | Essential Splice Site | 900 | 999 | 19 | 21 |
ENSDART00000135808 | Essential Splice Site | 875 | 974 | 19 | 21 |
Genomic Location (Zv9):
Chromosome 25 (position 6584000)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 6103442 |
GRCz11 | 25 | 6230844 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGGCTCAGGCAGCTCACGGGACTGGGCTGCCAAAGGACCTTATTTACTG[G/A]TAGGAGACGTATAAACCTTGAAATCAAAAAGTATTGAGCTGCGATTCACT
Long Flanking Sequence:
TAAATAATATTTTAGATATATTCAAGACACTTCTATACAGCTTAAAGTGACATTTAAAGGCTTAACTAGGGTAATTAGGCAAGTTGGGGTTATTAGGCTAGTTATTGTACAACAGTGGTTTGTTCTGTAGACTATAGAAACCAATATTGCTGAAGGAGGCTAATAATATTGAATAATATGATTATAGAAAAATTTCAAACTGTTTTTATTCTAGACAAAATAAAACAAAAGACTTTCTCCAGAAGAAAAAATATTATAGGAAATACTGTGAAAATTTCCTTGCTCTGTTAAACATCATTTGGGAAATATTTAAAAAAGAAAAAAAATCCCAGGAGAGTGAATAATGTTGACTTTAACTGTGTGTTTTCCCACTGCAGCTGGATGTGTTTGAAGCTGCTGAGCGCTATCAAAGAGACGGAGTTCCTCTCATCATCCTGGCTGGAAAGGAGTACGGCTCAGGCAGCTCACGGGACTGGGCTGCCAAAGGACCTTATTTACTG[G/A]TAGGAGACGTATAAACCTTGAAATCAAAAAGTATTGAGCTGCGATTCACTCACTACTCAACACACTGACTGTCTTTGTTGTGTTTCTCAGGGCGTGCGTGCGGTGATAGCTGAGAGCTTTGAAAAGATTCATAGGAATCATTTGGTGGGGATGGGAATCGCTCCTCTTCAGTTTTTGCCAGGACAGAATGCAGACTCACTGGAGCTGTGTGGAAAAGAGCGATTCACCATCGACATCCCAGAGGAGCTCACGGCCAGACAGCAGATCACTGTACAGGTAGATGTCCCCGCCAACTGCACAAAACAACAGCATGACTAGTGTAGTCTGATTCATGATCCTTATGAACAGGTTCTGTGTTAAACTGATTCACATACAAATGACTCTCATGAGCCATTTCTTTATAGTGAACAATAAACATACAGCATAACCAGTGCACTTTGATTTACAAACAAGTGACTCTTATGAACCAGTTCTTTAAGTATTTTAAATAATGGTTTGTT
Associated Phenotype:
Not determined