ZMP
il11ra
Ensembl ID:
ZFIN ID:
Description:
interleukin 11 receptor, alpha [Source:RefSeq peptide;Acc:NP_001106971]
Human Orthologue:
IL11RA
Human Description:
interleukin 11 receptor, alpha [Source:HGNC Symbol;Acc:5967]
Mouse Orthologues:
Gm13305, Gm2002, Il11ra1, Il11ra2
Mouse Descriptions:
interleukin 11 receptor, alpha chain 1 Gene [Source:MGI Symbol;Acc:MGI:107426]
interleukin 11 receptor, alpha chain 2 Gene [Source:MGI Symbol;Acc:MGI:109123]
predicted gene 13305 Gene [Source:MGI Symbol;Acc:MGI:3801997]
predicted gene 2002 Gene [Source:MGI Symbol;Acc:MGI:3780172]
interleukin 11 receptor, alpha chain 2 Gene [Source:MGI Symbol;Acc:MGI:109123]
predicted gene 13305 Gene [Source:MGI Symbol;Acc:MGI:3801997]
predicted gene 2002 Gene [Source:MGI Symbol;Acc:MGI:3780172]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45398 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12313 | Nonsense | Available for shipment | Available now |
sa34862 | Nonsense | Available for shipment | Available now |
sa45397 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45398
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000030976 | Nonsense | 132 | 402 | 4 | 10 |
ENSDART00000135941 | Nonsense | 132 | 402 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 10 (position 13295875)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 13373966 |
GRCz11 | 10 | 13332085 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTGTCTTGTCGTGTGCCGAATCATATGAAAATCTCCTGCTCCTGGGAA[C/T]AAACCAAGAGGACAAACTTGCCCACATCATACAGAGCCTCATACAGGTGC
Long Flanking Sequence:
GGGTCATTTTAACCCATAGGTCAACAGGAGGGTTAAAGTACATTAAGTCTTGATAATTGCTGGATGTGTCTGAAATGGCACTTGTATTGGACAGATTTCTGGAAGGCCAGGAAATGTTTTAGTAAAAAGGAAACTCTTTGAGCTCAGGGAGCTGCAAAAGAAAGTTGTACGCCCTATTCTGTTTAACTCAAGGCACTTCCTCTAACAGGAAGTCAATACATCACAGCTCCACAGTTTCCTGATAGGAAGGGTGAGATTGCAGGGTAGAGTGAAGAATAGTAAAGTATAGTAAAGAATTAATGTACAGCCTTGATGTTCATGAGCTGAACAGTTCTCCAGTGCTGTTTAAATGATTCGACTTGTGTTCACAGATACTGAATGATATTTTGTGTGAAGTTATCTCATGAGATTTTCTTTGTCTTCTACATCTAGACCCACCTCATTTCGTCAGTGTGTCTTGTCGTGTGCCGAATCATATGAAAATCTCCTGCTCCTGGGAA[C/T]AAACCAAGAGGACAAACTTGCCCACATCATACAGAGCCTCATACAGGTGCAGCTTCATCTTGTTCTTTACTTCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCTGTCTGTCTGTCTGTCTGTCTGTCTGTCCATTCGTCTGTTCGTCTTCCATCCAATCAAAAGAAAAGTCTTAAAAGTAACCTAGGACATGTTAGCAGTCTCATAAAAGATGGTAGTGGTGAGTTAAAAATTCTAGTGATGTAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12313
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 |
---|---|---|---|---|---|
ENSDART00000030976 | Nonsense | 161 | 402 | 5 | 10 |
ENSDART00000135941 | Nonsense | 161 | 402 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 10 (position 13294272)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 13372363 |
GRCz11 | 10 | 13330482 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATACAGTCAGAAGGGCCAGGGCCGCAAGCAAATTCCCAGTGAACCCTG[T/A]GAACAGAAGGATWCCGGGGTAAATGAGTGYACAATTAMAGACCCACCTTT
Long Flanking Sequence:
AGTTTATGTAATTTCGGGTGTTTCATTTTTAATTTGTTGACTTTAACTGCATTTTGGCAAGAGTATTGTTTTAATGGAATATGATACCACCTGTCGTATGGGAAATAAAATCTCTGCATTTCATGATGCAGGTGTCTGTGATCCTTCACTGACTTCTTAGGTGCAGATAATAGTGTCAAACAGCCATGCATGGAAAATCCTGTTGCAAAATGCGAAAATCATAGACGACAGTAATAGTTTGATTATGGTGTTTACATGTCTGTTCTGTTCTTCAATTATGCGACTAAAATCGGCATACATCAGATGTCCTAATTCCATTTCTGACTTTAGTCAGATTAAATTAATGAAAAATCATTGTTGACATGGTAGACTCTTAATCAGAGTATTGTCTTAATTGTATTAAAAAATTATTATTGGTGTTCATGTAAACATACTCTCTGTTACTTGATTCCATACAGTCAGAAGGGCCAGGGCCGCAAGCAAATTCCCAGTGAACCCTG[T/A]GAACAGAAGGATACCGGGGTAAATGAGTGCACAATTACAGACCCACCTTTCTGGAGCTCCTCGAAGATCCTGGTGAACATCACTGAAATCAACCCGCTGGGATCTAACTCCACCATCATCCAAATAGATCTCCGTGAACTCTGTAAGTCAATGAACCCTCTTATTCTTTTTTAAAACCTTCTTTTTCGTAGTATCTTCCCCACCTTACAGAGTATTAGAGTATCTTAGACAGTTTAACATACTGATACACGTGCAATTTGTTCTCCAGCTGTGTAAATTCACTGACATAAACACAAGTTTGCATAATGTTGGTTTTAACTTAAACATTTATGTATTTTACATCTGCTGTGAAAGAGTGCTTAGTTCAAATCTGAGTGACAGACATTTTTCAGCGCTCGTAATTGCAATTTTTTTGCTCGCATATGGACCTAAAATTTTATCTGTGCGACCTTAAAATATATTGGGAGCATATGTGCGACTGCGTAAAATTGTTGTCGTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34862
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000030976 | Nonsense | 239 | 402 | 6 | 10 |
ENSDART00000135941 | Nonsense | 239 | 402 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 10 (position 13290529)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 13368620 |
GRCz11 | 10 | 13326739 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGGGTGAGCCTACACAGTTACTGGTCCAGTGGAACTGTCCCCCATCAT[G/A]GCTGGTTGGCATGTCTGCTTTTTCATTGACATATTTACTGCGCTACCGGC
Long Flanking Sequence:
TGAGAGAAATTTGTGTGTACACACGGAAATTAAAACTACAAAAAAAAAAGTATCTCCTGGAACGCATTTTGCGTTTATTCTGTCCAGAAATGTATACAAGGGTACGTGCCAGTAAAGAGCCTGGGTTGTGTACCCTATAAAGTAGCCAAGGCATGTTGATTGTAAAAACAATGGCAAAATACAAATTCAGATTTTTGTTGCCTGATTTGCTGAGGTTCCGCACTTTTTTGGAAAGGGGGCGGGGAGCATTAGCTAATTTGAATTAAAAAAAGACACATAAACACCAAGCTGCAATAAATGATTAAAGGTATATTTTTTGTTAATATTACACAGAGATGTATGTAGTGTCTTGTAAAATTGGCCAAAATAAAGTGCATCATAATTAAATGTTTTTAATAATGGTGTTTTAGTGAAACCAGATCCCCCAGAAGATGTTCAAGTCTCTCAGGTGGAGGGTGAGCCTACACAGTTACTGGTCCAGTGGAACTGTCCCCCATCAT[G/A]GCTGGTTGGCATGTCTGCTTTTTCATTGACATATTTACTGCGCTACCGGCCAATTGGCTCCAACTACTGGTCAAAGGTAAGAACTTTCAACCTCAGCAACTTGTTATTGGTTGTATTGTATTGTTAGTTGGACACAAACAATGACATACTCTCTATCTCTCGATTTTGACTGAGGGAGTCTGCTTCATATGTTCCAGAATGCAGTGCAACTGTGATATCACAACAGTGTAATTTCCAAGTGCCCAAGGGTTTAGAGCATTTCATTTAACCCCATTCAGATGTTCCGCAAGTAGTGGACACTCGTGTAAAGTAATTAATAACATACATCTGAGGGAATGAGACAAAGGGAAGGGCTTAAAATAAATTGGAATGAAATGTAGCCATTCTCTGTAAACAGGAGACCAATCACAAACCTCTGACCAATCAGAGCGGAGGAGACTTTTTGAAAAGTGGGGCTTAAAAAGGATCCTTTAATAAACTTTAAAATTCTGAGAGAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45397
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000030976 | Nonsense | 389 | 402 | 10 | 10 |
ENSDART00000135941 | Nonsense | 389 | 402 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 10 (position 13279483)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 13357574 |
GRCz11 | 10 | 13315693 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTATTCTCCTCACAGGGTGAGACAAAGGAAACAAGACAATGTGAAGAAA[C/T]AAGAACTGACTTCTATGCTGAAGATGAAGTCCATACCAATCTAAAGTAAG
Long Flanking Sequence:
GTTGTTTGTATTTTGTTGTTTAATATAATGTGGTTTTAACTCGTCTTATTTGGTATGATTTTAATGTTTTGTTTAATTTTGTTTCTTTTGTTGTTTAATATGTTGCGTAATGTTTTATTTAAATTTGTTTTGTTTGTTTTATAATTGTCATTATTGTTTTCATTTGATTACACTTTGTTTTGTGCTTGATATTGTATTACTTCTGTTTTATACGTGCTTTTTATTTTGTTTGTGTCTCATTCCATTTCTGTCTTAGATTCGTCTTCAAACCATAATGGAAATGTTGGACTGTTGGTTTTGTTGGGGCTGTTTGCAGCGATCATGGTGGCTGTCTTATTAACAATCATCACGCTTCTTTGGTGAAAAATTGTTTTACATTAACCTATATTTTACAATACAAACCAAATAAATGGCATTCAATAATAAGACAATGTGTGACCTGATATCGCAACTATTCTCCTCACAGGGTGAGACAAAGGAAACAAGACAATGTGAAGAAA[C/T]AAGAACTGACTTCTATGCTGAAGATGAAGTCCATACCAATCTAAAGTAAGCTGGCACAGACACTTGTTTCCATTCCCACATTCCCTTCTGCCGTTTTGGCGATTTGCCCATTTTTAGTTCAAACTGTTTAGAAAAAAAAAGCCCTGCTAAACTATCCATTTATTTTTATTTACTGTGTTGACTTTAAACTAACAGAAATCTAAGTCCGCCAAACATGCAGTCAACAAAACCAACCAGATTACCAACTAGAGGAATAACAAATCAATTTTTTCATACTCACTTAATTTAGGGAGTGACAGCTGCCTATGTGGCATTGGATCTCCTAAATGACTGTTTTGGGTGTGTGTGGAATATAGTGACATAATCAAAACCAAAGCACTGTTTTTTCATCTCACAACTACGCACAAAGCAGCAGCTTACAAACATGAGAATATTGAGTTGTTGATATTAGTAGCTTGAGATGTTTTATATTTAGAAACACTGTAAACAAGAACATCGCA
Associated Phenotype:
Not determined