Busch Lab

ZMP

il13ra2

Ensembl ID:
ENSDARG00000039436
ZFIN ID:
ZDB-GENE-030521-10
Description:
interleukin-13 receptor subunit alpha-2 [Source:RefSeq peptide;Acc:NP_001107203]
Human Orthologues:
IL13RA1, IL13RA2, IL5RA
Human Descriptions:
interleukin 13 receptor, alpha 1 [Source:HGNC Symbol;Acc:5974]
interleukin 13 receptor, alpha 2 [Source:HGNC Symbol;Acc:5975]
interleukin 5 receptor, alpha [Source:HGNC Symbol;Acc:6017]
Mouse Orthologues:
Il13ra1, Il13ra2, Il5ra
Mouse Descriptions:
interleukin 13 receptor, alpha 1 Gene [Source:MGI Symbol;Acc:MGI:105052]
interleukin 13 receptor, alpha 2 Gene [Source:MGI Symbol;Acc:MGI:1277954]
interleukin 5 receptor, alpha Gene [Source:MGI Symbol;Acc:MGI:96558]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa40503 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa14818 Nonsense Available for shipment Available now
sa25305 Nonsense Mutation detected in F1 DNA Not yet available
sa33654 Nonsense Mutation detected in F1 DNA Not yet available
sa40502 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa40503
Status:
Mutation detected in F1 DNA
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
ENSDART00000057613 Essential Splice Site 85 407 2 10
Genomic Location (Zv9):
Chromosome 5 (position 38714309)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 36513993
GRCz11 5 37114146
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTGCGATACCAGCTCCGATACTTTGACACCTACGAGGAGCGATGGAGG[G/A]TGAGAATCCACCCACAAAACAGGCCTCACACACATTTATTTTCATTTCAA
Long Flanking Sequence:
AGAATAGAGTCCCCTTCACTATACTGGGACATTAAGACCCACACAGACCACAGGTTCAGTGCCCTGCTTAGCTTAAGTGAGCAAAAATGTGATAGTTGCAAAGAGCTAGCTACTAGCTGATTGAAGTGTAGCATTACCAAAACATTACTTGTGACTTCAGTGGTCCAGCTGTAATCATATGAAGCTTAAACAACACTTTTGAGTGTGTTTCCTGTGTGCAATATAATGTATTTGCATTAGAATCATGAGGGTGAGTGATTAATAACCAAATTAAAATTTTTGGGTGAACTAATCCATTAACAGTGCAACAAATATTGCTCGTTAACTTACACTATTCCTTCCTTACAGTGGATCCACCTGCTAATATTGAGATAACAGATCCTGGCTTTCTGGGTTACCTCAATATCCAGTGGACTCGTCCAGCTAGCCTTCAGAACCTCACGGGCTGCACAGTGCGATACCAGCTCCGATACTTTGACACCTACGAGGAGCGATGGAGG[G/A]TGAGAATCCACCCACAAAACAGGCCTCACACACATTTATTTTCATTTCAATTAGTAAACTTTCATTCTGCTGCATATTCTGCCACAAAAACAAACACGTTTTGCCTATTTCACACTTCATGCATGCTTCACTCTTTGGCATGATTTGAATGATTTGCTTTGATTAACAGAAGATTTCTTTTATGCTGATTTTTGTGGAAATTCCTCGTTGAAGATCTTTATTATCATAGCTCAATATCAGCCATCGGAATAAAACTGTGTTTTCAAAGCAACTGAATGGCATGACAAATATTATCTAAAAACTGAGAATGGTCACATTGGTTTTACCTCCATTTCATTGCTTCATTTAATGAATCACACTTAAGTGCACTCTAAGGTCCATTGCAAGCACAAGTGAAACAACAGTGTAGAGTTCCAGGGAACTCCAAAAAGCCGAGCCAAATCTTTGTTTAATTTAATGCAATCCTTCTGTGACCACAACCACCTGCAGGCAATCTTCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14818
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000057613 Nonsense 212 407 5 10
Genomic Location (Zv9):
Chromosome 5 (position 38707036)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 36506720
GRCz11 5 37106873
KASP Assay ID:
2259-6195.1 (used for ordering genotyping assays)
KASP Sequence:
ACAATGAGAGAGGATGCAGGTTTCCTCGCCAATCACTCTTGGAGTTTTCC[A/T]AGTTTAATATGTGTGTCAACGGATCTTCTTCAACAGGGAGTCTAAGACCA
Long Flanking Sequence:
CTGGGGTGGTACCTTTTTGAAAGGAACAAATTTGTACCAATAAGGTCCATATTAATACCTCAAGGGTACATATTAGTACCTAAAAAGTACAAAAGTGTTCCACCTAAAATTTTTAGGTAATAATATATACTTTTGGGGTACCAATATGGACCCTTCAAGTACAAATTTGTACCTTTTAAAAAGGTACCACCGTAGTGACAGCTTGCGTACCTTTATATCTGAGAGTGTAGAGAGTGTCCCCACCAATGTCAAGAGCGAATCTACGCCCTTTGTGTATATATAAACATATATCTTACACATAGACTTAGACATAAGTCACTTTGGATAAAAGTGTTTGCTAAATTAATCAATGTAAATGTAAAGTAAGTGCACTCAATAAGTGTATCTGTTTTTCCAGGCACAGGGAAATGGAAGAAACAAAGGAATGTCCAGAATACATTGTATCATCAAACAATGAGAGAGGATGCAGGTTTCCTCGCCAATCACTCTTGGAGTTTTCC[A/T]AGTTTAATATGTGTGTCAACGGATCTTCTTCAACAGGGAGTCTAAGACCAGCCTACTTCTCCATTGAGATCCAAAACTATGGTAATTACACTGACAGAACAAATTGCATATATACTGCAGAATAACTAGGGACACATAAGCAGTTGATTTGACCCAAAGTGCATAATGGAACATTGTCTTCTGTCTGCAGTAAAGCCTGCAGCGGTCTCTTCTCTGGACGTGTTAGAGACTGATGGACGGTTGAAGTTAGAATGGGCGCCACCTAGCGGTCAGGTGCCAGAACACTGCTTGGATTATGAGGTGGAGAGCAGCACTCTAATGGCAAATGGCAAAGAACTGAAGGTATTCTAATCCTTTTATCTTACTTCCTTCTATACAGCGATCTTCTGTTTTGTGTGCAAACTGTGGTGCATTTTTGAGCTTGCTGGTTCATGTTTTAGACGTTTCACAACAGTCACACAAAAATTTGGTTGTGCAAGATGTCTATAGATATTATGATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25305
Status:
Mutation detected in F1 DNA
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
ENSDART00000057613 Nonsense 266 407 6 10
Genomic Location (Zv9):
Chromosome 5 (position 38706765)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 36506449
GRCz11 5 37106602
KASP Assay ID:
554-7499.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTAGAGACTGATGGACGGTTGAAGTTAGAATGGGCGCCACCTAGCGGT[C/T]AGGTGCCAGAACACTGCTTGGATTATGAGGTGGAGAGCAGCACTCTAATG
Long Flanking Sequence:
GTGTATATATAAACATATATCTTACACATAGACTTAGACATAAGTCACTTTGGATAAAAGTGTTTGCTAAATTAATCAATGTAAATGTAAAGTAAGTGCACTCAATAAGTGTATCTGTTTTTCCAGGCACAGGGAAATGGAAGAAACAAAGGAATGTCCAGAATACATTGTATCATCAAACAATGAGAGAGGATGCAGGTTTCCTCGCCAATCACTCTTGGAGTTTTCCAAGTTTAATATGTGTGTCAACGGATCTTCTTCAACAGGGAGTCTAAGACCAGCCTACTTCTCCATTGAGATCCAAAACTATGGTAATTACACTGACAGAACAAATTGCATATATACTGCAGAATAACTAGGGACACATAAGCAGTTGATTTGACCCAAAGTGCATAATGGAACATTGTCTTCTGTCTGCAGTAAAGCCTGCAGCGGTCTCTTCTCTGGACGTGTTAGAGACTGATGGACGGTTGAAGTTAGAATGGGCGCCACCTAGCGGT[C/T]AGGTGCCAGAACACTGCTTGGATTATGAGGTGGAGAGCAGCACTCTAATGGCAAATGGCAAAGAACTGAAGGTATTCTAATCCTTTTATCTTACTTCCTTCTATACAGCGATCTTCTGTTTTGTGTGCAAACTGTGGTGCATTTTTGAGCTTGCTGGTTCATGTTTTAGACGTTTCACAACAGTCACACAAAAATTTGGTTGTGCAAGATGTCTATAGATATTATGATATCTCAGGACTTTATTTAAAACTAACTTCAACATAAAATACATCCCAAGTGTAAATATAAGCCATCAGCTCCACTTGATTGCAATGCTTCAGATTTCAATTCTGCAGATTTAAAGCTTGTATATTCCCCCTTAAGAAATCACATTGAGATGGGTAGAGTTCACCAAACGTGAACTTCATGGTTGCAATCTATTTGGCTTTCAGGCGCATGCTTGTAAACTCCCCAAGCACTTCTATTCAGGGAATTCTCTCTGGTCTTTTAAAAACTGTTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33654
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000057613 Nonsense 295 407 7 10
Genomic Location (Zv9):
Chromosome 5 (position 38703404)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 36503088
GRCz11 5 37103241
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCCAATCTGTGTTATTTTTATTTTCTTCTTTCAGCAAACGGAGATTCTG[G/T]AGAATCTGGATCTGGGCACATCTTATGAGCTCCCGAGAGAAGCAGAAAGT
Long Flanking Sequence:
TTAGTGAGAAAGGGGTGCTAAAAAATGAACTGGAACTGTAATACAGCCAAACTCAAAATAGGTCCCCTTTAGCTTGTGTTTCTGCTGTCCTTCATTCACATGCCTGACAAAGTGCTTTGTAACCACCCCTTTCCACTCGCAGATCACTTTCTGTGAGCACTCTGCTAATGTGCTGATAAGAATCAGGTGTATTTGATAAGAAGAACATCCAAAACGCCTTTAGCAGCACAGCAGAGGAAAACTGATGACAGGACTCTCAATATTTTCGTTGCGGTGCAAGAGCTAGTAATTAGTAAACAGCTCTTGAACATGAATGACTTGAACAAATACCACTCACTCGCATTTCATTCTGAATCTTGGCATGCACCGTTAAACAAATGTTTGATTAAGGTTGTGTGCCAAACCAAGCAATAAAAAAGAAAGAAAGAAAGCCAAGAATCCCATCTGTCAAGCCAATCTGTGTTATTTTTATTTTCTTCTTTCAGCAAACGGAGATTCTG[G/T]AGAATCTGGATCTGGGCACATCTTATGAGCTCCCGAGAGAAGCAGAAAGTAAGAAAACCTGCTTTAATCTCAGATCGAAAGTGAATATGTACTGCGCTGATGGAGGATTCTGGAGCGACTGGAGCCAAACAAAATGTACAGGTGAGACAGGTTTTTAAAATTGACCTTGATTAATTTCATTCATTCGTTTATTCTTTCCAATTTGTCTTTTTATTTTTTCAGAACATTTATATTAAGATGGGATTTTAATTTTATATAAGATTCATCAGCATGAACCACGCCACACTTTGAGCTAGACTTTATTATAAGGATGTAGGGGATGGTAAGAGAACAGGGGGATGAAGGGAAAGAGAAGTAAGAGGATGAACAGTGAACATTTAGATAGGTAGGTTGATCAGGTGTCCTACAATGATGCCCAGAGTCTTAGAGTGGGGGTACCATCTTTGTAATATTTTGGTTGAGGGATTGGATCCCCCGATTCAACCTAGGAGTGAAGAGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40502
Status:
Mutation detected in F1 DNA
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
ENSDART00000057613 Nonsense 390 407 10 10
Genomic Location (Zv9):
Chromosome 5 (position 38702356)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 36502040
GRCz11 5 37102193
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACAGCTGCATAAAGCCGTGCAGCAAGAAGGATGTCATCTACACGCTGTA[C/A]AAGCAGAAGGTCAACGAGAACATGCCTTCAATCTTCAGCCCCATTTTCAA
Long Flanking Sequence:
TTCAAAAGAATGAGAAGAATAGTGCTAGAGGGCTGGTCTGCCTTAATTAAGTTTTAGGGAGTAGGTGATTGGTTAAGGAGACAAAGTGAGGCGGGGTTCCTCTGCCGAACTTTTGTTAACAAGTTAACTCCATTAAAAATTGTACCATGACAAGCTTTTCAGCTTTTGGGAATATTTTTTTTATGAATAATGTAAATGTGTCTGCTAAAATGTTTGATGTTAAATAGTTCTTTGCGGTTTGATCATTTAATCATGTATTTTTCCTCAAAGTCAAACCAACATTGAATTATCGTTTGCTGGACCTGGTGATGATTGGCACTGCTGGAGTCATCATCTTCTGTCTTTCCTTATGGATATTAACGAGGATGTGAGTTTTCAGCCAATAGAAAAAAATTTATGCATACACCATTATCTTTGCCGTTTGTTGACACTCAATCTCATTTTTGTTCTGACAGCTGCATAAAGCCGTGCAGCAAGAAGGATGTCATCTACACGCTGTA[C/A]AAGCAGAAGGTCAACGAGAACATGCCTTCAATCTTCAGCCCCATTTTCAAGTGATGATGCTTCCTATGACCTGCTTTTGCTGCATTACCATTCATACCTAATACTACATCACTAAATGCACACTACTCAGAGAAATAAACACGAGAATTGAGACTCGTCAGAGCCCTCGCACAGTTTACCTGGTAGTGGATTCAAAGTGAGCGCTGAGAGGCTTGTGGAGCAGATTTGTGGAAAACCAAAAGAACCAAAGCACTGACCTGAATGTAGAATCCACTTTGTTGTTTACCAAGCCACTCTACTATTAGCTAATGTGTTTACACAAATGTTATGTGCCTGTTAAAGTTACTCATATATAAATATGAATTATATTATAATATATTTTATTTCAAATGCCAGTGGTCTTGCCAGTTTTGCCCAGTTTTCAATAGCATCTATTCAGTCTTGAATATTTGTTCTTAATGTCAATGATCTTGCCAGACATGGCGTACTGTACAGTTTCA
Associated Phenotype:
Not determined