ZMP

il23r

Ensembl ID:

ENSDARG00000052158

ZFIN ID:

ZDB-GENE-080107-5

Description:

interleukin 23 receptor [Source:RefSeq peptide;Acc:NP_001106978]

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 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa33896	Nonsense	Mutation detected in F1 DNA	Not yet available
sa40728	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa20741	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa33896

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000073956	Nonsense	201	818	5	13

Genomic Location (Zv9):

Chromosome 6 (position 34949400)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	34892128
GRCz11	6	34875511

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AATTTGCCCGCAACATGAACTGACTATTTTATTCCATCTTCCAGAGCTAT[A/T]GACCAGAATATTACAATGGAGAATTATTATATTACAAGTTGTCCTATAAA

Long Flanking Sequence:

TCCATATAGCAAACAGTATGTGTGTAACGTTTGTTTTTTTAAATAAAAAAGTCTTAAAATGTAAACAACTTATTAAAAAACATCCCGTAAAGTAAATAAGTTGTTATGTATGAAGAATATGTCATTAACTCAAGGTGCCAAACTATATTGTGACCAAAGTCCTTTGGAGTTGGAGCTCACTGTTTTGTTTCTCAAGATAATTTCCACTGTGTATTTCCTACAATATCATTCCTGTAAATATAGTTTGAGGTTTTGTGATTATTCATGGTCTGCTGTAAGTAGAATTTATTTTGGATGCATGAACTGTGTTGAGAATAGTGCCACATTAACTCAGTTTTTAAAAACATTTCACAGATTTGTATTATTTGCTTTTGATTTACAGAAGTTACTCCCATTATTTAAGCAAAGCATAATGTCATGAAATAAGAAAAGGTGGATAATGAAAAAAGGAATTTGCCCGCAACATGAACTGACTATTTTATTCCATCTTCCAGAGCTAT[A/T]GACCAGAATATTACAATGGAGAATTATTATATTACAAGTTGTCCTATAAACAAGAAGGCAAGATCCAGGAGGTGATTTGCTCACCTGAGCTCACTCAGCAGACTCTTCAGCTGAACGTGGCAGACGTCAACATCAGTGTTGTGATGTCATATGGCTCCTCCCCTCCTGCACAAGTCAACTTCAAACGCACAGGTCAGACCTTTTGTGGCTGCTGTTTCCAAATCTTCATCATTGTGATTATTTTGCGCCTCATGATGCTTTGTCTGATTCATGGGTGTAGATGTTGTTGAAAAATTGGGATTAAGGATGTGGCATTATTCTCCTCACTGTTCATTTACCGAATACTGCAACTTATTAGAATCAACAATTTACTTTCACCAGATCATGAATAATGCCAAAAACTCAAAAAGATCTTTCTACAGACATATATTGAATATTACTTTTAATAATACAAAACACAAAAACTCAGTGAACTCAAAAAAGCTTTACCTACATTAAGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa40728

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:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000073956	Essential Splice Site	329	818	7	13

Genomic Location (Zv9):

Chromosome 6 (position 34947121)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	34894407
GRCz11	6	34877790

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATATGTGAGGGTAAAACTAATGTCCTTGAACTGTTCTGAAACTCTTTTGC[A/T]GGTATGCAAGCTGGTGTCTTGTATAATTTTTCTTTGTATGCTGAAGAAGC

Long Flanking Sequence:

AATAATAACTATAATTACTAATATAAATAATTATCATTATAATTACTGTTTTTACATTATTGTGAGCAGGGGAAGACTGTGAGGGTTGGGATTAGGGATGGGGTTGATGTTAAAAAAACACAATTTAATGGGTAATTTAATAAATAATATAAATTATTATTTAGATAACAATAGATAACAGCTGTATCTCAATGTGTATTTCTGTATGTGTTACAGGTAAAGCAGCTCCAGTGATTACAAATGTAATTCCGGCAGCATCTGGCATCTTAACTCTGTCCTGGAACGTGTCTCATTACACTGAGGAAGAGCAGAAGGGCATTCTGGGTTTTGTTGTACAGTGGCAATTTAACCCACAGCACCTAGAATGGAAGCGATTTGGAAAAGACTGCACTTTTACATCCCTACAAGGTACGAAACAGCTTTATAAACACATGACTGGTGGTCTTAATAATATGTGAGGGTAAAACTAATGTCCTTGAACTGTTCTGAAACTCTTTTGC[A/T]GGTATGCAAGCTGGTGTCTTGTATAATTTTTCTTTGTATGCTGAAGAAGCCAATGGCATTTCACACCCTGCCTTGGTCCAGGTTTATGCAAAACAAGAGCGTAAGTACATCTTTACTTGTACTGTAGGTGTAGTTTCTCTCTCCTGCTTTTGACTTTGAACTATTTCATTTTAATATTTATTTCTGGTTGTTTTATTGAATTATGACTTATTTTATGTATTAGATTTTTAAATTCTTTTTCTTCCTCTTCTTTTTATTATTATTTTTATTATTATTATTATTATTCTCATCATTATTATGTCCTGTAAAACTTTTGACATTAAAATGTAATATTGTTAATAACTTAAAGCTCATTACTTTGAATATACCTAATCTATGTCAGTAACTGATAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAATGTGTGTGCATG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa20741

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000073956	Essential Splice Site	412	818	8	13

Genomic Location (Zv9):

Chromosome 6 (position 34945255)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	34896273
GRCz11	6	34879656

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAACTACACCATTTACTTCCAGAGGCACAGAGACAAGCCACTTGAAACCC[G/A]TGAGTAAAAACTTGTTTATGAGTGTGACGGCTGTGGTTTGTGTCTATATG

Long Flanking Sequence:

TTCAAATGTTAATGAATTTCTTTCTTCACTTGAACACCCAAAAAGAAAAAACAATCCGTAATTATCAATGTTTATAGTAGAAAGAAAATACTGTGGAAGTCATTGGTTGCAGGTTTTTAGCATTTAAAAAAAAACTTCTTTTGTGTTCAACAGAAGAAACTCAAGCAGGTTTGAAACAAGTAAAGGGGATTAAATGACTGACAGAATGCTCAGTTTTAATGTTCAGTTTCTATCCCTTCAAATGCAGAAGCATATAATATAGTTAAGAAGCTTTATATCTTAACTGTTCAACAAATTTCTGCTCAGTGATTGAAGGCTAACTTAATCCTCCTCTGTTTCTTTCTCAGAGCCTCTAGCTGGTCCAGATGTATCAGTAACCAATGTAGGAGAAGGGCAGATTTTAATTCAATGGGATGAACTGAGCCAAGAAAAGCAAAGGGGATTTATCACAAACTACACCATTTACTTCCAGAGGCACAGAGACAAGCCACTTGAAACCC[G/A]TGAGTAAAAACTTGTTTATGAGTGTGACGGCTGTGGTTTGTGTCTATATGTGCTCAAGAGGAGGAGTCATATGGTTTGTGCAGACAGAATCAGAATTTTTTTTTGTTCATTAACACCTTCTCAAAGTAAAAAACAAAAACAAAGAAAAAAATGGCCACAACCCAGGTGTCTTTAACCTCATCCCACAAGTGATGCAGTGCACCTTCATGCATTTAACACAGTGGAAAGACACTACCTGTGTCTGGTTGGAGACTCATCACAGTCACACCCACAGTTCTGCTGCAGGGTTTTCCACCATTTACTGAAAGAGATCACATCCTCTTCCAGTAACTCTACTCCCCTTCACGTCTACATTAATGGTCTAAAACTAATGTATTCTTACTGCAAAGCGTCTCCTTTGAATTGGGTGTTTTGGAAATGAGTTGGTAATCACTTTTAAAAGAGTGAGTTTTATGTGTTTTGGGTTGGTAGTGGATCATTTCAGTTGTCTAAACAATACC

Associated Phenotype:

Not determined