ZMP
irx2a
Ensembl ID:
ZFIN ID:
Description:
iroquois-class homeodomain protein IRX-2 [Source:RefSeq peptide;Acc:NP_957351]
Human Orthologue:
IRX2
Human Description:
iroquois homeobox 2 [Source:HGNC Symbol;Acc:14359]
Mouse Orthologue:
Irx2
Mouse Description:
Iroquois related homeobox 2 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1197526]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17696 | Essential Splice Site | Available for shipment | Available now |
sa22736 | Nonsense | Available for shipment | Available now |
sa10776 | Nonsense | Available for shipment | Available now |
sa19128 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17696
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016303 | Essential Splice Site | 74 | 432 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 568818)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 542626 |
GRCz11 | 16 | 561858 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAAAACACAAATWCAAGAACATTTGACTGRCCCCGAATKTTATTTTTGA[A/G]GGGCYCTCCGTATGACGCGCACACTACGGGAATGGCAGGAGCCAYAAGTT
Long Flanking Sequence:
AATTGATGAATTGCCATGCTAATGACATGGCACATGAAAGCGCGTGGAAAAAAAGCCAGTCCATATCCAGTGGTTTTCTAATAGGATTTGTAATGCTGCGCTTCACTGATATGCTTCTGACACTGAAAGAGCACTGGGAAAGTCAGCCTGGTGATTATGCAAAATGGCTGCAATTACCCATTATCTGTTATCCACCCCGGTCCCGTGTAATTGTGCATTCTGATAATTGCGTAGAGGATTAATCGTTGTTTATTGGCTTAATTATTATTAGTATTATATTTCTGGATACACTTTAGAATGGCGATCATTAATGACATTAACTTTATAAAAACGCAGAATGGATCATTGGTTAATTTGCATTTGAATTGTTTTATTATTATTATTATTATTATTCATCCTACATTATTTTTGTTTTAAATTAAGCTATTTATTTTTAAAGTGTTTGCAAAGCAAAAACACAAATACAAGAACATTTGACTGACCCCGAATGTTATTTTTGA[A/G]GGGCTCTCCGTATGACGCGCACACTACGGGAATGGCAGGAGCCATAAGTTATCACCCGTACGGGAGTCCCGGTTACCCGTACCAGCTCAACGATCCCGCTTACCGGAAAAACGCCACTCGGGACGCAACAGCGACGTTAAAAGCGTGGCTGCAGGAGCACAGGAAAAACCCCTATCCCACTAAAGGAGAGAAGATCATGCTGGCCATCATCACCAAAATGACCCTCACGCAAGTGTCCACCTGGTTCGCCAATGCACGACGGAGACTCAAGAAGGAGAACAAGATGACCTGGGCACCGCGGAATAAAAGTGAAGACGAAGACGAAGATGACGGAGATGGAGAGAGAAAAGACGAGCGCACGGATAAAAACATGGACAACAGCGAAGCGTCAGCTGAGGACGAAGGTGCGTTACTAATATTAATAATAATAATAACATCAGCTGATTTATTTTAAATGTATGACACTTTAAACAATGTATTGCATGGCATGAGATGTTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22736
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 |
---|---|---|---|---|---|
ENSDART00000016303 | Nonsense | 159 | 432 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 568561)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 542369 |
GRCz11 | 16 | 561601 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATCACCAAAATGACCCTCACGCAAGTGTCCACCTGGTTCGCCAATGCA[C/T]GACGGAGACTCAAGAAGGAGAACAAGATGACCTGGGCACCGCGGAATAAA
Long Flanking Sequence:
TTAATTATTATTAGTATTATATTTCTGGATACACTTTAGAATGGCGATCATTAATGACATTAACTTTATAAAAACGCAGAATGGATCATTGGTTAATTTGCATTTGAATTGTTTTATTATTATTATTATTATTATTCATCCTACATTATTTTTGTTTTAAATTAAGCTATTTATTTTTAAAGTGTTTGCAAAGCAAAAACACAAATACAAGAACATTTGACTGACCCCGAATGTTATTTTTGAAGGGCTCTCCGTATGACGCGCACACTACGGGAATGGCAGGAGCCATAAGTTATCACCCGTACGGGAGTCCCGGTTACCCGTACCAGCTCAACGATCCCGCTTACCGGAAAAACGCCACTCGGGACGCAACAGCGACGTTAAAAGCGTGGCTGCAGGAGCACAGGAAAAACCCCTATCCCACTAAAGGAGAGAAGATCATGCTGGCCATCATCACCAAAATGACCCTCACGCAAGTGTCCACCTGGTTCGCCAATGCA[C/T]GACGGAGACTCAAGAAGGAGAACAAGATGACCTGGGCACCGCGGAATAAAAGTGAAGACGAAGACGAAGATGACGGAGATGGAGAGAGAAAAGACGAGCGCACGGATAAAAACATGGACAACAGCGAAGCGTCAGCTGAGGACGAAGGTGCGTTACTAATATTAATAATAATAATAACATCAGCTGATTTATTTTAAATGTATGACACTTTAAACAATGTATTGCATGGCATGAGATGTTATAAGATTTGATTGATGGATCTATTTCACTTTAAAATTGCAGGGTTGATGGTTCAAATATGTACAAAACCAATATTATGTTGAGTTATTTTTTATTTAAATTATACATTTTAACCCAACCGCTGTGTGTGTTTATATTTAACCCAAGATTTTAGCTCTAAGAAATGCTGGGTTATTTTAAACCCAAATTTAATACACTTCAGACTAATCCAAACATTGCGTTAATTTCGGCCCTATTTATTTAATTTAAAAATAACCCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10776
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 |
---|---|---|---|---|---|
ENSDART00000016303 | Nonsense | 260 | 432 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 567751)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 541559 |
GRCz11 | 16 | 560791 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGAAATCCAGGACAAATGCGAGGCGACGGATCTCGGGGAGGAAAGGCAG[C/T]GAGGCGCGTCACCCAAACCGGTGACCTCTTCTCCTYTGACCGGGGTGGAG
Long Flanking Sequence:
CAATATTATGTTGAGTTATTTTTTATTTAAATTATACATTTTAACCCAACCGCTGTGTGTGTTTATATTTAACCCAAGATTTTAGCTCTAAGAAATGCTGGGTTATTTTAAACCCAAATTTAATACACTTCAGACTAATCCAAACATTGCGTTAATTTCGGCCCTATTTATTTAATTTAAAAATAACCCAGCAGTGTGTGTACCCCGTATTACACCAATAATTATTAGAGTGCATTAACGCTAATATGGATTCATATTTCTAAAATGCATCAGTGCAATTTTATGACTGTTTTATTATTAGTTTTTAACGCAATAATCTCACTGCGGTGCCGCTTCTGTCTCCAGGCATCAGTTTGCACGTCGATGCCCTGACAGACCACTCGTGCTCGGTGGAGTCGGACGGGGAGAAGGTCACGTGTCGGACCGGAGACCTTGTTTGCGATTCTGGAGCTGAAATCCAGGACAAATGCGAGGCGACGGATCTCGGGGAGGAAAGGCAG[C/T]GAGGCGCGTCACCCAAACCGGTGACCTCTTCTCCTCTGACCGGGGTGGAGGCGCCTCTATTGACCCATCATCACCGGGAGAACAGCACCAACAAAACATGCCTGGACGGTCAAAACCAAACCGTCAAGCCTAAGCTGTGGTCATTAGCAGAGATCGCCACTTCGGACCCCAAGCAGCAGAACTGTCCCCCGGGTGTCGGCCTTCTGACCTCCAGCGCGCCCGGCGCGTCCCCGGCGGGCGCGGTTTACCCCGCCACCTCCATACTAGGAAGACCTCTTTATTACACTTCTCCGTTTTATAGTAATTACACAAACTATGGCAACTTCAGCCCGCTTCAGGGCCAGGGGATACTGCGCTACAACTCCGCCGCAGAGGGACTCCTTCATAAACAGACTGGAGAGCCGCTAATAAAGACTAATCCAAACCAGACTGAAGCTCACTTCAGGGCCTCCAATGCAGAATCCAAAAAAGGTGCGTAGGCTGTTAATCTCTGACAGCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19128
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016303 | Nonsense | 429 | 432 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 566835)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 540643 |
GRCz11 | 16 | 559875 |
KASP Assay ID:
2260-9074.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATTTCCTGCAGACCCCAGCGAGGTTTTCACAGTAAGATCCCAATCTTA[C/A]CTGTCGAGTTAAGACGAGGAAGATCTTCCAAGTAAGTCGCTAATTTGAGC
Long Flanking Sequence:
TAATCCAAACCAGACTGAAGCTCACTTCAGGGCCTCCAATGCAGAATCCAAAAAAGGTGCGTAGGCTGTTAATCTCTGACAGCTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATTAGACCCTTTTTACAGAATCGGTCGCGGTTTTAAAATGATTTCAACGCAAATTGTGTATGCATAAACTGCTGGATTGTTAATTTCAATTCATTCATAACCAGATTGATTGAGTTTGTCTTATATTCTACCTTAAATTGTGTTTAAAAAACTTATAAATGTTAACCAGATTCCGCAGTTCCCTCGTTTATATTGTTGTTTGCACTTGACATGCATTTCCCCTACTGTTTATTCCCTCAATCGATCGCGGAATACGAAGTAGCCCATTTAAGCTGTCAAAACGATTCCCTTCACTAAATTGGGTGTGTATTTCCTGCAGACCCCAGCGAGGTTTTCACAGTAAGATCCCAATCTTA[C/A]CTGTCGAGTTAAGACGAGGAAGATCTTCCAAGTAAGTCGCTAATTTGAGCATTTCAGTGCTGATTATTATTATTCTGTATGCTTCTGAAGGCCACGTCCTCATATTTGACACCTGTCAACATACGCTATAAATAATGCTGAGATGTTTTATCCAAATATTGGATTTATTTTTTATTTTTTTGTAATTAAATTTATTTTACGATTTTGCTTTTTGCAAATTTGTCCTTATCTGACCCAGCGTTGGGTTACAATAACCCAGCATATTTAGAGTGCATGAATATGACACTTCCCATCGACTCAAAGGTTGCTTCATGAAGTGTGTGTATTTCTAAATGTCATGCTGTAGTTTTATTTCATTCACTTTCTCTGGAAAAATCGACTGATGTAGGTTTTGTTTCCTTGGTTCACAGGTAGGTGTCACAATTGCTTTGAACAAAGCGAACAAGCCATCACCCCTTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCCCT
Associated Phenotype:
Not determined