ZMP
irx4a
Ensembl ID:
ZFIN ID:
Description:
iroquois-class homeodomain protein IRX-4 [Source:RefSeq peptide;Acc:NP_991261]
Human Orthologue:
IRX4
Human Description:
iroquois homeobox 4 [Source:HGNC Symbol;Acc:6129]
Mouse Orthologue:
Irx4
Mouse Description:
Iroquois related homeobox 4 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1355275]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17695 | Nonsense | Available for shipment | Available now |
sa17778 | Nonsense | Available for shipment | Available now |
sa45557 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17695
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 |
---|---|---|---|---|---|
ENSDART00000051693 | Nonsense | 126 | 440 | 3 | 5 |
ENSDART00000051693 | Nonsense | 126 | 440 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 279615)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 290131 |
GRCz11 | 16 | 381459 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGGGWTAACACCGGCTGCCRCATATTACCCATACGATCCCACCCTGGGA[C/T]AGTACCAGTATGACAGGTATTGAAMWKCGGCCATCATAAGAGTCTTCTGW
Long Flanking Sequence:
TGCTTGTTTTACAGTATACTAATAAAGCAGATAATCTGCATGATTTTATTCTACAGGGTGGGTCATTTATATGGAGACACCTTAATAAACTGGGGATTTCACAAGAAAAGCAATGGTGTGCTTGGTTACATAACTTTTTTCTGTCATGAGTTATTTACAAGCCCCCTCACCTATACTAATGTGGCATAAACAGGACGATAATATCACCAACCATTCATATTTTAAGGTGTATCTATATAAATGGCCCACCCTGTATATCTCTATAACTCATGCTGACTATTAACACACGTTTGCTGCAGGAAAAGGTTTTAGTTGCTGGTTTGTTAATAGTGAGAATTGCACATCAAGTTTTGCACTTGACAGCAGTGTTAAGTTAACTGCATGAGTGTTATTCTTGTGTTTATTTGCAGGGAACATTTGACGCCAAAGATGGAAGCGCGTCTGCGCATGCGGGGATAACACCGGCTGCCGCATATTACCCATACGATCCCACCCTGGGA[C/T]AGTACCAGTATGACAGGTATTGAACAGCGGCCATCATAAGAGTCTTCTGATTGCTAATTAACAAGTGCAGGAAGTTCAGCAGGATCAATTGCGCAGGCAGCGCTCAACACATTTGATGGAATCATATTTAGCTCAATCATTCAAACGCGTTTTTCCGAAAAATTAAAATTACCCAGTGACATTTTCAGTTCACTAATGTATATTTGATGTTATATCATGCACTTGACGCTTTACCCTTCAGGGTTTTCCCTGAAGTGCTTTAATGGACGGTCAGAGCAGTCTGTGTGCACTCGATCAAGCAATTCATACGCTCTGTTATGCCTCTAAAAATATCATGAAAGGAAGTTTAGAGCTTATGGAAACAGCCTCGAATGTCTTATTAACATCAATAACTTCTCTGCTAACTGCAGGTACGGCTCTATGGAGGGCGGGACCCGCAGGAAAAACGCCACCCGGGAGACCACGAGCACGCTGAAGGCCTGGCTGCAGGAGCACCGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17778
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 |
---|---|---|---|---|---|
ENSDART00000051693 | Nonsense | 126 | 440 | 3 | 5 |
ENSDART00000051693 | Nonsense | 126 | 440 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 279615)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 290131 |
GRCz11 | 16 | 381459 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGGGWTAACACCGGCTGCCRCATATTACCCATACGATCCCACCCTGGGA[C/T]AGTACCAGTATGACAGGTATTGAAMWKCGGCCATCATAAGAGTCTTCTGW
Long Flanking Sequence:
TGCTTGTTTTACAGTATACTAATAAAGCAGATAATCTGCATGATTTTATTCTACAGGGTGGGTCATTTATATGGAGACACCTTAATAAACTGGGGATTTCACAAGAAAAGCAATGGTGTGCTTGGTTACATAACTTTTTTCTGTCATGAGTTATTTACAAGCCCCCTCACCTATACTAATGTGGCATAAACAGGACGATAATATCACCAACCATTCATATTTTAAGGTGTATCTATATAAATGGCCCACCCTGTATATCTCTATAACTCATGCTGACTATTAACACACGTTTGCTGCAGGAAAAGGTTTTAGTTGCTGGTTTGTTAATAGTGAGAATTGCACATCAAGTTTTGCACTTGACAGCAGTGTTAAGTTAACTGCATGAGTGTTATTCTTGTGTTTATTTGCAGGGAACATTTGACGCCAAAGATGGAAGCGCGTCTGCGCATGCGGGGATAACACCGGCTGCCGCATATTACCCATACGATCCCACCCTGGGA[C/T]AGTACCAGTATGACAGGTATTGAACAGCGGCCATCATAAGAGTCTTCTGATTGCTAATTAACAAGTGCAGGAAGTTCAGCAGGATCAATTGCGCAGGCAGCGCTCAACACATTTGATGGAATCATATTTAGCTCAATCATTCAAACGCGTTTTTCCGAAAAATTAAAATTACCCAGTGACATTTTCAGTTCACTAATGTATATTTGATGTTATATCATGCACTTGACGCTTTACCCTTCAGGGTTTTCCCTGAAGTGCTTTAATGGACGGTCAGAGCAGTCTGTGTGCACTCGATCAAGCAATTCATACGCTCTGTTATGCCTCTAAAAATATCATGAAAGGAAGTTTAGAGCTTATGGAAACAGCCTCGAATGTCTTATTAACATCAATAACTTCTCTGCTAACTGCAGGTACGGCTCTATGGAGGGCGGGACCCGCAGGAAAAACGCCACCCGGGAGACCACGAGCACGCTGAAGGCCTGGCTGCAGGAGCACCGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45557
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000051693 | Nonsense | 194 | 440 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 280213)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 289533 |
GRCz11 | 16 | 380861 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAGATGACCCTCACTCAGGTGTCCACCTGGTTCGCCAACGCCAGAAGG[A/T]GACTCAAGAAGGAGAACAAGATGACCTGGCCACCGAGGAACAAGGGCTCG
Long Flanking Sequence:
CAGCGCTCAACACATTTGATGGAATCATATTTAGCTCAATCATTCAAACGCGTTTTTCCGAAAAATTAAAATTACCCAGTGACATTTTCAGTTCACTAATGTATATTTGATGTTATATCATGCACTTGACGCTTTACCCTTCAGGGTTTTCCCTGAAGTGCTTTAATGGACGGTCAGAGCAGTCTGTGTGCACTCGATCAAGCAATTCATACGCTCTGTTATGCCTCTAAAAATATCATGAAAGGAAGTTTAGAGCTTATGGAAACAGCCTCGAATGTCTTATTAACATCAATAACTTCTCTGCTAACTGCAGGTACGGCTCTATGGAGGGCGGGACCCGCAGGAAAAACGCCACCCGGGAGACCACGAGCACGCTGAAGGCCTGGCTGCAGGAGCACCGGAAAAACCCCTACCCGACCAAAGGAGAGAAGATCATGCTGGCCATCATCACCAAGATGACCCTCACTCAGGTGTCCACCTGGTTCGCCAACGCCAGAAGG[A/T]GACTCAAGAAGGAGAACAAGATGACCTGGCCACCGAGGAACAAGGGCTCGGACGAGAAGAAGTATGATGATGATGAGGATGGATCACCAGAGGAGCAGATCAAGAGTGAAACCAATGATGACGGTCAGCAGCATCCCACTCTCTAAACAATACTCTAAAATGCTGGGTTGAGTTAACCTTATGGGGACAATATGGACAAAATTATCAGTTGGGTTAAAATAAAAGTCATTCAAATGTACTTTTAAAAAGATATTTCACACAATATTTGCTTAATACAATCTAGCAGCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGTTTATTGCTTCTCCACCTTCAGCTGTCAGATTTCAGATTTTACGTTTAAAGAGCTTCCTGAATATATAAAAAAATATATATATATATACATAATTTTAACATCCATGGAAC
Associated Phenotype:
Not determined