Busch Lab

ZMP

crfb4

Ensembl ID:
ENSDARG00000068711
ZFIN ID:
ZDB-GENE-070905-3
Description:
interleukin-10 receptor subunit beta [Source:RefSeq peptide;Acc:NP_001077337]
Human Orthologues:
AP000295.9, IFNGR2, IL10RB
Human Descriptions:
interferon gamma receptor 2 (interferon gamma transducer 1) [Source:HGNC Symbol;Acc:5440]
interleukin 10 receptor, beta [Source:HGNC Symbol;Acc:5965]
Mouse Orthologues:
Ifngr2, Il10rb
Mouse Descriptions:
interferon gamma receptor 2 Gene [Source:MGI Symbol;Acc:MGI:107654]
interleukin 10 receptor, beta Gene [Source:MGI Symbol;Acc:MGI:109380]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa38728 Nonsense Mutation detected in F1 DNA Not yet available
sa21454 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa38728
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
ENSDART00000099479 Nonsense 133 313 4 7
ENSDART00000127448 Nonsense 133 313 4 7
Genomic Location (Zv9):
Chromosome 9 (position 16631803)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 16018366
GRCz11 9 15955632
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACAGCTGAGATTAGTGCTCCTCATGTAGAACTGAGAAGTAACAATGGA[C/T]AAACAGAAGTTGATATCACTGATCCACCGATGAAAAGAAAAAACCTGAGA
Long Flanking Sequence:
CAAAATGTTGTACAGTGCCATATATATTTTTTTTTCAATTTATGGCATAAGAAGCTACTATGCATCGGTTTACAAGACATATTATGCATTCCCTGAATTTTCAAGAGAGACTGTGTTAACATTTTTTCAATTAAAAAAAATCACCAAAATCTGTTATTTATCATGGGGTGGCTAATCTTTTGCATAGGACTGTACCATTATGCAGGAAAATGACTTTTCTGAACCATAAGAAGGCAAAACTCAGGAAGATCATAAGACAATTCGAGTCACTCATATTTCTATATGAAGAACATTTTTTAAAAAGGCTGCAAAAAAATCAAATGTATATATAAAAAACTTTATGACTTCATTATATATGAAATACTGCGTTTTTTATACTTAAACATTTCATTTATTTTTTACTTGAAATGAATATTTTTTAGTACTATGTTTTAAAACATTGCTGTGTGTCTACAGCTGAGATTAGTGCTCCTCATGTAGAACTGAGAAGTAACAATGGA[C/T]AAACAGAAGTTGATATCACTGATCCACCGATGAAAAGAAAAAACCTGAGAGACGTCTTTGGGAATATTTCTTACCTCATACGTTTTTGGAAAAAAGGAGAATCAAATAAGGTAAAGAACGTTTCCTCAAAAGTATTTTAAATTTTTTATTTTGCAGTTGGAAAAAAAATGTGGCTCACTCCACTTAGTATATTACACTTTGTGTTTACTTTAAAACTATGGAGTTTTACATCACTACAACAATATAAACACCTGTTCATAATGCTGATGTGTCCTCATTACAGTTACACTTGACATTAATTTAACAATTTACAATGTGCATAAACATTTCACAGGACAATAATGGATGCTATGAGTGAAAAAAGAACACTTTAAAGTAAATTGTTTAGAAAAACTGACTGCTCTTGACTACTTCAATATAATAGGGCTGTATATTGGCAAGGGCCTCACGATATGATACATATCACGATACATGGGTCATGGTATCACAGTATATTGCGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21454
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
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000099479 Essential Splice Site 269 313 6 7
ENSDART00000127448 Essential Splice Site 269 313 6 7
Genomic Location (Zv9):
Chromosome 9 (position 16650288)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 15999881
GRCz11 9 15937147
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATACAGAATTGTATTCCCTAATGATAATCTGCCAGAGCATCTAAAACAGG[T/A]AGCAAAATTATAAAAGGCAACTGACTTACTGTTAATCTGTTACTGACTTT
Long Flanking Sequence:
CTATATCTGTTTAACCAAGTTGTGTAATTTAATCTTTTTGTAATTCATTTTTAACAGGTCAAACTAAAAAGAGAACAGAGCAGAGTCATGTTACCAAAAGTGAAGCCTCTGGAAAACTACTGTGTCGAAGTAGAGGTTTTGTATTTGAAGAATAAAACAAGCCAGCCCAGCAACATGACCTGTTTAAAAAATTCGCCCAGCAGTAAGTATTCCACTATATAAAGTCTGTATTCTCTTTTTTTTTCCAAATTAATTTACTGAATGTTTATTATGATGATGCTTTAATCCTTTTTCTTTTGTTTTTAATATTTAACATAAAATACTGATTTGTATGTTTTTTTTAGATGAGACAGAACCCTGGCTTATAGCTGTGATGCTTTTGATCAGTTTTCTAGTGGTGTTAGTTGCGGTTCTCCTGATCTTTATGGCTGTGTGGTACAGTTACAAAGGATACAGAATTGTATTCCCTAATGATAATCTGCCAGAGCATCTAAAACAGG[T/A]AGCAAAATTATAAAAGGCAACTGACTTACTGTTAATCTGTTACTGACTTTTTTCTCTTGCTGTCTTCTCTTAAAGTATTTGGCACAACGGTCCCAGTCACCTGCACCTTTACCCATACATGAGGGAACTCACCTGAAGGAGCCCATTCATGAGTTAATGATATATGAAAAGAAACTTAACAGCTCTCAGGACAATCAGCAAATAATATAACAATTATCGTTTCAGACAAATAGGAGGATTGTATTTGAGGTAATGTAAATAAATGTAATGATAAATGTAATAAAGAGAAACTTTTTTTTTTTTTTTACACAACAGAAGTTTTGCTTACCATAATCATATTACAGTTTTTAAAATTGCTAGCATACATTTGCCCAATCTGTAGCCACATTTTCAAAACACTAAGTGAAGTTTAATAAACTAATTTCAAGAGGAGCACGTGATATGCACCGCTGGCCACTCATCCGTAATCAGTAAAAATCCAATCAGAATGATCCTAGCTT
Associated Phenotype:
Not determined