Busch Lab

ZMP

IL17RA (4 of 4)

Ensembl ID:
ENSDARG00000089153
Description:
interleukin 17 receptor A [Source:HGNC Symbol;Acc:5985]
Human Orthologue:
IL17RA
Human Description:
interleukin 17 receptor A [Source:HGNC Symbol;Acc:5985]
Mouse Orthologue:
Il17ra
Mouse Description:
interleukin 17 receptor A Gene [Source:MGI Symbol;Acc:MGI:107399]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa24666 Nonsense Available for shipment Available now
sa13496 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa24666
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127168 Nonsense 164 420 4 4
Genomic Location (Zv9):
Chromosome 25 (position 20544882)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 19955671
GRCz11 25 20053325
KASP Assay ID:
2261-9658.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGGCTCAGCACAATCGGCAGAATTCAATGGCTGGATATGCAAAGGGAA[C/T]GAATCGCCAAGTCCTCTGATAAAGTCCTGATTCTGTGCTCTCCGGGAGTG
Long Flanking Sequence:
TGGAAACGGGTCATTAGAAAAGGGTTCCAAAAAGTAGCAAGGTTGCAATTAGCTATTCTTTGGTACTTCAGTAGAATTGGAAATAATATGTACTGTATGTACAGTACCGAACCATATTGCTCAGTAAAAATGAGCCACTTTGTGTTCCAAAGATTTCTTAGCATTTCTAATTTTTCGACTGTTTGTCTGATCTTTCATTCACTCTCCATTAATTTAATCCATTCTGCTTCTGTATCTCAACCTTTATATTTTTAATAGAAACCCCATCCTCAGACACCTCCACCTGTGCAAAGAGTAAACTGGAGATGAATCCTGTTCAGCAGGAACATAAGAAGCTCATCATCATCTACTCTCTAGATCATCCCCTGTACAAAGAGATCGTCTTGAAGTTATGTGCCTTCCTCAGGGCTAAATGTGGCACAGACGTCACACTGGATCTTCTGGACTCCACCTGGCTCAGCACAATCGGCAGAATTCAATGGCTGGATATGCAAAGGGAA[C/T]GAATCGCCAAGTCCTCTGATAAAGTCCTGATTCTGTGCTCTCCGGGAGTGTATGCGAAGTGGAAGTCAATGTGCGGTAAACACCAAGTAAGACTAAAAGAGGACGAACGTTCACCAATGGGAGATATGCTCACTCCAGCTTTGAGCCTCATTATACCGGATTTTATTCACGCTTCATCTTTCAACAAATACATGGTGGCTTATTTTGATGATGTTTGCAGCGAGGTTGATGTTCCAGCACCTTTTAATGTTCTGGTGAAGTACAAGCTCATGAACCACTTTGAGGAACTTTACTTCCGGATCCTAGACATGGAAAAACACGAGCCAGGACGGATTAAATGCATTGAAGGCATTAGGGAGAATGATTACTTCTGCTGTCCGTCAGGACGAGCCCTTCGGGATGCAATTGAGGTGTTTCGAAATTACCAGGTGAAGAATCCAAACTGGTTTGAAATGGAGCTTCTGGACTCTGATGATGAAGATGAAAGCATCATGGAGTCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13496
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127168 Nonsense 292 420 4 4
Genomic Location (Zv9):
Chromosome 25 (position 20544498)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 19955287
GRCz11 25 20052941
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTAAATSCATTGAAGGCATTWGGGAGAAYGATTACTTCTGCTGTCCGTCA[G/T]GACGAGCCCTTCGGGATGCAATTGAGGWGTTTCGAAAYTACCAGGTGAAG
Long Flanking Sequence:
TGAAGTTATGTGCCTTCCTCAGGGCTAAATGTGGCACAGACGTCACACTGGATCTTCTGGACTCCACCTGGCTCAGCACAATCGGCAGAATTCAATGGCTGGATATGCAAAGGGAACGAATCGCCAAGTCCTCTGATAAAGTCCTGATTCTGTGCTCTCCGGGAGTGTATGCGAAGTGGAAGTCAATGTGCGGTAAACACCAAGTAAGACTAAAAGAGGACGAACGTTCACCAATGGGAGATATGCTCACTCCAGCTTTGAGCCTCATTATACCGGATTTTATTCACGCTTCATCTTTCAACAAATACATGGTGGCTTATTTTGATGATGTTTGCAGCGAGGTTGATGTTCCAGCACCTTTTAATGTTCTGGTGAAGTACAAGCTCATGAACCACTTTGAGGAACTTTACTTCCGGATCCTAGACATGGAAAAACACGAGCCAGGACGGATTAAATGCATTGAAGGCATTAGGGAGAATGATTACTTCTGCTGTCCGTCA[G/T]GACGAGCCCTTCGGGATGCAATTGAGGTGTTTCGAAATTACCAGGTGAAGAATCCAAACTGGTTTGAAATGGAGCTTCTGGACTCTGATGATGAAGATGAAAGCATCATGGAGTCGATGTTTCCAAAGGATGTTAAATGTAATCCTTATCAGCTAGTTGAAAATTATAAACCTCATGCGTTTGTCAACGTGATTCAGATTGATGAAGACGTTTTTAAAAATGCTTCCATTGCAGAGACAGCCATAATATTGAGTGAGCATTCTTCAGTTTCCACTACAGGTGTTCATTCTAGGGGTCCAGGATTGAGTAGCTTGACAACTATTGATGTGAAAGGTTTGGCAGCAACTAAACCTGTGGCACAGCATGCTTTATGCTTACAGGCTCTGTGAATGCCTCTAAATTTGTAGCTGTAAATAATCAGTCATGTTCAGGCTTAAAGCATTACAAGTTTTCTAATCAGGTTACATTTTCACATAATACTAAAGTAATCCATTAATTTT
Associated Phenotype:
Not determined