Busch Lab

ZMP

il12rb2l

Ensembl ID:
ENSDARG00000074850
ZFIN IDs:
ZDB-GENE-080107-6, ZDB-GENE-091204-58
Description:
Interleukin 12 receptor beta 2.b [Source:UniProtKB/TrEMBL;Acc:A8WHA9]
Human Orthologue:
IL12RB2
Human Description:
interleukin 12 receptor, beta 2 [Source:HGNC Symbol;Acc:5972]
Mouse Orthologue:
Il12rb2
Mouse Description:
interleukin 12 receptor, beta 2 Gene [Source:MGI Symbol;Acc:MGI:1270861]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa33137 Nonsense Mutation detected in F1 DNA Not yet available
sa30603 Essential Splice Site, Missense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa33137
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
ENSDART00000110287 Nonsense 308 761 7 15
ENSDART00000134433 Nonsense 308 674 7 14
Genomic Location (Zv9):
Chromosome 3 (position 19050034)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 19078396
GRCz11 3 19228136
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACTGACAAAGACTTTTTCTTTTCTCATATGTTTTCAATAGCTCCAGTT[G/T]GACAGCTGGATGTTTGGAGTGACTGCGCACCTAATTCTGACAAATCATCT
Long Flanking Sequence:
TCCCTAATCCTACACTAAAAATAGATTCGTTGGATTTACAAAATATTTTTAAGGTAAGTGGTTGCAAACAATTTATATGGGCTGATTTTAAACAAACTTGACCAAAGTTGACCATTACTAAATTAAATTTGTTACCTAAACCCAACTTCTGCCTTACTAACTATTAATAAAGAGCTAATTAGTAGTTTCTTGAACAAGTAATGTTAGTTAATGGTTTGTTAAAACCTTGAATTGTGACCTAAACACCGCTATGGCGACCCCTGATAAATAATAAAATAATAGTGAGTTAATTATTTACACAATGAAGACTATGCAATGCTATTTTGCATTTGATGATTCTATCTCTGCACCTGAAATCTTACCCAATAGAGCTTTTTAACCCATCTGGTGAAATTTTACTAAATGCAATGTCAGATTTTTCTAATATCGTGCAGCCCTAATTCCAACTAAAAACTGACAAAGACTTTTTCTTTTCTCATATGTTTTCAATAGCTCCAGTT[G/T]GACAGCTGGATGTTTGGAGTGACTGCGCACCTAATTCTGACAAATCATCTTGTAACGTTTATTGGAAGGTAGATTATGCTCCTATAACTTAGTTACTTAACTTTGCTACCGTTCAAAAGGTTCAGTACATTATGAATGTGCTTTTGAAATGTTTCTGTCTATTCTTTCCTGTCTCAGGAAATGCCCCTGTCTCAGGCTCGAGGGGAAGTTACGAGTTATATTGTAACGCTGACGCTTAAAAATGGCACTGAGATTAAGCAGGTTGCGAGGCAGAAGAGAGACGCTGGAAACCAGCATCGCACTGAACACAGCTGCCCACAGCTCAGACACTTCCCTTTAAAACCCAGCGTTGTGGGGGTTTTTGTGTCTGCCAGCACCTCAATGGGCACATCCGACCCCACACTCATGCCATTTCCTGAGAGGGGTATGTAAAAAAAAAAAGTAGGGTTATATGGTTTACTGCTACTATGGTAGTGCTGCAATACTATGGCTACTAAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30603
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:
Essential Splice Site, Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110287 Essential Splice Site 628 761 14 15
ENSDART00000134433 Missense 641 674 14 14
Genomic Location (Zv9):
Chromosome 3 (position 19060189)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 19088551
GRCz11 3 19238291
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATTAAATTAGACACATCATGGTAAATTTATTTCTGCTGTTTACCCGCA[G/T]GTTATCTTACTGTCACTGTTTTGAGAAGATTCCAGATCCAATAAACAGCA
Long Flanking Sequence:
TCCCAGGAAAAATATTCTAATCACTTTTCAAATTATATATTAAAATCATAAATCATATATGATTTCCTTCACATTTTTCTGCTGTTCAGCATTTCACTTCACTGGCATTGTAAACCCAAATTTATCATCTTTATCATGCGTTTACCAAACTAAAAAACAAAATCAAAAATCTAAAATCTTTCCTCTGGGTGCTCCGGTTTCCCCCACAGTCCAAAGACATGTGGTACAGGTGAATTGGGTAAGCTAAATTGGTCGTAGTGTCATGAGTGTGAATGCAAGAGTGTATGGGTATTTCCCAGTAATGGGTTACAGCTGGAAGGGTAAAAACATATGCTGGATAAGTTGGTGGTTCATTCCGCTGTGGCGCCCCCAGATTAATAAAGGAACTGAGCTAAATGAAAATGAATGAATAAATGAATAAAAAGAGCTGCAAGCAATCCATGATTTTACCTATTAAATTAGACACATCATGGTAAATTTATTTCTGCTGTTTACCCGCA[G/T]GTTATCTTACTGTCACTGTTTTGAGAAGATTCCAGATCCAATAAACAGCAAATCATTTAAACACATGAACTTACAGGTGAGAATCTACTTTTTTGTGTTATAAATGAAAGAGATTAGCTGTGATTCCATCCAAAGATGCAAATTAGACTTTGCAAAACTGGAATGTCACATAAAACATTCGTGAATACAGCACCGTTTCCTTTCAAAAACAAAGTCAAAAACAACAAAATCGTCACTTCCTGATAAAATGGTGGCAAATATTAAACAAAAAAAGGAATTTGCTGCTGCAGGAGAAGATACTGGACCTTTTCTCTTCAGTCACATGACTTTTCTTTTAATGGGCTAGCTGGGAATTCTTTTTTTCATGGTTGTTTAGTCACATTTTCTTTCTTATTGGGTATAAAATTATCTTATTTAATTGTGCGCAAAAGTTTTTTTTTTTTTTTTGCACATATTTAATATTTATGTATATATGCATATTGGCATTTCCATTAGGCTTT
Associated Phenotype:
Not determined