ZMP
crfb9
Ensembl ID:
ZFIN ID:
Description:
interleukin-22 receptor subunit alpha-2 [Source:RefSeq peptide;Acc:NP_001038744]
Human Orthologues:
IL22RA1, IL22RA2
Human Descriptions:
interleukin 22 receptor, alpha 1 [Source:HGNC Symbol;Acc:13700]
interleukin 22 receptor, alpha 2 [Source:HGNC Symbol;Acc:14901]
interleukin 22 receptor, alpha 2 [Source:HGNC Symbol;Acc:14901]
Mouse Orthologues:
Il22ra1, Il22ra2
Mouse Descriptions:
interleukin 22 receptor, alpha 1 Gene [Source:MGI Symbol;Acc:MGI:2663588]
interleukin 22 receptor, alpha 2 Gene [Source:MGI Symbol;Acc:MGI:2665114]
interleukin 22 receptor, alpha 2 Gene [Source:MGI Symbol;Acc:MGI:2665114]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13952 | Essential Splice Site | Available for shipment | Available now |
sa18241 | Nonsense | Available for shipment | Available now |
sa18524 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13952
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057619 | Essential Splice Site | 28 | 238 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 23847696)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23493356 |
GRCz11 | 13 | 23623806 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AYAAACCATCYRCTGYATTTCAATRAAAARCTGCATTTCTWCTCTCTTCC[A/T]GGTAGCMCCACTCAGCAGGAAGAARTGGCTCCAACCGAAGTACAGTTTCA
Long Flanking Sequence:
AAGTGGCATGGTTTAAAGGTGTCAGAGCCGAACCACAATAATGCCTTTTAACATGCTCACCTTGACCGGTCATCAATGCCTGGACATCGTTTTTGCGATTTCCCTTCTGTGTTGGGCAGAATGTAAGTTTACCAGCTTGTCACTTGCACTGAATTTTGATTTTGAAAGATGGTAATAGATGCAAAACTTTTAAATTTGAATCGATGCAATACAATACAATTTTATACAATTTAAAACAAATTTTACGCTTATTTAGCTTCAAATCAAGCTTTTTTGCTTATAGCCTGCATGCTTTTAAAATGTTTACAAACCATAATGCTTTTTAAAGTATAATTTATATTAGAAAATGCTCTTTAAATATTGTTCACTGAGGAGAAATGCTCTGAAAGATTCTTTGGAAAAACTTCAATGGCACTGCTGCAAAAACCCTTATTTAGAAGAGCTTAAACAACAAACCATCTGCTGTATTTCAATGAAAAGCTGCATTTCTTCTCTCTTCC[A/T]GGTAGCCCCACTCAGCAGGAAGAAATGGCTCCAACCGAAGTACAGTTTCAATCTTTGGACTTCCGAAATGTCTTACATTGGAAACATCAGCACAAAGCTTCCAAAAACTTGAAATATTTTGTTCAGCATAAAATGTAAGCCTGCGTCTCTCAACCCTACGCGATGAGAAATGACTTGATGAATTCTCAAAATGTTCATGCATATCCCTCACCTTCATTTTAGACATGGAGACAAAGAGTGGAGCAATTCCAAACATTGTCAGGGCATCCGGACGCTACAGTGTGACCTGACGCAGGAGACATCGGACCCCAGAGAATGGTACTACGCCAGGGTCCGCTCGCTCTCCCCTGAGGGCTTCTCTTCATGGGCCATCAGCCACAGGTTCTACCCTCAGTGGGAAAGTGAGTTCCTTTAGAAACGCTTATAATTGTGTAACACTTGTTAGTTCATTTGCACAATGTAAATAAGTATAAAGCATAACAAATATTAGTCTTCACAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18241
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 |
---|---|---|---|---|---|
ENSDART00000057619 | Nonsense | 64 | 238 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 23847806)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23493466 |
GRCz11 | 13 | 23623916 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTCCGAAWTGTCTTACATTGGAAACATCAGYACAAAGCTTCCAAAAACT[T/A]GAAATATTTTSTTCAGCATAAAATGTAAGCCTGCGTCTCTCAASCCTACG
Long Flanking Sequence:
GTTGGGCAGAATGTAAGTTTACCAGCTTGTCACTTGCACTGAATTTTGATTTTGAAAGATGGTAATAGATGCAAAACTTTTAAATTTGAATCGATGCAATACAATACAATTTTATACAATTTAAAACAAATTTTACGCTTATTTAGCTTCAAATCAAGCTTTTTTGCTTATAGCCTGCATGCTTTTAAAATGTTTACAAACCATAATGCTTTTTAAAGTATAATTTATATTAGAAAATGCTCTTTAAATATTGTTCACTGAGGAGAAATGCTCTGAAAGATTCTTTGGAAAAACTTCAATGGCACTGCTGCAAAAACCCTTATTTAGAAGAGCTTAAACAACAAACCATCTGCTGTATTTCAATGAAAAGCTGCATTTCTTCTCTCTTCCAGGTAGCCCCACTCAGCAGGAAGAAATGGCTCCAACCGAAGTACAGTTTCAATCTTTGGACTTCCGAAATGTCTTACATTGGAAACATCAGCACAAAGCTTCCAAAAACT[T/A]GAAATATTTTGTTCAGCATAAAATGTAAGCCTGCGTCTCTCAACCCTACGCGATGAGAAATGACTTGATGAATTCTCAAAATGTTCATGCATATCCCTCACCTTCATTTTAGACATGGAGACAAAGAGTGGAGCAATTCCAAACATTGTCAGGGCATCCGGACGCTACAGTGTGACCTGACGCAGGAGACATCGGACCCCAGAGAATGGTACTACGCCAGGGTCCGCTCGCTCTCCCCTGAGGGCTTCTCTTCATGGGCCATCAGCCACAGGTTCTACCCTCAGTGGGAAAGTGAGTTCCTTTAGAAACGCTTATAATTGTGTAACACTTGTTAGTTCATTTGCACAATGTAAATAAGTATAAAGCATAACAAATATTAGTCTTCACAATTACAATATGAAAATTTACTTTCAAAAGTGACATTGCTGAATGCCTGTTAACATTAAAAATGTGCAGGTTTTATTAATTAATATTCGATTACTAAATGTAGACACACTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18524
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 |
---|---|---|---|---|---|
ENSDART00000057619 | Essential Splice Site | 72 | 238 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 23847917)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23493577 |
GRCz11 | 13 | 23624027 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGACTTGATGAAWTCTCAAAATGTTCATGCATWTCCCTCAYCTTCATTTT[A/G]GACATGGAGACAAAGAGTGGAGCAATTCCAAACAYTGTCAGGGCATCCGG
Long Flanking Sequence:
TTATACAATTTAAAACAAATTTTACGCTTATTTAGCTTCAAATCAAGCTTTTTTGCTTATAGCCTGCATGCTTTTAAAATGTTTACAAACCATAATGCTTTTTAAAGTATAATTTATATTAGAAAATGCTCTTTAAATATTGTTCACTGAGGAGAAATGCTCTGAAAGATTCTTTGGAAAAACTTCAATGGCACTGCTGCAAAAACCCTTATTTAGAAGAGCTTAAACAACAAACCATCTGCTGTATTTCAATGAAAAGCTGCATTTCTTCTCTCTTCCAGGTAGCCCCACTCAGCAGGAAGAAATGGCTCCAACCGAAGTACAGTTTCAATCTTTGGACTTCCGAAATGTCTTACATTGGAAACATCAGCACAAAGCTTCCAAAAACTTGAAATATTTTGTTCAGCATAAAATGTAAGCCTGCGTCTCTCAACCCTACGCGATGAGAAATGACTTGATGAATTCTCAAAATGTTCATGCATATCCCTCACCTTCATTTT[A/G]GACATGGAGACAAAGAGTGGAGCAATTCCAAACATTGTCAGGGCATCCGGACGCTACAGTGTGACCTGACGCAGGAGACATCGGACCCCAGAGAATGGTACTACGCCAGGGTCCGCTCGCTCTCCCCTGAGGGCTTCTCTTCATGGGCCATCAGCCACAGGTTCTACCCTCAGTGGGAAAGTGAGTTCCTTTAGAAACGCTTATAATTGTGTAACACTTGTTAGTTCATTTGCACAATGTAAATAAGTATAAAGCATAACAAATATTAGTCTTCACAATTACAATATGAAAATTTACTTTCAAAAGTGACATTGCTGAATGCCTGTTAACATTAAAAATGTGCAGGTTTTATTAATTAATATTCGATTACTAAATGTAGACACACTGCTGTTAGTTAATGCATCAACAAGCAGTGAGAGGTGTGCAATATTTATAGTATATAATACTGTATTTGTTGATTAAATAATTTCTTACATTCAACAAAAACAGATCGTTTGAGT
Associated Phenotype:
Not determined